NUCLEOBASE EDITORS AND USES THEREOF

Abstract

Some aspects of this disclosure provide strategies, systems, reagents, methods, and kits that are useful for the targeted editing of nucleic acids, including editing a single site within the genome of a cell or subject, e.g., within the human genome. In some embodiments, fusion proteins of Cas9 and nucleic acid editing proteins or protein domains, e.g., deaminase domains, are provided. In some embodiments, methods for targeted nucleic acid editing are provided. In some embodiments, reagents and kits for the generation of targeted nucleic acid editing proteins, e.g., fusion proteins of Cas9 and nucleic acid editing proteins or domains, are provided.

Description

BACKGROUND OF THE INVENTION

Targeted editing of nucleic acid sequences, for example, the targeted cleavage or the targeted introduction of a specific modification into genomic DNA, is a highly promising approach for the study of gene function and also has the potential to provide new therapies for human genetic diseases.¹ An ideal nucleic acid editing technology possesses three characteristics: (1) high efficiency of installing the desired modification; (2) minimal off-target activity; and (3) the ability to be programmed to edit precisely any site in a given nucleic acid, e.g., any site within the human genome.² Current genome engineering tools, including engineered zinc finger nucleases (ZFNs),³ transcription activator like effector nucleases (TALENs),⁴ and most recently, the RNA-guided DNA endonuclease Cas9,⁵ effect sequence-specific DNA cleavage in a genome. This programmable cleavage can result in mutation of the DNA at the cleavage site via non-homologous end joining (NHEJ) or replacement of the DNA surrounding the cleavage site via homology-directed repair (HDR).^6,7

One drawback to the current technologies is that both NHEJ and HDR are stochastic processes that typically result in modest gene editing efficiencies as well as unwanted gene alterations that can compete with the desired alteration.⁸ Since many genetic diseases in principle can be treated by effecting a specific nucleotide change at a specific location in the genome (for example, a C to T change in a specific codon of a gene associated with a disease),⁹ the development of a programmable way to achieve such precision gene editing would represent both a powerful new research tool, as well as a potential new approach to gene editing-based human therapeutics.

SUMMARY OF THE INVENTION

The clustered regularly interspaced short palindromic repeat (CRISPR) system is a recently discovered prokaryotic adaptive immune system¹⁰ that has been modified to enable robust and general genome engineering in a variety of organisms and cell lines.¹¹ CRISPR-Cas (CRISPR associated) systems are protein-RNA complexes that use an RNA molecule (sgRNA) as a guide to localize the complex to a target DNA sequence via base-pairing.¹² In the natural systems, a Cas protein then acts as an endonuclease to cleave the targeted DNA sequence.¹³ The target DNA sequence must be both complementary to the sgRNA, and also contain a “protospacer-adjacent motif” (PAM) at the 3′-end of the complementary region in order for the system to function.¹⁴

Among the known Cas proteins, S. pyogenes Cas9 has been mostly widely used as a tool for genome engineering.¹⁵ This Cas9 protein is a large, multi-domain protein containing two distinct nuclease domains. Point mutations can be introduced into Cas9 to abolish nuclease activity, resulting in a dead Cas9 (dCas9) that still retains its ability to bind DNA in a sgRNA-programmed manner.¹⁶ In principle, when fused to another protein or domain, dCas9 can target that protein to virtually any DNA sequence simply by co-expression with an appropriate sgRNA.

The potential of the dCas9 complex for genome engineering purposes is immense. Its unique ability to bring proteins to specific sites in a genome programmed by the sgRNA in theory can be developed into a variety of site-specific genome engineering tools beyond nucleases, including transcriptional activators, transcriptional repressors, histone-modifying proteins, integrases, and recombinases.¹¹ Some of these potential applications have recently been implemented through dCas9 fusions with transcriptional activators to afford RNA-guided transcriptional activators,^17,18 transcriptional repressors,^16,19,20 and chromatin modification enzymes.²¹ Simple co-expression of these fusions with a variety of sgRNAs results in specific expression of the target genes. These seminal studies have paved the way for the design and construction of readily programmable sequence-specific effectors for the precise manipulation of genomes.

Significantly, 80-90% of protein mutations responsible for human disease arise from the substitution, deletion, or insertion of only a single nucleotide.⁶ Most current strategies for single-base gene correction include engineered nucleases (which rely on the creation of double-strand breaks, DSBs, followed by stochastic, inefficient homology-directed repair, HDR), and DNA-RNA chimeric oligonucleotides.²² The latter strategy involves the design of a RNA/DNA sequence to base pair with a specific sequence in genomic DNA except at the nucleotide to be edited. The resulting mismatch is recognized by the cell's endogenous repair system and fixed, leading to a change in the sequence of either the chimera or the genome. Both of these strategies suffer from low gene editing efficiencies and unwanted gene alterations, as they are subject to both the stochasticity of HDR and the competition between HDR and non-homologous end-joining, NHEJ.^23-25 HDR efficiencies vary according to the location of the target gene within the genome,²⁶ the state of the cell cycle,²⁷ and the type of cell/tissue.²⁸ The development of a direct, programmable way to install a specific type of base modification at a precise location in genomic DNA with enzyme-like efficiency and no stochasticity therefore represents a powerful new approach to gene editing-based research tools and human therapeutics.

Some aspects of the disclosure are based on the recognition that certain configurations of a dCas9 domain, and a cytidine deaminase domain fused by a linker are useful for efficiently deaminating target cytidine residues. Other aspects of this disclosure relate to the recognition that a nucleobase editing fusion protein with a cytidine deaminase domain fused to the N-terminus of a nuclease inactive Cas9 (dCas9) via a linker was capable of efficiently deaminating target nucleic acids in a double stranded DNA target molecule. See for example, Examples 3 and 4 below, which demonstrate that the fusion proteins, which are also referred to herein as base editors, generate less indels and more efficiently deaminate target nucleic acids than other base editors, such as base editors without a UGI domain. In some embodiments, the fusion protein comprises a nuclease-inactive Cas9 (dCas9) domain and an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain, where the deaminase domain is fused to the N-terminus of the dCas9 domain via a linker comprising the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7). In some embodiments, the nuclease-inactive Cas9 (dCas9) domain of comprises the amino acid sequence set forth in SEQ ID NO: 263. In some embodiments, the deaminase is rat APOBEC1 (SEQ ID NO: 284). In some embodiments, the deaminase is human APOBEC1 (SEQ ID NO: 282). In some embodiments, the deaminase is pmCDA1 (SEQ ID NO: 5738). In some embodiments, the deaminase is human APOBEC3G (SEQ ID NO: 275). In some embodiments, the deaminase is a human APOBEC3G variant of any one of (SEQ ID NOs: 5739-5741).

Some aspects of the disclosure are based on the recognition that certain configurations of a dCas9 domain, and a cytidine deaminase domain fused by a linker are useful for efficiently deaminating target cytidine residues. Other aspects of this disclosure relate to the recognition that a nucleobase editing fusion protein with an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain fused to the N-terminus of a nuclease inactive Cas9 (dCas9) via a linker comprising the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7) was capable of efficiently deaminating target nucleic acids in a double stranded DNA target molecule. In some embodiments, the fusion protein comprises a nuclease-inactive Cas9 (dCas9) domain and an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain, where the deaminase domain is fused to the N-terminus of the dCas9 domain via a linker comprising the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7).

In some embodiments, the fusion protein comprises the amino acid residues 11-1629 of the amino acid sequence set forth in SEQ ID NO: 591. In some embodiments, the fusion protein comprises the amino acid sequence set forth in SEQ ID NO: 591. In some embodiments, the fusion protein comprises the amino acid sequence of any one of SEQ ID NOs: 5737, 5743, 5745, and 5746.

Some aspects of this disclosure provide strategies, systems, reagents, methods, and kits that are useful for the targeted editing of nucleic acids, including editing a single site within a subject's genome, e.g., a human's genome. In some embodiments, fusion proteins of Cas9 (e.g., dCas9, nuclease active Cas9, or Cas9 nickase) and deaminases or deaminase domains, are provided. In some embodiments, methods for targeted nucleic acid editing are provided. In some embodiments, reagents and kits for the generation of targeted nucleic acid editing proteins, e.g., fusion proteins of Cas9 and deaminases or deaminase domains, are provided.

Some aspects of this disclosure provide fusion proteins comprising a Cas9 protein as provided herein that is fused to a second protein (e.g., an enzymatic domain such as a cytidine deaminase domain), thus forming a fusion protein. In some embodiments, the second protein comprises an enzymatic domain, or a binding domain. In some embodiments, the enzymatic domain is a nuclease, a nickase, a recombinase, a deaminase, a methyltransferase, a methylase, an acetylase, an acetyltransferase, a transcriptional activator, or a transcriptional repressor domain. In some embodiments, the enzymatic domain is a nucleic acid editing domain. In some embodiments, the nucleic acid editing domain is a deaminase domain. In some embodiments, the deaminase is a cytosine deaminase or a cytidine deaminase. In some embodiments, the deaminase is an apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the deaminase is an APOBEC1 deaminase. In some embodiments, the deaminase is an APOBEC2 deaminase. In some embodiments, the deaminase is an APOBEC3 deaminase. In some embodiments, the deaminase is an APOBEC3A deaminase. In some embodiments, the deaminase is an APOBEC3B deaminase. In some embodiments, the deaminase is an APOBEC3C deaminase. In some embodiments, the deaminase is an APOBEC3D deaminase. In some embodiments, the deaminase is an APOBEC3E deaminase. In some embodiments, the deaminase is an APOBEC3F deaminase. In some embodiments, the deaminase is an APOBEC3G deaminase. In some embodiments, the deaminase is an APOBEC3H deaminase. In some embodiments, the deaminase is an APOBEC4 deaminase. In some embodiments, the deaminase is an activation-induced deaminase (AID). It should be appreciated that the deaminase may be from any suitable organism (e.g., a human or a rat). In some embodiments, the deaminase is from a human, chimpanzee, gorilla, monkey, cow, dog, rat, or mouse. In some embodiments, the deaminase is rat APOBEC1 (SEQ ID NO: 284). In some embodiments, the deaminase is human APOBEC1 (SEQ ID NO: 282). In some embodiments, the deaminase is pmCDA1.

Some aspects of this disclosure provide fusion proteins comprising: (i) a nuclease-inactive Cas9 (dCas9) domain comprising the amino acid sequence of SEQ ID NO: 263; and (ii) an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain, wherein the deaminase domain is fused to the N-terminus of the dCas9 domain via a linker comprising the amino acid sequence of SGSETPGTSESATPES (SEQ ID NO: 7). In some embodiments, the deaminase is rat APOBEC1 (SEQ ID NO: 284). In some embodiments, the deaminase is human APOBEC1 (SEQ ID NO: 282). In some embodiments, the fusion protein comprises the amino acid sequence of SEQ ID NO: 591. In some embodiments, the fusion protein comprises the amino acid sequence of SEQ ID NO: 5737. In some embodiments, the deaminase is pmCDA1 (SEQ ID NO: 5738). In some embodiments, the deaminase is human APOBEC3G (SEQ ID NO: 275). In some embodiments, the deaminase is a human APOBEC3G variant of any one of SEQ ID NOs: 5739-5741.

Some aspects of this disclosure provide fusion proteins comprising: (i) a Cas9 nickase domain and (ii) an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain, wherein the deaminase domain is fused to the N-terminus of the Cas9 nickase domain. In some embodiments, the Cas9 nickase domain comprises a D10X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for D. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a histidine at amino acid position 840 of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding amino acid position in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises the amino acid sequence as set forth in SEQ ID NO: 267. In some embodiments, the deaminase is rat APOBEC1 (SEQ ID NO: 284). In some embodiments, the deaminase is human APOBEC1 (SEQ ID NO: 282). In some embodiments, the deaminase is pmCDA1.

Some aspects of this disclosure provide fusion proteins comprising: (i) a Cas9 nickase domain and (ii) an apolipoprotein B mRNA-editing complex 1 (APOBEC1) deaminase domain, wherein the deaminase domain is fused to the N-terminus of the Cas9 nickase domain. In some embodiments, the Cas9 nickase domain comprises a D10X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for D. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a histidine at amino acid position 840 of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding amino acid position in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises the amino acid sequence as set forth in SEQ ID NO: 267. In some embodiments, the deaminase is rat APOBEC1 (SEQ ID NO: 284). In some embodiments, the deaminase is human APOBEC1 (SEQ ID NO: 282). In some embodiments, the deaminase is pmCDA1.

Other aspects of this disclosure relate to the recognition that fusion proteins comprising a deaminase domain, a dCas9 domain and a uracil glycosylase inhibitor (UGI) domain demonstrate improved efficiency for deaminating target nucleotides in a nucleic acid molecule. Without wishing to be bound by any particular theory, cellular DNA-repair response to the presence of U:G heteroduplex DNA may be responsible for a decrease in nucleobase editing efficiency in cells. Uracil DNA glycosylase (UDG) catalyzes removal of U from DNA in cells, which may initiate base excision repair, with reversion of the U:G pair to a C:G pair as the most common outcome. As demonstrated herein, Uracil DNA Glycosylase Inhibitor (UGI) may inhibit human UDG activity. Without wishing to be bound by any particular theory, base excision repair may be inhibited by molecules that bind the single strand, block the edited base, inhibit UGI, inhibit base excision repair, protect the edited base, and/or promote “fixing” of the non-edited strand, etc. Thus, this disclosure contemplates fusion proteins comprising a dCas9-cytidine deaminase domain that is fused to a UGI domain.

In some embodiments, the fusion protein comprises a nuclease-inactive Cas9 (dCas9) domain; a nucleic acid editing domain; and a uracil glycosylase inhibitor (UGI) domain. In some embodiments, the dCas9 domain comprises a D10X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for D. In some embodiments, the amino acid sequence of the dCas9 domain comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the dCas9 domain comprises an H840X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for H. In some embodiments, the amino acid sequence of the dCas9 domain comprises an H840A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the dCas9 domain comprises the amino acid sequence as set forth in SEQ ID NO: 263.

Further aspects of this disclosure relate to the recognition that fusion proteins using a Cas9 nickase as the Cas9 domain demonstrate improved efficiency for editing nucleic acids. For example, aspects of this disclosure relate to the recognition that fusion proteins comprising a Cas9 nickase, a deaminase domain and a UGI domain demonstrate improved efficiency for editing nucleic acids. For example, the improved efficiency for editing nucleotides is described below in the Examples section.

Some aspects of the disclosure are based on the recognition that any of the base editors provided herein are capable of modifying a specific nucleotide base without generating a significant proportion of indels. An “indel”, as used herein, refers to the insertion or deletion of a nucleotide base within a nucleic acid. Such insertions or deletions can lead to frame shift mutations within a coding region of a gene. In some embodiments, it is desirable to generate base editors that efficiently modify (e.g. mutate or deaminate) a specific nucleotide within a nucleic acid, without generating a large number of insertions or deletions (i.e., indels) in the nucleic acid. In certain embodiments, any of the base editors provided herein are capable of generating a greater proportion of intended modifications (e.g., point mutations or deaminations) versus indels.

Some aspects of the disclosure are based on the recognition that any of the base editors provided herein are capable of efficiently generating an intended mutation, such as a point mutation, in a nucleic acid (e.g. a nucleic acid within a genome of a subject) without generating a significant number of unintended mutations, such as unintended point mutations.

In some embodiments, a fusion protein comprises a Cas9 nickase domain, a nucleic acid editing domain; and a uracil glycosylase inhibitor (UGI) domain. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a D10X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for D. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises a histidine at amino acid position 840 of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding amino acid position in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the amino acid sequence of the Cas9 nickase domain comprises the amino acid sequence as set forth in SEQ ID NO: 267.

In some embodiments, the deaminase domain of the fusion protein is fused to the N-terminus of the dCas9 domain or the Cas9 nickase. In some embodiments, the UGI domain is fused to the C-terminus of the dCas9 domain or the Cas9 nickase. In some embodiments, the dCas9 domain or the Cas9 nickase and the nucleic acid editing domain are fused via a linker. In some embodiments, the dCas9 domain or the Cas9 nickase and the UGI domain are fused via a linker.

In certain embodiments, linkers may be used to link any of the peptides or peptide domains of the invention. The linker may be as simple as a covalent bond, or it may be a polymeric linker many atoms in length. In certain embodiments, the linker is a polypeptide or based on amino acids. In other embodiments, the linker is not peptide-like. In certain embodiments, the linker is a covalent bond (e.g., a carbon-carbon bond, disulfide bond, carbon-heteroatom bond, etc.). In certain embodiments, the linker is a carbon-nitrogen bond of an amide linkage. In certain embodiments, the linker is a cyclic or acyclic, substituted or unsubstituted, branched or unbranched aliphatic or heteroaliphatic linker. In certain embodiments, the linker is polymeric (e.g., polyethylene, polyethylene glycol, polyamide, polyester, etc.). In certain embodiments, the linker comprises a monomer, dimer, or polymer of aminoalkanoic acid. In certain embodiments, the linker comprises an aminoalkanoic acid (e.g., glycine, ethanoic acid, alanine, beta-alanine, 3-aminopropanoic acid, 4-aminobutanoic acid, 5-pentanoic acid, etc.). In certain embodiments, the linker comprises a monomer, dimer, or polymer of aminohexanoic acid (Ahx). In certain embodiments, the linker is based on a carbocyclic moiety (e.g., cyclopentane, cyclohexane). In other embodiments, the linker comprises a polyethylene glycol moiety (PEG). In other embodiments, the linker comprises amino acids. In certain embodiments, the linker comprises a peptide. In certain embodiments, the linker comprises an aryl or heteroaryl moiety. In certain embodiments, the linker is based on a phenyl ring. The linker may included funtionalized moieties to facilitate attachment of a nucleophile (e.g., thiol, amino) from the peptide to the linker. Any electrophile may be used as part of the linker. Exemplary electrophiles include, but are not limited to, activated esters, activated amides, Michael acceptors, alkyl halides, aryl halides, acyl halides, and isothiocyanates.

In some embodiments, the linker comprises the amino acid sequence (GGGGS)_n (SEQ ID NO: 5), (G)_n, (EAAAK)_n (SEQ ID NO: 6), (GGS)_n, (SGGS)_n (SEQ ID NO: 4288), SGSETPGTSESATPES (SEQ ID NO: 7), (XP)_n, or any combination thereof, wherein n is independently an integer between 1 and 30, and wherein X is any amino acid. In some embodiments, the linker comprises the amino acid sequence (GGS)_n, wherein n is 1, 3, or 7. In some embodiments, the linker comprises the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7).

In some embodiments, the fusion protein comprises the structure [nucleic acid editing domain]-[optional linker sequence]-[dCas9 or Cas9 nickase]-[optional linker sequence]-[UGI]. In some embodiments, the fusion protein comprises the structure [nucleic acid editing domain]-[optional linker sequence]-[UGI]-[optional linker sequence]-[dCas9 or Cas9 nickase]; [UGI]-[optional linker sequence]-[nucleic acid editing domain]-[optional linker sequence]-[dCas9 or Cas9 nickase]; [UGI]-[optional linker sequence]-[dCas9 or Cas9 nickase]-[optional linker sequence]-[nucleic acid editing domain]; [dCas9 or Cas9 nickase]-[optional linker sequence]-[UGI]-[optional linker sequence]-[nucleic acid editing domain]; or [dCas9 or Cas9 nickase]-[optional linker sequence]-[nucleic acid editing domain]-[optional linker sequence]-[UGI].

In some embodiments, the nucleic acid editing domain comprises a deaminase. In some embodiments, the nucleic acid editing domain comprises a deaminase. In some embodiments, the deaminase is a cytidine deaminase. In some embodiments, the deaminase is an apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the deaminase is an APOBEC1 deaminase, an APOBEC2 deaminase, an APOBEC3A deaminase, an APOBEC3B deaminase, an APOBEC3C deaminase, an APOBEC3D deaminase, an APOBEC3F deaminase, an APOBEC3G deaminase, an APOBEC3H deaminase, or an APOBEC4 deaminase. In some embodiments, the deaminase is an activation-induced deaminase (AID). In some embodiments, the deaminase is a Lamprey CDA1 (pmCDA1) deaminase.

In some embodiments, the deaminase is from a human, chimpanzee, gorilla, monkey, cow, dog, rat, or mouse. In some embodiments, the deaminase is from a human. In some embodiments the deaminase is from a rat. In some embodiments, the deaminase is a rat APOBEC1 deaminase comprising the amino acid sequence set forth in (SEQ ID NO: 284). In some embodiments, the deaminase is a human APOBEC1 deaminase comprising the amino acid sequence set forth in (SEQ ID NO: 282). In some embodiments, the deaminase is pmCDA1 (SEQ ID NO: 5738). In some embodiments, the deaminase is human APOBEC3G (SEQ ID NO: 275). In some embodiments, the deaminase is a human APOBEC3G variant of any one of (SEQ ID NOs: 5739-5741). In some embodiments, the deaminase is at least 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of the amino acid sequences set forth in SEQ ID NOs: 266-284 or 5725-5741.

In some embodiments, the UGI domain comprises an amino acid sequence that is at least 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to SEQ ID NO: 600. In some embodiments, the UGI domain comprises the amino acid sequence as set forth in SEQ ID NO: 600.

Some aspects of this disclosure provide complexes comprising a Cas9 protein or a Cas9 fusion protein as provided herein, and a guide RNA bound to the Cas9 protein or the Cas9 fusion protein.

Some aspects of this disclosure provide methods of using the Cas9 proteins, fusion proteins, or complexes provided herein. For example, some aspects of this disclosure provide methods comprising contacting a DNA molecule (a) with a Cas9 protein or a fusion protein as provided herein and with a guide RNA, wherein the guide RNA is about 15-100 nucleotides long and comprises a sequence of at least 10 contiguous nucleotides that is complementary to a target sequence; or (b) with a Cas9 protein, a Cas9 fusion protein, or a Cas9 protein or fusion protein complex with a gRNA as provided herein.

Some aspects of this disclosure provide kits comprising a nucleic acid construct, comprising (a) a nucleotide sequence encoding a Cas9 protein or a Cas9 fusion protein as provided herein; and (b) a heterologous promoter that drives expression of the sequence of (a). In some embodiments, the kit further comprises an expression construct encoding a guide RNA backbone, wherein the construct comprises a cloning site positioned to allow the cloning of a nucleic acid sequence identical or complementary to a target sequence into the guide RNA backbone.

Some aspects of this disclosure provide polynucleotides encoding a Cas9 protein of a fusion protein as provided herein. Some aspects of this disclosure provide vectors comprising such polynucleotides. In some embodiments, the vector comprises a heterologous promoter driving expression of polynucleotide.

Some aspects of this disclosure provide cells comprising a Cas9 protein, a fusion protein, a nucleic acid molecule, and/or a vector as provided herein.

The description of exemplary embodiments of the reporter systems above is provided for illustration purposes only and not meant to be limiting. Additional reporter systems, e.g., variations of the exemplary systems described in detail above, are also embraced by this disclosure.

The summary above is meant to illustrate, in a non-limiting manner, some of the embodiments, advantages, features, and uses of the technology disclosed herein. Other embodiments, advantages, features, and uses of the technology disclosed herein will be apparent from the Detailed Description, the Drawings, the Examples, and the Claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the deaminase activity of deaminases on single stranded DNA substrates. Single stranded DNA substrates using randomized PAM sequences (NNN PAM) were used as negative controls. Canonical PAM sequences used (NGG PAM)

FIG. 2 shows activity of Cas9:deaminase fusion proteins on single stranded DNA substrates. (GGS)₃ corresponds to SEQ ID NO: 596.

FIG. 3 illustrates double stranded DNA substrate binding by Cas9:deaminase:sgRNA complexes.

FIG. 4 illustrates a double stranded DNA deamination assay.

FIG. 5 demonstrates that Cas9 fusions can target positions 3-11 of double-stranded DNA target sequences (numbered according to the schematic in FIG. 5). Upper Gel: 1 μM rAPOBEC1-GGS-dCas9, 125 nM dsDNA, 1 equivalent sgRNA. Mid Gel: 1 μM rAPOBEC1-(GGS)₃(SEQ ID NO: 596)-dCas9, 125 nM dsDNA, 1 equivalent sgRNA. Lower Gel: 1.85 μM rAPOBEC1-XTEN-dCas9, 125 nM dsDNA, 1 equivalent sgRNA.

FIG. 6 demonstrates that the correct guide RNA, e.g., the correct sgRNA, is required for deaminase activity. (GGS)₃ corresponds to SEQ ID NO: 596.

FIG. 7 illustrates the mechanism of target DNA binding of in vivo target sequences by deaminase-dCas9:sgRNA complexes.

FIG. 8 shows successful deamination of exemplary disease-associated target sequences.

FIG. 9 shows in vitro C→T editing efficiencies using His6-rAPOBEC1-XTEN-dCas9.

FIG. 10 shows C→T editing efficiencies in HEK293T cells is greatly enhanced by fusion with UGI.

FIGS. 11A to 11C show NBE1 mediates specific, guide RNA-programmed C to U conversion in vitro. FIG. 11A: Nucleobase editing strategy. DNA with a target C (red) at a locus specified by a guide RNA (green) is bound by dCas9 (blue), which mediates the local denaturation of the DNA substrate. Cytidine deamination by a tethered APOBEC1 enzyme (orange) converts the target C to U. The resulting G:U heteroduplex can be permanently converted to an A:T base pair following DNA replication or repair. If the U is in the template DNA strand, it will also result in an RNA transcript containing a G to A mutation following transcription. FIG. 11B: Deamination assay showing an activity window of approximately five nucleotides. Following incubation of NBE1-sgRNA complexes with dsDNA substrates at 37° C. for 2 h, the 5′ fluorophore-labeled DNA was isolated and incubated with USER enzyme (uracil DNA glycosylase and endonuclease VIII) at 37° C. for 1 h to induce DNA cleavage at the site of any uracils. The resulting DNA was resolved on a denaturing polyacrylamide gel, and any fluorophore-linked strands were visualized. Each lane is labeled according to the position of the target C within the protospacer, or with “-” if no target C is present, counting the base distal from the PAM as position 1. FIG. 11C: Deaminase assay showing the sequence specificity and sgRNA-dependence of NBE1. The DNA substrate with a target C at position 7 was incubated with NBE1 as in FIG. 11B with either the correct sgRNA, a mismatched sgRNA, or no sgRNA. No C to U editing is observed with the mismatched sgRNA or with no sgRNA. The positive control sample contains a DNA sequence with a U synthetically incorporated at position 7.

FIGS. 12A to 12B show effects of sequence context and target C position on nucleobase editing efficiency in vitro. FIG. 12A: Effect of changing the sequence surrounding the target C on editing efficiency in vitro. The deamination yield of 80% of targeted strands (40% of total sequencing reads from both strands) for C₇ in the protospacer sequence 5′-TTATTTCGTGGATTTATTTA-3′(SEQ ID NO: 264) was defined as 1.0, and the relative deamination efficiencies of substrates containing all possible single-base mutations at positions 1-6 and 8-13 are shown. Values and error bars reflect the mean and standard deviation of two or more independent biological replicates performed on different days. FIG. 12B: Positional effect of each NC motif on editing efficiency in vitro. Each NC target motif was varied from positions 1 to 8 within the protospacer as indicated in the sequences shown on the right (the PAM shown in red, the protospacer plus one base 5′ to the protospacer are also shown). The percentage of total sequence reads containing T at each of the numbered target C positions following incubation with NBE1 is shown in the graph. Note that the maximum possible deamination yield in vitro is 50% of total sequencing reads (100% of targeted strands). Values and error bars reflect the mean and standard deviation of two or three independent biological replicates performed on different days. FIG. 12B depicts SEQ ID NOs: 5750 through 5757 from top to bottom, respectively.

FIGS. 13A to 13C show nucleobase editing in human cells. FIG. 13A: Protospacer (black) and PAM (red) sequences of the six mammalian cell genomic loci targeted by nucleobase editors. Target Cs are indicated with subscripted numbers corresponding to their positions within the protospacer. FIG. 13A depicts SEQ ID NOs: 293 through 298 from top to bottom, respectively. FIG. 13B: HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and an appropriate sgRNA. Three days after transfection, genomic DNA was extracted and analyzed by high-throughput DNA sequencing at the six loci. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown for NBE1, NBE2, and NBE3 at all six genomic loci, and for wt Cas9 with a donor HDR template at three of the six sites (EMX1, HEK293 site 3, and HEK293 site 4). Values and error bars reflect the mean and standard deviation of three independent biological replicates performed on different days. FIG. 13C: Frequency of indel formation, calculated as described in the Methods, is shown following treatment of HEK293T cells with NBE2 and NBE3 for all six genomic loci, or with wt Cas9 and a single-stranded DNA template for HDR at three of the six sites (EMX1, HEK293 site 3, and HEK293 site 4). Values reflect the mean of at least three independent biological replicates performed on different days.

FIGS. 14A to 14C show NBE2- and NBE3-mediated correction of three disease-relevant mutations in mammalian cells. For each site, the sequence of the protospacer is indicated to the right of the name of the mutation, with the PAM highlighted in green and the base responsible for the mutation indicated in bold with a subscripted number corresponding to its position within the protospacer. The amino acid sequence above each disease-associated allele is shown, together with the corrected amino acid sequence following nucleobase editing in red. Underneath each sequence are the percentages of total sequencing reads with the corresponding base. Cells were nucleofected with plasmids encoding NBE2 or NBE3 and an appropriate sgRNA. Two days after nucleofection, genomic DNA was extracted and analyzed by HTS to assess pathogenic mutation correction. FIG. 14A: The Alzheimer's disease-associated APOE4 allele is converted to APOE3′ in mouse astrocytes by NBE3 in 11% of total reads (44% of nucleofected astrocytes). Two nearby Cs are also converted to Ts, but with no change to the predicted sequence of the resulting protein (SEQ ID NO: 299). The DNA sequence in FIG. 14A corresponds to SEQ ID NO: 5747. FIG. 14B The cancer-associated p53 N239D mutation is corrected by NBE2 in 11% of treated human lymphoma cells (12% of nucleofected cells) that are heterozygous for the mutation (SEQ ID NO: 300). The DNA sequence in FIG. 14B corresponds to SEQ ID NO: 5748. FIG. 14C The p53 Y163C mutation is corrected by NBE3 in 7.6% of nucleofected human breast cancer cells (SEQ ID NO: 301). The DNA sequence FIG. 14C corresponds to SEQ ID NO: 5749.

FIGS. 15A to 15D show effects of deaminase-dCas9 linker length and composition on nucleobase editing. Gel-based deaminase assay showing the deamination window of nucleobase editors with deaminase-Cas9 linkers of GGS (FIG. 15A), (GGS)₃ (SEQ ID NO: 596) (FIG. 15B), XTEN (FIG. 15C), or (GGS)₇ (SEQ ID NO: 597) (FIG. 15D). Following incubation of 1.85 μM editor-sgRNA complexes with 125 nM dsDNA substrates at 37° C. for 2 h, the dye-conjugated DNA was isolated and incubated with USER enzyme (uracil DNA glycosylase and endonuclease VIII) at 37° C. for an additional hour to cleave the DNA backbone at the site of any uracils. The resulting DNA was resolved on a denaturing polyacrylamide gel, and the dye-conjugated strand was imaged. Each lane is numbered according to the position of the target C within the protospacer, or with—if no target C is present. 8U is a positive control sequence with a U synthetically incorporated at position 8.

FIGS. 16A to 16B show NBE1 is capable of correcting disease-relevant mutations in vitro. FIG. 16A: Protospacer and PAM sequences (red) of seven disease-relevant mutations. The disease-associated target C in each case is indicated with a subscripted number reflecting its position within the protospacer. For all mutations except both APOE4 SNPs, the target C resides in the template (non-coding) strand. FIG. 16A depicts SEQ ID NOs: 5760, 5747, and 5761 through 5765 from top to bottom, respectively. FIG. 16B: Deaminase assay showing each dsDNA oligonucleotide before (−) and after (+) incubation with NBE1, DNA isolation, and incubation with USER enzymes to cleave DNA at positions containing U. Positive control lanes from incubation of synthetic oligonucleotides containing U at various positions within the protospacer with USER enzymes are shown with the corresponding number indicating the position of the U.

FIG. 17 shows processivity of NBE1. The protospacer and PAM (red) of a 60-mer DNA oligonucleotide containing eight consecutive Cs is shown at the top. The oligonucleotide (125 nM) was incubated with NBE1 (2 μM) for 2 h at 37° C. The DNA was isolated and analyzed by high-throughput sequencing. Shown are the percent of total reads for the most frequent nine sequences observed. The vast majority of edited strands (>93%) have more than one C converted to T. This figure depicts SEQ ID NO: 5766.

FIGS. 18A to 18H show the effect of fusing UGI to NBE1 to generate NBE2. FIG. 18A: Protospacer and PAM (red) sequences of the six mammalian cell genomic loci targeted with nucleobase editors. Editable Cs are indicated with labels corresponding to their positions within the protospacer. FIG. 18A depicts SEQ ID NOs: 293 through 298 from top to bottom, respectively. FIGS. 18B to 18G: HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE1 and UGI, and an appropriate sgRNA. Three days after transfection, genomic DNA was extracted and analyzed by high-throughput DNA sequencing at the six loci. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown for NBE1, NBE1 and UGI, and. NBE2 at all six genomic loci. FIG. 18H: C to T mutation rates at 510 Cs surrounding the protospacers of interest for NBE1, NBE1 plus UGI on a separate plasmid, NBE2, and untreated cells are shown. The data show the results of 3,000,000 DNA sequencing reads from 1.5×106 cells. Values reflect the mean of at least two biological experiments conducted on different days.

FIG. 19 shows nucleobase editing efficiencies of NBE2 in U2OS and HEK293T cells. Cellular C to T conversion percentages by NBE2 are shown for each of the six targeted genomic loci in HEK293T cells and U2OS cells. HEK293T cells were transfected using lipofectamine 2000, and U2OS cells were nucleofected. U2OS nucleofection efficiency was 74%. Three days after plasmid delivery, genomic DNA was extracted and analyzed for nucleobase editing at the six genomic loci by FITS. Values and error bars reflect the mean and standard deviation of at least two biological experiments done on different days.

FIG. 20 shows nucleobase editing persists over multiple cell divisions. Cellular C to T conversion percentages by NBE2 are displayed at two genomic loci in HEK293T cells before and after passaging the cells. HEK293T cells were transfected using Lipofectamine 2000. Three days post transfection, the cells were harvested and split in half. One half was subjected to HTS analysis, and the other half was allowed to propagate for approximately five cell divisions, then harvested and subjected to HTS analysis.

FIG. 21 shows genetic variants from ClinVar that can be corrected in principle by nucleobase editing. The NCBI ClinVar database of human genetic variations and their corresponding phenotypes⁶⁸ was searched for genetic diseases that can be corrected by current nucleobase editing technologies. The results were filtered by imposing the successive restrictions listed on the left. The x-axis shows the number of occurrences satisfying that restriction and all above restrictions on a logarithmic scale.

FIG. 22 shows in vitro identification of editable Cs in six genomic loci. Synthetic 80-mers with sequences matching six different genomic sites were incubated with NBE1 then analyzed for nucleobase editing via FITS. For each site, the sequence of the protospacer is indicated to the right of the name of the site, with the PAM highlighted in red. Underneath each sequence are the percentages of total DNA sequencing reads with the corresponding base. A target C was considered as “editable” if the in vitro conversion efficiency is >10%. Note that maximum yields are 50% of total DNA sequencing reads since the non-targeted strand is not a substrate for nucleobase editing. This figure depicts SEQ ID NOs: 293 through 298 from top to bottom, respectively.

FIG. 23 shows activities of NBE1, NBE2, and NBE3 at EMX1 off-targets. HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and a sgRNA matching the EMX1 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus the top ten known Cas9 off-target loci for the EMX1 sgRNA, as previously determined using the GUIDE-seq method⁵⁵. EMX1 off-target 5 locus did not amplify and is not shown. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for NBE1, NBE2, and NBE3. On the far right are displayed the total number of sequencing reads reported for each sequence. This figure depicts SEQ ID NOs: 293, and 5767 through 5775 from top to bottom, respectively.

FIG. 24 shows activities of NBE1, NBE2, and NBE3 at FANCF off-targets. HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and a sgRNA matching the FANCF sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus all of the known Cas9 off-target loci for the FANCF sgRNA, as previously determined using the GUIDE-seq method⁵⁵. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for NBE1, NBE2, and NBE3. On the far right are displayed the total number of sequencing reads reported for each sequence. This figure depicts SEQ ID NOs: 294 and 5776 through 5781, 5777, and 5782 from top to bottom, respectively.

FIG. 25 shows activities of NBE1, NBE2, and NBE3 at HEK293 site 2 off-targets. HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and a sgRNA matching the HEK293 site 2 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus all of the known Cas9 off-target loci for the HEK293 site 2 sgRNA, as previously determined using the GUIDE-seq method⁵⁵. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for NBE1, NBE2, and NBE3. On the far right are displayed the total number of sequencing reads reported for each sequence. This figure depicts SEQ ID NOs: 295, 327, and 328 from top to bottom, respectively.

FIG. 26 shows activities of NBE1, NBE2, and NBE3 at HEK293 site 3 off-targets. HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and a sgRNA matching the HEK293 site 3 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus all of the known Cas9 off-target loci for the HEK293 site 3 sgRNA, as previously determined using the GUIDE-seq method⁵⁵. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for NBE1, NBE2, and NBE3. On the far right are displayed the total number of sequencing reads reported for each sequence. This figure depicts SEQ ID NOs: 296 and 659 through 663 from top to bottom, respectively.

FIG. 27 shows activities of NBE1, NBE2, and NBE3 at HEK293 site 4 off-targets. HEK293T cells were transfected with plasmids expressing NBE1, NBE2, or NBE3 and a sgRNA matching the HEK293 site 4 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus the top ten known Cas9 off-target loci for the HEK293 site 4 sgRNA, as previously determined using the GUIDE-seq method⁵⁵. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for NBE1, NBE2, and NBE3. On the far right are displayed the total number of sequencing reads reported for each sequence. This figure depicts SEQ ID NOs: 297 and 664 through 673 from top to bottom, respectively.

FIG. 28 shows non-target C mutation rates. Shown here are the C to T mutation rates at 2,500 distinct cytosines surrounding the six on-target and 34 off-target loci tested, representing a total of 14,700,000 sequence reads derived from approximately 1.8×106 cells.

FIGS. 29A to 29C show base editing in human cells. FIG. 29A shows possible base editing outcomes in mammalian cells. Initial editing resulted in a U:G mismatch. Recognition and excision of the U by uracil DNA glycosylase (UDG) initiated base excision repair (BER), which lead to reversion to the C:G starting state. BER was impeded by BE2 and BE3, which inhibited UDG. The U:G mismatch was also processed by mismatch repair (MMR), which preferentially repaired the nicked strand of a mismatch. BE3 nicked the non-edited strand containing the G, favoring resolution of the U:G mismatch to the desired U:A or T:A outcome. FIG. 29B shows HEK293T cells treated as described in the Materials and Methods in the Examples below. The percentage of total DNA sequencing read with Ts at the target positions indicated show treatment with BE1, BE2, or BE3, or for treatment with wt Cas9 with a donor HDR template. FIG. 29C shows frequency of indel formation following the treatment in FIG. 29B. Values are listed in FIG. 34. For FIGS. 29B and 29C, values and error bars reflect the mean and s.d. of three independent biological replicates performed on different days.

FIGS. 30A to 30B show BE3-mediated correction of two disease-relevant mutations in mammalian cells. The sequence of the protospacer is shown to the right of the mutation, with the PAM in blue and the target base in red with a subscripted number indicating its position within the protospacer. Underneath each sequence are the percentages of total sequencing reads with the corresponding base. Cells were treated as described in the Materials and Methods. FIG. 30A shows the Alzheimer's disease-associated APOE4 allele converted to APOE3r in mouse astrocytes by BE3 in 74.9% of total reads. Two nearby Cs were also converted to Ts, but with no change to the predicted sequence of the resulting protein. Identical treatment of these cells with wt Cas9 and donor ssDNA results in only 0.3% correction, with 26.1% indel formation. FIG. 30B shows the cancer associated p53 Y163C mutation corrected by BE3 in 7.6% of nucleofected human breast cancer cells with 0.7% indel formation. Identical treatment of these cells with wt Cas9 and donor ssDNA results in no mutation correction with 6.1% indel formation. The amino acid sequences in FIG. 30A correspond to SEQ ID NOs: 675, 299, and 299 from top to bottom, respectively. The three DNA sequences in FIG. 30A correspond to SEQ ID NO: 5747. The amino acid sequences in FIG. 30B correspond to SEQ ID NOs: 678, 301, and 301 from top to bottom, respectively. The three DNA sequences in FIG. 30B correspond to SEQ ID NO: 5749.

FIG. 31 shows activities of BE1, BE2, and BE3 at HEK293 site 2 off-targets. HEK293T cells were transfected with plasmids expressing BE1, BE2, or BE3 and a sgRNA matching the HEK293 site 2 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus all of the known Cas9 and dCas9 off-target loci for the HEK293 site 2 sgRNA, as previously determined by Joung and coworkers using the GUIDE-seq method (63), and Adli and coworkers using chromatin immunoprecipitation high-throughput sequencing (ChIP-seq) experiments (18). Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for BE1, BE2, and BE3. On the far right are displayed the total number of sequencing reads reported, and the ChIP-seq intensity reported for each sequence. This figure depicts SEQ ID NOs: 295, 327 through 328 and 684 through 688 from top to bottom, respectively.

FIG. 32 shows activities of BE1, BE2, a signal

nd BE3 at HEK293 site 3 off-targets. HEK293T cells were transfected with plasmids expressing BE1, BE2, or BE3 and a sgRNA matching the HEK293 site 3 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus all of the known Cas9 off-target loci and the top five known dCas9 off-target loci for the HEK293 site 3 sgRNA, as previously determined by Joung and coworkers using the GUIDE-seq method⁵⁴, and using chromatin immunoprecipitation high-throughput sequencing (ChIP-seq) experiments⁶¹. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for BE1, BE2, and BE3. On the far right are displayed the total number of sequencing reads reported, and the ChIP-seq signal intensity reported for each sequence. This figure depicts SEQ ID NOs: 296, 659 through 663 and 695 through 699 from top to bottom, respectively.

FIG. 33 shows activities of BE1, BE2, and BE3 at HEK293 site 4 off-targets. HEK293T cells were transfected with plasmids expressing BE1, BE2, or BE3 and a sgRNA matching the HEK293 site 4 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci, plus the top ten known Cas9 off-target loci and the top five known dCas9 off-target loci for the HEK293 site 4 sgRNA, as previously determined using the GUIDE-seq method⁵⁴, and using chromatin immunoprecipitation high-throughput sequencing (ChIP-seq) experiments⁶¹. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for BE1, BE2, and BE3. On the far right are displayed the total number of sequencing reads reported, and the ChIP-seq signal intensity reported for each sequence. This figure depicts SEQ ID NOs: 297, 664 through 673, 5783, and 5784 from top to bottom, respectively.

FIG. 34 shows mutation rates of non-protospacer bases following BE3-mediated correction of the Alzheimer's disease-associated APOE4 allele to APOE3r in mouse astrocytes. The DNA sequence of the 50 bases on either side of the protospacer from FIG. 30A and FIG. 34B is shown with each base's position relative to the protospacer. The side of the protospacer distal to the PAM is designated with positive numbers, while the side that includes the PAM is designated with negative numbers, with the PAM shown in blue. Underneath each sequence are the percentages of total DNA sequencing reads with the corresponding base for untreated cells, for cells treated with BE3 and an sgRNA targeting the APOE4 C158R mutation, or for cells treated with BE3 and an sgRNA targeting the VEGFA locus. Neither BE3-treated sample resulted in mutation rates above those of untreated controls. This figure depicts SEQ ID NOs: 713 to 716 from top to bottom, respectively.

FIG. 35 shows mutation rates of non-protospacer bases following BE3-mediated correction of the cancer-associated p53 Y163C mutation in HCC1954 human cells. The DNA sequence of the 50 bases on either side of the protospacer from FIG. 30B and FIG. 39Bis shown with each base's position relative to the protospacer. The side of the protospacer distal to the PAM is designated with positive numbers, while the side that includes the PAM is designated with negative numbers, with the PAM shown in blue. Underneath each sequence are the percentages of total sequencing reads with the corresponding base for untreated cells, for cells treated with BE3 and an sgRNA targeting the TP53 Y163C mutation, or for cells treated with BE3 and an sgRNA targeting the VEGFA locus. Neither BE3-treated sample resulted in mutational rates above those of untreated controls. This figure depicts SEQ ID NOs: 717 to 720 from top to bottom, respectively.

FIGS. 36A to 36F show the effects of deaminase, linker length, and linker composition on base editing. FIG. 36A shows a gel-based deaminase assay showing activity of rAPOBEC1, pmCDA1, hAID, hAPOBEC3G, rAPOBEC1-GGS-dCas9, rAPOBEC1-(GGS)₃(SEQ ID NO: 596)-dCas9, and dCas9-(GGS)₃(SEQ ID NO: 596)-rAPOBEC1 on ssDNA. Enzymes were expressed in a mammalian cell lysate-derived in vitro transcription-translation system and incubated with 1.8 μM dye-conjugated ssDNA and USER enzyme (uracil DNA glycosylase and endonuclease VIII) at 37° C. for 2 hours. The resulting DNA was resolved on a denaturing polyacrylamide gel and imaged. The positive control is a sequence with a U synthetically incorporated at the same position as the target C. FIG. 36B shows coomassie-stained denaturing PAGE gel of the expressed and purified proteins used in FIGS. 36C to 36F. FIGS. 36C to 36F show gel-based deaminase assay showing the deamination window of base editors with deaminase-Cas9 linkers of GGS (FIG. 36C), (GGS)₃ (SEQ ID NO: 596) (FIG. 36D), XTEN (FIG. 36E), or (GGS)₇ (SEQ ID NO: 597) (FIG. 36F). Following incubation of 1.85 μM deaminase-dCas9 fusions complexed with sgRNA with 125 nM dsDNA substrates at 37° C. for 2 hours, the dye-conjugated DNA was isolated and incubated with USER enzyme at 37° C. for 1 hour to cleave the DNA backbone at the site of any uracils. The resulting DNA was resolved on a denaturing polyacrylamide gel, and the dye-conjugated strand was imaged. Each lane is numbered according to the position of the target C within the protospacer, or with—if no target C is present. 8U is a positive control sequence with a U synthetically incorporated at position 8.

FIGS. 37A to 37C show BE1 base editing efficiencies are dramatically decreased in mammalian cells. FIG. 37A Protospacer (black and red) and PAM (blue) sequences of the six mammalian cell genomic loci targeted by base editors. Target Cs are indicated in red with subscripted numbers corresponding to their positions within the protospacer. FIG. 37B shows synthetic 80-mers with sequences matching six different genomic sites were incubated with BE1 then analyzed for base editing by HTS. For each site, the sequence of the protospacer is indicated to the right of the name of the site, with the PAM highlighted in blue. Underneath each sequence are the percentages of total DNA sequencing reads with the corresponding base. We considered a target C as “editable” if the in vitro conversion efficiency is >10%. Note that maximum yields are 50% of total DNA sequencing reads since the non-targeted strand is unaffected by BEL Values are shown from a single experiment. FIG. 37C shows HEK293T cells were transfected with plasmids expressing BE1 and an appropriate sgRNA. Three days after transfection, genomic DNA was extracted and analyzed by high-throughput DNA sequencing at the six loci. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown for BE1 at all six genomic loci. Values and error bars of all data from HEK293T cells reflect the mean and standard deviation of three independent biological replicates performed on different days. FIG. 37A depicts SEQ ID NOs: 293 through 298 from top to bottom, respectively. FIG. 37B depicts SEQ ID NOs: 293 through 298 from top to bottom, respectively.

FIG. 38 shows base editing persists over multiple cell divisions. Cellular C to T conversion percentages by BE2 and BE3 are shown for HEK293 sites 3 and 4 in HEK293T cells before and after passaging the cells. HEK293T cells were nucleofected with plasmids expressing BE2 or BE3 and an sgRNA targeting HEK293 site 3 or 4. Three days after nucleofection, the cells were harvested and split in half. One half was subjected to HTS analysis, and the other half was allowed to propagate for approximately five cell divisions, then harvested and subjected to HTS analysis. Values and error bars reflect the mean and standard deviation of at least two biological experiments.

FIGS. 39A to 39C show non-target C/G mutation rates. Shown here are the C to T and G to A mutation rates at 2,500 distinct cytosines and guanines surrounding the six on-target and 34 off-target loci tested, representing a total of 14,700,000 sequence reads derived from approximately 1.8×10⁶ cells. FIGS. 39A and 39B show cellular non-target C to T and G to A conversion percentages by BE1, BE2, and BE3 are plotted individually against their positions relative to a protospacer for all 2,500 cytosines/guanines. The side of the protospacer distal to the PAM is designated with positive numbers, while the side that includes the PAM is designated with negative numbers. FIG. 39C shows average non-target cellular C to T and G to A conversion percentages by BE1, BE2, and BE3 are shown, as well as the highest and lowest individual conversion percentages.

FIGS. 40A to 40B show additional data sets of BE3-mediated correction of two disease-relevant mutations in mammalian cells. For each site, the sequence of the protospacer is indicated to the right of the name of the mutation, with the PAM highlighted in blue and the base responsible for the mutation indicated in red bold with a subscripted number corresponding to its position within the protospacer. The amino acid sequence above each disease-associated allele is shown, together with the corrected amino acid sequence following base editing in green. Underneath each sequence are the percentages of total sequencing reads with the corresponding base. Cells were nucleofected with plasmids encoding BE3 and an appropriate sgRNA. Two days after nucleofection, genomic DNA was extracted from the nucleofected cells and analyzed by HTS to assess pathogenic mutation correction. FIG. 40A shows the Alzheimer's disease-associated APOE4 allele is converted to APOE3r in mouse astrocytes by BE3 in 58.3% of total reads only when treated with the correct sgRNA. Two nearby Cs are also converted to Ts, but with no change to the predicted sequence of the resulting protein. Identical treatment of these cells with wt Cas9 and donor ssDNA results in 0.2% correction, with 26.7% indel formation. FIG. 40B shows the cancer-associated p53 Y163C mutation is corrected by BE3 in 3.3% of nucleofected human breast cancer cells only when treated with the correct sgRNA. Identical treatment of these cells with wt Cas9 and donor ssDNA results in no detectable mutation correction with 8.0% indel formation. The amino acid sequences in FIG. 40A correspond to SEQ ID NOs: 675, 299, 675, and 299 from top to bottom, respectively. The nucleotide sequence is given by SEQ ID NO: 5747. The amino acid sequences in FIG. 40B correspond to SEQ ID NOs: 678, 301, 678, and 301 from top to bottom, respectively. The nucleotide sequence is given by SEQ ID NO: 5749.

FIG. 41 shows a schematic representation of an exemplary USER (Uracil-Specific Excision Reagent) Enzyme-based assay, which may be used to test the activity of various deaminases on single-stranded DNA (ssDNA) substrates.

FIG. 42 is a schematic of the pmCDA-nCas9-UGI-NLS construct and its activity at the HeK-3 site relative to the base editor (rAPOBEC1) and the negative control (untreated). The sequence corresponds to SEQ ID NO: 4139.

FIG. 43 is a schematic of the pmCDA1-XTEN-nCas9-UGI-NLS construct and its activity at the HeK-3 site relative to the base editor (rAPOBEC1) and the negative control (untreated). The sequence corresponds to SEQ ID NO: 4140.

FIG. 44 shows the percent of total sequencing reads with target C converted to T using cytidine deaminases (CDA) or APOBEC.

FIG. 45 shows the percent of total sequencing reads with target C converted to A using deaminases (CDA) or APOBEC.

FIG. 46 shows the percent of total sequencing reads with target C converted to G using deaminases (CDA) or APOBEC.

FIG. 47 is a schematic of the huAPOBEC3G-XTEN-nCas9-UGI-NLS construct and its activity at the HeK-2 site relative to a mutated form (huAPOBEC3G*(D316R_D317R)-XTEN-nCas9-UGI-NLS, the base editor (rAPOBEC1) and the negative control (untreated). The sequence corresponds to SEQ ID NO: 4141.

FIG. 48 shows the schematic of the LacZ construct used in the selection assay of Example 7. The sequence corresponds to SEQ ID NO: 4142.

FIG. 49 shows reversion data from different plasmids and constructs.

FIG. 50 shows the verification of lacZ reversion (the sequences correspond to SEQ ID NO: 4143 (the nucleotide sequence) and SEQ ID NO: 4144 (the amino acid sequence) from the MP6 plasmid) and the purification of reverted clones (the sequences correspond to SEQ ID NO: 4145 (the nucleotide sequence) and SEQ ID NO: 4146 (the amino acid sequence) from the CDA plasmid).

FIG. 51 is a schematic depicting a deamination selection plasmid used in Example 7.

FIG. 52 shows the results of a chloramphenicol reversion assay (pmCDA1 fusion).

FIGS. 53A to 53B demonstrated DNA correction induction of two constructs. The sequences in FIG. 53A from top to bottom correspond to SEQ ID NOs: 4147 (the nucleotide sequence), 4148 (the amino acid sequence), 4149 (the nucleotide sequence), 4150 (the amino acid sequence), 4147 (the nucleotide sequence) and 4151 (the truncated nucleotide sequence). The sequences in FIG. 53B from top to bottom correspond to SEQ ID NOs: 5785 (the nucleotide sequence), 5787 (the amino acid sequence), 5786 (the nucleotide sequence), 5788 (the amino acid sequence), 5785 (the nucleotide sequence), and 5806 (the truncated nucleotide sequence).

FIG. 54 shows the results of a chloramphenicol reversion assay (huAPOBEC3G fusion). The sequences correspond to SEQ ID NOs: 5802 (the nucleotide sequence), 5803 (the amino acid sequence), 5804 (the nucleotide sequence), 5805 (the amino acid sequence), and 5802 (the nucleotide sequence).

FIG. 55 shows the activities of BE3 and HF-BE3 at EMX1 off-targets. This figure depicts SEQ ID NOs: 293, and 5767 through 5775 from top to bottom, respectively.

FIG. 56 shows on-target base editing efficiencies of BE3 and HF-BE3.

FIG. 57 is a graph demonstrating that mutations affect cytidine deamination with varying degrees. Combinations of mutations that each slightly impairs catalysis allow selective deamination at one position over others. The FANCF site was GGAATC₆C₇C₈TTC₁₁TGCAGCACCTGG (SEQ ID NO: 303).

FIG. 58 is a schematic depicting next generation base editors.

FIG. 59 is a schematic illustrating new base editors made from Cas9 variants.

FIG. 60 shows the base-edited percentage of different NGA PAM sites.

FIG. 61 shows the base-edited percentage of cytidines using NGCG PAM EMX (VRER BE3) and the C₁TC₃C₄C₅ATC₈AC₁₀ATCAACCGGT (SEQ ID NO: 304) spacer.

FIG. 62 shows the based-edited percentages resulting from different NNGRRT PAM sites.

FIG. 63 shows the based-edited percentages resulting from different NNHRRT PAM sites.

FIGS. 64A to 64C show the base-edited percentages resulting from different TTTN PAM sites using Cpf1 BE2. The spacers used were:

• TTTCCTC₃C₄C₅C₆C₇C₈C₉AC₁₁AGGTAGAACAT (FIG. 64A, SEQ ID NO: 305),
• TTTCC₁C₂TC₄TGTC₈C₉AC₁₁ACCCTCATCCTG (FIG. 64B, SEQ ID NO: 306), and
• TTTCC₁C₂C₃AGTC₇C₈TC₁₀C₁₁AC_BAC₁₅C₁₆C₁₇TGAAAC (FIG. 64C, SEQ ID NO: 307).

FIG. 65 is a schematic depicting selective deamination as achieved through kinetic modulation of cytidine deaminase point mutagenesis.

FIG. 66 is a graph showing the effect of various mutations on the deamination window probed in cell culture with multiple cytidines in the spacer. The spacer used was: TGC₃C₄C₅C₆TC₈C₉C₁₀TC₁₂C₁₃C₁₄TGGCCC (SEQ ID NO: 308).

FIG. 67 is a graph showing the effect of various mutations on the deamination window probed in cell culture with multiple cytidines in the spacer. The spacer used was: AGAGC₅C₆C₇C₈C₉C₁₀C₁₁TC_BAAAGAGA (SEQ ID NO: 309).

FIG. 68 is a graph showing the effect of various mutations on the FANCF site with a limited number of cytidines. The spacer used was: GGAATC₆C₇C₈TTC₁₁TGCAGCACCTGG (SEQ ID NO: 303). Note that the triple mutant (W90Y, R126E, R132E) preferentially edits the cytidine at the sixth position.

FIG. 69 is a graph showing the effect of various mutations on the HEK3 site with a limited number of cytidines. The spacer used was: GGCC₄C₅AGACTGAGCACGTGATGG (SEQ ID NO: 310). Note that the double and triple mutants preferentially edit the cytidine at the fifth position over the cytidine in the fourth position.

FIG. 70 is a graph showing the effect of various mutations on the EMX1 site with a limited number of cytidines. The spacer used was: GAGTC₅C₆GAGCAGAAGAAGAAGGG (SEQ ID NO: 311). Note that the triple mutant only edits the cytidine at the fifth position, not the sixth.

FIG. 71 is a graph showing the effect of various mutations on the HEK2 site with a limited number of cytidines. The spacer used was: GAAC₄AC₆AAAGCATAGACTGCGGG (SEQ ID NO: 312).

FIG. 72 shows on-target base editing efficiencies of BE3 and BE3 comprising mutations W90Y R132E in immortalized astrocytes. The amino acid sequences correspond to SEQ ID NO: 5789. The nucleic acid sequences correspond to SEQ ID NO: 5790.

FIG. 73 depicts a schematic of three Cpf1 fusion constructs.

FIG. 74 shows a comparison of plasmid delivery of BE3 and HF-BE3 (EMX1, FANCF, and RNF2).

FIG. 75 shows a comparison of plasmid delivery of BE3 and HF-BE3 (HEK3 and HEK 4).

FIG. 76 shows off-target editing of EMX-1 at all 10 sites. This figure depicts SEQ ID NOs: 293 and 5767 through 5775 from top to bottom, respectively.

FIG. 77 shows deaminase protein lipofection to HEK cells using a GAGTCCGAGCAGAAGAAGAAG (SEQ ID NO: 313) spacer. The EMX-1 on-target and EMX-1 off target site 2 were examined.

FIG. 78 shows deaminase protein lipofection to HEK cells using a GGAATCCCTTCTGCAGCACCTGG (SEQ ID NO: 314) spacer. The FANCF on target and FANCF off target site 1 were examined.

FIG. 79 shows deaminase protein lipofection to HEK cells using a GGCCCAGACTGAGCACGTGA (SEQ ID NO: 315) spacer. The HEK-3 on target site was examined.

FIG. 80 shows deaminase protein lipofection to HEK cells using a GGCACTGCGGCTGGAGGTGGGGG (SEQ ID NO: 316) spacer. The HEK-4 on target, off target site 1, site 3, and site 4.

FIG. 81 shows the results of an in vitro assay for sgRNA activity for sgHR_13 (GTCAGGTCGAGGGTTCTGTC (SEQ ID NO: 317) spacer; C8 target: G51 to STOP), sgHR_14 (GGGCCGCAGTATCCTCACTC (SEQ ID NO: 318) spacer; C7 target; C7 target: Q68 to STOP), and sgHR_15 (CCGCCAGTCCCAGTACGGGA (SEQ ID NO: 319) spacer; C10 and C11 are targets: W239 or W237 to STOP).

FIG. 82 shows the results of an in vitro assay for sgHR_17 (CAACCACTGCTCAAAGATGC (SEQ ID NO: 320) spacer; C4 and C5 are targets: W410 to STOP), and sgHR_16 (CTTCCAGGATGAGAACACAG (SEQ ID NO: 321) spacer; C4 and C5 are targets: W273 to STOP).

FIG. 83 shows the direct injection of BE3 protein complexed with sgHR_13 in zebrafish embryos.

FIG. 84 shows the direct injection of BE3 protein complexed with sgHR_16 in zebrafish embryos.

FIG. 85 shows the direct injection of BE3 protein complexed with sgHR_17 in zebrafish embryos.

FIG. 86 shows exemplary nucleic acid changes that may be made using base editors that are capable of making a cytosine to thymine change.

FIG. 87 shows an illustration of apolipoprotein E (APOE) isoforms, demonstrating how a base editor (e.g., BE3) may be used to edit one APOE isoform (e.g., APOE4) into another APOE isoform (e.g., APOE3r) that is associated with a decreased risk of Alzheimer's disease.

FIG. 88 shows base editing of APOE4 to APOE3r in mouse astrocytes. The amino acid sequences correspond to SEQ ID NOs: 675, 299, and 299 from top to bottom, respectively. The nucleic acid sequences correspond to SEQ ID NO: 5747.

FIG. 89 shows base editing of PRNP to cause early truncation of the protein at arginine residue 37. The sequences correspond to SEQ ID NOs: 5791 (the amino acid sequence) and 4126 (the nucleic acid sequence).

FIG. 90 shows that knocking out UDG (which UGI inhibits) dramatically improves the cleanliness of efficiency of C to T base editing.

FIG. 91 shows that use of a base editor with the nickase but without UGI leads to a mixture of outcomes, with very high indel rates.

FIGS. 92A to 92G show that SaBE3, SaKKH-BE3, VQR-BE3, EQR-BE3, and VRER-BE3 mediate efficient base editing at target sites containing non-NGG PAMs in human cells. FIG. 92A shows base editor architectures using S. pyogenes and S. aureus Cas9. FIG. 92B shows recently characterized Cas9 variants with alternate or relaxed PAM requirements. FIGS. 92C and 92D show HEK293T cells treated with the base editor variants shown as described in Example 12. The percentage of total DNA sequencing reads (with no enrichment for transfected cells) with C converted to T at the target positions indicated are shown. The PAM sequence of each target tested is shown below the X-axis. The charts show the results for SaBE3 and SaKKH-BE3 at genomic loci with NNGRRT PAMs (FIG. 92C), SaBE3 and SaKKH-BE3 at genomic loci with NNNRRT PAMs (FIG. 92D), VQR-BE3 and EQR-BE3 at genomic loci with NGAG PAMs (FIG. 92E), and with NGAH PAMs (FIG. 92F), and VRER-BE3 at genomic loci with NGCG PAMs (FIG. 92G). Values and error bars reflect the mean and standard deviation of at least two biological replicates.

FIGS. 93A to 93C demonstrate that base editors with mutations in the cytidine deaminase domain exhibit narrowed editing windows. FIGS. 93A to 93C show HEK293T cells transfected with plasmids expressing mutant base editors and an appropriate sgRNA. Three days after transfection, genomic DNA was extracted and analyzed by high-throughput DNA sequencing at the indicated loci. The percentage of total DNA sequencing reads (without enrichment for transfected cells) with C changed to T at the target positions indicated are shown for the EMX1 site, HEK293 site 3, FANCF site, HEK293 site 2, site A, and site B loci. FIG. 93A illustrates certain cytidine deaminase mutations which narrow the base editing window. The sequences in FIG. 93A correspond to SEQ ID NOs: 5792 and 5793 from top to bottom, respectively. See FIG. 98 for the characterization of additional mutations. FIG. 93B shows the effect of cytidine deaminase mutations which effect the editing window width on genomic loci. Combining beneficial mutations has an additive effect on narrowing the editing window. The sequences correspond to SEQ ID NOs: 296, 295, 293, and 294 from left to right and top to bottom, respectively. FIG. 93C shows that YE1-BE3, YE2-BE3, EE-BE3, and YEE-BE3 effect the product distribution of base editing, producing predominantly singly-modified products in contrast with BE3. Values and error bars reflect the mean and standard deviation of at least two biological replicates.

FIGS. 94A and 94B show genetic variants from ClinVar that in principle can be corrected by the base editors developed in this work. The NCBI ClinVar database of human genetic variations and their corresponding phenotypes was searched for genetic diseases that in theory can be corrected by base editing. FIG. 94A demonstrates improvement in base editing targeting scope among all pathogenic T→C mutations in the ClinVar database through the use of base editors with altered PAM specificities. The white fractions denote the proportion of pathogenic T→C mutations accessible on the basis of the PAM requirements of either BE3, or BE3 together with the five modified-PAM base editors developed in this work. FIG. 94B shows improvement in base editing targeting scope among all pathogenic T→C mutations in the ClinVar database through the use of base editors with narrowed activity windows. BE3 was assumed to edit Cs in positions 4-8 with comparable efficiency as shown in FIGS. 93A to 93C. YEE-BE3 was assumed to edit with C5>C6>C7>others preference within its activity window. The white fractions denote the proportion of pathogenic T→C mutations that can be edited BE3 without comparable editing of other Cs (left), or that can be edited BE3 or YEE-BE3 without comparable editing of other Cs (right).

FIGS. 95A to 95C show the effect of truncated guide RNAs on base editing window width. HEK293T cells were transfected with plasmids expressing BE3 and sgRNAs of different 5′ truncation lengths. The treated cells were analyzed as described in the Examples. FIG. 95A shows protospacer and PAM sequence (top, SEQ ID NO: 5792) and cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, at a site within the EMX1 genomic locus. At this site, the base editing window was altered through the use of a 17-nt truncated gRNA. FIG. 95B shows protospacer and PAM sequences (top, SEQ ID NOs: 5794 and 5795 from left to right, respectively) and cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, at sites within the HEK site 3 and site 4 genomic loci. At these sites, no change in the base editing window was observed, but a linear decrease in editing efficiency for all substrate bases as the sgRNA is truncated was noted.

FIG. 96 shows the effect of APOBEC1-Cas9 linker lengths on base editing window width. HEK293T cells were transfected with plasmids expressing base editors with rAPOBEC1-Cas9 linkers of XTEN, GGS, (GGS)₃ (SEQ ID NO: 596), (GGS)₅ (SEQ ID NO: 4271), or (GGS)₇ (SEQ ID NO: 597) and an sgRNA. The treated cells were analyzed as described in the Examples. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown for the various base editors with different linkers. The sequence corresponds to SEQ ID NO: 5792.

FIGS. 97A to 97C show the effect of rAPOBEC mutations on base editing window width. FIG. 97C shows HEK293T cells transfected with plasmids expressing an sgRNA targeting either Site A or Site B and the BE3 point mutants indicated. The treated cells were analyzed as described in the Examples. All C′s in the protospacer and within three basepairs of the protospacer are displayed and the cellular C to T conversion percentages are shown. The ‘editing window widths’, defined as the calculated number of nucleotides within which editing efficiency exceeds the half-maximal value, are displayed for all tested mutants. The sequences in FIG. 97C correspond to SEQ ID NOs: 5792 and 5793 from left to right, respectively.

FIG. 98 shows the effect of APOBEC1 mutation son product distributions of base editing in mammalian cells. HEK293T cells were transfected with plasmids expressing BE3 or its mutants and an appropriate sgRNAs. The treated cells were analyzed as described in the Examples. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown (left). Percent of total sequencing reads containing the C to T conversion is shown on the right. The BE3 point mutants do not significantly affect base editing efficiencies at HEK site 4, a site with only one target cytidine. The sequence corresponds to SEQ ID NO: 297.

FIG. 99 shows a comparison of on-target editing plasma delivery in BE3 and HF-BE3.

FIG. 100 shows a comparison of on-target editing in protein and plasma delivery of BE3.

FIG. 101 shows a comparison of on-target editing in protein and plasma delivery of HF-BE3.

FIG. 102 shows that both lipofection and installing HF mutations decrease off-target deamination events. The diamond indicates no off targets were detected and the specificity ratio was set to 100.

FIG. 103 shows in vitro C to T editing on a synthetic substrate with Cs placed at even positions in the protospacer (NNNNTC₂TC₄TC₆TC₈TC₁₀TC₁₂TC₁₄TC₁₆TC₁₈TC₂₀NGG, SEQ ID NO: 4272).

FIG. 104 shows in vitro C to T editing on a synthetic substrate with Cs placed at odd positions in the protospacer (NNNNTC₂TC₄TC₆TC₈TC₁₀TC₁₂TC₁₄TC₁₆TC₁₈TC₂₀NGG, SEQ ID NO: 4272).

FIG. 105 includes two graphs depicting the specificity ratio of base editing with plasmid vs. protein delivery.

FIGS. 106A to 106B shows BE3 activity on non-NGG PAM sites. HEK293T cells were transfected with plasmids expressing BE3 and appropriate sgRNA. The treated cells were analyzed as described in the Examples. FIG. 106A shows BE3 activity on sites can be efficiently targeted by SaBE3 or SaKKH-BE3. BE3 shows low but significant activity on the NAG PAM. The sequences correspond to SEQ ID NOs: 5796 and 5797 from left to right, respectively. FIG. 106B shows BE3 has significantly reduced editing at sites with NGA or NGCG PAMs, in contrast to VQR-BE3 or VRER-BE3. The sequences correspond to SEQ ID NOs: 5798 and 5799 from left to right, respectively.

FIGS. 107A to 107B show the effect of APOBEC1 mutations on VQR-BE3 and SaKKH-BE3. HEK293T cells were transfected with plasmids expressing VQR-BE3, SaKKH-BE3 or its mutants and an appropriate sgRNAs. The treated cells were analyzed as described in the Methods. Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with Ts at the target positions indicated, are shown. FIG. 107A shows that the window-modulating mutations can be applied to VQR-BE3 to enable selective base editing at sites targetable by NGA PAM. The sequences correspond to SEQ ID NOs: 5800 and 5798 from left to right, respectively. FIG. 107B shows that, when applied to SaKKH-BE3, the mutations cause overall decrease in base editing efficiency without conferring base selectivity within the target window. The sequences correspond to SEQ ID NOs: 5796 and 5801 from left to right, respectively.

FIG. 108 shows a schematic representation of nucleotide editing. The following abbreviations are used: (MMR)—mismatch repair, (BE3 Nickase)—refers to base editor 3, which comprises a Cas9 nickase domain, (UGI)—uracil glycosylase inhibitor, UDG)—uracil DNA glycosylase, (APOBEC)—refers to an APOBEC cytidine deaminase.

DEFINITIONS

As used herein and in the claims, the singular forms “a,” “an,” and “the” include the singular and the plural reference unless the context clearly indicates otherwise. Thus, for example, a reference to “an agent” includes a single agent and a plurality of such agents.

The term “Cas9” or “Cas9 nuclease” refers to an RNA-guided nuclease comprising a Cas9 protein, or a fragment thereof (e.g., a protein comprising an active, inactive, or partially active DNA cleavage domain of Cas9, and/or the gRNA binding domain of Cas9). A Cas9 nuclease is also referred to sometimes as a casn1 nuclease or a CRISPR (clustered regularly interspaced short palindromic repeat)-associated nuclease. CRISPR is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and a Cas9 protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently, Cas9/crRNA/tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer. The target strand not complementary to crRNA is first cut endonucleolytically, then trimmed 3′-5′ exonucleolytically. In nature, DNA-binding and cleavage typically requires protein and both RNAs. However, single guide RNAs (“sgRNA”, or simply “gNRA”) can be engineered so as to incorporate aspects of both the crRNA and tracrRNA into a single RNA species. See, e.g., Jinek M., Chylinski K., Fonfara I., Hauer M., Doudna J. A., Charpentier E. Science 337:816-821(2012), the entire contents of which is hereby incorporated by reference. Cas9 recognizes a short motif in the CRISPR repeat sequences (the PAM or protospacer adjacent motif) to help distinguish self versus non-self. Cas9 nuclease sequences and structures are well known to those of skill in the art (see, e.g., “Complete genome sequence of an M1 strain of Streptococcus pyogenes.” Ferretti et al., J. J., McShan W. M., Ajdic D. J., Savic D. J., Savic G., Lyon K., Primeaux C., Sezate S., Suvorov A. N., Kenton S., Lai H. S., Lin S. P., Qian Y., Jia H. G., Najar F. Z., Ren Q., Zhu H., Song L., White J., Yuan X., Clifton S. W., Roe B. A., McLaughlin R. E., Proc. Natl. Acad. Sci. U.S.A. 98:4658-4663(2001); “CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III.” Deltcheva E., Chylinski K., Sharma C. M., Gonzales K., Chao Y., Pirzada Z. A., Eckert M. R., Vogel J., Charpentier E., Nature 471:602-607(2011); and “A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.” Jinek M., Chylinski K., Fonfara I., Hauer M., Doudna J. A., Charpentier E. Science 337:816-821(2012), the entire contents of each of which are incorporated herein by reference). Cas9 orthologs have been described in various species, including, but not limited to, S. pyogenes and S. thermophilus. Additional suitable Cas9 nucleases and sequences will be apparent to those of skill in the art based on this disclosure, and such Cas9 nucleases and sequences include Cas9 sequences from the organisms and loci disclosed in Chylinski, Rhun, and Charpentier, “The tracrRNA and Cas9 families of type II CRISPR-Cas immunity systems” (2013) RNA Biology 10:5, 726-737; the entire contents of which are incorporated herein by reference. In some embodiments, a Cas9 nuclease has an inactive (e.g., an inactivated) DNA cleavage domain, that is, the Cas9 is a nickase.

A nuclease-inactivated Cas9 protein may interchangeably be referred to as a “dCas9” protein (for nuclease-“dead” Cas9). Methods for generating a Cas9 protein (or a fragment thereof) having an inactive DNA cleavage domain are known (See, e.g., Jinek et al., Science. 337:816-821(2012); Qi et al., “Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression” (2013) Cell. 28; 152(5):1173-83, the entire contents of each of which are incorporated herein by reference). For example, the DNA cleavage domain of Cas9 is known to include two subdomains, the HNH nuclease subdomain and the RuvC1 subdomain. The HNH subdomain cleaves the strand complementary to the gRNA, whereas the RuvC1 subdomain cleaves the non-complementary strand. Mutations within these subdomains can silence the nuclease activity of Cas9. For example, the mutations D10A and H840A completely inactivate the nuclease activity of S. pyogenes Cas9 (Jinek et al., Science. 337:816-821(2012); Qi et al., Cell. 28; 152(5):1173-83 (2013)). In some embodiments, proteins comprising fragments of Cas9 are provided. For example, in some embodiments, a protein comprises one of two Cas9 domains: (1) the gRNA binding domain of Cas9; or (2) the DNA cleavage domain of Cas9. In some embodiments, proteins comprising Cas9 or fragments thereof are referred to as “Cas9 variants.” A Cas9 variant shares homology to Cas9, or a fragment thereof. For example a Cas9 variant is at least about 70% identical, at least about 80% identical, at least about 90% identical, at least about 95% identical, at least about 96% identical, at least about 97% identical, at least about 98% identical, at least about 99% identical, at least about 99.5% identical, or at least about 99.9% identical to wild type Cas9. In some embodiments, the Cas9 variant may have 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 21, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50 or more amino acid changes compared to wild type Cas9. In some embodiments, the Cas9 variant comprises a fragment of Cas9 (e.g., a gRNA binding domain or a DNA-cleavage domain), such that the fragment is at least about 70% identical, at least about 80% identical, at least about 90% identical, at least about 95% identical, at least about 96% identical, at least about 97% identical, at least about 98% identical, at least about 99% identical, at least about 99.5% identical, or at least about 99.9% identical to the corresponding fragment of wild type Cas9. In some embodiments, the fragment is at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% identical, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% of the amino acid length of a corresponding wild type Cas9.

In some embodiments, the fragment is at least 100 amino acids in length. In some embodiments, the fragment is at least 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, or at least 1300 amino acids in length. In some embodiments, wild type Cas9 corresponds to Cas9 from Streptococcus pyogenes (NCBI Reference Sequence: NC_017053.1, SEQ ID NO:1 (nucleotide); SEQ ID NO:2 (amino acid)).

(SEQ ID NO: 1)
ATGGATAAGAAATACTCAATAGGCTTAGATATCGGCACAAATAGCGTCGG
ATGGGCGGTGATCACTGATGATTATAAGGTTCCGTCTAAAAAGTTCAAGG
TTCTGGGAAATACAGACCGCCACAGTATCAAAAAAAATCTTATAGGGGCT
CTTTTATTTGGCAGTGGAGAGACAGCGGAAGCGACTCGTCTCAAACGGAC
AGCTCGTAGAAGGTATACACGTCGGAAGAATCGTATTTGTTATCTACAGG
AGATTTTTTCAAATGAGATGGCGAAAGTAGATGATAGTTTCTTTCATCGA
CTTGAAGAGTCTTTTTTGGTGGAAGAAGACAAGAAGCATGAACGTCATCC
TATTTTTGGAAATATAGTAGATGAAGTTGCTTATCATGAGAAATATCCAA
CTATCTATCATCTGCGAAAAAAATTGGCAGATTCTACTGATAAAGCGGAT
TTGCGCTTAATCTATTTGGCCTTAGCGCATATGATTAAGTTTCGTGGTCA
TTTTTTGATTGAGGGAGATTTAAATCCTGATAATAGTGATGTGGACAAAC
TATTTATCCAGTTGGTACAAATCTACAATCAATTATTTGAAGAAAACCCT
ATTAACGCAAGTAGAGTAGATGCTAAAGCGATTCTTTCTGCACGATTGAG
TAAATCAAGACGATTAGAAAATCTCATTGCTCAGCTCCCCGGTGAGAAGA
GAAATGGCTTGTTTGGGAATCTCATTGCTTTGTCATTGGGATTGACCCCT
AATTTTAAATCAAATTTTGATTTGGCAGAAGATGCTAAATTACAGCTTTC
AAAAGATACTTACGATGATGATTTAGATAATTTATTGGCGCAAATTGGAG
ATCAATATGCTGATTTGTTTTTGGCAGCTAAGAATTTATCAGATGCTATT
TTACTTTCAGATATCCTAAGAGTAAATAGTGAAATAACTAAGGCTCCCCT
ATCAGCTTCAATGATTAAGCGCTACGATGAACATCATCAAGACTTGACTC
TTTTAAAAGCTTTAGTTCGACAACAACTTCCAGAAAAGTATAAAGAAATC
TTTTTTGATCAATCAAAAAACGGATATGCAGGTTATATTGATGGGGGAGC
TAGCCAAGAAGAATTTTATAAATTTATCAAACCAATTTTAGAAAAAATGG
ATGGTACTGAGGAATTATTGGTGAAACTAAATCGTGAAGATTTGCTGCGC
AAGCAACGGACCTTTGACAACGGCTCTATTCCCCATCAAATTCACTTGGG
TGAGCTGCATGCTATTTTGAGAAGACAAGAAGACTTTTATCCATTTTTAA
AAGACAATCGTGAGAAGATTGAAAAAATCTTGACTTTTCGAATTCCTTAT
TATGTTGGTCCATTGGCGCGTGGCAATAGTCGTTTTGCATGGATGACTCG
GAAGTCTGAAGAAACAATTACCCCATGGAATTTTGAAGAAGTTGTCGATA
AAGGTGCTTCAGCTCAATCATTTATTGAACGCATGACAAACTTTGATAAA
AATCTTCCAAATGAAAAAGTACTACCAAAACATAGTTTGCTTTATGAGTA
TTTTACGGTTTATAACGAATTGACAAAGGTCAAATATGTTACTGAGGGAA
TGCGAAAACCAGCATTTCTTTCAGGTGAACAGAAGAAAGCCATTGTTGAT
TTACTCTTCAAAACAAATCGAAAAGTAACCGTTAAGCAATTAAAAGAAGA
TTATTTCAAAAAAATAGAATGTTTTGATAGTGTTGAAATTTCAGGAGTTG
AAGATAGATTTAATGCTTCATTAGGCGCCTACCATGATTTGCTAAAAATT
ATTAAAGATAAAGATTTTTTGGATAATGAAGAAAATGAAGATATCTTAGA
GGATATTGTTTTAACATTGACCTTATTTGAAGATAGGGGGATGATTGAGG
AAAGACTTAAAACATATGCTCACCTCTTTGATGATAAGGTGATGAAACAG
CTTAAACGTCGCCGTTATACTGGTTGGGGACGTTTGTCTCGAAAATTGAT
TAATGGTATTAGGGATAAGCAATCTGGCAAAACAATATTAGATTTTTTGA
AATCAGATGGTTTTGCCAATCGCAATTTTATGCAGCTGATCCATGATGAT
AGTTTGACATTTAAAGAAGATATTCAAAAAGCACAGGTGTCTGGACAAGG
CCATAGTTTACATGAACAGATTGCTAACTTAGCTGGCAGTCCTGCTATTA
AAAAAGGTATTTTACAGACTGTAAAAATTGTTGATGAACTGGTCAAAGTA
ATGGGGCATAAGCCAGAAAATATCGTTATTGAAATGGCACGTGAAAATCA
GACAACTCAAAAGGGCCAGAAAAATTCGCGAGAGCGTATGAAACGAATCG
AAGAAGGTATCAAAGAATTAGGAAGTCAGATTCTTAAAGAGCATCCTGTT
GAAAATACTCAATTGCAAAATGAAAAGCTCTATCTCTATTATCTACAAAA
TGGAAGAGACATGTATGTGGACCAAGAATTAGATATTAATCGTTTAAGTG
ATTATGATGTCGATCACATTGTTCCACAAAGTTTCATTAAAGACGATTCA
ATAGACAATAAGGTACTAACGCGTTCTGATAAAAATCGTGGTAAATCGGA
TAACGTTCCAAGTGAAGAAGTAGTCAAAAAGATGAAAAACTATTGGAGAC
AACTTCTAAACGCCAAGTTAATCACTCAACGTAAGTTTGATAATTTAACG
AAAGCTGAACGTGGAGGTTTGAGTGAACTTGATAAAGCTGGTTTTATCAA
ACGCCAATTGGTTGAAACTCGCCAAATCACTAAGCATGTGGCACAAATTT
TGGATAGTCGCATGAATACTAAATACGATGAAAATGATAAACTTATTCGA
GAGGTTAAAGTGATTACCTTAAAATCTAAATTAGTTTCTGACTTCCGAAA
AGATTTCCAATTCTATAAAGTACGTGAGATTAACAATTACCATCATGCCC
ATGATGCGTATCTAAATGCCGTCGTTGGAACTGCTTTGATTAAGAAATAT
CCAAAACTTGAATCGGAGTTTGTCTATGGTGATTATAAAGTTTATGATGT
TCGTAAAATGATTGCTAAGTCTGAGCAAGAAATAGGCAAAGCAACCGCAA
AATATTTCTTTTACTCTAATATCATGAACTTCTTCAAAACAGAAATTACA
CTTGCAAATGGAGAGATTCGCAAACGCCCTCTAATCGAAACTAATGGGGA
AACTGGAGAAATTGTCTGGGATAAAGGGCGAGATTTTGCCACAGTGCGCA
AAGTATTGTCCATGCCCCAAGTCAATATTGTCAAGAAAACAGAAGTACAG
ACAGGCGGATTCTCCAAGGAGTCAATTTTACCAAAAAGAAATTCGGACAA
GCTTATTGCTCGTAAAAAAGACTGGGATCCAAAAAAATATGGTGGTTTTG
ATAGTCCAACGGTAGCTTATTCAGTCCTAGTGGTTGCTAAGGTGGAAAAA
GGGAAATCGAAGAAGTTAAAATCCGTTAAAGAGTTACTAGGGATCACAAT
TATGGAAAGAAGTTCCTTTGAAAAAAATCCGATTGACTTTTTAGAAGCTA
AAGGATATAAGGAAGTTAAAAAAGACTTAATCATTAAACTACCTAAATAT
AGTCTTTTTGAGTTAGAAAACGGTCGTAAACGGATGCTGGCTAGTGCCGG
AGAATTACAAAAAGGAAATGAGCTGGCTCTGCCAAGCAAATATGTGAATT
TTTTATATTTAGCTAGTCATTATGAAAAGTTGAAGGGTAGTCCAGAAGAT
AACGAACAAAAACAATTGTTTGTGGAGCAGCATAAGCATTATTTAGATGA
GATTATTGAGCAAATCAGTGAATTTTCTAAGCGTGTTATTTTAGCAGATG
CCAATTTAGATAAAGTTCTTAGTGCATATAACAAACATAGAGACAAACCA
ATACGTGAACAAGCAGAAAATATTATTCATTTATTTACGTTGACGAATCT
TGGAGCTCCCGCTGCTTTTAAATATTTTGATACAACAATTGATCGTAAAC
GATATACGTCTACAAAAGAAGTTTTAGATGCCACTCTTATCCATCAATCC
ATCACTGGTCTTTATGAAACACGCATTGATTTGAGTCAGCTAGGAGGTGA
CTGA
(SEQ ID NO: 2)
MDKKYSIGLDIGTNSVGWAVITDDYKVPSKKFKVLGNTDRHSIKKNLIG
ALLFGSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSF
FHRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLAD
STDKADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQI
YNQLFEENPINASRVDAKAILSARLSKSRRLENLIAQLPGEKRNGLF
GNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQ
YADLFLAAKNLSDAILLSDILRVNSEITKAPLSASMIKRYDEHHQDL
TLLKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPI
LEKMDGTEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQ
EDFYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETI
TPWNFEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTV
YNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKED
YFKKIECFDSVEISGVEDRFNASLGAYHDLLKIIKDKDFLDNEENE
DILEDIVLTLTLFEDRGMIEERLKTYAHLFDDKVMKQLKRRRYTGW
GRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFK
EDIQKAQVSGQGHSLHEQIANLAGSPAIKKGILQTVKIVDELVKVM
GHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKE
HPVENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQ
SFIKDDSIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAK
LITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQITKHVAQILD
SRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVREINNYH
HAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQE
IGKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVW
DKGRDFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLI
ARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGI
TIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKR
MLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQLF
VEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIRE
QAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQ
SITGLYETRIDLSQLGGD

(single underline: HNH domain; double underline: RuvC domain)

In some embodiments, wild type Cas9 corresponds to, or comprises SEQ ID NO:3 (nucleotide) and/or SEQ ID NO: 4 (amino acid):

(SEQ ID NO: 3)
ATGGATAAAAAGTATTCTATTGGTTTAGACATCGGCACTAATTCCGTTG
GATGGGCTGTCATAACCGATGAATACAAAGTACCTTCAAAGAAATTTAA
GGTGTTGGGGAACACAGACCGTCATTCGATTAAAAAGAATCTTATCGGT
GCCCTCCTATTCGATAGTGGCGAAACGGCAGAGGCGACTCGCCTGAAAC
GAACCGCTCGGAGAAGGTATACACGTCGCAAGAACCGAATATGTTACTT
ACAAGAAATTTTTAGCAATGAGATGGCCAAAGTTGACGATTCTTTCTTT
CACCGTTTGGAAGAGTCCTTCCTTGTCGAAGAGGACAAGAAACATGAAC
GGCACCCCATCTTTGGAAACATAGTAGATGAGGTGGCATATCATGAAAA
GTACCCAACGATTTATCACCTCAGAAAAAAGCTAGTTGACTCAACTGAT
AAAGCGGACCTGAGGTTAATCTACTTGGCTCTTGCCCATATGATAAAGT
TCCGTGGGCACTTTCTCATTGAGGGTGATCTAAATCCGGACAACTCGGA
TGTCGACAAACTGTTCATCCAGTTAGTACAAACCTATAATCAGTTGTTT
GAAGAGAACCCTATAAATGCAAGTGGCGTGGATGCGAAGGCTATTCTTA
GCGCCCGCCTCTCTAAATCCCGACGGCTAGAAAACCTGATCGCACAATT
ACCCGGAGAGAAGAAAAATGGGTTGTTCGGTAACCTTATAGCGCTCTCA
CTAGGCCTGACACCAAATTTTAAGTCGAACTTCGACTTAGCTGAAGATG
CCAAATTGCAGCTTAGTAAGGACACGTACGATGACGATCTCGACAATCT
ACTGGCACAAATTGGAGATCAGTATGCGGACTTATTTTTGGCTGCCAAA
AACCTTAGCGATGCAATCCTCCTATCTGACATACTGAGAGTTAATACTG
AGATTACCAAGGCGCCGTTATCCGCTTCAATGATCAAAAGGTACGATGA
ACATCACCAAGACTTGACACTTCTCAAGGCCCTAGTCCGTCAGCAACTG
CCTGAGAAATATAAGGAAATATTCTTTGATCAGTCGAAAAACGGGTACG
CAGGTTATATTGACGGCGGAGCGAGTCAAGAGGAATTCTACAAGTTTAT
CAAACCCATATTAGAGAAGATGGATGGGACGGAAGAGTTGCTTGTAAAA
CTCAATCGCGAAGATCTACTGCGAAAGCAGCGGACTTTCGACAACGGTA
GCATTCCACATCAAATCCACTTAGGCGAATTGCATGCTATACTTAGAAG
GCAGGAGGATTTTTATCCGTTCCTCAAAGACAATCGTGAAAAGATTGAG
AAAATCCTAACCTTTCGCATACCTTACTATGTGGGACCCCTGGCCCGAG
GGAACTCTCGGTTCGCATGGATGACAAGAAAGTCCGAAGAAACGATTAC
TCCATGGAATTTTGAGGAAGTTGTCGATAAAGGTGCGTCAGCTCAATCG
TTCATCGAGAGGATGACCAACTTTGACAAGAATTTACCGAACGAAAAAG
TATTGCCTAAGCACAGTTTACTTTACGAGTATTTCACAGTGTACAATGA
ACTCACGAAAGTTAAGTATGTCACTGAGGGCATGCGTAAACCCGCCTTT
CTAAGCGGAGAACAGAAGAAAGCAATAGTAGATCTGTTATTCAAGACCA
ACCGCAAAGTGACAGTTAAGCAATTGAAAGAGGACTACTTTAAGAAAAT
TGAATGCTTCGATTCTGTCGAGATCTCCGGGGTAGAAGATCGATTTAAT
GCGTCACTTGGTACGTATCATGACCTCCTAAAGATAATTAAAGATAAGG
ACTTCCTGGATAACGAAGAGAATGAAGATATCTTAGAAGATATAGTGTT
GACTCTTACCCTCTTTGAAGATCGGGAAATGATTGAGGAAAGACTAAAA
ACATACGCTCACCTGTTCGACGATAAGGTTATGAAACAGTTAAAGAGGC
GTCGCTATACGGGCTGGGGACGATTGTCGCGGAAACTTATCAACGGGAT
AAGAGACAAGCAAAGTGGTAAAACTATTCTCGATTTTCTAAAGAGCGAC
GGCTTCGCCAATAGGAACTTTATGCAGCTGATCCATGATGACTCTTTAA
CCTTCAAAGAGGATATACAAAAGGCACAGGTTTCCGGACAAGGGGACTC
ATTGCACGAACATATTGCGAATCTTGCTGGTTCGCCAGCCATCAAAAAG
GGCATACTCCAGACAGTCAAAGTAGTGGATGAGCTAGTTAAGGTCATGG
GACGTCACAAACCGGAAAACATTGTAATCGAGATGGCACGCGAAAATCA
AACGACTCAGAAGGGGCAAAAAAACAGTCGAGAGCGGATGAAGAGAATA
GAAGAGGGTATTAAAGAACTGGGCAGCCAGATCTTAAAGGAGCATCCTG
TGGAAAATACCCAATTGCAGAACGAGAAACTTTACCTCTATTACCTACA
AAATGGAAGGGACATGTATGTTGATCAGGAACTGGACATAAACCGTTTA
TCTGATTACGACGTCGATCACATTGTACCCCAATCCTTTTTGAAGGACG
ATTCAATCGACAATAAAGTGCTTACACGCTCGGATAAGAACCGAGGGAA
AAGTGACAATGTTCCAAGCGAGGAAGTCGTAAAGAAAATGAAGAACTAT
TGGCGGCAGCTCCTAAATGCGAAACTGATAACGCAAAGAAAGTTCGATA
ACTTAACTAAAGCTGAGAGGGGTGGCTTGTCTGAACTTGACAAGGCCGG
ATTTATTAAACGTCAGCTCGTGGAAACCCGCCAAATCACAAAGCATGTT
GCACAGATACTAGATTCCCGAATGAATACGAAATACGACGAGAACGATA
AGCTGATTCGGGAAGTCAAAGTAATCACTTTAAAGTCAAAATTGGTGTC
GGACTTCAGAAAGGATTTTCAATTCTATAAAGTTAGGGAGATAAATAAC
TACCACCATGCGCACGACGCTTATCTTAATGCCGTCGTAGGGACCGCAC
TCATTAAGAAATACCCGAAGCTAGAAAGTGAGTTTGTGTATGGTGATTA
CAAAGTTTATGACGTCCGTAAGATGATCGCGAAAAGCGAACAGGAGATA
GGCAAGGCTACAGCCAAATACTTCTTTTATTCTAACATTATGAATTTCT
TTAAGACGGAAATCACTCTGGCAAACGGAGAGATACGCAAACGACCTTT
AATTGAAACCAATGGGGAGACAGGTGAAATCGTATGGGATAAGGGCCGG
GACTTCGCGACGGTGAGAAAAGTTTTGTCCATGCCCCAAGTCAACATAG
TAAAGAAAACTGAGGTGCAGACCGGAGGGTTTTCAAAGGAATCGATTCT
TCCAAAAAGGAATAGTGATAAGCTCATCGCTCGTAAAAAGGACTGGGAC
CCGAAAAAGTACGGTGGCTTCGATAGCCCTACAGTTGCCTATTCTGTCC
TAGTAGTGGCAAAAGTTGAGAAGGGAAAATCCAAGAAACTGAAGTCAGT
CAAAGAATTATTGGGGATAACGATTATGGAGCGCTCGTCTTTTGAAAAG
AACCCCATCGACTTCCTTGAGGCGAAAGGTTACAAGGAAGTAAAAAAGG
ATCTCATAATTAAACTACCAAAGTATAGTCTGTTTGAGTTAGAAAATGG
CCGAAAACGGATGTTGGCTAGCGCCGGAGAGCTTCAAAAGGGGAACGAA
CTCGCACTACCGTCTAAATACGTGAATTTCCTGTATTTAGCGTCCCATT
ACGAGAAGTTGAAAGGTTCACCTGAAGATAACGAACAGAAGCAACTTTT
TGTTGAGCAGCACAAACATTATCTCGACGAAATCATAGAGCAAATTTCG
GAATTCAGTAAGAGAGTCATCCTAGCTGATGCCAATCTGGACAAAGTAT
TAAGCGCATACAACAAGCACAGGGATAAACCCATACGTGAGCAGGCGGA
AAATATTATCCATTTGTTTACTCTTACCAACCTCGGCGCTCCAGCCGCA
TTCAAGTATTTTGACACAACGATAGATCGCAAACGATACACTTCTACCA
AGGAGGTGCTAGACGCGACACTGATTCACCAATCCATCACGGGATTATA
TGAAACTCGGATAGATTTGTCACAGCTTGGGGGTGACGGATCCCCCAAG
AAGAAGAGGAAAGTCTCGAGCGACTACAAAGACCATGACGGTGATTATA
AAGATCATGACATCGATTACAAGGATGACGATGACAAGGCTGCAGGA
(SEQ ID NO: 4)
MDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIG
ALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFF
HRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTD
KADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLF
EENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALS
LGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAK
NLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQL
PEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVK
LNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIE
KILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQS
FIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAF
LSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFN
ASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLK
TYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSD
GFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKK
GILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKGQKNSRERMKRI
EEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDMYVDQELDINRL
SDYDVDHIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNY
WRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQITKHV
AQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVREINN
YHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQEI
GKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDKGR
DFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEK
NPIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNE
LALPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQIS
EFSKRVILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAA
FKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGD

(single underline: HNH domain; double underline: RuvC domain)

In some embodiments, wild type Cas9 corresponds to Cas9 from Streptococcus pyogenes (NCBI Reference Sequence: NC_002737.2, SEQ ID NO: 8 (nucleotide); and Uniport Reference Sequence: Q99ZW2, SEQ ID NO: 10 (amino acid).

(SEQ ID NO: 8)
ATGGATAAGAAATACTCAATAGGCTTAGATATCGGCACAAATAGCGTCGG
ATGGGCGGTGATCACTGATGAATATAAGGTTCCGTCTAAAAAGTTCAAGG
TTCTGGGAAATACAGACCGCCACAGTATCAAAAAAAATCTTATAGGGGCT
CTTTTATTTGACAGTGGAGAGACAGCGGAAGCGACTCGTCTCAAACGGAC
AGCTCGTAGAAGGTATACACGTCGGAAGAATCGTATTTGTTATCTACAGG
AGATTTTTTCAAATGAGATGGCGAAAGTAGATGATAGTTTCTTTCATCGA
CTTGAAGAGTCTTTTTTGGTGGAAGAAGACAAGAAGCATGAACGTCATCC
TATTTTTGGAAATATAGTAGATGAAGTTGCTTATCATGAGAAATATCCAA
CTATCTATCATCTGCGAAAAAAATTGGTAGATTCTACTGATAAAGCGGAT
TTGCGCTTAATCTATTTGGCCTTAGCGCATATGATTAAGTTTCGTGGTCA
TTTTTTGATTGAGGGAGATTTAAATCCTGATAATAGTGATGTGGACAAAC
TATTTATCCAGTTGGTACAAACCTACAATCAATTATTTGAAGAAAACCCT
ATTAACGCAAGTGGAGTAGATGCTAAAGCGATTCTTTCTGCACGATTGAG
TAAATCAAGACGATTAGAAAATCTCATTGCTCAGCTCCCCGGTGAGAAGA
AAAATGGCTTATTTGGGAATCTCATTGCTTTGTCATTGGGTTTGACCCCT
AATTTTAAATCAAATTTTGATTTGGCAGAAGATGCTAAATTACAGCTTTC
AAAAGATACTTACGATGATGATTTAGATAATTTATTGGCGCAAATTGGAG
ATCAATATGCTGATTTGTTTTTGGCAGCTAAGAATTTATCAGATGCTATT
TTACTTTCAGATATCCTAAGAGTAAATACTGAAATAACTAAGGCTCCCCT
ATCAGCTTCAATGATTAAACGCTACGATGAACATCATCAAGACTTGACTC
TTTTAAAAGCTTTAGTTCGACAACAACTTCCAGAAAAGTATAAAGAAATC
TTTTTTGATCAATCAAAAAACGGATATGCAGGTTATATTGATGGGGGAGC
TAGCCAAGAAGAATTTTATAAATTTATCAAACCAATTTTAGAAAAAATGG
ATGGTACTGAGGAATTATTGGTGAAACTAAATCGTGAAGATTTGCTGCGC
AAGCAACGGACCTTTGACAACGGCTCTATTCCCCATCAAATTCACTTGGG
TGAGCTGCATGCTATTTTGAGAAGACAAGAAGACTTTTATCCATTTTTAA
AAGACAATCGTGAGAAGATTGAAAAAATCTTGACTTTTCGAATTCCTTAT
TATGTTGGTCCATTGGCGCGTGGCAATAGTCGTTTTGCATGGATGACTCG
GAAGTCTGAAGAAACAATTACCCCATGGAATTTTGAAGAAGTTGTCGATA
AAGGTGCTTCAGCTCAATCATTTATTGAACGCATGACAAACTTTGATAAA
AATCTTCCAAATGAAAAAGTACTACCAAAACATAGTTTGCTTTATGAGTA
TTTTACGGTTTATAACGAATTGACAAAGGTCAAATATGTTACTGAAGGAA
TGCGAAAACCAGCATTTCTTTCAGGTGAACAGAAGAAAGCCATTGTTGAT
TTACTCTTCAAAACAAATCGAAAAGTAACCGTTAAGCAATTAAAAGAAGA
TTATTTCAAAAAAATAGAATGTTTTGATAGTGTTGAAATTTCAGGAGTTG
AAGATAGATTTAATGCTTCATTAGGTACCTACCATGATTTGCTAAAAATT
ATTAAAGATAAAGATTTTTTGGATAATGAAGAAAATGAAGATATCTTAGA
GGATATTGTTTTAACATTGACCTTATTTGAAGATAGGGAGATGATTGAGG
AAAGACTTAAAACATATGCTCACCTCTTTGATGATAAGGTGATGAAACAG
CTTAAACGTCGCCGTTATACTGGTTGGGGACGTTTGTCTCGAAAATTGAT
TAATGGTATTAGGGATAAGCAATCTGGCAAAACAATATTAGATTTTTTGA
AATCAGATGGTTTTGCCAATCGCAATTTTATGCAGCTGATCCATGATGAT
AGTTTGACATTTAAAGAAGACATTCAAAAAGCACAAGTGTCTGGACAAGG
CGATAGTTTACATGAACATATTGCAAATTTAGCTGGTAGCCCTGCTATTA
AAAAAGGTATTTTACAGACTGTAAAAGTTGTTGATGAATTGGTCAAAGTA
ATGGGGCGGCATAAGCCAGAAAATATCGTTATTGAAATGGCACGTGAAAA
TCAGACAACTCAAAAGGGCCAGAAAAATTCGCGAGAGCGTATGAAACGAA
TCGAAGAAGGTATCAAAGAATTAGGAAGTCAGATTCTTAAAGAGCATCCT
GTTGAAAATACTCAATTGCAAAATGAAAAGCTCTATCTCTATTATCTCCA
AAATGGAAGAGACATGTATGTGGACCAAGAATTAGATATTAATCGTTTAA
GTGATTATGATGTCGATCACATTGTTCCACAAAGTTTCCTTAAAGACGAT
TCAATAGACAATAAGGTCTTAACGCGTTCTGATAAAAATCGTGGTAAATC
GGATAACGTTCCAAGTGAAGAAGTAGTCAAAAAGATGAAAAACTATTGGA
GACAACTTCTAAACGCCAAGTTAATCACTCAACGTAAGTTTGATAATTTA
ACGAAAGCTGAACGTGGAGGTTTGAGTGAACTTGATAAAGCTGGTTTTAT
CAAACGCCAATTGGTTGAAACTCGCCAAATCACTAAGCATGTGGCACAAA
TTTTGGATAGTCGCATGAATACTAAATACGATGAAAATGATAAACTTATT
CGAGAGGTTAAAGTGATTACCTTAAAATCTAAATTAGTTTCTGACTTCCG
AAAAGATTTCCAATTCTATAAAGTACGTGAGATTAACAATTACCATCATG
CCCATGATGCGTATCTAAATGCCGTCGTTGGAACTGCTTTGATTAAGAAA
TATCCAAAACTTGAATCGGAGTTTGTCTATGGTGATTATAAAGTTTATGA
TGTTCGTAAAATGATTGCTAAGTCTGAGCAAGAAATAGGCAAAGCAACCG
CAAAATATTTCTTTTACTCTAATATCATGAACTTCTTCAAAACAGAAATT
ACACTTGCAAATGGAGAGATTCGCAAACGCCCTCTAATCGAAACTAATGG
GGAAACTGGAGAAATTGTCTGGGATAAAGGGCGAGATTTTGCCACAGTGC
GCAAAGTATTGTCCATGCCCCAAGTCAATATTGTCAAGAAAACAGAAGTA
CAGACAGGCGGATTCTCCAAGGAGTCAATTTTACCAAAAAGAAATTCGGA
CAAGCTTATTGCTCGTAAAAAAGACTGGGATCCAAAAAAATATGGTGGTT
TTGATAGTCCAACGGTAGCTTATTCAGTCCTAGTGGTTGCTAAGGTGGAA
AAAGGGAAATCGAAGAAGTTAAAATCCGTTAAAGAGTTACTAGGGATCAC
AATTATGGAAAGAAGTTCCTTTGAAAAAAATCCGATTGACTTTTTAGAAG
CTAAAGGATATAAGGAAGTTAAAAAAGACTTAATCATTAAACTACCTAAA
TATAGTCTTTTTGAGTTAGAAAACGGTCGTAAACGGATGCTGGCTAGTGC
CGGAGAATTACAAAAAGGAAATGAGCTGGCTCTGCCAAGCAAATATGTGA
ATTTTTTATATTTAGCTAGTCATTATGAAAAGTTGAAGGGTAGTCCAGAA
GATAACGAACAAAAACAATTGTTTGTGGAGCAGCATAAGCATTATTTAGA
TGAGATTATTGAGCAAATCAGTGAATTTTCTAAGCGTGTTATTTTAGCAG
ATGCCAATTTAGATAAAGTTCTTAGTGCATATAACAAACATAGAGACAAA
CCAATACGTGAACAAGCAGAAAATATTATTCATTTATTTACGTTGACGAA
TCTTGGAGCTCCCGCTGCTTTTAAATATTTTGATACAACAATTGATCGTA
AACGATATACGTCTACAAAAGAAGTTTTAGATGCCACTCTTATCCATCAA
TCCATCACTGGTCTTTATGAAACACGCATTGATTTGAGTCAGCTAGGAGG
TGACTGA
(SEQ ID NO: 10)
MDKKYSIGLDIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGA
LLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHR
LEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKAD
LRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENP
INASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTP
NFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAI
LLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEI
FFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLR
KQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPY
YVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDK
NLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVD
LLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKI
IKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQ
LKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDD
SLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKV
MGRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHP
VENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDD
SIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNL
TKAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLI
REVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKK
YPKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEI
TLANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEV
QTGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVE
KGKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPK
YSLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPE
DNEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDK
PIREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQ
SITGLYETRIDLSQLGGD

10) (single underline: HNH domain; double underline: RuvC domain)

In some embodiments, Cas9 refers to Cas9 from: Corynebacterium ulcerans (NCBI Refs: NC_015683.1, NC_017317.1); Corynebacterium diphtheria (NCBI Refs: NC_016782.1, NC_016786.1); Spiroplasma syrphidicola (NCBI Ref: NC_021284.1); Prevotella intermedia (NCBI Ref: NC_017861.1); Spiroplasma taiwanense (NCBI Ref: NC_021846.1); Streptococcus iniae (NCBI Ref: NC_021314.1); Belliella baltica (NCBI Ref: NC_018010.1); Psychroflexus torquisI (NCBI Ref: NC_018721.1); Streptococcus thermophilus (NCBI Ref: YP_820832.1), Listeria innocua (NCBI Ref: NP_472073.1), Campylobacter jejuni (NCBI Ref: YP_002344900.1) or Neisseria. meningitidis (NCBI Ref: YP_002342100.1) or to a Cas9 from any of the organisms listed in Example 5.

In some embodiments, dCas9 corresponds to, or comprises in part or in whole, a Cas9 amino acid sequence having one or more mutations that inactivate the Cas9 nuclease activity. For example, in some embodiments, a dCas9 domain comprises D10A and/or H840A mutation.

(SEQ ID NO: 9)
dCas9 (D10A and H840A):
MDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDS
GET              AEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFLVEEDKK
HERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYLALAHMIKFRGHFLI
EGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIAQ
LPGEKKNGLFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQ
YADLFLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQL
PEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLARGNSR
FAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYF
TVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIEC
FDSVEISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFEDREMIEE
RLKTYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFAN
NTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDAIVPQSFLKDDSIDNKV
TVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLI
IKLPKYSLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDN
EQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQAENIIH
LFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGD

(single underline: HNH domain; double underline: RuvC domain).

In some embodiments, the Cas9 domain comprises a D10A mutation, while the residue at position 840 remains a histidine in the amino acid sequence provided in SEQ ID NO: 10, or at corresponding positions in any of the amino acid sequences provided in SEQ ID NOs: 11-260. Without wishing to be bound by any particular theory, the presence of the catalytic residue H840 restores the acvitity of the Cas9 to cleave the non-edited (e.g., non-deaminated) strand containing a G opposite the targeted C. Restoration of H840 (e.g., from A840) does not result in the cleavage of the target strand containing the C. Such Cas9 variants are able to generate a single-strand DNA break (nick) at a specific location based on the gRNA-defined target sequence, leading to repair of the non-edited strand, ultimately resulting in a G to A change on the non-edited strand. A schematic representation of this process is shown in FIG. 108. Briefly, the C of a C-G basepair can be deaminated to a U by a deaminase, e.g., an APOBEC deamonase. Nicking the non-edited strand, having the G, facilitates removal of the G via mismatch repair mechanisms. UGI inhibits UDG, which prevents removal of the U.

In other embodiments, dCas9 variants having mutations other than D10A and H840A are provided, which, e.g., result in nuclease inactivated Cas9 (dCas9). Such mutations, by way of example, include other amino acid substitutions at D10 and H820, or other substitutions within the nuclease domains of Cas9 (e.g., substitutions in the HNH nuclease subdomain and/or the RuvC1 subdomain). In some embodiments, variants or homologues of dCas9 (e.g., variants of SEQ ID NO: 10) are provided which are at least about 70% identical, at least about 80% identical, at least about 90% identical, at least about 95% identical, at least about 98% identical, at least about 99% identical, at least about 99.5% identical, or at least about 99.9% identical to SEQ ID NO: 10. In some embodiments, variants of dCas9 (e.g., variants of SEQ ID NO: 10) are provided having amino acid sequences which are shorter, or longer than SEQ ID NO: 10, by about 5 amino acids, by about 10 amino acids, by about 15 amino acids, by about 20 amino acids, by about 25 amino acids, by about 30 amino acids, by about 40 amino acids, by about 50 amino acids, by about 75 amino acids, by about 100 amino acids or more.

In some embodiments, Cas9 fusion proteins as provided herein comprise the full-length amino acid sequence of a Cas9 protein, e.g., one of the Cas9 sequences provided herein. In other embodiments, however, fusion proteins as provided herein do not comprise a full-length Cas9 sequence, but only a fragment thereof. For example, in some embodiments, a Cas9 fusion protein provided herein comprises a Cas9 fragment, wherein the fragment binds crRNA and tracrRNA or sgRNA, but does not comprise a functional nuclease domain, e.g., in that it comprises only a truncated version of a nuclease domain or no nuclease domain at all. Exemplary amino acid sequences of suitable Cas9 domains and Cas9 fragments are provided herein, and additional suitable sequences of Cas9 domains and fragments will be apparent to those of skill in the art.

In some embodiments, Cas9 refers to Cas9 from: Corynebacterium ulcerans (NCBI Refs: NC_015683.1, NC_017317.1); Corynebacterium diphtheria (NCBI Refs: NC_016782.1, NC_016786.1); Spiroplasma syrphidicola (NCBI Ref: NC_021284.1); Prevotella intermedia (NCBI Ref: NC_017861.1); Spiroplasma taiwanense (NCBI Ref: NC_021846.1); Streptococcus iniae (NCBI Ref: NC_021314.1); Belliella baltica (NCBI Ref: NC_018010.1); Psychroflexus torquisI (NCBI Ref: NC_018721.1); Streptococcus thermophilus (NCBI Ref: YP_820832.1); Listeria innocua (NCBI Ref: NP_472073.1); Campylobacter jejuni (NCBI Ref: YP_002344900.1); or Neisseria. meningitidis (NCBI Ref: YP_002342100.1).

The term “deaminase” or “deaminase domain,” as used herein, refers to a protein or enzyme that catalyzes a deamination reaction. In some embodiments, the deaminase or deaminase domain is a cytidine deaminase, catalyzing the hydrolytic deamination of cytidine or deoxycytidine to uridine or deoxyuridine, respectively. In some embodiments, the deaminase or deaminase domain is a cytidine deaminase domain, catalyzing the hydrolytic deamination of cytosine to uracil. In some embodiments, the deaminase or deaminase domain is a naturally-occuring deaminase from an organism, such as a human, chimpanzee, gorilla, monkey, cow, dog, rat, or mouse. In some embodiments, the deaminase or deaminase domain is a variant of a naturally-occuring deaminase from an organism, that does not occur in nature. For example, in some embodiments, the deaminase or deaminase domain is at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75% at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to a naturally-occuring deaminase from an organism.

The term “effective amount,” as used herein, refers to an amount of a biologically active agent that is sufficient to elicit a desired biological response. For example, in some embodiments, an effective amount of a nuclease may refer to the amount of the nuclease that is sufficient to induce cleavage of a target site specifically bound and cleaved by the nuclease. In some embodiments, an effective amount of a fusion protein provided herein, e.g., of a fusion protein comprising a nuclease-inactive Cas9 domain and a nucleic acid editing domain (e.g., a deaminase domain) may refer to the amount of the fusion protein that is sufficient to induce editing of a target site specifically bound and edited by the fusion protein. As will be appreciated by the skilled artisan, the effective amount of an agent, e.g., a fusion protein, a nuclease, a deaminase, a recombinase, a hybrid protein, a protein dimer, a complex of a protein (or protein dimer) and a polynucleotide, or a polynucleotide, may vary depending on various factors as, for example, on the desired biological response, e.g., on the specific allele, genome, or target site to be edited, on the cell or tissue being targeted, and on the agent being used.

The term “linker,” as used herein, refers to a chemical group or a molecule linking two molecules or moieties, e.g., two domains of a fusion protein, such as, for example, a nuclease-inactive Cas9 domain and a nucleic acid editing domain (e.g., a deaminase domain). In some embodiments, a linker joins a gRNA binding domain of an RNA-programmable nuclease, including a Cas9 nuclease domain, and the catalytic domain of anucleic-acid editing protein. In some embodiments, a linker joins a dCas9 and a nucleic-acid editing protein. Typically, the linker is positioned between, or flanked by, two groups, molecules, or other moieties and connected to each one via a covalent bond, thus connecting the two. In some embodiments, the linker is an amino acid or a plurality of amino acids (e.g., a peptide or protein). In some embodiments, the linker is an organic molecule, group, polymer, or chemical moiety. In some embodiments, the linker is 5-100 amino acids in length, for example, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 30-35, 35-40, 40-45, 45-50, 50-60, 60-70, 70-80, 80-90, 90-100, 100-150, or 150-200 amino acids in length. Longer or shorter linkers are also contemplated.

The term “mutation,” as used herein, refers to a substitution of a residue within a sequence, e.g., a nucleic acid or amino acid sequence, with another residue, or a deletion or insertion of one or more residues within a sequence. Mutations are typically described herein by identifying the original residue followed by the position of the residue within the sequence and by the identity of the newly substituted residue. Various methods for making the amino acid substitutions (mutations) provided herein are well known in the art, and are provided by, for example, Green and Sambrook, Molecular Cloning: A Laboratory Manual (4^th ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2012)).

The terms “nucleic acid” and “nucleic acid molecule,” as used herein, refer to a compound comprising a nucleobase and an acidic moiety, e.g., a nucleoside, a nucleotide, or a polymer of nucleotides. Typically, polymeric nucleic acids, e.g., nucleic acid molecules comprising three or more nucleotides are linear molecules, in which adjacent nucleotides are linked to each other via a phosphodiester linkage. In some embodiments, “nucleic acid” refers to individual nucleic acid residues (e.g. nucleotides and/or nucleosides). In some embodiments, “nucleic acid” refers to an oligonucleotide chain comprising three or more individual nucleotide residues. As used herein, the terms “oligonucleotide” and “polynucleotide” can be used interchangeably to refer to a polymer of nucleotides (e.g., a string of at least three nucleotides). In some embodiments, “nucleic acid” encompasses RNA as well as single and/or double-stranded DNA. Nucleic acids may be naturally occurring, for example, in the context of a genome, a transcript, an mRNA, tRNA, rRNA, siRNA, snRNA, a plasmid, cosmid, chromosome, chromatid, or other naturally occurring nucleic acid molecule. On the other hand, a nucleic acid molecule may be a non-naturally occurring molecule, e.g., a recombinant DNA or RNA, an artificial chromosome, an engineered genome, or fragment thereof, or a synthetic DNA, RNA, DNA/RNA hybrid, or including non-naturally occurring nucleotides or nucleosides. Furthermore, the terms “nucleic acid,” “DNA,” “RNA,” and/or similar terms include nucleic acid analogs, e.g., analogs having other than a phosphodiester backbone. Nucleic acids can be purified from natural sources, produced using recombinant expression systems and optionally purified, chemically synthesized, etc. Where appropriate, e.g., in the case of chemically synthesized molecules, nucleic acids can comprise nucleoside analogs such as analogs having chemically modified bases or sugars, and backbone modifications. A nucleic acid sequence is presented in the 5′ to 3′ direction unless otherwise indicated. In some embodiments, a nucleic acid is or comprises natural nucleosides (e.g. adenosine, thymidine, guanosine, cytidine, uridine, deoxyadenosine, deoxythymidine, deoxyguanosine, and deoxycytidine); nucleoside analogs (e.g., 2-aminoadenosine, 2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyl adenosine, 5-methylcytidine, 2-aminoadenosine, C5-bromouridine, C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine, C5-propynyl-cytidine, C5-methylcytidine, 2-aminoadenosine, 7-deazaadenosine, 7-deazaguanosine, 8-oxoadenosine, 8-oxoguanosine, O(6)-methylguanine, and 2-thiocytidine); chemically modified bases; biologically modified bases (e.g., methylated bases); intercalated bases; modified sugars (e.g.,2′-fluororibose, ribose, 2′-deoxyribose, arabinose, and hexose); and/or modified phosphate groups (e.g., phosphorothioates and 5′-N-phosphoramidite linkages).

The term “nucleic acid editing domain,” as used herein refers to a protein or enzyme capable of making one or more modifications (e.g., deamination of a cytidine residue) to a nucleic acid (e.g., DNA or RNA). Exemplary nucleic acid editing domains include, but are not limited to a deaminase, a nuclease, a nickase, a recombinase, a methyltransferase, a methylase, an acetylase, an acetyltransferase, a transcriptional activator, or a transcriptional repressor domain. In some embodiments the nucleic acid editing domain is a deaminase (e.g., a cytidine deaminase, such as an APOBEC or an AID deaminase).

The term “proliferative disease,” as used herein, refers to any disease in which cell or tissue homeostasis is disturbed in that a cell or cell population exhibits an abnormally elevated proliferation rate. Proliferative diseases include hyperproliferative diseases, such as pre-neoplastic hyperplastic conditions and neoplastic diseases. Neoplastic diseases are characterized by an abnormal proliferation of cells and include both benign and malignant neoplasias. Malignant neoplasia is also referred to as cancer.

The terms “protein,” “peptide,” and “polypeptide” are used interchangeably herein, and refer to a polymer of amino acid residues linked together by peptide (amide) bonds. The terms refer to a protein, peptide, or polypeptide of any size, structure, or function. Typically, a protein, peptide, or polypeptide will be at least three amino acids long. A protein, peptide, or polypeptide may refer to an individual protein or a collection of proteins. One or more of the amino acids in a protein, peptide, or polypeptide may be modified, for example, by the addition of a chemical entity such as a carbohydrate group, a hydroxyl group, a phosphate group, a farnesyl group, an isofarnesyl group, a fatty acid group, a linker for conjugation, functionalization, or other modification, etc. A protein, peptide, or polypeptide may also be a single molecule or may be a multi-molecular complex. A protein, peptide, or polypeptide may be just a fragment of a naturally occurring protein or peptide. A protein, peptide, or polypeptide may be naturally occurring, recombinant, or synthetic, or any combination thereof. The term “fusion protein” as used herein refers to a hybrid polypeptide which comprises protein domains from at least two different proteins. One protein may be located at the amino-terminal (N-terminal) portion of the fusion protein or at the carboxy-terminal (C-terminal) protein thus forming an “amino-terminal fusion protein” or a “carboxy-terminal fusion protein,” respectively. A protein may comprise different domains, for example, a nucleic acid binding domain (e.g., the gRNA binding domain of Cas9 that directs the binding of the protein to a target site) and a nucleic acid cleavage domain or a catalytic domain of a nucleic-acid editing protein. In some embodiments, a protein comprises a proteinaceous part, e.g., an amino acid sequence constituting a nucleic acid binding domain, and an organic compound, e.g., a compound that can act as a nucleic acid cleavage agent. In some embodiments, a protein is in a complex with, or is in association with, a nucleic acid, e.g., RNA. Any of the proteins provided herein may be produced by any method known in the art. For example, the proteins provided herein may be produced via recombinant protein expression and purification, which is especially suited for fusion proteins comprising a peptide linker. Methods for recombinant protein expression and purification are well known, and include those described by Green and Sambrook, Molecular Cloning: A Laboratory Manual (4^th ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2012)), the entire contents of which are incorporated herein by reference.

The term “RNA-programmable nuclease,” and “RNA-guided nuclease” are used interchangeably herein and refer to a nuclease that forms a complex with (e.g., binds or associates with) one or more RNA that is not a target for cleavage. In some embodiments, an RNA-programmable nuclease, when in a complex with an RNA, may be referred to as a nuclease:RNA complex. Typically, the bound RNA(s) is referred to as a guide RNA (gRNA). gRNAs can exist as a complex of two or more RNAs, or as a single RNA molecule. gRNAs that exist as a single RNA molecule may be referred to as single-guide RNAs (sgRNAs), though “gRNA” is used interchangeably to refer to guide RNAs that exist as either single molecules or as a complex of two or more molecules. Typically, gRNAs that exist as single RNA species comprise two domains: (1) a domain that shares homology to a target nucleic acid (e.g., and directs binding of a Cas9 complex to the target); and (2) a domain that binds a Cas9 protein. In some embodiments, domain (2) corresponds to a sequence known as a tracrRNA, and comprises a stem-loop structure. For example, in some embodiments, domain (2) is identical or homologous to a tracrRNA as provided in Jinek et al., Science 337:816-821(2012), the entire contents of which is incorporated herein by reference. Other examples of gRNAs (e.g., those including domain 2) can be found in U.S. Provisional Patent Application, U.S. Ser. No. 61/874,682, filed Sep. 6, 2013, entitled “Switchable Cas9 Nucleases And Uses Thereof,” and U.S. Provisional Patent Application, U.S. Ser. No. 61/874,746, filed Sep. 6, 2013, entitled “Delivery System For Functional Nucleases,” the entire contents of each are hereby incorporated by reference in their entirety. In some embodiments, a gRNA comprises two or more of domains (1) and (2), and may be referred to as an “extended gRNA.” For example, an extended gRNA will, e.g., bind two or more Cas9 proteins and bind a target nucleic acid at two or more distinct regions, as described herein. The gRNA comprises a nucleotide sequence that complements a target site, which mediates binding of the nuclease/RNA complex to said target site, providing the sequence specificity of the nuclease:RNA complex. In some embodiments, the RNA-programmable nuclease is the (CRISPR-associated system) Cas9 endonuclease, for example Cas9 (Csn1) from Streptococcus pyogenes (see, e.g., “Complete genome sequence of an M1 strain of Streptococcus pyogenes.” Ferretti J. J., McShan W. M., Ajdic D. J., Savic D. J., Savic G., Lyon K., Primeaux C., Sezate S., Suvorov A. N., Kenton S., Lai H. S., Lin S. P., Qian Y., Jia H. G., Najar F. Z., Ren Q., Zhu H., Song L., White J., Yuan X., Clifton S. W., Roe B. A., McLaughlin R. E., Proc. Natl. Acad. Sci. U.S.A. 98:4658-4663(2001); “CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III.” Deltcheva E., Chylinski K., Sharma C. M., Gonzales K., Chao Y., Pirzada Z. A., Eckert M. R., Vogel J., Charpentier E., Nature 471:602-607(2011); and “A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.” Jinek M., Chylinski K., Fonfara I., Hauer M., Doudna J. A., Charpentier E. Science 337:816-821(2012), the entire contents of each of which are incorporated herein by reference.

Because RNA-programmable nucleases (e.g., Cas9) use RNA:DNA hybridization to target DNA cleavage sites, these proteins are able to be targeted, in principle, to any sequence specified by the guide RNA. Methods of using RNA-programmable nucleases, such as Cas9, for site-specific cleavage (e.g., to modify a genome) are known in the art (see e.g., Cong, L. et al. Multiplex genome engineering using CRISPR/Cas systems. Science 339, 819-823 (2013); Mali, P. et al. RNA-guided human genome engineering via Cas9. Science 339, 823-826 (2013); Hwang, W. Y. et al. Efficient genome editing in zebrafish using a CRISPR-Cas system. Nature biotechnology 31, 227-229 (2013); Jinek, M. et al. RNA-programmed genome editing in human cells. eLife 2, e00471 (2013); Dicarlo, J. E. et al. Genome engineering in Saccharomyces cerevisiae using CRISPR-Cas systems. Nucleic acids research (2013); Jiang, W. et al. RNA-guided editing of bacterial genomes using CRISPR-Cas systems. Nature biotechnology 31, 233-239 (2013); the entire contents of each of which are incorporated herein by reference).

The term “subject,” as used herein, refers to an individual organism, for example, an individual mammal. In some embodiments, the subject is a human. In some embodiments, the subject is a non-human mammal. In some embodiments, the subject is a non-human primate. In some embodiments, the subject is a rodent. In some embodiments, the subject is a sheep, a goat, a cattle, a cat, or a dog. In some embodiments, the subject is a vertebrate, an amphibian, a reptile, a fish, an insect, a fly, or a nematode. In some embodiments, the subject is a research animal. In some embodiments, the subject is genetically engineered, e.g., a genetically engineered non-human subject. The subject may be of either sex and at any stage of development.

The term “target site” refers to a sequence within a nucleic acid molecule that is deaminated by a deaminase or a fusion protein comprising a deaminase, (e.g., a dCas9-deaminase fusion protein provided herein).

The terms “treatment,” “treat,” and “treating,” refer to a clinical intervention aimed to reverse, alleviate, delay the onset of, or inhibit the progress of a disease or disorder, or one or more symptoms thereof, as described herein. As used herein, the terms “treatment,” “treat,” and “treating” refer to a clinical intervention aimed to reverse, alleviate, delay the onset of, or inhibit the progress of a disease or disorder, or one or more symptoms thereof, as described herein. In some embodiments, treatment may be administered after one or more symptoms have developed and/or after a disease has been diagnosed. In other embodiments, treatment may be administered in the absence of symptoms, e.g., to prevent or delay onset of a symptom or inhibit onset or progression of a disease. For example, treatment may be administered to a susceptible individual prior to the onset of symptoms (e.g., in light of a history of symptoms and/or in light of genetic or other susceptibility factors). Treatment may also be continued after symptoms have resolved, for example, to prevent or delay their recurrence.

The term “recombinant” as used herein in the context of proteins or nucleic acids refers to proteins or nucleic acids that do not occur in nature, but are the product of human engineering. For example, in some embodiments, a recombinant protein or nucleic acid molecule comprises an amino acid or nucleotide sequence that comprises at least one, at least two, at least three, at least four, at least five, at least six, or at least seven mutations as compared to any naturally occurring sequence.

The term “nucleobase editors (NBEs)” or “base editors (BEs),” as used herein, refers to the Cas9 fusion proteins described herein. In some embodiments, the fusion protein comprises a nuclease-inactive Cas9 (dCas9) fused to a deaminase. In some embodiments, the fusion protein comprises a Cas9 nickase fused to a deaminase. In some embodiments, the fusion protein comprises a nuclease-inactive Cas9 fused to a deaminase and further fused to a UGI domain. In some embodiments, the fusion protein comprises a Cas9 nickase fused to a deaminase and further fused to a UGI domain. In some embodiments, the dCas9 of the fusion protein comprises a D10A and a H840A mutation of SEQ ID NO: 10, or a corresponding mutation in any of SEQ ID NOs: 11-260, which inactivates nuclease activity of the Cas9 protein. In some embodiments, the fusion protein comprises a D10A mutation and comprises a histidine at residue 840 of SEQ ID NO: 10, or a corresponding mutation in any of SEQ ID NOs: 11-260, which renders Cas9 capable of cleaving only one strand of a nucleic acid duplex. An example of a Cas9 nickase is shown below in SEQ ID NO: 674. The terms “nucleobase editors (NBEs)” and “base editors (BEs)” may be used interchangeably.

The term “uracil glycosylase inhibitor” or “UGI,” as used herein, refers to a protein that is capable of inhibiting a uracil-DNA glycosylase base-excision repair enzyme.

The term “Cas9 nickase,” as used herein, refers to a Cas9 protein that is capable of cleaving only one strand of a duplexed nucleic acid molecule (e.g., a duplexed DNA molecule). In some embodiments, a Cas9 nickase comprises a D10A mutation and has a histidine at position H840 of SEQ ID NO: 10, or a corresponding mutation in any of SEQ ID NOs: 11-260. For example, a Cas9 nickase may comprise the amino acid sequence as set forth in SEQ ID NO: 674. Such a Cas9 nickase has an active HNH nuclease domain and is able to cleave the non-targeted strand of DNA, i.e., the strand bound by the gRNA. Further, such a Cas9 nickase has an inactive RuvC nuclease domain and is not able to cleave the targeted strand of the DNA, i.e., the strand where base editing is desired.

Exemplary Cas9 nickase (Cloning vector pPlatTET-gRNA2; Accession No. BAV54124).

(SEQ ID NO: 674)
MDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIG
ALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFF
HRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTD
KADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLF
EENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALS
LGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAK
NLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQL
PEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVK
LNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIE
KILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQS
FIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAF
LSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFN
ASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLK
TYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSD
GFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKK
GILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKGQKNSRERMKRI
EEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDMYVDQELDINRL
SDYDVDHIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNY
WRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQITKHV
AQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVREINN
YHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQEI
GKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDKGR
DFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEK
NPIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNE
LALPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQIS
EFSKRVILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAA
FKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGD

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS OF THE INVENTION

Some aspects of this disclosure provide fusion proteins that comprise a domain capable of binding to a nucleotide sequence (e.g., a Cas9, or a Cpf1 protein) and an enzyme domain, for example, a DNA-editing domain, such as, e.g., a deaminase domain. The deamination of a nucleobase by a deaminase can lead to a point mutation at the respective residue, which is referred to herein as nucleic acid editing. Fusion proteins comprising a Cas9 variant or domain and a DNA editing domain can thus be used for the targeted editing of nucleic acid sequences. Such fusion proteins are useful for targeted editing of DNA in vitro, e.g., for the generation of mutant cells or animals; for the introduction of targeted mutations, e.g., for the correction of genetic defects in cells ex vivo, e.g., in cells obtained from a subject that are subsequently re-introduced into the same or another subject; and for the introduction of targeted mutations, e.g., the correction of genetic defects or the introduction of deactivating mutations in disease-associated genes in a subject. Typically, the Cas9 domain of the fusion proteins described herein does not have any nuclease activity but instead is a Cas9 fragment or a dCas9 protein or domain. Methods for the use of Cas9 fusion proteins as described herein are also provided.

Cas9 Domains of Nucleobase Editors

Non-limiting, exemplary Cas9 domains are provided herein. The Cas9 domain may be a nuclease active Cas9 domain, a nucleasae inactive Cas9 domain, or a Cas9 nickase. In some embodiments, the Cas9 domain is a nuclease active domain. For example, the Cas9 domain may be a Cas9 domain that cuts both strands of a duplexed nucleic acid (e.g., both strands of a duplexed DNA molecule). In some embodiments, the Cas9 domain comprises any one of the amino acid sequences as set forth in SEQ ID NOs: 11-260. In some embodiments the Cas9 domain comprises an amino acid sequence that is at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of the amino acid sequences set forth in SEQ ID NOs: 11-260. In some embodiments, the Cas9 domain comprises an amino acid sequence that has 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 21, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50 or more or more mutations compared to any one of the amino acid sequences set forth in SEQ ID NOs: 11-260. In some embodiments, the Cas9 domain comprises an amino acid sequence that has at least 10, at least 15, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90, at least 100, at least 150, at least 200, at least 250, at least 300, at least 350, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1100, or at least 1200 identical contiguous amino acid residues as compared to any one of the amino acid sequences set forth in SEQ ID NOs: 11-260.

In some embodiments, the Cas9 domain is a nuclease-inactive Cas9 domain (dCas9). For example, the dCas9 domain may bind to a duplexed nucleic acid molecule (e.g., via a gRNA molecule) without cleaving either strand of the duplexed nucleic acid molecule. In some embodiments, the nuclease-inactive dCas9 domain comprises a D10X mutation and a H840X mutation of the amino acid sequence set forth in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid change. In some embodiments, the nuclease-inactive dCas9 domain comprises a D10A mutation and a H840A mutation of the amino acid sequence set forth in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. As one example, a nuclease-inactive Cas9 domain comprises the amino acid sequence set forth in SEQ ID NO: 263 (Cloning vector pPlatTET-gRNA2, Accession No. BAV54124).

(SEQ ID NO: 263
MDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGA
LLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHR
LEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKAD
LRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENP
INASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTP
NFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAI
LLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEI
FFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLR
KQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPY
YVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDK
NLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVD
LLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKI
IKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQ
LKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDD
SLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKV
MGRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHP
VENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDAIVPQSFLKDD
SIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNL
TKAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLI
REVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKK
YPKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEI
TLANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEV
QTGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVE
KGKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPK
YSLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPE
DNEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDK
PIREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQ
SITGLYETRIDLSQLGGD;

see, e.g., Qi et al., Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression. Cell. 2013; 152(5):1173-83, the entire contents of which are incorporated herein by reference).

Additional suitable nuclease-inactive dCas9 domains will be apparent to those of skill in the art based on this disclosure and knowledge in the field, and are within the scope of this disclosure. Such additional exemplary suitable nuclease-inactive Cas9 domains include, but are not limited to, D10A/H840A, D10A/D839A/H840A, and D10A/D839A/H840A/N863A mutant domains (See, e.g., Prashant et al., CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering. Nature Biotechnology. 2013; 31(9): 833-838, the entire contents of which are incorporated herein by reference). In some embodiments the dCas9 domain comprises an amino acid sequence that is at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of the dCas9 domains provided herein. In some embodiments, the Cas9 domain comprises an amino acid sequences that has 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 21, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50 or more or more mutations compared to any one of the amino acid sequences set forth in SEQ ID NOs: 11-260. In some embodiments, the Cas9 domain comprises an amino acid sequence that has at least 10, at least 15, at least 20, at least 30, at least 40, at least 50, at least 60, at least 70, at least 80, at least 90, at least 100, at least 150, at least 200, at least 250, at least 300, at least 350, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1100, or at least 1200 identical contiguous amino acid residues as compared to any one of the amino acid sequences set forth in SEQ ID NOs: 11-260.

In some embodiments, the Cas9 domain is a Cas9 nickase. The Cas9 nickase may be a Cas9 protein that is capable of cleaving only one strand of a duplexed nucleic acid molecule (e.g., a duplexed DNA molecule). In some embodiments the Cas9 nickase cleaves the target strand of a duplexed nucleic acid molecule, meaning that the Cas9 nickase cleaves the strand that is base paired to (complementary to) a gRNA (e.g., an sgRNA) that is bound to the Cas9. In some embodiments, a Cas9 nickase comprises a D10A mutation and has a histidine at position 840 of SEQ ID NO: 10, or a mutation in any of SEQ ID NOs: 11-260. For example, a Cas9 nickase may comprise the amino acid sequence as set forth in SEQ ID NO: 674. In some embodiments the Cas9 nickase cleaves the non-target, non-base-edited strand of a duplexed nucleic acid molecule, meaning that the Cas9 nickase cleaves the strand that is not base paired to a gRNA (e.g., an sgRNA) that is bound to the Cas9. In some embodiments, a Cas9 nickase comprises an H840A mutation and has an aspartic acid residue at position 10 of SEQ ID NO: 10, or a corresponding mutation in any of SEQ ID NOs: 11-260. In some embodiments the Cas9 nickase comprises an amino acid sequence that is at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of the Cas9 nickases provided herein. Additional suitable Cas9 nickases will be apparent to those of skill in the art based on this disclosure and knowledge in the field, and are within the scope of this disclosure.

Cas9 Domains with Reduced PAM Exclusivity

Some aspects of the disclosure provide Cas9 domains that have different PAM specificities. Typically, Cas9 proteins, such as Cas9 from S. pyogenes (spCas9), require a canonical NGG PAM sequence to bind a particular nucleic acid region. This may limit the ability to edit desired bases within a genome. In some embodiments, the base editing fusion proteins provided herein may need to be placed at a precise location, for example where a target base is placed within a 4 base region (e.g., a “deamination window”), which is approximately 15 bases upstream of the PAM. See Komor, A. C., et al., “Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage” Nature 533, 420-424 (2016), the entire contents of which are hereby incorporated by reference. Accordingly, in some embodiments, any of the fusion proteins provided herein may contain a Cas9 domain that is capable of binding a nucleotide sequence that does not contain a canonical (e.g., NGG) PAM sequence. Cas9 domains that bind to non-canonical PAM sequences have been described in the art and would be apparent to the skilled artisan. For example, Cas9 domains that bind non-canonical PAM sequences have been described in Kleinstiver, B. P., et al., “Engineered CRISPR-Cas9 nucleases with altered PAM specificities” Nature 523, 481-485 (2015); and Kleinstiver, B. P., et al., “Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition” Nature Biotechnology 33, 1293-1298 (2015); the entire contents of each are hereby incorporated by reference.

In some embodiments, the Cas9 domain is a Cas9 domain from Staphylococcus aureus (SaCas9). In some embodiments, the SaCas9 domain is a nuclease active SaCas9, a nuclease inactive SaCas9 (SaCas9d), or a SaCas9 nickase (SaCas9n). In some embodiments, the SaCas9 comprises the amino acid sequence SEQ ID NO: 4273. In some embodiments, the SaCas9 comprises a N579X mutation of SEQ ID NO: 4273, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for N. In some embodiments, the SaCas9 comprises a N579A mutation of SEQ ID NO: 4273, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SaCas9 domain, the SaCas9d domain, or the SaCas9n domain can bind to a nucleic acid sequence having a non-canonical PAM. In some embodiments, the SaCas9 domain, the SaCas9d domain, or the SaCas9n domain can bind to a nucleic acid sequence having a NNGRRT PAM sequence. In some embodiments, the SaCas9 domain comprises one or more of a E781X, a N967X, and a R1014X mutation of SEQ ID NO: 4273, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid. In some embodiments, the SaCas9 domain comprises one or more of a E781K, a N967K, and a R1014H mutation of SEQ ID NO: 4273, or one or more corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SaCas9 domain comprises a E781K, a N967K, or a R1014H mutation of SEQ ID NO: 4273, or corresponding mutations in any of the amino acid sequences provided in SEQ ID NOs: 11-260.

In some embodiments, the Cas9 domain of any of the fusion proteins provided herein comprises an amino acid sequence that is at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of SEQ ID NOs: 4273-4275. In some embodiments, the Cas9 domain of any of the fusion proteins provided herein comprises the amino acid sequence of any one of SEQ ID NOs: 4273-4275. In some embodiments, the Cas9 domain of any of the fusion proteins provided herein consists of the amino acid sequence of any one of SEQ ID NOs: 4273-4275.

Exemplary SaCas9 sequence

(SEQ ID NO: 4273)
KRNYILGLDIGITSVGYGIIDYETRDVIDAGVRLFKEANVENNEGRRSKR
GARRLKRRRRHRIQRVKKLLFDYNLLTDHSELSGINPYEARVKGLSQKLS
EEEFSAALLHLAKRRGVHNVNEVEEDTGNELSTKEQISRNSKALEEKYVA
ELQLERLKKDGEVRGS1NRFKTSDYVKEAKQLLKVQKAYHQLDQSFIDTY
IDLLETRRTYYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPEELRSVKYAY
NADLYNALNDLNNLVITRDENEKLEYYEKFQIIENVFKQKKKPTLKQIAK
EILVNEEDIKGYRVTSTGKPEFTNLKVYHDIKDITARKEIIENAELLDQI
AKILTIYQSSEDIQEELTNLNSELTQEEIEQISNLKGYTGTHNLSLKAIN
LILDELWHTNDNQIAIFNRLKLVPKKVDLSQQKEIPTTLVDDFILSPVVK
RSFIQSIKVINAIIKKYGLPNDIIIELAREKNSKDAQKMINEMQKRNRQT
NERIEEIIRTTGKENAKYLIEKIKLHDMQEGKCLYSLEAIPLEDLLNNPF
NYEVDHIIPRSVSFDNSFNNKVLVKQEENSKKGNRTPFQYLSSSDSKISY
ETFKKHILNLAKGKGRISKTKKEYLLEERDINRFSVQKDFINRNLVDTRY
ATRGLMNLLRSYFRVNNLDVKVKSINGGFTSFLRRKWKFKKERNKGYKHH
AEDALIIANADFIFKEWKKLDKAKKVMENQMFEEKQAESMPEIETEQEYK
EIFITPHQIKHIKDFKDYKYSHRVDKKPNRELINDTLYSTRKDDKGNTLI
VNNLNGLYDKDNDKLKKLINKSPEKLLMYHHDPQTYQKLKLIMEQYGDEK
NPLYKYYEETGNYLTKYSKKDNGPVIKKIKYYGNKLNAHLDITDDYPNSR
NKVVKLSLKPYRFDVYLDNGVYKFVTVKNLDVIKKENYYEVNSKCYEEAK
KLKKISNQAEFIASFYNNDLIKINGELYRVIGVNNDLLNRIEVNMIDITY
REYLENMNDKRPPRIIKTIASKTQSIKKYSTDILGNLYEVKSKKHPQIIK
KG

Residue N579 of SEQ ID NO: 4273, which is underlined and in bold, may be mutated (e.g., to a A579) to yield a SaCas9 nickase.

Exemplary SaCas9n Sequence

(SEQ ID NO: 4274)
KRNYILGLDIGITSVGYGIIDYETRDVIDAGVRLFKEANVENNEGRRSKR
GARRLKRRRRHRIQRVKKLLFDYNLLTDHSELSGINPYEARVKGLSQKLS
EEEFSAALLHLAKRRGVHNVNEVEEDTGNELSTKEQISRNSKALEEKYVA
ELQLERLKKDGEVRGSINRFKTSDYVKEAKQLLKVQKAYHQLDQSFIDTY
IDLLETRRTYYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPEELRSVKYAY
NADLYNALNDLNNLVITRDENEKLEYYEKFQIIENVFKQKKKPTLKQIAK
EILVNEEDIKGYRVTSTGKPEFTNLKVYHDIKDITARKEIIENAELLDQI
AKILTIYQSSEDIQEELTNLNSELTQEEIEQISNLKGYTGTHNLSLKAIN
LILDELWHTNDNQIAIFNRLKLVPKKVDLSQQKEIPTTLVDDFILSPVVK
RSFIQSIKVINAIIKKYGLPNDIIIELAREKNSKDAQKMINEMQKRNRQT
NERIEEIIRTTGKENAKYLIEKIKLHDMQEGKCLYSLEAIPLEDLLNNPF
NYEVDHIIPRSVSFDNSFNNKVLVKQEEASKKGNRTPFQYLSSSDSKISY
ETFKKHILNLAKGKGRISKTKKEYLLEERDINRFSVQKDFINRNLVDTRY
ATRGLMNLLRSYFRVNNLDVKVKSINGGFTSFLRRKWKFKKERNKGYKHH
AEDALIIANADFIFKEWKKLDKAKKVMENQMFEEKQAESMPEIETEQEYK
EIFITPHQIKHIKDFKDYKYSHRVDKKPNRELINDTLYSTRKDDKGNTLI
VNNLNGLYDKDNDKLKKLINKSPEKLLMYHHDPQTYQKLKLIMEQYGDEK
NPLYKYYEETGNYLTKYSKKDNGPVIKKIKYYGNKLNAHLDITDDYPNSR
NKVVKLSLKPYRFDVYLDNGVYKFVTVKNLDVIKKENYYEVNSKCYEEAK
KLKKISNQAEFIASFYNNDLIKINGELYRVIGVNNDLLNRIEVNMIDITY
REYLENMNDKRPPRIIKTIASKTQSIKKYSTDILGNLYEVKSKKHPQIIK
KG.

Residue A579 of SEQ ID NO: 4274, which can be mutated from N579 of SEQ ID NO: 4273 to yield a SaCas9 nickase, is underlined and in bold.

Exemplary SaKKH Cas9

(SEQ ID NO: 4275)
KRNYILGLDIGITSVGYGIIDYETRDVIDAGVRLFKEANVENNEGRRSK
RGARRLKRRRRHRIQRVKKLLFDYNLLTDHSELSGINPYEARVKGLSQK
LSEEEFSAALLHLAKRRGVHNVNEVEEDTGNELSTKEQISRNSKALEEK
YVAELQLERLKKDGEVRGSINRFKTSDYVKEAKQLLKVQKAYHQLDQSF
IDTYIDLLETRRTYYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPEELRS
VKYAYNADLYNALNDLNNLVITRDENEKLEYYEKFQIIENVFKQKKKPT
LKQIAKEILVNEEDIKGYRVTSTGKPEFTNLKVYHDIKDITARKEIIEN
AELLDQIAKILTIYQSSEDIQEELTNLNSELTQEEIEQISNLKGYTGTH
NLSLKAINLILDELWHTNDNQIAIFNRLKLVPKKVDLSQQKEIPTTLVD
DFILSPVVKRSFIQSIKVINAIIKKYGLPNDIIIELAREKNSKDAQKMI
NEMQKRNRQTNERIEEIIRTTGKENAKYLIEKIKLHDMQEGKCLYSLEA
IPLEDLLNNPFNYEVDHIIPRSVSFDNSFNNKVLVKQEEASKKGNRTPF
QYLSSSDSKISYETFKKHILNLAKGKGRISKTKKEYLLEERDINRFSVQ
KDFINRNLVDTRYATRGLMNLLRSYFRVNNLDVKVKSINGGFTSFLRRK
WKFKKERNKGYKHHAEDALIIANADFIFKEWKKLDKAKKVMENQMFEEK
QAESMPEIETEQEYKEIFITPHQIKHIKDFKDYKYSHRVDKKPNRKLIN
DTLYSTRKDDKGNTLIVNNLNGLYDKDNDKLKKLINKSPEKLLMYHHDP
QTYQKLKLIMEQYGDEKNPLYKYYEETGNYLTKYSKKDNGPVIKKIKYY
GNKLNAHLDITDDYPNSRNKVVKLSLKPYRFDVYLDNGVYKFVTVKNLD
VIKKENYYEVNSKCYEEAKKLKKISNQAEFIASFYKNDLIKINGELYRV
IGVNNDLLNRIEVNMIDITYREYLENMNDKRPPHIIKTIASKTQSIKKY
STDILGNLYEVKSKKHPQIIKKG.

Residue A579 of SEQ ID NO: 4275, which can be mutated from N579 of SEQ ID NO: 4273 to yield a SaCas9 nickase, is underlined and in bold. Residues K781, K967, and H1014 of SEQ ID NO: 4275, which can be mutated from E781, N967, and R1014 of SEQ ID NO: 4273 to yield a SaKKH Cas9 are underlined and in italics.

In some embodiments, the Cas9 domain is a Cas9 domain from Streptococcus pyogenes (SpCas9). In some embodiments, the SpCas9 domain is a nuclease active SpCas9, a nuclease inactive SpCas9 (SpCas9d), or a SpCas9 nickase (SpCas9n). In some embodiments, the SpCas9 comprises the amino acid sequence SEQ ID NO: 4276. In some embodiments, the SpCas9 comprises a D9X mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid except for D. In some embodiments, the SpCas9 comprises a D9A mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain, the SpCas9d domain, or the SpCas9n domain can bind to a nucleic acid sequence having a non-canonical PAM. In some embodiments, the SpCas9 domain, the SpCas9d domain, or the SpCas9n domain can bind to a nucleic acid sequence having a NGG, a NGA, or a NGCG PAM sequence. In some embodiments, the SpCas9 domain comprises one or more of a D1134X, a R1334X, and a T1336X mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid. In some embodiments, the SpCas9 domain comprises one or more of a D1134E, R1334Q, and T1336R mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain comprises a D1134E, a R1334Q, and a T1336R mutation of SEQ ID NO: 4276, or corresponding mutations in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain comprises one or more of a D1134X, a R1334X, and a T1336X mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid. In some embodiments, the SpCas9 domain comprises one or more of a D1134V, a R1334Q, and a T1336R mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain comprises a D1134V, a R1334Q, and a T1336R mutation of SEQ ID NO: 4276, or corresponding mutations in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain comprises one or more of a D1134X, a G1217X, a R1334X, and a T1336X mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid. In some embodiments, the SpCas9 domain comprises one or more of a D1134V, a G1217R, a R1334Q, and a T1336R mutation of SEQ ID NO: 4276, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the SpCas9 domain comprises a D1134V, a G1217R, a R1334Q, and a T1336R mutation of SEQ ID NO: 4276, or corresponding mutations in any of the amino acid sequences provided in SEQ ID NOs: 11-260.

In some embodiments, the Cas9 domain of any of the fusion proteins provided herein comprises an amino acid sequence that is at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to any one of SEQ ID NOs: 4276-4280. In some embodiments, the Cas9 domain of any of the fusion proteins provided herein comprises the amino acid sequence of any one of SEQ ID NOs: 4276-4280. In some embodiments, the Cas9 domain of any of the fusion proteins provided herein consists of the amino acid sequence of any one of SEQ ID NOs: 4276-4280.

Exemplary SpCas9

(SEQ ID NO: 4276)
DKKYSIGLDIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGD

Exemplary SpCas9n

(SEQ ID NO: 4277)
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGD

Exemplary SpEQR Cas9

(SEQ ID NO: 4278)
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFESPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKQYRSTKEVLDATLIHQS
ITGLYETRIDLSQLGGD

Residues E1134, Q1334, and R1336 of SEQ ID NO: 4278, which can be mutated from D1134, R1334, and T1336 of SEQ ID NO: 4276 to yield a SpEQR Cas9, are underlined and in bold.

Exemplary SpVQR Cas9

(SEQ ID NO: 4279)
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIG
ALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSF
FHRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDS
TDKADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYN
QLFEENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNL
IALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADL
FLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKA
LVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDG
TEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFL
KDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEV
VDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKY
VTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDS
VEISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTL
FEDREMIEERLKTYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDK
QSGKTILDFLKSDGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLH
EHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKPENIVIEMARENQT
TQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQLQNEKLYLYYLQ
NGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKVLTRSDKNRG
KSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERGGLSELDK
AGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVITLKSK
LVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLESEFV
YGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGEI
RKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGF
SKESILPKRNSDKLIARKKDWDPKKYGGFVSPTVAYSVLVVAKVEKGK
SKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSP
EDNEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKH
RDKPIREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKQYRSTKEVLDA
TLIHQSITGLYETRIDLSQLGGD

Residues V1134, Q1334, and R1336 of SEQ ID NO: 4279, which can be mutated from D1134, R1334, and T1336 of SEQ ID NO: 4276 to yield a SpVQR Cas9, are underlined and in bold.

Exemplary SpVRER Cas9

(SEQ ID NO: 4280)
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFVSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASARELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKEYRSTKEVLDATLIHQS
ITGLYETRIDLSQLGGD

Residues V1134, R1217, Q1334, and R1336 of SEQ ID NO: 4280, which can be mutated from D1134, G1217, R1334, and T1336 of SEQ ID NO: 4276 to yield a SpVRER Cas9, are underlined and in bold.

The following are exemplary fusion proteins (e.g., base editing proteins) capable of binding to a nucleic acid sequence having a non-canonical (e.g., a non-NGG) PAM sequence:

Exemplary SaBE3 (rAPOBEC1-XTEN-SaCas9n-UGI-NLS)

(SEQ ID NO: 4281)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESKRNYI
LGLDIGITSVGYGIIDYETRDVIDAGVRLFKEANVENNEGRRSKRGARRL
KRRRRHRIQRVKKLLFDYNLLTDHSELSGINPYEARVKGLSQKLSEEEFS
AALLHLAKRRGVHNVNEVEEDTGNELSTKEQISRNSKALEEKYVAELQLE
RLKKDGEVRGSINRFKTSDYVKEAKQLLKVQKAYHQLDQSFIDTYIDLLE
TRRTYYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPEELRSVKYAYNADLY
NALNDLNNLVITRDENEKLEYYEKFQIIENVFKQKKKPTLKQIAKEILVN
EEDIKGYRVTSTGKPEFTNLKVYHDIKDITARKEIIENAELLDQIAKILT
IYQSSEDIQEELTNLNSELTQEEIEQISNLKGYTGTHNLSLKAINLILDE
LWHTNDNQIAIFNRLKLVPKKVDLSQQKEIPTTLVDDFILSPVVKRSFIQ
SIKVINAIIKKYGLPNDIIIELAREKNSKDAQKMINEMQKRNRQTNERIE
EIIRTTGKENAKYLIEKIKLHDMQEGKCLYSLEAIPLEDLLNNPFNYEVD
HIIPRSVSFDNSFNNKVLVKQEEASKKGNRTPFQYLSSSDSKISYETFKK
HILNLAKGKGRISKTKKEYLLEERDINRFSVQKDFINRNLVDTRYATRGL
MNLLRSYFRVNNLDVKVKSINGGFTSFLRRKWKFKKERNKGYKHHAEDAL
IIANADFIFKEWKKLDKAKKVMENQMFEEKQAESMPEIETEQEYKEIFIT
PHQIKHIKDFKDYKYSHRVDKKPNRELINDTLYSTRKDDKGNTLIVNNLN
GLYDKDNDKLKKLINKSPEKLLMYHHDPQTYQKLKLIMEQYGDEKNPLYK
YYEETGNYLTKYSKKDNGPVIKKIKYYGNKLNAHLDITDDYPNSRNKVVK
LSLKPYRFDVYLDNGVYKFVTVKNLDVIKKENYYEVNSKCYEEAKKLKKI
SNQAEFIASFYNNDLIKINGELYRVIGVNNDLLNRIEVNMIDITYREYLE
NMNDKRPPRIIKTIASKTQSIKKYSTDILGNLYEVKSKKHPQIIKKGSGG
STNLSDIIEKETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDES
TDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLSGGSPKKKRKV

Exemplary SaKKH-BE3 (rAPOBEC1-XTEN-SaCas9n-UGI-NLS)

(SEQ ID NO: 4282)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESKRNYI
LGLDIGITSVGYGIIDYETRDVIDAGVRLFKEANVENNEGRRSKRGARRL
KRRRRHRIQRVKKLLFDYNLLTDHSELSGINPYEARVKGLSQKLSEEEFS
AALLHLAKRRGVHNVNEVEEDTGNELSTKEQISRNSKALEEKYVAELQLE
RLKKDGEVRGSINRFKTSDYVKEAKQLLKVQKAYHQLDQSFIDTYIDLLE
TRRTYYEGPGEGSPFGWKDIKEWYEMLMGHCTYFPEELRSVKYAYNADLY
NALNDLNNLVITRDENEKLEYYEKFQIIENVFKQKKKPTLKQIAKEILVN
EEDIKGYRVTSTGKPEFTNLKVYHDIKDITARKEIIENAELLDQIAKILT
IYQSSEDIQEELTNLNSELTQEEIEQISNLKGYTGTHNLSLKAINLILDE
LWHTNDNQIAIFNRLKLVPKKVDLSQQKEIPTTLVDDFILSPVVKRSFIQ
SIKVINAIIKKYGLPNDIIIELAREKNSKDAQKMINEMQKRNRQTNERIE
EIIRTTGKENAKYLIEKIKLHDMQEGKCLYSLEAIPLEDLLNNPFNYEVD
HIIPRSVSFDNSFNNKVLVKQEEASKKGNRTPFQYLSSSDSKISYETFKK
HILNLAKGKGRISKTKKEYLLEERDINRFSVQKDFINRNLVDTRYATRGL
MNLLRSYFRVNNLDVKVKSINGGFTSFLRRKWKFKKERNKGYKHHAEDAL
IIANADFIFKEWKKLDKAKKVMENQMFEEKQAESMPEIETEQEYKEIFIT
PHQIKHIKDFKDYKYSHRVDKKPNRKLINDTLYSTRKDDKGNTLIVNNLN
GLYDKDNDKLKKLINKSPEKLLMYHHDPQTYQKLKLIMEQYGDEKNPLYK
YYEETGNYLTKYSKKDNGPVIKKIKYYGNKLNAHLDITDDYPNSRNKVVK
LSLKPYRFDVYLDNGVYKFVTVKNLDVIKKENYYEVNSKCYEEAKKLKKI
SNQAEFIASFYKNDLIKINGELYRVIGVNNDLLNRIEVNMIDITYREYLE
NMNDKRPPHIIKTIASKTQSIKKYSTDILGNLYEVKSKKHPQIIKKGSGG
STNLSDIIEKETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDES
TDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLSGGSPKKKRKV

Exemplary EOR-BE3 (rAPOBEC1-XTEN-Cas9n-UGI-NLS)

(SEQ ID NO: 4283)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGE
IRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGFS
KESILPKRNSDKLIARKKDWDPKKYGGFESPTVAYSVLVVAKVEKGKSKK
LKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFEL
ENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQ
LFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQA
ENIIHLFTLTNLGAPAAFKYFDTTIDRKQYRSTKEVLDATLIHQSITGLY
ETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGN
KPESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLS
GGSPKKKRKV

VQR-BE3 (rAPOBEC1-XTEN-Cas9n-UGI-NLS)

(SEQ ID NO: 4284)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGE
IRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGFS
KESILPKRNSDKLIARKKDWDPKKYGGFVSPTVAYSVLVVAKVEKGKSKK
LKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFEL
ENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQ
LFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQA
ENIIHLFTLTNLGAPAAFKYFDTTIDRKQYRSTKEVLDATLIHQSITGLY
ETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGN
KPESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLS
GGSPKKKRKV

VRER-BE3 (rAPOBEC1-XTEN-Cas9n-UGI-NLS)

(SEQ ID NO: 4285)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGE
IRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGFS
KESILPKRNSDKLIARKKDWDPKKYGGFVSPTVAYSVLVVAKVEKGKSKK
LKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFEL
ENGRKRMLASARELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQ
LFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQA
ENIIHLFTLTNLGAPAAFKYFDTTIDRKEYRSTKEVLDATLIHQSITGLY
ETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGN
KPESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLS
GGSPKKKRKV

High Fidelity Base Editors

Some aspects of the disclosure provide Cas9 fusion proteins (e.g., any of the fusion proteins provided herein) comprising a Cas9 domain that has high fidelity. Additional aspects of the disclosure provide Cas9 fusion proteins (e.g., any of the fusion proteins provided herein) comprising a Cas9 domain with decreased electrostatic interactions between the Cas9 domain and a sugar-phosphate backbone of a DNA, as compared to a wild-type Cas9 domain. In some embodiments, a Cas9 domain (e.g., a wild type Cas9 domain) comprises one or more mutations that decreases the association between the Cas9 domain and a sugar-phosphate backbone of a DNA. In some embodiments, any of the Cas9 fusion proteins provided herein comprise one or more of a N497X, a R661X, a Q695X, and/or a Q926X mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, wherein X is any amino acid. In some embodiments, any of the Cas9 fusion proteins provided herein comprise one or more of a N497A, a R661A, a Q695A, and/or a Q926A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the Cas9 domain comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the Cas9 domain (e.g., of any of the fusion proteins provided herein) comprises the amino acid sequence as set forth in SEQ ID NO: 325. In some embodiments, the fusion protein comprises the amino acid sequence as set forth in SEQ ID NO: 285. Cas9 domains with high fidelity are known in the art and would be apparent to the skilled artisan. For example, Cas9 domains with high fidelity have been described in Kleinstiver, B. P., et al. “High-fidelity CRISPR-Cas9 nucleases with no detectable genome-wide off-target effects.” Nature 529, 490-495 (2016); and Slaymaker, I. M., et al. “Rationally engineered Cas9 nucleases with improved specificity.” Science 351, 84-88 (2015); the entire contents of each are incorporated herein by reference.

It should be appreciated that the base editors provided herein, for example base editor 2 (BE2) or base editor 3 (BE3), may be converted into high fidelity base editors by modifying the Cas9 domain as described herein to generate high fidelity base editors, for example high fidelity base editor 2 (HF-BE2) or high fidelity base editor 3 (HF-BE3). In some embodiments, base editor 2 (BE2) comprises a deaminase domain, a dCas9, and a UGI domain. In some embodiments, base editor 3 (BE3) comprises a deaminase domain an nCas9 domain and a UGI domain.

Cas9 Domain where Mutations Relative to Cas9 of SEQ ID NO: 10 are Shown in Bold and Underlines

(SEQ ID NO: 325)
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTAFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGALSRKLINGIRDKQSGKTILDFLKSDGFANRNFMALIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRAITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGD

HF-BE3

(SEQ ID NO: 5808)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETALATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQLEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTAFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGALSRKLINGIRDKQSGKTILDFLKSDGFANRNFMALIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLONGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRAITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGE
IRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGFS
KESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKGKSKK
LKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFEL
ENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQ
LFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQA
ENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSITGLY
ETRIDLSQLGGD

Cas9 Fusion Proteins

Any of the Cas9 domains (e.g., a nuclease active Cas9 protein, a nuclease-inactive dCas9 protein, or a Cas9 nickase protein) disclosed herein may be fused to a second protein, thus fusion proteins provided herein comprise a Cas9 domain as provided herein and a second protein, or a “fusion partner”. In some embodiments, the second protein is fused to the N-terminus of the Cas9 domain. However, in other embodiments, the second protein is fused to the C-terminus of the Cas9 domain. In some embodiments, the second protein that is fused to the Cas9 domain is a nucleic acid editing domain. In some embodiments, the Cas9 domain and the nucleic acid editing domain are fused via a linker, while in other embodiments the Cas9 domain and the nucleic acid editing domain are fused directly to one another. In some embodiments, the linker comprises (GGGS)_n (SEQ ID NO: 265), (GGGGS)_n (SEQ ID NO: 5), (G)_n, (EAAAK)_n (SEQ ID NO: 6), (GGS)_n, (SGGS)_n (SEQ ID NO: 4288), SGSETPGTSESATPES (SEQ ID NO: 7), or (XP)_n motif, or a combination of any of these, wherein n is independently an integer between 1 and 30, and wherein X is any amino acid. In some embodiments, the linker comprises a (GGS)_n motif, wherein n is 1, 3, or 7. In some embodiments, the linker comprises a (GGS)_n motif, wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15. In some embodiments, the linker comprises an amino acid sequence of SGSETPGTSESATPES (SEQ ID NO: 7),also referred to as the XTEN linker in the Examples). The length of the linker can influence the base to be edited, as illustrated in the Examples. For example, a linker of 3-amino-acid long (e.g., (GGS)₁) may give a 2-5, 2-4, 2-3, 3-4 base editing window relative to the PAM sequence, while a 9-amino-acid linker (e.g., (GGS)₃ (SEQ ID NO: 596)) may give a 2-6, 2-5, 2-4, 2-3, 3-6, 3-5, 3-4, 4-6, 4-5, 5-6 base editing window relative to the PAM sequence. A 16-amino-acid linker (e.g., the XTEN linker) may give a 2-7, 2-6, 2-5, 2-4, 2-3, 3-7, 3-6, 3-5, 3-4, 4-7, 4-6, 4-5, 5-7, 5-6, 6-7 base window relative to the PAM sequence with exceptionally strong activity, and a 21-amino-acid linker (e.g., (GGS)₇ (SEQ ID NO: 597)) may give a 3-8, 3-7, 3-6, 3-5, 3-4, 4-8, 4-7, 4-6, 4-5, 5-8, 5-7, 5-6, 6-8, 6-7, 7-8 base editing window relative to the PAM sequence. The novel finding that varying linker length may allow the dCas9 fusion proteins of the disclosure to edit nucleobases different distances from the PAM sequence affords siginicant clinical importance, since a PAM sequence may be of varying distance to the disease-causing mutation to be corrected in a gene. It is to be understood that the linker lengths described as examples here are not meant to be limiting.

In some embodiments, the second protein comprises an enzymatic domain. In some embodiments, the enzymatic domain is a nucleic acid editing domain. Such a nucleic acid editing domain may be, without limitation, a nuclease, a nickase, a recombinase, a deaminase, a methyltransferase, a methylase, an acetylase, or an acetyltransferase. Non-limiting exemplary binding domains that may be used in accordance with this disclosure include transcriptional activator domains and transcriptional repressor domains.

Deaminase Domains

In some embodiments, second protein comprises a nucleic acid editing domain. In some embodiments, the nucleic acid editing domain can catalyze a C to U base change. In some embodiments, the nucleic acid editing domain is a deaminase domain. In some embodiments, the deaminase is a cytidine deaminase or a cytidine deaminase. In some embodiments, the deaminase is an apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the deaminase is an APOBEC1 deaminase. In some embodiments, the deaminase is an APOBEC2 deaminase. In some embodiments, the deaminase is an APOBEC3 deaminase. In some embodiments, the deaminase is an APOBEC3A deaminase. In some embodiments, the deaminase is an APOBEC3B deaminase. In some embodiments, the deaminase is an APOBEC3C deaminase. In some embodiments, the deaminase is an APOBEC3D deaminase. In some embodiments, the deaminase is an APOBEC3E deaminase. In some embodiments, the deaminase is an APOBEC3F deaminase. In some embodiments, the deaminase is an APOBEC3G deaminase. In some embodiments, the deaminase is an APOBEC3H deaminase. In some embodiments, the deaminase is an APOBEC4 deaminase. In some embodiments, the deaminase is an activation-induced deaminase (AID). In some embodiments, the deaminase is a vertebrate deaminase. In some embodiments, the deaminase is an invertebrate deaminase. In some embodiments, the deaminase is a human, chimpanzee, gorilla, monkey, cow, dog, rat, or mouse deaminase. In some embodiments, the deaminase is a human deaminase. In some embodiments, the deaminase is a rat deaminase, e.g., rAPOBEC1. In some embodiments, the deaminase is a Petromyzon marinus cytidine deaminase 1 (pmCDA1). In some embodiments, the deminase is a human APOBEC3G (SEQ ID NO: 275). In some embodiments, the deaminase is a fragment of the human APOBEC3G (SEQ ID NO: 5740). In some embodiments, the deaminase is a human APOBEC3G variant comprising a D316R_D317R mutation (SEQ ID NO: 5739). In some embodiments, the deaminase is a frantment of the human APOBEC3G and comprising mutations corresponding to the D316R_D317R mutations in SEQ ID NO: 275 (SEQ ID NO: 5741).

In some embodiments, the nucleic acid editing domain is at least 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to the deaminase domain of any one of SEQ ID NOs: 266-284, 607-610, 5724-5736, or 5738-5741. In some embodiments, the nucleic acid editing domain comprises the amino acid sequence of any one of SEQ ID NOs: 266-284, 607-610, 5724-5736, or 5738-5741.

Deaminase Domains that Modulate the Editing Window of Base Editors

Some aspects of the disclosure are based on the recognition that modulating the deaminase domain catalytic activity of any of the fusion proteins provided herein, for example by making point mutations in the deaminase domain, affect the processivity of the fusion proteins (e.g., base editors). For example, mutations that reduce, but do not eliminate, the catalytic activity of a deaminase domain within a base editing fusion protein can make it less likely that the deaminase domain will catalyze the deamination of a residue adjacent to a target residue, thereby narrowing the deamination window. The ability to narrow the deaminataion window may prevent unwanted deamination of residues adjacent of specific target residues, which may decrease or prevent off-target effects.

In some embodiments, any of the fusion proteins provided herein comprise a deaminase domain (e.g., a cytidine deaminase domain) that has reduced catalytic deaminase activity. In some embodiments, any of the fusion proteins provided herein comprise a deaminase domain (e.g., a cytidine deaminase domain) that has a reduced catalytic deaminase activity as compared to an appropriate control. For example, the appropriate control may be the deaminase activity of the deaminase prior to introducing one or more mutations into the deaminase. In other embodiments, the appropriate control may be a wild-type deaminase. In some embodiments, the appropriate control is a wild-type apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the appropriate control is an APOBEC1 deaminase, an APOBEC2 deaminase, an APOBEC3A deaminase, an APOBEC3B deaminase, an APOBEC3C deaminase, an APOBEC3D deaminase, an APOBEC3F deaminase, an APOBEC3G deaminase, or an APOBEC3H deaminase. In some embodiments, the appropriate control is an activation induced deaminase (AID). In some embodiments, the appropriate control is a cytidine deaminase 1 from Petromyzon marinus (pmCDA1). In some embodiments, the deaminase domain may be a deaminase domain that has at least 1%, at least 5%, at least 15%, at least 20%, at least 25%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or at least 95% less catalytic deaminase activity as compared to an appropriate control.

In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising one or more mutations selected from the group consisting of H121X, H122X, R126X, R126X, R118X, W90X, W90X, and R132X of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase, wherein X is any amino acid. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising one or more mutations selected from the group consisting of H121R, H122R, R126A, R126E, R118A, W90A, W90Y, and R132E of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase.

In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising one or more mutations selected from the group consisting of D316X, D317X, R320X, R320X, R313X, W285X, W285X, R326X of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase, wherein X is any amino acid. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising one or more mutations selected from the group consisting of D316R, D317R, R320A, R320E, R313A, W285A, W285Y, R326E of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase.

In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a H121R and a H122R mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R126A mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R126E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R118A mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W90A mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W90Y mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R132E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W90Y and a R126E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R126E and a R132E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W90Y and a R132E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W90Y, R126E, and R132E mutation of rAPOBEC1 (SEQ ID NO: 284), or one or more corresponding mutations in another APOBEC deaminase.

In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a D316R and a D317R mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R320A mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R320E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R313A mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W285A mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W285Y mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R326E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W285Y and a R320E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a R320E and a R326E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W285Y and a R326E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase. In some embodiments, any of the fusion proteins provided herein comprise an APOBEC deaminase comprising a W285Y, R320E, and R326E mutation of hAPOBEC3G (SEQ ID NO: 275), or one or more corresponding mutations in another APOBEC deaminase.

Some aspects of this disclosure provide fusion proteins comprising (i) a nuclease-inactive Cas9 domain; and (ii) a nucleic acid editing domain. In some embodiments, a nuclease-inactive Cas9 domain (dCas9), comprises an amino acid sequence that is at least 80%, at least 85%, at least 90%, at least 92%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% identical to the amino acid sequence of a Cas9 as provided by any one of SEQ ID NOs: 11-260, and comprises mutations that inactivate the nuclease activity of Cas9. Mutations that render the nuclease domains of Cas9 inactive are well-known in the art. For example, the DNA cleavage domain of Cas9 is known to include two subdomains, the HNH nuclease subdomain and the RuvC1 subdomain. The HNH subdomain cleaves the strand complementary to the gRNA, whereas the RuvC1 subdomain cleaves the non-complementary strand. Mutations within these subdomains can silence the nuclease activity of Cas9. For example, the mutations D10A and H840A completely inactivate the nuclease activity of S. pyogenes Cas9 (Jinek et al., Science. 337:816-821(2012); Qi et al., Cell. 28; 152(5):1173-83 (2013)). In some embodiments, the dCas9 of this disclosure comprises a D10A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the dCas9 of this disclosure comprises a H840A mutation of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the dCas9 of this disclosure comprises both D10A and H840A mutations of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. In some embodiments, the Cas9 further comprises a histidine residue at position 840 of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. The presence of the catalytic residue H840 restores the acvitity of the Cas9 to cleave the non-edited strand containing a G opposite the targeted C. Restoration of H840 does not result in the cleavage of the target strand containing the C. In some embodiments, the dCas9 comprises an amino acid sequence of SEQ ID NO: 263. It is to be understood that other mutations that inactivate the nuclease domains of Cas9 may also be included in the dCas9 of this disclosure.

The Cas9 or dCas9 domains comprising the mutations disclosed herein, may be a full-length Cas9, or a fragment thereof. In some embodiments, proteins comprising Cas9, or fragments thereof, are referred to as “Cas9 variants.” A Cas9 variant shares homology to Cas9, or a fragment thereof. For example a Cas9 variant is at least about 70% identical, at least about 80% identical, at least about 90% identical, at least about 95% identical, at least about 96% identical, at least about 97% identical, at least about 98% identical, at least about 99% identical, at least about 99.5% identical, or at least about 99.9% to wild type Cas9. In some embodiments, the Cas9 variant comprises a fragment of Cas9 (e.g., a gRNA binding domain or a DNA-cleavage domain), such that the fragment is at least about 70% identical, at least about 80% identical, at least about 90% identical, at least about 95% identical, at least about 96% identical, at least about 97% identical, at least about 98% identical, at least about 99% identical, at least about 99.5% identical, or at least about 99.9% identical to the corresponding fragment of wild type Cas9, e.g., a Cas9 comprising the amino acid sequence of SEQ ID NO: 10.

Any of the Cas9 fusion proteins of this disclosure may further comprise a nucleic acid editing domain (e.g., an enzyme that is capable of modifying nucleic acid, such as a deaminase). In some embodiments, the nucleic acid editing domain is a DNA-editing domain. In some embodiments, the nucleic acid editing domain has deaminase activity. In some embodiments, the nucleic acid editing domain comprises or consists of a deaminase or deaminase domain. In some embodiments, the deaminase is a cytidine deaminase. In some embodiments, the deaminase is an apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the deaminase is an APOBEC1 family deaminase. In some embodiments, the deaminase is an activation-induced cytidine deaminase (AID). Some nucleic-acid editing domains as well as Cas9 fusion proteins including such domains are described in detail herein. Additional suitable nucleic acid editing domains will be apparent to the skilled artisan based on this disclosure and knowledge in the field.

Some aspects of the disclosure provide a fusion protein comprising a Cas9 domain fused to a nucleic acid editing domain, wherein the nucleic acid editing domain is fused to the N-terminus of the Cas9 domain. In some embodiments, the Cas9 domain and the nucleic acid editing-editing domain are fused via a linker. In some embodiments, the linker comprises a (GGGS)_n (SEQ ID NO: 265), a (GGGGS)_n (SEQ ID NO: 5), a (G)_n, an (EAAAK)_n (SEQ ID NO: 6), a (GGS)_n, (SGGS)_n (SEQ ID NO: 4288), an SGSETPGTSESATPES (SEQ ID NO: 7) motif (see, e.g., Guilinger J P, Thompson D B, Liu D R. Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification. Nat. Biotechnol. 2014; 32(6): 577-82; the entire contents are incorporated herein by reference), or an (XP)_n motif, or a combination of any of these, wherein n is independently an integer between 1 and 30. In some embodiments, n is independently 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30, or, if more than one linker or more than one linker motif is present, any combination thereof. In some embodiments, the linker comprises a (GGS)_n motif, wherein n is 1,2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15. In some embodiments, the linker comprises a (GGS)_n motif, wherein n is 1, 3, or 7. In some embodiments, the linker comprises the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7). Additional suitable linker motifs and linker configurations will be apparent to those of skill in the art. In some embodiments, suitable linker motifs and configurations include those described in Chen et al., Fusion protein linkers: property, design and functionality. Adv Drug Deliv Rev. 2013; 65(10):1357-69, the entire contents of which are incorporated herein by reference. Additional suitable linker sequences will be apparent to those of skill in the art based on the instant disclosure. In some embodiments, the general architecture of exemplary Cas9 fusion proteins provided herein comprises the structure:

• • [NH₂]-[nucleic acid editing domain]-[Cas9]-[COOH] or
  • [NH₂]-[nucleic acid editing domain]-[linker]-[Cas9]-[COOH],wherein NH₂ is the N-terminus of the fusion protein, and COOH is the C-terminus of the fusion protein.

The fusion proteins of the present disclosure may comprise one or more additional features. For example, in some embodiments, the fusion protein comprises a nuclear localization sequence (NLS). In some embodiments, the NLS of the fusion protein is localized between the nucleic acid editing domain and the Cas9 domain. In some embodiments, the NLS of the fusion protein is localized C-terminal to the Cas9 domain.

Other exemplary features that may be present are localization sequences, such as cytoplasmic localization sequences, export sequences, such as nuclear export sequences, or other localization sequences, as well as sequence tags that are useful for solubilization, purification, or detection of the fusion proteins. Suitable protein tags provided herein include, but are not limited to, biotin carboxylase carrier protein (BCCP) tags, myc-tags, calmodulin-tags, FLAG-tags, hemagglutinin (HA)-tags, polyhistidine tags, also referred to as histidine tags or His-tags, maltose binding protein (MBP)-tags, nus-tags, glutathione-S-transferase (GST)-tags, green fluorescent protein (GFP)-tags, thioredoxin-tags, S-tags, Softags (e.g., Softag 1, Softag 3), strep-tags, biotin ligase tags, FlAsH tags, V5 tags, and SBP-tags. Additional suitable sequences will be apparent to those of skill in the art. In some embodiments, the fusion protein comprises one or more His tags.

In some embodiments, the nucleic acid editing domain is a deaminase. For example, in some embodiments, the general architecture of exemplary Cas9 fusion proteins with a deaminase domain comprises the structure:

• • [NH₂]-[NLS]-[deaminase]-[Cas9]-[COOH],
  • [NH₂]-[Cas9]-[deaminase]-[COOH],
  • [NH₂]-[deaminase]-[Cas9]-[COOH], or
  • [NH₂]-[deaminase]-[Cas9]-[NLS]-[COOH]wherein NLS is a nuclear localization sequence, NH₂ is the N-terminus of the fusion protein, and COOH is the C-terminus of the fusion protein. Nuclear localization sequences are known in the art and would be apparent to the skilled artisan. For example, NLS sequences are described in Plank et al., PCT/EP2000/011690, the contents of which are incorporated herein by reference for their disclosure of exemplary nuclear localization sequences. In some embodiments, a NLS comprises the amino acid sequence PKKKRKV (SEQ ID NO: 741) or MDSLLMNRRKFLYQFKNVRWAKGRRETYLC (SEQ ID NO: 742). In some embodiments, a linker is inserted between the Cas9 and the deaminase. In some embodiments, the NLS is located C-terminal of the Cas9 domain. In some embodiments, the NLS is located N-terminal of the Cas9 domain. In some embodiments, the NLS is located between the deaminase and the Cas9 domain. In some embodiments, the NLS is located N-terminal of the deaminase domain. In some embodiments, the NLS is located C-terminal of the deaminase domain.

One exemplary suitable type of nucleic acid editing domain is a cytidine deaminase, for example, of the APOBEC family. The apolipoprotein B mRNA-editing complex (APOBEC) family of cytidine deaminase enzymes encompasses eleven proteins that serve to initiate mutagenesis in a controlled and beneficial manner.²⁹ One family member, activation-induced cytidine deaminase (AID), is responsible for the maturation of antibodies by converting cytosines in ssDNA to uracils in a transcription-dependent, strand-biased fashion.³⁰ The apolipoprotein B editing complex 3 (APOBEC3) enzyme provides protection to human cells against a certain HIV-1 strain via the deamination of cytosines in reverse-transcribed viral ssDNA.³¹ These proteins all require a Zn²⁺-coordinating motif (His-X-Glu-X_23-26-Pro-Cys-X_2-4-Cys; SEQ ID NO: 598) and bound water molecule for catalytic activity. The Glu residue acts to activate the water molecule to a zinc hydroxide for nucleophilic attack in the deamination reaction. Each family member preferentially deaminates at its own particular “hotspot”, ranging from WRC (W is A or T, R is A or G) for hAID, to TTC for hAPOBEC3F.³² A recent crystal structure of the catalytic domain of APOBEC3G revealed a secondary structure comprised of a five-stranded β-sheet core flanked by six α-helices, which is believed to be conserved across the entire family.³³ The active center loops have been shown to be responsible for both ssDNA binding and in determining “hotspot” identity.³⁴ Overexpression of these enzymes has been linked to genomic instability and cancer, thus highlighting the importance of sequence-specific targeting.³⁵

Some aspects of this disclosure relate to the recognition that the activity of cytidine deaminase enzymes such as APOBEC enzymes can be directed to a specific site in genomic DNA. Without wishing to be bound by any particular theory, advantages of using Cas9 as a recognition agent include (1) the sequence specificity of Cas9 can be easily altered by simply changing the sgRNA sequence; and (2) Cas9 binds to its target sequence by denaturing the dsDNA, resulting in a stretch of DNA that is single-stranded and therefore a viable substrate for the deaminase. It should be understood that other catalytic domains, or catalytic domains from other deaminases, can also be used to generate fusion proteins with Cas9, and that the disclosure is not limited in this regard.

Some aspects of this disclosure are based on the recognition that Cas9:deaminase fusion proteins can efficiently deaminate nucleotides at positions 3-11 according to the numbering scheme in FIG. 3. In view of the results provided herein regarding the nucleotides that can be targeted by Cas9:deaminase fusion proteins, a person of skill in the art will be able to design suitable guide RNAs to target the fusion proteins to a target sequence that comprises a nucleotide to be deaminated.

In some embodiments, the deaminase domain and the Cas9 domain are fused to each other via a linker. Various linker lengths and flexibilities between the deaminase domain (e.g., AID) and the Cas9 domain can be employed (e.g., ranging from very flexible linkers of the form (GGGGS)_n (SEQ ID NO: 5), (GGS)_n, and (G)_n to more rigid linkers of the form (EAAAK)_n (SEQ ID NO: 6), (SGGS)_n (SEQ ID NO: 4288), SGSETPGTSESATPES (SEQ ID NO: 7) (see, e.g., Guilinger J P, Thompson D B, Liu D R. Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification. Nat. Biotechnol. 2014; 32(6): 577-82; the entire contents are incorporated herein by reference) and (XP)_n)³⁶ in order to achieve the optimal length for deaminase activity for the specific application. In some embodiments, the linker comprises a (GGS)_n motif, wherein n is 1, 3, or 7. In some embodiments, the linker comprises a (an SGSETPGTSESATPES (SEQ ID NO: 7) motif.

Some exemplary suitable nucleic-acid editing domains, e.g., deaminases and deaminase domains, that can be fused to Cas9 domains according to aspects of this disclosure are provided below. It should be understood that, in some embodiments, the active domain of the respective sequence can be used, e.g., the domain without a localizing signal (nuclear localization sequence, without nuclear export signal, cytoplasmic localizing signal).

Human AID:

(SEQ ID NO: 266)
MDSLLMNRRKFLYQFKNVRWAKGRRETYLCYVVKRRDSATSFSLDFGY
LRNKNGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVAD
FLRGNPNLSLRIFTARLYFCEDRKAEPEGLRRLHRAGVQIAIMTFKDY
FYCWNTFVENHERTFKAWEGLHENSVRLSRQLRRTLLPLYEVDDLRDA
FRTLGL

(underline: nuclear localization sequence; double underline: nuclear export signal)

Mouse AID:

(SEQ ID NO: 267)
MDSLLMKQKKFLYHFKNVRWAKGRHETYLCYVVKRRDSATSCSLDFGH
LRNKSGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVAE
FLRWNPNLSLRIFTARLYFCEDRKAEPEGLRRLHRAGVQIGIMTFKDY
FYCWNTFVENRERTFKAWEGLHENSVRLTRQLRRILLPLYEVDDLRDA
FRMLGF

(underline: nuclear localization sequence; double underline: nuclear export signal)

Dog AID:

(SEQ ID NO: 268)
MDSLLMKQRKFLYHFKNVRWAKGRHETYLCYVVKRRDSATSFSLDFGH
LRNKSGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVAD
FLRGYPNLSLRIFAARLYFCEDRKAEPEGLRRLHRAGVQIAIMTFKDY
FYCWNTFVENREKTFKAWEGLHENSVRLSRQLRRILLPLYEVDDLRDA
FRTLGL

(underline: nuclear localization sequence; double underline: nuclear export signal)

Bovine AID:

(SEQ ID NO: 269)
MDSLLKKQRQFLYQFKNVRWAKGRHETYLCYVVKRRDSPTSFSLDFGH
LRNKAGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVAD
FLRGYPNLSLRIFTARLYFCDKERKAEPEGLRRLHRAGVQIAIMTFKD
YFYCWNTFVENHERTFKAWEGLHENSVRKSRQLRRILLPLYEVDDLRD
AFRTLGL

(underline: nuclear localization sequence; double underline: nuclear export signal)

Rat AID

(SEQ ID NO: 5725)
MAVGSKPKAALVGPHWERERIWCFLCSTGLGTQQTGQTSRWLRPAATQ
DPVSPPRSLLMKQRKFLYHFKNVRWAKGRHETYLCYVVKRRDSATSFS
LDFGYLRNKSGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCA
RHVADFLRGNPNLSLRIFTARLTGWGALPAGLMSPARPSDYFYCWNTF
VENHERTFKAWEGLHENSVRLSRRLRRILLPLYEVDDLRDAFRTLGL

(underline: nuclear localization sequence; double underline: nuclear export signal)

Mouse APOBEC-3:

(SEQ ID NO: 270)
MGPFCLGCSHRKCYSPIRNLISQETFKFHFKNLGYAKGRKDTFLCYEV
TRKDCDSPVSLHHGVFKNKDNIHAEICFLYWFHDKVLKVLSPREEFKI
TWYMSWSPCFECAEQIVRFLATHHNLSLDIFSSRLYNVQDPETQQNLC
RLVQEGAQVAAMDLYEFKKCWKKFVDNGGRRFRPWKRLLTNFRYQDSK
LQEILRPCYIPVPSSSSSTLSNICLTKGLPETRFCVEGRRMDPLSEEE
FYSQFYNQRVKHLCYYHRMKPYLCYQLEQFNGQAPLKGCLLSEKGKQH
AEILFLDKIRSMELSQVTITCYLTWSPCPNCAWQLAAFKRDRPDLILH
IYTSRLYFHWKRPFQKGLCSLWQSGILVDVMDLPQFTDCWTNFVNPKR
PFWPWKGLEIISRRTQRRLRRIKESWGLQDLVNDFGNLQLGPPMS

(italic: nucleic acid editing domain)

Rat APOBEC-3:

(SEQ ID NO: 271)
MGPFCLGCSHRKCYSPIRNLISQETFKFHFKNLRYAIDRKDTFLCYEV
TRKDCDSPVSLHHGVFKNKDNIHAEICFLYWFHDKVLKVLSPREEFKI
TWYMSWSPCFECAEQVLRFLATHHNLSLDIFSSRLYNIRDPENQQNLC
RLVQEGAQVAAMDLYEFKKCWKKFVDNGGRRFRPWKKLLTNFRYQDSK
LQEILRPCYIPVPSSSSSTLSNICLTKGLPETRFCVERRRVHLLSEEE
FYSQFYNQRVKHLCYYHGVKPYLCYQLEQFNGQAPLKGCLLSEKGKQH
AEILFLDKIRSMELSQVIITCYLTWSPCPNCAWQLAAFKRDRPDLILH
IYTSRLYFHWKRPFQKGLCSLWQSGILVDVMDLPQFTDCWTNFVNPKR
PFWPWKGLEIISRRTQRRLHRIKESWGLQDLVNDFGNLQLGPPMS

(italic: nucleic acid editing domain)

Rhesus macaque APOBEC-3G:

(SEQ ID NO: 272)
MVEPMDPRTFVSNFNNRPILSGLNTVWLCCEVKTKDPSGPPLDAKIFQ
GKVYSKAKYHPEM              RFLRWFHKWRQLHHDQEYKVTWYVSWSPCTRCANS
VATFLAKDPKYTLTIFVARLYYFWKPDYQQALRILCQKRGGPHATMKI
MNYNEFQDCWNKFVDGRGKPFKPRNNLPKHYTLLQATLGELLRHLMDP
GTFTSNFNNKPWVSGQHETYLCYKVERLHNDTWVPLNQHRGFLRNQAP
NIHGFPKGRHAELCFLDLIPFWKLDGQQYRVTCFTSWSPCFSCAQEMA
KFISNNEHVSLCIFAARIYDDQGRYQEGLRALHRDGAKIAMMNYSEFE
YCWDTFVDRQGRPFQPWDGLDEHSQALSGRLRAI

(italic: nucleic acid editing domain; underline: cytoplasmic localization signal)

Chimpanzee APOBEC-3G:

(SEQ ID NO: 273)
MKPHFRNPVERMYQDTFSDNFYNRPILSHRNTVWLCYEVKTKGPSRPP
LDAKIFRGQVYSKLKYHPEMRFFHWFSKWRKLHRDQEYEVTWYISWSP
CTKCTRDVATFLAEDPKVTLTIFVARLYYFWDPDYQEALRSLCQKRDG
PRATMKIMNYDEFQHCWSKFVYSQRELFEPWNNLPKYYILLHIMLGEI
LRHSMDPPTFTSNFNNELWVRGRHETYLCYEVERLHNDTWVLLNQRRG
FLCNQAPHKHGFLEGRHAELCFLDVIPFWKLDLHQDYRVTCFTSWSPC
FSCAQEMAKFISNNKHVSLCIFAARIYDDQGRCQEGLRTLAKAGAKIS
IMTYSEFKHCWDTFVDHQGCPFQPWDGLEEHSQALSGRLRAILQNQGN

(italic: nucleic acid editing domain; underline: cytoplasmic localization signal)

Green monkey APOBEC-3G:

(SEQ ID NO: 274)
MNPQIRNMVEQMEPDIFVYYFNNRPILSGRNTVWLCYEVKTKDPSGPP
LDANIFQGKLYPEAKDHPEMKFLHWFRKWRQLHRDQEYEVTWYVSWSP
CTRCANSVATFLAEDPKVTLTIFVARLYYFWKPDYQQALRILCQERGG
PHATMKIMNYNEFQHCWNEFVDGQGKPFKPRKNLPKHYTLLHATLGEL
LRHVMDPGTFTSNFNNKPWVSGQRETYLCYKVERSHNDTWVLLNQHRG
FLRNQAPDRHGFPKGRHAELCFLDLIPFWKLDDQQYRVTCFTSWSPCF
SCAQKMAKFISNNKHVSLCIFAARIYDDQGRCQEGLRTLHRDGAKIAV
MNYSEFEYCWDTFVDRQGRPFQPWDGLDEHSQALSGRLRAI

(italic: nucleic acid editing domain; underline: cytoplasmic localization signal)

Human APOBEC-3G:

(SEQ ID NO: 275)
MKPHFRNTVERMYRDTFSYNFYNRPILSRRNTVWLCYEVKTKGPSRPPLD
AKIFRGQVYSELKYHPEMRFFHWFSKWRKLHRDQEYEVTWYISWSPCTKC
TRDMATFLAEDPKVTLTIFVARLYYFWDPDYQEALRSLCQKRDGPRATMK
IMNYDEFQHCWSKFVYSQRELFEPWNNLPKYYILLHIMLGEILRHSMDPP
TFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQAPHKH
GFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFIS
KNKHVSLCIFTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHCWDTF
VDHQGCPFQPWDGLDEHSQDLSGRLRAILQNQEN

(italic: nucleic acid editing domain; underline: cytoplasmic localization signal)

Human APOBEC-3F:

(SEQ ID NO: 276)
MKPHFRNTVERMYRDTFSYNFYNRPILSRRNTVWLCYEVKTKGPSRPRL
DAKIFRGQVYSQPEHHAEMCFLSWFCGNQLPAYKCFQITWFVSWTPCPD
CVAKLAEFLAEHPNVTLTISAARLYYYWERDYRRALCRLSQAGARVKIM
DDEEFAYCWENFVYSEGQPFMPWYKFDDNYAFLHRTLKEILRNPMEAMY
PHIFYFHFKNLRKAYGRNESWLCFTMEVVKHHSPVSWKRGVFRNQVDPE
THCHAERCFLSWFCDDILSPNTNYEVTWYTSWSPCPECAGEVAEFLARH
SNVNLTIFTARLYYFWDTDYQEGLRSLSQEGASVEIMGYKDFKYCWENF
VYNDDEPFKPWKGLKYNFLFLDSKLQEILE

(italic: nucleic acid editing domain)

Human APOBEC-3B:

(SEQ ID NO: 277)
MNPQIRNPMERMYRDTFYDNFENEPILYGRSYTWLCYEVKIKRGRSNLL
WDTGVFRGQVYFKPQYHAEMCFLSWFCGNQLPAYKCFQITWFVSWTPCP
DCVAKLAEFLSEHPNVTLTISAARLYYYWERDYRRALCRLSQAGARVTI
MDYEEFAYCWENFVYNEGQQFMPWYKFDENYAFLHRTLKEILRYLMDPD
TFTFNFNNDPLVLRRRQTYLCYEVERLDNGTWVLMDQHMGFLCNEAKNL
LCGFYGRHAELRFLDLVPSLQLDPAQIYRVTWFISWSPCFSWGCAGEVR
AFLQENTHVRLRIFAARIYDYDPLYKEALQMLRDAGAQVSIMTYDEFEY
CWDTFVYRQGCPFQPWDGLEEHSQALSGRLRAILQNQGN

(italic: nucleic acid editing domain)

Rat APOBEC-3B:

(SEQ ID NO: 5729)
MQPQGLGPNAGMGPVCLGCSHRRPYSPIRNPLKKLYQQTFYFHFKNVRY
AWGRKNNFLCYEVNGMDCALPVPLRQGVFRKQGHIHAELCFIYWFHDKV
WLRVLSPMEEFKVTYMSWSPCSKCAEQVARFLAAHRNLSLAIFSSRLYY
YLRNPNYQQKLCRLIQEGVHVAAMDLPEFKKCWNKFVDNDGQPFRPWMR
LRINFSFYDCKLQEIFSRMNLLREDVFYLQFNNSHRVKPVQNRYYRRKS
YLCYQLERANGQEPLKGYLLYKKGEQHVEILFLEKMRSMELSQVRITCY
LTWSPCPNCARQLAAFKKDHPDLILRIYTSRLYFYWRKKFQKGLCTLWR
SGIHVDVMDLPQFADCWTNFVNPQRPFRPWNELEKNSWRIQRRLRRIKE
SWGL

Bovine APOBEC-3B:

(SEQ ID NO: 5730)
DGWEVAFRSGTVLKAGVLGVSMTEGWAGSGHPGQGACVWTPGTRNTMN
LLREVLFKQQFGNQPRVPAPYYRRKTYLCYQLKQRNDLTLDRGCFRNK
KQRHAEIRFIDKINSLDLNPSQSYKIICYITWSPCPNCANELVNFITR
NNHLKLEIFASRLYFHWIKSFKMGLQDLQNAGISVAVMTHTEFEDCWE
QFVDNQSRPFQPWDKLEQYSASIRRRLQRILTAPI

Chimpanzee APOBEC-3B:

(SEQ ID NO: 5731)
MNPQIRNPMEWMYQRTFYYNFENEPILYGRSYTWLCYEVKIRRGHSNLLW
DTGVFRGQMYSQPEHHAEMCFLSWFCGNQLSAYKCFQITWFVSWTPCPDC
VAKLAKFLAEHPNVTLTISAARLYYYWERDYRRALCRLSQAGARVKIMDD
EEFAYCWENFVYNEGQPFMPWYKFDDNYAFLHRTLKEIIRHLMDPDTFTF
NFNNDPLVLRRHQTYLCYEVERLDNGTWVLMDQHMGFLCNEAKNLLCGFY
GRHAELRFLDLVPSLQLDPAQIYRVTWFISWSPCFSWGCAGQVRAFLQEN
THVRLRIFAARIYDYDPLYKEALQMLRDAGAQVSIMTYDEFEYCWDTFVY
RQGCPFQPWDGLEEHSQALSGRLRAILQVRASSLCMVPHRPPPPPQSPGP
CLPLCSEPPLGSLLPTGRPAPSLPFLLTASFSFPPPASLPPLPSLSLSPG
HLPVPSFHSLTSCSIQPPCSSRIRETEGWASVSKEGRDLG

Human APOBEC-3C:

(SEQ ID NO: 278)
MNPQRNPMKAMYPGTFYFQFKNLWEANDRNETWLCFTVEGIKRRSVVSW
KTGVFRNQVDSETHCHAERCFLSWFCDDILSPNTKYQVTWYTSWSPCPD
CAGEVAEFLARHSNVNLTIFTARLYYFQYPCYQEGLRSLSQEGVAVEIM
DYEDFKYCWENFVYNDNEPFKPWKGLKTNFRLLKRRLRESLQ

(italic: nucleic acid editing domain)

Gorilla APOBEC3C

(SEQ ID NO: 5726)
MNPQRNPMKAMYPGTFYFQFKNLWEANDRNETWLCFTVEGIKRRSVVSWK
TGVFRNQVDSETHCHAERCFLSWFCDDILSPNTNYQVTWYTSWSPCPECA
GEVAEFLARHSNVNLTIFTARLYYFQDTDYQEGLRSLSQEGVAVKIMDYK
DFKYCWENFVYNDDEPFKPWKGLKYNFRFLKRRLQEILE

(italic: nucleic acid editing domain)

Human APOBEC-3A:

(SEQ ID NO: 279)
MEASPASGPRHLMDPHIFTSNFNNGIGRHKTYLCYEVERLDNGTSVKMDQ
HRGFLHNQAKNLLCGFYGRHAELRFLDLVPSLQLDPAQIYRVTWFISWSP
CFSWGCAGEVRAFLQENTHVRLRIFAARIYDYDPLYKEALQMLRDAGAQV
SIMTYDEFKHCWDTFVDHQGCPFQPWDGLDEHSQALSGRLRAILQNQGN

(italic: nucleic acid editing domain)

Rhesus macaque APOBEC-3A:

(SEQ ID NO: 5727)
MDGSPASRPRHLMDPNTFTFNFNNDLSVRGRHQTYLCYEVERLDNGTWVP
MDERRGFLCNKAKNVPCGDYGCHVELRFLCEVPSWQLDPAQTYRVTWFIS
WSPCFRRGCAGQVRVFLQENKHVRLRIFAARIYDYDPLYQEALRTLRDAG
AQVSIMTYEEFKHCWDTFVDRQGRPFQPWDGLDEHSQALSGRLRAILQNQ
GN

(italic: nucleic acid editing domain)

Bovine APOBEC-3A:

(SEQ ID NO: 5728)
MDEYTFTENFNNQGWPSKTYLCYEMERLDGDATIPLDEYKGFVRNKGLDQ
PEKPCHAELYFLGKIHSWNLDRNQHYRLTCFISWSPCYDCAQKLTTFLKE
NHHISLHILASRIYTHNRFGCHQSGLCELQAAGARITIMTFEDFKHCWET
FVDHKGKPFQPWEGLNVKSQALCTELQAILKTQQN

(italic: nucleic acid editing domain)

Human APOBEC-3H:

(SEQ ID NO: 280)
MALLTAETFRLQFNNKRRLRRPYYPRKALLCYQLTPQNGSTPTRGYFENK
KKCHAEICFINEIKSMGLDETQCYQVTCYLTWSPCSSCAWELVDFIKAHD
HLNLGIFASRLYYHWCKPQQKGLRLLCGSQVPVEVMGFPKFADCWENFVD
HEKPLSFNPYKMLEELDKNSRAIKRRLERIKIPGVRAQGRYMDILCDAEV

(italic: nucleic acid editing domain)

Rhesus macaque APOBEC-3H:

(SEQ ID NO: 5732)
MALLTAKTFSLQFNNKRRVNKPYYPRKALLCYQLTPQNGSTPTRGHLKNK
KKDHAEIRFINKIKSMGLDETQCYQVTCYLTWSPCPSCAGELVDFIKAHR
HLNLRIFASRLYYHWRPNYQEGLLLLCGSQVPVEVMGLPEFTDCWENFVD
HKEPPSFNPSEKLEELDKNSQAIKRRLERIKSRSVDVLENGLRSLQLGPV
TPSSSIRNSR

Human APOBEC-3D:

(SEQ ID NO: 281)
MNPQRNPMERMYRDTFYDNFENEPILYGRSYTWLCYEVKIKRGRSNLLW
DTGVFRGPVLPKRQSNHRQEVYFRFENHAEMCFLSWFCGNRLPANRRFQ
ITWFVSWNPCLPCVVKVTKFLAEHPNVTLTISAARLYYYRDRDWRWVLL
RLHKAGARVKIMDYEDFAYCWENFVCNEGQPFMPWYKFDDNYASLHRTL
KEILRNPMEAMYPHIFYFHFKNLLKACGRNESWLCFTMEVTKHHSAVFR
KRGVFRNQVDPETHCHAERCFLSWFCDDILSPNTNYEVTWYTSWSPCPE
CAGEVAEFLARHSNVNLTIFTARLCYFWDTDYQEGLCSLSQEGASVKIM
GYKDFVSCWKNFVYSDDEPFKPWKGLQTNFRLLKRRLREILQ

(italic: nucleic acid editing domain)

Human APOBEC-1:

(SEQ ID NO: 282)
MTSEKGPSTGDPTLRRRIEPWEFDVFYDPRELRKEACLLYEIKWGMSRKI
WRSSGKNTTNHVEVNFIKKFTSERDFHPSMSCSITWFLSWSPCWECSQAI
REFLSRHPGVTLVIYVARLFWHMDQQNRQGLRDLVNSGVTIQIMRASEYY
HCWRNFVNYPPGDEAHWPQYPPLWMMLYALELHCIILSLPPCLKISRRWQ
NHLTFFRLHLQNCHYQTIPPHILLATGLIHPSVAWR

Mouse APOBEC-1:

(SEQ ID NO: 283)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSV
WRHTSQNTSNHVEVNFLEKFTTERYFRPNTRCSITWFLSWSPCGECSRAI
TEFLSRHPYVTLFIYIARLYHHTDQRNRQGLRDLISSGVTIQIMTEQEYC
YCWRNFVNYPPSNEAYWPRYPHLWVKLYVLELYCIILGLPPCLKILRRKQ
PQLTFFTITLQTCHYQRIPPHLLWATGLK

Rat APOBEC-1:

(SEQ ID NO: 284)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHS
IWRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSR
AITEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQ
ESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNIL
RRKQPQLTFFTIALQSCHYQRLPPHILWATGLK

Human APOBEC-2:

(SEQ ID NO: 5733)
MAQKEEAAVATEAASQNGEDLENLDDPEKLKELIELPPFEIVTGERLPAN
FFKFQFRNVE
YSSGRNKTFLCYVVEAQGKGGQVQASRGYLEDEHAAAHAEEAFFNTILPA
FDPALRYNVTWYVSSSPCAACADRIIKTLSKTKNLRLLILVGRLFMWEEP
EIQAALKKLKEAGCKLRIMKPQDFEYVWQNFVEQEEGESKAFQPWEDIQE
NFLYYEEKLADILK

Mouse APOBEC-2:

(SEQ ID NO: 5734)
MAQKEEAAEAAAPASQNGDDLENLEDPEKLKELIDLPPFEIVTGVRLPVN
FFKFQFRNVEYSSGRNKTFLCYVVEVQSKGGQAQATQGYLEDEHAGAHAE
EAFFNTILPAFDPALKYNVTWYVSSSPCAACADRILKTLSKTKNLRLLIL
VSRLFMWEEPEVQAALKKLKEAGCKLRIMKPQDFEYIWQNFVEQEEGESK
AFEPWEDIQENFLYYEEKLADILK

Rat APOBEC-2:

(SEQ ID NO: 5735)
MAQKEEAAEAAAPASQNGDDLENLEDPEKLKELIDLPPFEIVTGVRLPV
NFFKFQFRNVEYSSGRNKTFLCYVVEAQSKGGQVQATQGYLEDEHAGAH
AEEAFFNTILPAFDPALKYNVTWYVSSSPCAACADRILKTLSKTKNLRL
LILVSRLFMWEEPEVQAALKKLKEAGCKLRIMKPQDFEYLWQNFVEQEE
GESKAFEPWEDIQENFLYYEEKLADILK

Bovine APOBEC-2:

(SEQ ID NO: 5736)
MAQKEEAAAAAEPASQNGEEVENLEDPEKLKELIELPPFEIVTGERLPAH
YFKFQFRNVE
YSSGRNKTFLCYVVEAQSKGGQVQASRGYLEDEHATNHAEEAFFNSIMPT
FDPALRYMVTWYVSSSPCAACADRIVKTLNKTKNLRLLILVGRLFMWEEP
EIQAALRKLKEAGCRLRIMKPQDFEYIWQNFVEQEEGESKAFEPWEDIQE
NFLYYEEKLADILK

Petromyzon marinus CDA1 (pmCDA1)

(SEQ ID NO: 5738)
MTDAEYVRIHEKLDIYTFKKQFFNNKKSVSHRCYVLFELKRRGERRACF
WGYAVNKPQSGTERGIHAEIFSIRKVEEYLRDNPGQFTINWYSSWSPCA
DCAEKILEWYNQELRGNGHTLKIWACKLYYEKNARNQIGLWNLRDNGVG
LNVMVSEHYQCCRKIFIQSSHNQLNENRWLEKTLKRAEKRRSELSIMIQ
VKILHTTKSPAV

Human APOBEC3G D316R_D317R

(SEQ ID NO: 5739)
MKPHFRNTVERMYRDTFSYNFYNRPILSRRNTVWLCYEVKTKGPSRPPL
DAKIFRGQVYSELKYHPEMRFFHWFSKWRKLHRDQEYEVTWYISWSPCT
KCTRDMATFLAEDPKVTLTIFVARLYYFWDPDYQEALRSLCQKRDGPRA
TMKIMNYDEFQHCWSKFVYSQRELFEPWNNLPKYYILLHIMLGEILRHS
MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQ
APHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQE
MAKFISKNKHVSLCIFTARIYRRQGRCQEGLRTLAEAGAKISIMTYSEF
KHCWDTFVDHQGCPFQPWDGLDEHSQDLSGRLRAILQNQEN

Human APOBEC3G chain A

(SEQ ID NO: 5740)
MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQA
PHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMA
KFISKNKHVSLCIFTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHC
WDTFVDHQGCPFQPWDGLDEHSQDLSGRLRAILQ

Human APOBEC3G chain A D120R_D121R

(SEQ ID NO: 5741)
MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQ
APHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQE
MAKFISKNKHVSLFTARIYRRQGRCQEGLRTLAEAGAKISIMTYSEFKH
CWDTFVDHQGCPFQPWDGLDEHSQDLSGRLRAILQ

In some embodiments, fusion proteins as provided herein comprise the full-length amino acid of a nucleic acid editing enzyme, e.g., one of the sequences provided above. In other embodiments, however, fusion proteins as provided herein do not comprise a full-length sequence of a nucleic acid editing enzyme, but only a fragment thereof. For example, in some embodiments, a fusion protein provided herein comprises a Cas9 domain and a fragment of a nucleic acid editing enzyme, e.g., wherein the fragment comprises a nucleic acid editing domain. Exemplary amino acid sequences of nucleic acid editing domains are shown in the sequences above as italicized letters, and additional suitable sequences of such domains will be apparent to those of skill in the art.

Additional suitable nucleic-acid editing enzyme sequences, e.g., deaminase enzyme and domain sequences, that can be used according to aspects of this invention, e.g., that can be fused to a nuclease-inactive Cas9 domain, will be apparent to those of skill in the art based on this disclosure. In some embodiments, such additional enzyme sequences include deaminase enzyme or deaminase domain sequences that are at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% similar to the sequences provided herein. Additional suitable Cas9 domains, variants, and sequences will also be apparent to those of skill in the art. Examples of such additional suitable Cas9 domains include, but are not limited to, D10A, D10A/D839A/H840A, and D10A/D839A/H840A/N863A mutant domains (See, e.g., Prashant et al., CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering. Nature Biotechnology. 2013; 31(9): 833-838 the entire contents of which are incorporated herein by reference). In some embodiments, the Cas9 comprises a histidine residue at position 840 of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260. The presence of the catalytic residue H840 restores the acvitity of the Cas9 to cleave the non-edited strand containing a G opposite the targeted C. Restoration of H840 does not result in the cleavage of the target strand containing the C.

Additional suitable strategies for generating fusion proteins comprising a Cas9 domain and a deaminase domain will be apparent to those of skill in the art based on this disclosure in combination with the general knowledge in the art. Suitable strategies for generating fusion proteins according to aspects of this disclosure using linkers or without the use of linkers will also be apparent to those of skill in the art in view of the instant disclosure and the knowledge in the art. For example, Gilbert et al., CRISPR-mediated modular RNA-guided regulation of transcription in eukaryotes. Cell. 2013; 154(2):442-51, showed that C-terminal fusions of Cas9 with VP64 using 2 NLS's as a linker (SPKKKRKVEAS, SEQ ID NO: 599), can be employed for transcriptional activation. Mali et al., CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering. Nat Biotechnol. 2013; 31(9):833-8, reported that C-terminal fusions with VP64 without linker can be employed for transcriptional activation. And Maeder et al., CRISPR RNA-guided activation of endogenous human genes. Nat Methods. 2013; 10: 977-979, reported that C-terminal fusions with VP64 using a Gly₄Ser (SEQ ID NO: 5) linker can be used as transcriptional activators. Recently, dCas9-FokI nuclease fusions have successfully been generated and exhibit improved enzymatic specificity as compared to the parental Cas9 enzyme (In Guilinger J P, Thompson D B, Liu D R. Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification. Nat. Biotechnol. 2014; 32(6): 577-82, and in Tsai S Q, Wyvekens N, Khayter C, Foden J A, Thapar V, Reyon D, Goodwin M J, Aryee M J, Joung J K. Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing. Nat Biotechnol. 2014; 32(6):569-76. PMID: 24770325 a SGSETPGTSESATPES (SEQ ID NO: 7) or a GGGGS (SEQ ID NO: 5) linker was used in FokI-dCas9 fusion proteins, respectively).

Some aspects of this disclosure provide fusion proteins comprising (i) a Cas9 enzyme or domain (e.g., a first protein); and (ii) a nucleic acid-editing enzyme or domain (e.g., a second protein). In some aspects, the fusion proteins provided herein further include (iii) a programmable DNA-binding protein, for example, a zinc-finger domain, a TALE, or a second Cas9 protein (e.g., a third protein). Without wishing to be bound by any particular theory, fusing a programmable DNA-binding protein (e.g., a second Cas9 protein) to a fusion protein comprising (i) a Cas9 enzyme or domain (e.g., a first protein); and (ii) a nucleic acid-editing enzyme or domain (e.g., a second protein) may be useful for improving specificity of the fusion protein to a target nucleic acid sequence, or for improving specificity or binding affinity of the fusion protein to bind target nucleic acid sequence that does not contain a canonical PAM (NGG) sequence. In some embodiments, the third protein is a Cas9 protein (e.g, a second Cas9 protein). In some embodiments, the third protein is any of the Cas9 proteins provided herein. In some embodiments, the third protein is fused to the fusion protein N-terminal to the Cas9 protein (e.g., the first protein). In some embodiments, the third protein is fused to the fusion protein C-terminal to the Cas9 protein (e.g., the first protein). In some embodiments, the Cas9 domain (e.g., the first protein) and the third protein (e.g., a second Cas9 protein) are fused via a linker (e.g., a second linker). In some embodiments, the linker comprises a (GGGGS)n (SEQ ID NO: 5), a (G)n, an (EAAAK)n (SEQ ID NO: 6), a (GGS)n, (SGGS)_n (SEQ ID NO: 4288), an SGSETPGTSESATPES (SEQ ID NO: 7), or an (XP)n motif, or a combination of any of these, wherein n is independently an integer between 1 and 30. In some embodiments, the general architecture of exemplary Cas9 fusion proteins provided herein comprises the structure:

• • [NH2]-[nucleic acid-editing enzyme or domain]-[Cas9]-[third protein]-[COOH];
  • [NH2]-[third protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[COOH];
  • [NH2]-[Cas9]-[nucleic acid-editing enzyme or domain]-[third protein]-[COOH];
  • [NH2]-[third protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[COOH];
  • [NH2]-[UGI]-[nucleic acid-editing enzyme or domain]-[Cas9]-[third protein]-[COOH];
  • [NH2]-[UGI]-[third protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[COOH];
  • [NH2]-[UGI]-[Cas9]-[nucleic acid-editing enzyme or domain]-[third protein]-[COOH];
  • [NH2]-[UGI]-[third protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[COOH];
  • [NH2]-[nucleic acid-editing enzyme or domain]-[Cas9]-[third protein]-[UGI]-[COOH];
  • [NH2]-[third protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[UGI]-[COOH];
  • [NH2]-[Cas9]-[nucleic acid-editing enzyme or domain]-[third protein]-[UGI]-[COOH]; or
  • [NH2]-[third protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[UGI]-[COOH];wherein NH2 is the N-terminus of the fusion protein, and COOH is the C-terminus of the fusion protein. In some embodiments, the “]-[” used in the general architecture above indicates the presence of an optional linker sequence. In other examples, the general architecture of exemplary Cas9 fusion proteins provided herein comprises the structure:
  • [NH2]-[nucleic acid-editing enzyme or domain]-[Cas9]-[second Cas9 protein]-[COOH];
  • [NH2]-[second Cas9 protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[COOH];
  • [NH2]-[Cas9]-[nucleic acid-editing enzyme or domain]-[second Cas9 protein]-[COOH];
  • [NH2]-[second Cas9 protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[COOH];
  • [NH2]-[UGI]-[nucleic acid-editing enzyme or domain]-[Cas9]-[second Cas9 protein]-[COOH],
  • [NH2]-[UGI]-[second Cas9 protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[COOH];
  • [NH2]-[UGI]-[Cas9]-[nucleic acid-editing enzyme or domain]-[second Cas9 protein]-[COOH];
  • [NH2]-[UGI]-[second Cas9 protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[COOH];
  • [NH2]-[nucleic acid-editing enzyme or domain]-[Cas9]-[second Cas9 protein]-[UGI]-[COOH];
  • [NH2]-[second Cas9 protein]-[Cas9]-[nucleic acid-editing enzyme or domain]-[UGI]-[COOH];
  • [NH2]-[Cas9]-[nucleic acid-editing enzyme or domain]-[second Cas9 protein]-[UGI]-[COOH]; or
  • [NH2]-[second Cas9 protein]-[nucleic acid-editing enzyme or domain]-[Cas9]-[UGI]-[COOH];wherein NH₂ is the N-terminus of the fusion protein, and COOH is the C-terminus of the fusion protein. In some embodiments, the “]-[” used in the general architecture above indicates the presence of an optional linker sequence. In some embodiments, the second Cas9 is a dCas9 protein. In some examples, the general architecture of exemplary Cas9 fusion proteins provided herein comprises a structure as shown in FIG. 3. It should be appreciated that any of the proteins provided in any of the general architectures of exemplary Cas9 fusion proteins may be connected by one or more of the linkers provided herein. In some embodiments, the linkers are the same. In some embodiments, the linkers are different. In some embodiments, one or more of the proteins provided in any of the general architectures of exemplary Cas9 fusion proteins are not fused via a linker. In some embodiments, the fusion proteins further comprise a nuclear targeting sequence, for example a nuclear localization sequence. In some embodiments, fusion proteins provided herein further comprise a nuclear localization sequence (NLS). In some embodiments, the NLS is fused to the N-terminus of the fusion protein. In some embodiments, the NLS is fused to the C-terminus of the fusion protein. In some embodiments, the NLS is fused to the N-terminus of the third protein. In some embodiments, the NLS is fused to the C-terminus of the third protein. In some embodiments, the NLS is fused to the N-terminus of the Cas9 protein. In some embodiments, the NLS is fused to the C-terminus of the Cas9 protein. In some embodiments, the NLS is fused to the N-terminus of the nucleic acid-editing enzyme or domain. In some embodiments, the NLS is fused to the C-terminus of the nucleic acid-editing enzyme or domain. In some embodiments, the NLS is fused to the N-terminus of the UGI protein. In some embodiments, the NLS is fused to the C-terminus of the UGI protein. In some embodiments, the NLS is fused to the fusion protein via one or more linkers. In some embodiments, the NLS is fused to the fusion protein without a linker

Uracil Glycosylase Inhibitor Fusion Proteins

Some aspects of the disclosure relate to fusion proteins that comprise a uracil glycosylase inhibitor (UGI) domain. In some embodiments, any of the fusion proteins provided herein that comprise a Cas9 domain (e.g., a nuclease active Cas9 domain, a nuclease inactive dCas9 domain, or a Cas9 nickase) may be further fused to a UGI domain either directly or via a linker. Some aspects of this disclosure provide deaminase-dCas9 fusion proteins, deaminase-nuclease active Cas9 fusion proteins and deaminase-Cas9 nickase fusion proteins with increased nucleobase editing efficiency. Without wishing to be bound by any particular theory, cellular DNA-repair response to the presence of U:G heteroduplex DNA may be responsible for the decrease in nucleobase editing efficiency in cells. For example, uracil DNA glycosylase (UDG) catalyzes removal of U from DNA in cells, which may initiate base excision repair, with reversion of the U:G pair to a C:G pair as the most common outcome. As demonstrated in the Examples below, Uracil DNA Glycosylase Inhibitor (UGI) may inhibit human UDG activity. Thus, this disclosure contemplates a fusion protein comprising dCas9-nucleic acid editing domain further fused to a UGI domain. This disclosure also contemplates a fusion protein comprising a Cas9 nickase-nucleic acid editing domain further fused to a UGI domain. It should be understood that the use of a UGI domain may increase the editing efficiency of a nucleic acid editing domain that is capable of catalyzing a C to U change. For example, fusion proteins comprising a UGI domain may be more efficient in deaminating C residues. In some embodiments, the fusion protein comprises the structure:

• • [deaminase]-[optional linker sequence]-[dCas9]-[optional linker sequence]-[UGI];
  • [deaminase]-[optional linker sequence]-[UGI]-[optional linker sequence]-[dCas9];
  • [UGI]-[optional linker sequence]-[deaminase]-[optional linker sequence]-[dCas9];
  • [UGI]-[optional linker sequence]-[dCas9]-[optional linker sequence]-[deaminase];
  • [dCas9]-[optional linker sequence]-[deaminase]-[optional linker sequence]-[UGI]; or
  • [dCas9]-[optional linker sequence]-[UGI]-[optional linker sequence]-[deaminase].In other embodiments, the fusion protein comprises the structure:
  • [deaminase]-[optional linker sequence]-[Cas9 nickase]-[optional linker sequence]-[UGI];
  • [deaminase]-[optional linker sequence]-[UGI]-[optional linker sequence]-[Cas9 nickase];
  • [UGI]-[optional linker sequence]-[deaminase]-[optional linker sequence]-[Cas9 nickase];
  • [UGI]-[optional linker sequence]-[Cas9 nickase]-[optional linker sequence]-[deaminase];
  • [Cas9 nickase]-[optional linker sequence]-[deaminase]-[optional linker sequence]-[UGI]; or
  • [Cas9 nickase]-[optional linker sequence]-[UGI]-[optional linker sequence]-[deaminase].

In some embodiments, the fusion proteins provided herein do not comprise a linker sequence. In some embodiments, one or both of the optional linker sequences are present.

In some embodiments, the “-” used in the general architecture above indicates the presence of an optional linker sequence. In some embodiments, the fusion proteins comprising a UGI further comprise a nuclear targeting sequence, for example a nuclear localization sequence. In some embodiments, fusion proteins provided herein further comprise a nuclear localization sequence (NLS). In some embodiments, the NLS is fused to the N-terminus of the fusion protein. In some embodiments, the NLS is fused to the C-terminus of the fusion protein. In some embodiments, the NLS is fused to the N-terminus of the UGI protein. In some embodiments, the NLS is fused to the C-terminus of the UGI protein. In some embodiments, the NLS is fused to the N-terminus of the Cas9 protein. In some embodiments, the NLS is fused to the C-terminus of the Cas9 protein. In some embodiments, the NLS is fused to the N-terminus of the deaminase. In some embodiments, the NLS is fused to the C-terminus of the deaminase. In some embodiments, the NLS is fused to the N-terminus of the second Cas9. In some embodiments, the NLS is fused to the C-terminus of the second Cas9. In some embodiments, the NLS is fused to the fusion protein via one or more linkers. In some embodiments, the NLS is fused to the fusion protein without a linker. In some embodiments, the NLS comprises an amino acid sequence of any one of the NLS sequences provided or referenced herein. In some embodiments, the NLS comprises an amino acid sequence as set forth in SEQ ID NO: 741or SEQ ID NO: 742.

In some embodiments, a UGI domain comprises a wild-type UGI or a UGI as set forth in SEQ ID NO: 600. In some embodiments, the UGI proteins provided herein include fragments of UGI and proteins homologous to a UGI or a UGI fragment. For example, in some embodiments, a UGI domain comprises a fragment of the amino acid sequence set forth in SEQ ID NO: 600. In some embodiments, a UGI fragment comprises an amino acid sequence that comprises at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or at least 99.5% of the amino acid sequence as set forth in SEQ ID NO: 600. In some embodiments, a UGI comprises an amino acid sequence homologous to the amino acid sequence set forth in SEQ ID NO: 600 or an amino acid sequence homologous to a fragment of the amino acid sequence set forth in SEQ ID NO: 600. In some embodiments, proteins comprising UGI or fragments of UGI or homologs of UGI or UGI fragments are referred to as “UGI variants.” A UGI variant shares homology to UGI, or a fragment thereof. For example a UGI variant is at least 70% identical, at least 75% identical, at least 80% identical, at least 85% identical, at least 90% identical, at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, at least 99% identical, at least 99.5% identical, or at least 99.9% identical to a wild type UGI or a UGI as set forth in SEQ ID NO: 600. In some embodiments, the UGI variant comprises a fragment of UGI, such that the fragment is at least 70% identical, at least 80% identical, at least 90% identical, at least 95% identical, at least 96% identical, at least 97% identical, at least 98% identical, at least 99% identical, at least 99.5% identical, or at least 99.9% to the corresponding fragment of wild-type UGI or a UGI as set forth in SEQ ID NO: 600. In some embodiments, the UGI comprises the following amino acid sequence:

>sp|P14739|UNGI_BPPB2 Uracil-DNA glycosylase
inhibitor
(SEQ ID NO: 600)
MTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDES
TDENVMLLTSDAPEYKPWALVIQDSNGENKIKML

Suitable UGI protein and nucleotide sequences are provided herein and additional suitable UGI sequences are known to those in the art, and include, for example, those published in Wang et al., Uracil-DNA glycosylase inhibitor gene of bacteriophage PBS2 encodes a binding protein specific for uracil-DNA glycosylase. J. Biol. Chem. 264:1163-1171(1989); Lundquist et al., Site-directed mutagenesis and characterization of uracil-DNA glycosylase inhibitor protein. Role of specific carboxylic amino acids in complex formation with Escherichia coli uracil-DNA glycosylase. J. Biol. Chem. 272:21408-21419(1997); Ravishankar et al., X-ray analysis of a complex of Escherichia coli uracil DNA glycosylase (EcUDG) with a proteinaceous inhibitor. The structure elucidation of a prokaryotic UDG. Nucleic Acids Res. 26:4880-4887(1998); and Putnam et al., Protein mimicry of DNA from crystal structures of the uracil-DNA glycosylase inhibitor protein and its complex with Escherichia coli uracil-DNA glycosylase. J. Mol. Biol. 287:331-346(1999), the entire contents of each are incorporated herein by reference.

It should be appreciated that additional proteins may be uracil glycosylase inhibitors. For example, other proteins that are capable of inhibiting (e.g., sterically blocking) a uracil-DNA glycosylase base-excision repair enzyme are within the scope of this disclosure. Additionally, any proteins that block or inhibit base-excision repair as also within the scope of this disclosure. In some embodiments, a protein that binds DNA is used. In another embodiment, a substitute for UGI is used. In some embodiments, a uracil glycosylase inhibitor is a protein that binds single-stranded DNA. For example, a uracil glycosylase inhibitor may be a Erwinia tasmaniensis single-stranded binding protein. In some embodiments, the single-stranded binding protein comprises the amino acid sequence (SEQ ID NO: 322). In some embodiments, a uracil glycosylase inhibitor is a protein that binds uracil. In some embodiments, a uracil glycosylase inhibitor is a protein that binds uracil in DNA. In some embodiments, a uracil glycosylase inhibitor is a catalytically inactive uracil DNA-glycosylase protein. In some embodiments, a uracil glycosylase inhibitor is a catalytically inactive uracil DNA-glycosylase protein that does not excise uracil from the DNA. For example, a uracil glycosylase inhibitor is a UdgX. In some embodiments, the UdgX comprises the amino acid sequence (SEQ ID NO: 323). As another example, a uracil glycosylase inhibitor is a catalytically inactive UDG. In some embodiments, a catalytically inactive UDG comprises the amino acid sequence (SEQ ID NO: 324). It should be appreciated that other uracil glycosylase inhibitors would be apparent to the skilled artisan and are within the scope of this disclosure. In some embodiments, a uracil glycosylase inhibitor is a protein that is homologous to any one of SEQ ID NOs: 322-324. In some embodiments, a uracil glycosylase inhibitor is a protein that is at least 50% identical, at least 55% identical at least 60% identical, at least 65% identical, at least 70% identical, at least 75% identical, at least 80% identical at least 85% identical, at least 90% identical, at least 95% identical, at least 96% identical, at least 98% identical, at least 99% identical, or at least 99.5% identical to any one of SEQ ID NOs: 322-324.

Erwinia tasmaniensis SSB (themostable single-stranded DNA binding protein)

(SEQ ID NO: 322)
MASRGVNKVILVGNLGQDPEVRYMPNGGAVANITLATSESWRDKQTGETK
EKTEWHRVVLFGKLAEVAGEYLRKGSQVYIEGALQTRKWTDQAGVEKYTT
EVVVNVGGTMQMLGGRSQGGGASAGGQNGGSNNGWGQPQQPQGGNQFSGG
AQQQARPQQQPQQNNAPANNEPPIDFDDDIP

UdgX (binds to Uracil in DNA but does not excise)

(SEQ ID NO: 323)
MAGAQDFVPHTADLAELAAAAGECRGCGLYRDATQAVFGAGGRSARIMMI
GEQPGDKEDLAGLPFVGPAGRLLDRALEAADIDRDALYVTNAVKHFKFTR
AAGGKRRIHKTPSRTEVVACRPWLIAEMTSVEPDVVVLLGATAAKALLGN
DFRVTQHRGEVLHVDDVPGDPALVATVHPSSLLRGPKEERESAFAGLVDD
LRVAADVRP

UDG (catalytically inactive human UDG, binds to Uracil in DNA but does not excise)

(SEQ ID NO: 324)
MIGQKTLYSFFSPSPARKRHAPSPEPAVQGTGVAGVPEESGDAAAIPAK
KAPAGQEEPGTPPSSPLSAEQLDRIQRNKAAALLRLAARNVPVGFGESW
KKHLSGEFGKPYFIKLMGFVAEERKHYTVYPPPHQVFTWTQMCDIKDVK
VVILGQEPYHGPNQAHGLCFSVQRPVPPPPSLENIYKELSTDIEDFVHP
GHGDLSGWAKQGVLLLNAVLTVRAHQANSHKERGWEQFTDAVVSWLNQN
SNGLVFLLWGSYAQKKGSAIDRKRHHVLQTAHPSPLSVYRGFFGCRHFS
KTNELLQKSGKKPIDWKEL

In some embodiments, the nucleic acid editing domain is a deaminase domain. In some embodiments, the deaminase is a cytosine deaminase or a cytidine deaminase. In some embodiments, the deaminase is an apolipoprotein B mRNA-editing complex (APOBEC) family deaminase. In some embodiments, the deaminase is an APOBEC1 deaminase. In some embodiments, the deaminase is an APOBEC2 deaminase. In some embodiments, the deaminase is an APOBEC3 deaminase. In some embodiments, the deaminase is an APOBEC3A deaminase. In some embodiments, the deaminase is an APOBEC3B deaminase. In some embodiments, the deaminase is an APOBEC3C deaminase. In some embodiments, the deaminase is an APOBEC3D deaminase. In some embodiments, the deaminase is an APOBEC3E deaminase. In some embodiments, the deaminase is an APOBEC3F deaminase. In some embodiments, the deaminase is an APOBEC3G deaminase. In some embodiments, the deaminase is an APOBEC3H deaminase. In some embodiments, the deaminase is an APOBEC4 deaminase. In some embodiments, the deaminase is an activation-induced deaminase (AID). In some embodiments, the demianse is a rat APOBEC1 (SEQ ID NO: 282). In some embodiments, the deminase is a human APOBEC1 (SEQ ID No: 284). In some embodiments, the deaminase is a Petromyzon marinus cytidine deaminase 1 (pmCDA1). In some embodiments, the deminase is a human APOBEC3G (SEQ ID NO: 275). In some embodiments, the deaminase is a fragment of the human APOBEC3G (SEQ ID NO: 5740). In some embodiments, the deaminase is a human APOBEC3G variant comprising a D316R_D317R mutation (SEQ ID NO: 5739). In some embodiments, the deaminase is a frantment of the human APOBEC3G and comprising mutations corresponding to the D316R_D317R mutations in SEQ ID NO: 275 (SEQ ID NO: 5741).

In some embodiments, the linker comprises a (GGGS)_n (SEQ ID NO: 265), (GGGGS)_n (SEQ ID NO: 5), a (G)_n, an (EAAAK)_n (SEQ ID NO: 6), a (GGS)_n, an SGSETPGTSESATPES (SEQ ID NO: 7), or an (XP)_n motif, or a combination of any of these, wherein n is independently an integer between 1 and 30.

Suitable UGI protein and nucleotide sequences are provided herein and additional suitable UGI sequences are known to those in the art, and include, for example, those published in Wang et al., Uracil-DNA glycosylase inhibitor gene of bacteriophage PBS2 encodes a binding protein specific for uracil-DNA glycosylase. J. Biol. Chem. 264:1163-1171(1989); Lundquist et al., Site-directed mutagenesis and characterization of uracil-DNA glycosylase inhibitor protein. Role of specific carboxylic amino acids in complex formation with Escherichia coli uracil-DNA glycosylase. J. Biol. Chem. 272:21408-21419(1997); Ravishankar et al., X-ray analysis of a complex of Escherichia coli uracil DNA glycosylase (EcUDG) with a proteinaceous inhibitor. The structure elucidation of a prokaryotic UDG. Nucleic Acids Res. 26:4880-4887(1998); and Putnam et al., Protein mimicry of DNA from crystal structures of the uracil-DNA glycosylase inhibitor protein and its complex with Escherichia coli uracil-DNA glycosylase. J. Mol. Biol. 287:331-346(1999), the entire contents of which are incorporated herein by reference. In some embodiments, the optional linker comprises a (GGS)_n motif, wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 19, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20. In some embodiments, the optional linker comprises a (GGS)n motif, wherein n is 1, 3, or 7. In some embodiments, the optional linker comprises the amino acid sequence SGSETPGTSESATPES (SEQ ID NO: 7), which is also referred to as the XTEN linker in the Examples.

In some embodiments, a Cas9 nickase may further facilitate the removal of a base on the non-edited strand in an organism whose genome is edited in vivo. The Cas9 nickase, as described herein, may comprise a D10A mutation in SEQ ID NO: 10, or a corresponding mutation in any of SEQ ID NOs: 11-260. In some embodiments, the Cas9 nickase of this disclosure may comprise a histidine at mutation 840 of SEQ ID NO: 10, or a corresponding residue in any of SEQ ID NOs: 11-260. Such fusion proteins comprising the Cas9 nickase, can cleave a single strand of the target DNA sequence, e.g., the strand that is not being edited. Without wishing to be bound by any particular theory, this cleavage may inhibit mis-match repair mechanisms that reverse a C to U edit made by the deaminase.

Cas9 Complexes with Guide RNAs

Some aspects of this disclosure provide complexes comprising any of the fusion proteins provided herein, and a guide RNA bound to a Cas9 domain (e.g., a dCas9, a nuclease active Cas9, or a Cas9 nickase) of fusion protein.

In some embodiments, the guide RNA is from 15-100 nucleotides long and comprises a sequence of at least 10 contiguous nucleotides that is complementary to a target sequence. In some embodiments, the guide RNA is 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50 nucleotides long. In some embodiments, the guide RNA comprises a sequence of 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, or 40 contiguous nucleotides that is complementary to a target sequence. In some embodiments, the target sequence is a DNA sequence. In some embodiments, the target sequence is a sequence in the genome of a mammal. In some embodiments, the target sequence is a sequence in the genome of a human. In some embodiments, the 3′ end of the target sequence is immediately adjacent to a canonical PAM sequence (NGG). In some embodiments, the guide RNA is complementary to a sequence associated with a disease or disorder. In some embodiments, the guide RNA is complementary to a sequence associated with a disease or disorder having a mutation in a gene selected from the genes disclosed in any one of Tables 1-3. In some embodiments, the guide RNA comprises a nucleotide sequence of any one of the guide sequences provided in Table 2 or Table 3. Exemplary sequences in the human genome that may be targeted by the complexes of this disclosure are provided herein in Tables 1-3.

Methods of Using Cas9 Fusion Proteins

Some aspects of this disclosure provide methods of using the Cas9 proteins, fusion proteins, or complexes provided herein. For example, some aspects of this disclosure provide methods comprising contacting a DNA molecule (a) with any of the the Cas9 proteins or fusion proteins provided herein, and with at least one guide RNA, wherein the guide RNA is about 15-100 nucleotides long and comprises a sequence of at least 10 contiguous nucleotides that is complementary to a target sequence; or (b) with a Cas9 protein, a Cas9 fusion protein, or a Cas9 protein or fusion protein complex with at least one gRNA as provided herein. In some embodiments, the 3′ end of the target sequence is not immediately adjacent to a canonical PAM sequence (NGG). In some embodiments, the 3′ end of the target sequence is immediately adjacent to an AGC, GAG, TTT, GTG, or CAA sequence.

In some embodiments, the target DNA sequence comprises a sequence associated with a disease or disorder. In some embodiments, the target DNA sequence comprises a point mutation associated with a disease or disorder. In some embodiments, the activity of the Cas9 protein, the Cas9 fusion protein, or the complex results in a correction of the point mutation. In some embodiments, the target DNA sequence comprises a T→C point mutation associated with a disease or disorder, and wherein the deamination of the mutant C base results in a sequence that is not associated with a disease or disorder. In some embodiments, the target DNA sequence encodes a protein and wherein the point mutation is in a codon and results in a change in the amino acid encoded by the mutant codon as compared to the wild-type codon. In some embodiments, the deamination of the mutant C results in a change of the amino acid encoded by the mutant codon. In some embodiments, the deamination of the mutant C results in the codon encoding the wild-type amino acid. In some embodiments, the contacting is in vivo in a subject. In some embodiments, the subject has or has been diagnosed with a disease or disorder. In some embodiments, the disease or disorder is cystic fibrosis, phenylketonuria, epidermolytic hyperkeratosis (EHK), Charcot-Marie-Toot disease type 4J, neuroblastoma (NB), von Willebrand disease (vWD), myotonia congenital, hereditary renal amyloidosis, dilated cardiomyopathy (DCM), hereditary lymphedema, familial Alzheimer's disease, HIV, Prion disease, chronic infantile neurologic cutaneous particular syndrome (CINCA), desmin-related myopathy (DRM), a neoplastic disease associated with a mutant PI3KCA protein, a mutant CTNNB1 protein, a mutant HRAS protein, or a mutant p53 protein.

Some embodiments provide methods for using the Cas9 DNA editing fusion proteins provided herein. In some embodiments, the fusion protein is used to introduce a point mutation into a nucleic acid by deaminating a target nucleobase, e.g., a C residue. In some embodiments, the deamination of the target nucleobase results in the correction of a genetic defect, e.g., in the correction of a point mutation that leads to a loss of function in a gene product. In some embodiments, the genetic defect is associated with a disease or disorder, e.g., a lysosomal storage disorder or a metabolic disease, such as, for example, type I diabetes. In some embodiments, the methods provided herein are used to introduce a deactivating point mutation into a gene or allele that encodes a gene product that is associated with a disease or disorder. For example, in some embodiments, methods are provided herein that employ a Cas9 DNA editing fusion protein to introduce a deactivating point mutation into an oncogene (e.g., in the treatment of a proliferative disease). A deactivating mutation may, in some embodiments, generate a premature stop codon in a coding sequence, which results in the expression of a truncated gene product, e.g., a truncated protein lacking the function of the full-length protein.

In some embodiments, the purpose of the methods provide herein is to restore the function of a dysfunctional gene via genome editing. The Cas9 deaminase fusion proteins provided herein can be validated for gene editing-based human therapeutics in vitro, e.g., by correcting a disease-associated mutation in human cell culture. It will be understood by the skilled artisan that the fusion proteins provided herein, e.g., the fusion proteins comprising a Cas9 domain and a nucleic acid deaminase domain can be used to correct any single point T→C or A→G mutation. In the first case, deamination of the mutant C back to U corrects the mutation, and in the latter case, deamination of the C that is base-paired with the mutant G, followed by a round of replication, corrects the mutation.

An exemplary disease-relevant mutation that can be corrected by the provided fusion proteins in vitro or in vivo is the H1047R (A3140G) polymorphism in the PI3KCA protein. The phosphoinositide-3-kinase, catalytic alpha subunit (PI3KCA) protein acts to phosphorylate the 3-OH group of the inositol ring of phosphatidylinositol. The PI3KCA gene has been found to be mutated in many different carcinomas, and thus it is considered to be a potent oncogene.³⁷ In fact, the A3140G mutation is present in several NCI-60 cancer cell lines, such as, for example, the HCT116, SKOV3, and T47D cell lines, which are readily available from the American Type Culture Collection (ATCC).³⁸

In some embodiments, a cell carrying a mutation to be corrected, e.g., a cell carrying a point mutation, e.g., an A3140G point mutation in exon 20 of the PI3KCA gene, resulting in a H1047R substitution in the PI3KCA protein, is contacted with an expression construct encoding a Cas9 deaminase fusion protein and an appropriately designed sgRNA targeting the fusion protein to the respective mutation site in the encoding PI3KCA gene. Control experiments can be performed where the sgRNAs are designed to target the fusion enzymes to non-C residues that are within the PI3KCA gene. Genomic DNA of the treated cells can be extracted, and the relevant sequence of the PI3KCA genes PCR amplified and sequenced to assess the activities of the fusion proteins in human cell culture.

It will be understood that the example of correcting point mutations in PI3KCA is provided for illustration purposes and is not meant to limit the instant disclosure. The skilled artisan will understand that the instantly disclosed DNA-editing fusion proteins can be used to correct other point mutations and mutations associated with other cancers and with diseases other than cancer including other proliferative diseases.

The successful correction of point mutations in disease-associated genes and alleles opens up new strategies for gene correction with applications in therapeutics and basic research. Site-specific single-base modification systems like the disclosed fusions of Cas9 and deaminase enzymes or domains also have applications in “reverse” gene therapy, where certain gene functions are purposely suppressed or abolished. In these cases, site-specifically mutating Trp (TGG), Gln (CAA and CAG), or Arg (CGA) residues to premature stop codons (TAA, TAG, TGA) can be used to abolish protein function in vitro, ex vivo, or in vivo.

The instant disclosure provides methods for the treatment of a subject diagnosed with a disease associated with or caused by a point mutation that can be corrected by a Cas9 DNA editing fusion protein provided herein. For example, in some embodiments, a method is provided that comprises administering to a subject having such a disease, e.g., a cancer associated with a PI3KCA point mutation as described above, an effective amount of a Cas9 deaminase fusion protein that corrects the point mutation or introduces a deactivating mutation into the disease-associated gene. In some embodiments, the disease is a proliferative disease. In some embodiments, the disease is a genetic disease. In some embodiments, the disease is a neoplastic disease. In some embodiments, the disease is a metabolic disease. In some embodiments, the disease is a lysosomal storage disease. Other diseases that can be treated by correcting a point mutation or introducing a deactivating mutation into a disease-associated gene will be known to those of skill in the art, and the disclosure is not limited in this respect.

The instant disclosure provides methods for the treatment of additional diseases or disorders, e.g., diseases or disorders that are associated or caused by a point mutation that can be corrected by deaminase-mediated gene editing. Some such diseases are described herein, and additional suitable diseases that can be treated with the strategies and fusion proteins provided herein will be apparent to those of skill in the art based on the instant disclosure. Exemplary suitable diseases and disorders are listed below. It will be understood that the numbering of the specific positions or residues in the respective sequences depends on the particular protein and numbering scheme used. Numbering might be different, e.g., in precursors of a mature protein and the mature protein itself, and differences in sequences from species to species may affect numbering. One of skill in the art will be able to identify the respective residue in any homologous protein and in the respective encoding nucleic acid by methods well known in the art, e.g., by sequence alignment and determination of homologous residues. Exemplary suitable diseases and disorders include, without limitation, cystic fibrosis (see, e.g., Schwank et al., Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients. Cell stem cell. 2013; 13: 653-658; and Wu et. al., Correction of a genetic disease in mouse via use of CRISPR-Cas9. Cell stem cell. 2013; 13: 659-662, neither of which uses a deaminase fusion protein to correct the genetic defect); phenylketonuria—e.g., phenylalanine to serine mutation at position 835 (mouse) or 240 (human) or a homologous residue in phenylalanine hydroxylase gene (T>C mutation)—see, e.g., McDonald et al., Genomics. 1997; 39:402-405; Bernard-Soulier syndrome (BSS)—e.g., phenylalanine to serine mutation at position 55 or a homologous residue, or cysteine to arginine at residue 24 or a homologous residue in the platelet membrane glycoprotein IX (T>C mutation)—see, e.g., Noris et al., British Journal of Haematology. 1997; 97: 312-320, and Ali et al., Hematol. 2014; 93: 381-384; epidermolytic hyperkeratosis (EHK)—e.g., leucine to proline mutation at position 160 or 161 (if counting the initiator methionine) or a homologous residue in keratin 1 (T>C mutation)—see, e.g., Chipev et al., Cell. 1992; 70: 821-828, see also accession number P04264 in the UNIPROT database at www[dot]uniprot[dot]org; chronic obstructive pulmonary disease (COPD)—e.g., leucine to proline mutation at position 54 or 55 (if counting the initiator methionine) or a homologous residue in the processed form of α₁-antitrypsin or residue 78 in the unprocessed form or a homologous residue (T>C mutation)—see, e.g., Poller et al., Genomics. 1993; 17: 740-743, see also accession number P01011 in the UNIPROT database; Charcot-Marie-Toot disease type 4J—e.g., isoleucine to threonine mutation at position 41 or a homologous residue in FIG4 (T>C mutation)—see, e.g., Lenk et al., PLoS Genetics. 2011; 7: e1002104; neuroblastoma (NB)—e.g., leucine to proline mutation at position 197 or a homologous residue in Caspase-9 (T>C mutation)—see, e.g., Kundu et al., 3 Biotech. 2013, 3:225-234; von Willebrand disease (vWD)—e.g., cysteine to arginine mutation at position 509 or a homologous residue in the processed form of von Willebrand factor, or at position 1272 or a homologous residue in the unprocessed form of von Willebrand factor (T>C mutation)—see, e.g., Lavergne et al., Br. J. Haematol. 1992, see also accession number P04275 in the UNIPROT database; 82: 66-72; myotonia congenital—e.g., cysteine to arginine mutation at position 277 or a homologous residue in the muscle chloride channel gene CLCN1 (T>C mutation)—see, e.g., Weinberger et al., The J. of Physiology. 2012; 590: 3449-3464; hereditary renal amyloidosis—e.g., stop codon to arginine mutation at position 78 or a homologous residue in the processed form of apolipoprotein All or at position 101 or a homologous residue in the unprocessed form (T>C mutation)—see, e.g., Yazaki et al., Kidney Int. 2003; 64: 11-16; dilated cardiomyopathy (DCM)—e.g., tryptophan to Arginine mutation at position 148 or a homologous residue in the FOXD4 gene (T>C mutation), see, e.g., Minoretti et. al., Int. J. of Mol. Med. 2007; 19: 369-372; hereditary lymphedema—e.g., histidine to arginine mutation at position 1035 or a homologous residue in VEGFR3 tyrosine kinase (A>G mutation), see, e.g., Irrthum et al., Am. J. Hum. Genet. 2000; 67: 295-301; familial Alzheimer's disease—e.g., isoleucine to valine mutation at position 143 or a homologous residue in presenilin1 (A>G mutation), see, e.g., Gallo et. al., J. Alzheimer's disease. 2011; 25: 425-431; Prion disease—e.g., methionine to valine mutation at position 129 or a homologous residue in prion protein (A>G mutation)—see, e.g., Lewis et. al., J. of General Virology. 2006; 87: 2443-2449; chronic infantile neurologic cutaneous particular syndrome (CINCA)—e.g., Tyrosine to Cysteine mutation at position 570 or a homologous residue in cryopyrin (A>G mutation)—see, e.g., Fujisawa et. al. Blood. 2007; 109: 2903-2911; and desmin-related myopathy (DRM)—e.g., arginine to glycine mutation at position 120 or a homologous residue in αβ crystallin (A>G mutation)—see, e.g., Kumar et al., J. Biol. Chem. 1999; 274: 24137-24141. The entire contents of all references and database entries is incorporated herein by reference.

The instant disclosure provides lists of genes comprising pathogenic T>C or A>G mutations. Provided herein, are the names of these genes, their respective SEQ ID NOs, their gene IDs, and sequences flanking the mutation site. (Tables 2 and 3). In some instances, the gRNA sequences that can be used to correct the mutations in these genes are disclosed (Tables 2 and 3).

In some embodiments, a Cas9-deaminase fusion protein recognizes canonical PAMs and therefore can correct the pathogenic T>C or A>G mutations with canonical PAMs, e.g., NGG (listed in Tables 2 and 3, SEQ ID NOs: 2540-2702 and 5084-5260), respectively, in the flanking sequences. For example, the Cas9 proteins that recognize canonical PAMs comprise an amino acid sequence that is at least 90% identical to the amino acid sequence of Streptococcus pyogenes Cas9 as provided by SEQ ID NO: 10, or to a fragment thereof comprising the RuvC and HNH domains of SEQ ID NO: 10.

It will be apparent to those of skill in the art that in order to target a Cas9:nucleic acid editing enzyme/domain fusion protein as disclosed herein to a target site, e.g., a site comprising a point mutation to be edited, it is typically necessary to co-express the Cas9:nucleic acid editing enzyme/domain fusion protein together with a guide RNA, e.g., an sgRNA. As explained in more detail elsewhere herein, a guide RNA typically comprises a tracrRNA framework allowing for Cas9 binding, and a guide sequence, which confers sequence specificity to the Cas9:nucleic acid editing enzyme/domain fusion protein. In some embodiments, the guide RNA comprises a structure 5′-[guide sequence]-guuuuagagcuagaaauagcaaguuaaaauaaaggcuaguccguuaucaacuugaaaaaguggcaccgagucggugcuu uuu-3′ (SEQ ID NO: 601), wherein the guide sequence comprises a sequence that is complementary to the target sequence. The guide sequence is typically 20 nucleotides long. The sequences of suitable guide RNAs for targeting Cas9:nucleic acid editing enzyme/domain fusion proteins to specific genomic target sites will be apparent to those of skill in the art based on the instant disclosure. Such suitable guide RNA sequences typically comprise guide sequences that are complementary to a nucleic sequence within 50 nucleotides upstream or downstream of the target nucleotide to be edited. Some exemplary guide RNA sequences suitable for targeting Cas9:nucleic acid editing enzyme/domain fusion proteins to specific target sequences are provided below.

Base Editor Efficiency

Some aspects of the disclosure are based on the recognition that any of the base editors provided herein are capable of modifying a specific nucleotide base without generating a significant proportion of indels. An “indel”, as used herein, refers to the insertion or deletion of a nucleotide base within a nucleic acid. Such insertions or deletions can lead to frame shift mutations within a coding region of a gene. In some embodiments, it is desirable to generate base editors that efficiently modify (e.g. mutate or deaminate) a specific nucleotide within a nucleic acid, without generating a large number of insertions or deletions (i.e., indels) in the nucleic acid. In certain embodiments, any of the base editors provided herein are capable of generating a greater proportion of intended modifications (e.g., point mutations or deaminations) versus indels. In some embodiments, the base editors provided herein are capable of generating a ratio of intended point mutations to indels that is greater than 1:1. In some embodiments, the base editors provided herein are capable of generating a ratio of intended point mutations to indels that is at least 1.5:1, at least 2:1, at least 2.5:1, at least 3:1, at least 3.5:1, at least 4:1, at least 4.5:1, at least 5:1, at least 5.5:1, at least 6:1, at least 6.5:1, at least 7:1, at least 7.5:1, at least 8:1, at least 10:1, at least 12:1, at least 15:1, at least 20:1, at least 25:1, at least 30:1, at least 40:1, at least 50:1, at least 100:1, at least 200:1, at least 300:1, at least 400:1, at least 500:1, at least 600:1, at least 700:1, at least 800:1, at least 900:1, or at least 1000:1, or more. The number of intended mutations and indels may be determined using any suitable method, for example the methods used in the below Examples.

In some embodiments, the base editors provided herein are capable of limiting formation of indels in a region of a nucleic acid. In some embodiments, the region is at a nucleotide targeted by a base editor or a region within 2, 3, 4, 5, 6, 7, 8, 9, or 10 nucleotides of a nucleotide targeted by a base editor. In some embodiments, any of the base editors provided herein are capable of limiting the formation of indels at a region of a nucleic acid to less than 1%, less than 1.5%, less than 2%, less than 2.5%, less than 3%, less than 3.5%, less than 4%, less than 4.5%, less than 5%, less than 6%, less than 7%, less than 8%, less than 9%, less than 10%, less than 12%, less than 15%, or less than 20%. The number of indels formed at a nucleic acid region may depend on the amount of time a nucleic acid (e.g., a nucleic acid within the genome of a cell) is exposed to a base editor. In some embodiments, an number or proportion of indels is determined after at least 1 hour, at least 2 hours, at least 6 hours, at least 12 hours, at least 24 hours, at least 36 hours, at least 48 hours, at least 3 days, at least 4 days, at least 5 days, at least 7 days, at least 10 days, or at least 14 days of exposing a nucleic acid (e.g., a nucleic acid within the genome of a cell) to a base editor.

Some aspects of the disclosure are based on the recognition that any of the base editors provided herein are capable of efficiently generating an intended mutation, such as a point mutation, in a nucleic acid (e.g. a nucleic acid within a genome of a subject) without generating a significant number of unintended mutations, such as unintended point mutations. In some embodiments, a intended mutation is a mutation that is generated by a specific base editor bound to a gRNA, specifically designed to generate the intended mutation. In some embodiments, the intended mutation is a mutation associated with a disease or disorder. In some embodiments, the intended mutation is a cytosine (C) to thymine (T) point mutation associated with a disease or disorder. In some embodiments, the intended mutation is a guanine (G) to adenine (A) point mutation associated with a disease or disorder. In some embodiments, the intended mutation is a cytosine (C) to thymine (T) point mutation within the coding region of a gene. In some embodiments, the intended mutation is a guanine (G) to adenine (A) point mutation within the coding region of a gene. In some embodiments, the intended mutation is a point mutation that generates a stop codon, for example, a premature stop codon within the coding region of a gene. In some embodiments, the intended mutation is a mutation that eliminates a stop codon. In some embodiments, the intended mutation is a mutation that alters the splicing of a gene. In some embodiments, the intended mutation is a mutation that alters the regulatory sequence of a gene (e.g., a gene promotor or gene repressor). In some embodiments, any of the base editors provided herein are capable of generating a ratio of intended mutations to unintended mutations (e.g., intended point mutations:unintended point mutations) that is greater than 1:1. In some embodiments, any of the base editors provided herein are capable of generating a ratio of intended mutations to unintended mutations (e.g., intended point mutations:unintended point mutations) that is at least 1.5:1, at least 2:1, at least 2.5:1, at least 3:1, at least 3.5:1, at least 4:1, at least 4.5:1, at least 5:1, at least 5.5:1, at least 6:1, at least 6.5:1, at least 7:1, at least 7.5:1, at least 8:1, at least 10:1, at least 12:1, at least 15:1, at least 20:1, at least 25:1, at least 30:1, at least 40:1, at least 50:1, at least 100:1, at least 150:1, at least 200:1, at least 250:1, at least 500:1, or at least 1000:1, or more. It should be appreciated that the characterstics of the base editors described in the “Base Editor Efficiency” section, herein, may be applied to any of the fusion proteins, or methods of using the fusion proteins provided herein.

Methods for Editing Nucleic Acids

Some aspects of the disclosure provide methods for editing a nucleic acid. In some embodiments, the method is a method for editing a nucleobase of a nucleic acid (e.g., a base pair of a double-stranded DNA sequence). In some embodiments, the method comprises the steps of: a) contacting a target region of a nucleic acid (e.g., a double-stranded DNA sequence) with a complex comprising a base editor (e.g., a Cas9 domain fused to a cytidine deaminase domain) and a guide nucleic acid (e.g., gRNA), wherein the target region comprises a targeted nucleobase pair, b) inducing strand separation of said target region, c)converting a first nucleobase of said target nucleobase pair in a single strand of the target region to a second nucleobase, and d) cutting no more than one strand of said target region, where a third nucleobase complementary to the first nucleobase base is replaced by a fourth nucleobase complementary to the second nucleobase; and the method results in less than 20% indel formation in the nucleic acid. It should be appreciated that in some embodiments, step b is omitted. In some embodiments, the first nucleobase is a cytosine. In some embodiments, the second nucleobase is a deaminated cytosine, or a uracil. In some embodiments, the third nucleobase is a guanine. In some embodiments, the fourth nucleobase is an adenine. In some embodiments, the first nucleobase is a cytosine, the second nucleobase is a deaminated cytosine, or a uracil, the third nucleobase is a guanine, and the fourth nucleobase is an adenine. In some embodiments, the method results in less than 19%, 18%, 16%, 14%, 12%, 10%, 8%, 6%, 4%, 2%, 1%, 0.5%, 0.2%, or less than 0.1% indel formation. In some embodiments, the method further comprises replacing the second nucleobase with a fifth nucleobase that is complementary to the fourth nucleobase, thereby generating an intended edited base pair (e.g., C:G→T:A). In some embodiments, the fifth nucleobase is a thymine. In some embodiments, at least 5% of the intended basepaires are edited. In some embodiments, at least 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, or 50% of the intended basepaires are edited.

In some embodiments, the ratio of intended products to unintended products in the target nucleotide is at least 2:1, 5:1, 10:1, 20:1, 30:1, 40:1, 50:1, 60:1, 70:1, 80:1, 90:1, 100:1, or 200:1, or more. In some embodiments, the ratio of intended point mutation to indel formation is greater than 1:1, 10:1, 50:1, 100:1, 500:1, or 1000:1, or more. In some embodiments, the cut single strand (nicked strand) is hybridized to the guide nucleic acid. In some embodiments, the cut single strand is opposite to the strand comprising the first nucleobase. In some embodiments, the base editor comprises a Cas9 domain. In some embodiments, the first base is cytosine, and the second base is not a G, C, A, or T. In some embodiments, the second base is uracil. In some embodiments, the first base is cytosine. In some embodiments, the second base is not a G, C, A, or T. In some embodiments, the second base is uracil. In some embodiments, the base editor inhibits base escision repair of the edited strand. In some embodiments, the base editor protects or binds the non-edited strand. In some embodiments, the base editor comprises UGI activity. In some embodiments, the base editor comprises nickase activity. In some embodiments, the intended edited basepair is upstream of a PAM site. In some embodiments, the intended edited base pair is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides upstream of the PAM site. In some embodiments, the intended edited basepair is downstream of a PAM site. In some embodiments, the intended edited base pair is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides downstream stream of the PAM site. In some embodiments, the method does not require a canonical (e.g., NGG) PAM site. In some embodiments, the nucleobase editor comprises a linker. In some embodiments, the linker is 1-25 amino acids in length. In some embodiments, the linker is 5-20 amino acids in length. In some embodiments, linker is 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 amino acids in length. In some embodiments, the target region comprises a target window, wherein the target window comprises the target nucleobase pair. In some embodiments, the target window comprises 1-10 nucleotides. In some embodiments, the target window is 1-9, 1-8, 1-7, 1-6, 1-5, 1-4, 1-3, 1-2, or 1 nucleotides in length. In some embodiments, the target window is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides in length. In some embodiments, the intended edited base pair is within the target window. In some embodiments, the target window comprises the intended edited base pair. In some embodiments, the method is performed using any of the base editors provided herein. In some embodiments, a target windo is a deamination window

In some embodiments, the disclosure provides methods for editing a nucleotide. In some embodiments, the disclosure provides a method for editing a nucleobase pair of a double-stranded DNA sequence. In some embodiments, the method comprises a) contacting a target region of the double-stranded DNA sequence with a complex comprising a base editor and a guide nucleic acid (e.g., gRNA), where the target region comprises a target nucleobase pair, b) inducing strand separation of said target region, c) converting a first nucleobase of said target nucleobase pair in a single strand of the target region to a second nucleobase, d) cutting no more than one strand of said target region, wherein a third nucleobase complementary to the first nucleobase base is replaced by a fourth nucleobase complementary to the second nucleobase, and the second nucleobase is replaced with a fifth nucleobase that is complementary to the fourth nucleobase, thereby generating an intended edited basepair, wherein the efficiency of generating the intended edited basepair is at least 5%. It should be appreciated that in some embodiments, step b is omitted. In some embodiments, at least 5% of the intended basepaires are edited. In some embodiments, at least 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, or 50% of the intended basepaires are edited. In some embodiments, the method causes less than 19%, 18%, 16%, 14%, 12%, 10%, 8%, 6%, 4%, 2%, 1%, 0.5%, 0.2%, or less than 0.1% indel formation. In some embodiments, the ratio of intended product to unintended products at the target nucleotide is at least 2:1, 5:1, 10:1, 20:1, 30:1, 40:1, 50:1, 60:1, 70:1, 80:1, 90:1, 100:1, or 200:1, or more. In some embodiments, the ratio of intended point mutation to indel formation is greater than 1:1, 10:1, 50:1, 100:1, 500:1, or 1000:1, or more. In some embodiments, the cut single strand is hybridized to the guide nucleic acid. In some embodiments, the cut single strand is opposite to the strand comprising the first nucleobase. In some embodiments, the first base is cytosine. In some embodiments, the second nucleobase is not G, C, A, or T. In some embodiments, the second base is uracil. In some embodiments, the base editor inhibits base escision repair of the edited strand. In some embodiments, the base editor protects or binds the non-edited strand. In some embodiments, the nucleobase editor comprises UGI activity. In some embodiments, the nucleobase edit comprises nickase activity. In some embodiments, the intended edited basepair is upstream of a PAM site. In some embodiments, the intended edited base pair is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides upstream of the PAM site. In some embodiments, the intended edited basepair is downstream of a PAM site. In some embodiments, the intended edited base pair is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides downstream stream of the PAM site. In some embodiments, the method does not require a canonical (e.g., NGG) PAM site. In some embodiments, the nucleobase editor comprises a linker. In some embodiments, the linker is 1-25 amino acids in length. In some embodiments, the linker is 5-20 amino acids in length. In some embodiments, the linker is 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 amino acids in length. In some embodiments, the target region comprises a target window, wherein the target window comprises the target nucleobase pair. In some embodiments, the target window comprises 1-10 nucleotides. In some embodiments, the target window is 1-9, 1-8, 1-7, 1-6, 1-5, 1-4, 1-3, 1-2, or 1 nucleotides in length. In some embodiments, the target window is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides in length. In some embodiments, the intended edited base pair occurs within the target window. In some embodiments, the target window comprises the intended edited base pair. In some embodiments, the nucleobase editor is any one of the base editors provided herein.

Kits, Vectors, Cells

Some aspects of this disclosure provide kits comprising a nucleic acid construct, comprising (a) a nucleotide sequence encoding a Cas9 protein or a Cas9 fusion protein as provided herein; and (b) a heterologous promoter that drives expression of the sequence of (a). In some embodiments, the kit further comprises an expression construct encoding a guide RNA backbone, wherein the construct comprises a cloning site positioned to allow the cloning of a nucleic acid sequence identical or complementary to a target sequence into the guide RNA backbone.

Some aspects of this disclosure provide polynucleotides encoding a Cas9 protein of a fusion protein as provided herein. Some aspects of this disclosure provide vectors comprising such polynucleotides. In some embodiments, the vector comprises a heterologous promoter driving expression of polynucleotide.

Some aspects of this disclosure provide cells comprising a Cas9 protein, a fusion protein, a nucleic acid molecule encoding the fusion protein, a complex comprise the Cas9 protein and the gRNA, and/or a vector as provided herein.

The description of exemplary embodiments of the reporter systems above is provided for illustration purposes only and not meant to be limiting. Additional reporter systems, e.g., variations of the exemplary systems described in detail above, are also embraced by this disclosure.

EXAMPLES

Example 1

Cas9 Deaminase Fusion Proteins

A number of Cas9:Deaminase fusion proteins were generated and deaminase activity of the generated fusions was characterized. The following deaminases were tested: Human AID (hAID):

(SEQ ID NO: 607)
MDSLLMNRRKFLYQFKNVRWAKGRRETYLCYVVKRRDSATSFSLDFGYLRN
KNGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVADFLRGNP
YLSLRIFTARLYFCEDRKAEPEGLRRLHRAGVQIAIMTFKDYFYCWNTFVE
NHERTFKAWEGLHENSVRLSRQLRRILLPLYEVDDLRDAFRTLGLLD

Human AID-DC (hAID-DC, truncated version of hAID with 7-fold increased activity):

(SEQ ID NO: 608)
MDSLLMNRRKFLYQFKNVRWAKGRRETYLCYVVKRRDSATSFSLDFGYL
RNKNGCHVELLFLRYISDWDLDPGRCYRVTWFTSWSPCYDCARHVADFL
RGNPNLSLRIFTARLYFCEDRKAEPEGLRRLHRAGVQIAIMTFKDYFYC
WNTFVENHERTFKAWEGLHENSVRLSRQLRRILL

Rat APOBEC1 (rAPOBEC1):

(SEQ ID NO: 284)
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHS
IWRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSR
AITEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQ
ESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNIL
RRKQPQLTFFTIALQSCHYQRLPPHILWATGLK

Human APOBEC1 (hAPOBEC1)

(SEQ ID NO: 5724)
MTSEKGPSTGDPTLRRRIEPWEFDVFYDPRELRKEACLLYEIKWGMSRK
IWRSSGKNTTNHVEVNFIKKFTSERDFHPSMSCSITWFLSWSPCWECSQ
AIREFLSRHPGVTLVIYVARLFWHMDQQNRQGLRDLVNSGVTIQIMRAS
EYYHCWRNFVNYPPGDEAHWPQYPPLWMMLYALELHCIILSLPPCLKIS
RRWQNHLTFFRLHLQNCHYQTIPPHILLATGLIHPSVAWR

Petromyzon marinus (Lamprey) CDA1 (pmCDA1):

(SEQ ID NO: 609)
MTDAEYVRIHEKLDIYTFKKQFFNNKKSVSHRCYVLFELKRRGERRACFW
GYAVNKPQSGTERGIHAEIFSIRKVEEYLRDNPGQFTINWYSSWSPCADC
AEKILEWYNQELRGNGHTLKIWACKLYYEKNARNQIGLWNLRDNGVGLNV
MVSEHYQCCRKIFIQSSHNQLNENRWLEKTLKRAEKRRSELSIMIQVKIL
HTTKSPAV

Human APOBEC3G (hAPOBEC3G):

(SEQ ID NO: 610)
MELKYHPEMRFFHWFSKWRKLHRDQEYEVTWYISWSPCTKCTRDMATFLA
EDPKVTLTIFVARLYYFWDPDYQEALRSLCQKRDGPRATMKIMNYDEFQH
CWSKFVYSQRELFEPWNNLPKYYILLHIMLGEILRHSMDPPTFTFNFNNE
PWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQAPHKHGFLEGRHAE
LCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKFISKNKHVSLCI
FTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHCWDTFVDHQGCPFQ
PWDGLDEHSQDLSGRLRAILQNQEN

Deaminase Activity on ssDNA. A USER (Uracil-Specific Excision Reagent) Enzyme-based assay for deamination was employed to test the activity of various deaminases on single-stranded DNA (ssDNA) substrates. USER Enzyme was obtained from New England Biolabs. An ssDNA substrate was provided with a target cytosine residue at different positions. Deamination of the ssDNA cytosine target residue results in conversion of the target cytosine to a uracil. The USER Enzyme excises the uracil base and cleaves the ssDNA backbone at that position, cutting the ssDNA substrate into two shorter fragments of DNA. In some assays, the ssDNA substrate is labeled on one end with a dye, e.g., with a 5′ Cy3 label (the * in the scheme below). Upon deamination, excision, and cleavage of the strand, the substrate can be subjected to electrophoresis, and the substrate and any fragment released from it can be visualized by detecting the label. Where Cy5 is images, only the fragment with the label will be visible via imaging.

In one USER Enzyme assay, ssDNA substrates were used that matched the target sequences of the various deaminases tested. Expression cassettes encoding the deaminases tested were inserted into a CMV backbone plasmid that has been used previously in the lab (Addgene plasmid 52970). The deaminase proteins were expressed using a TNT Quick Coupled Transcription/Translation System (Promega) according to the manufacturers recommendations. After 90 min of incubation, 5 mL of lysate was incubated with 5′ Cy3-labeled ssDNA substrate and 1 unit of USER Enzyme (NEB) for 3 hours. The DNA was resolved on a 10% TBE PAGE gel and the DNA was imaged using Cy-dye imaging. A schematic representation of the USER Enzyme assay is shown in FIG. 41.

FIG. 1 shows the deaminase activity of the tested deaminases on ssDNA substrates, such as Doench 1, Doench 2, G7′ and VEGF Target 2. The rAPOBEC1 enzyme exhibited a substantial amount of deamination on the single-stranded DNA substrate with a canonical NGG PAM, but not with a negative control non-canonical NNN PAM. Cas9 fusion proteins with APOBEC family deaminases were generated. The following fusion architectures were constructed and tested on ssDNA:

(SEQ ID NO: 611)
rAPOBEC1-GGS-dCas9 primary sequence
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNT
NKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIAR
LYHHADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLW
(SEQ ID NO: 612)
rAPOBEC1-(GGS)3-dCas9 primary sequence
MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNT
NKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIAR
LYHHADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLW
(SEQ ID NO: 613)
VDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNTNKHVEVNFI
EKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIARLYHHADPR
NRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLEL
YCIILGLPPCLNILRRKQPQLTFFTIALQSCHYQRLPPHILWATGLK
(SEQ ID NO: 614)
ETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSTWRHTSQNTNKH
VEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIARLYH
HADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLWVRL
YVLELYCIILGLPPCLNILRRKQPQLTFFTIALQSCHYQRLPPHILWATGLK
(SEQ ID NO: 615)
MSSETFPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNT
NKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIAR
LYHHADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLW

FIG. 2 shows that the N-terminal deaminase fusions showed significant activity on the single stranded DNA substrates. For this reason, only the N-terminal architecture was chosen for further experiments.

FIG. 3 illustrates double stranded DNA substrate binding by deaminase-dCas9:sgRNA complexes. A number of double stranded deaminase substrate sequences were generated. The sequences are provided below. The structures according to FIG. 3 are identified in these sequences (36 bp: underlined, sgRNA target sequence: bold; PAM: boxed; 21 bp: italicized). All substrates were labeled with a 5′-Cy3 label:

(SEQ ID NO: 616)
2:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGTCCCGCGGATTTATTTATTT
(SEQ ID NO: 617)
3:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCTTCCGCGGATTTATTTATT
(SEQ ID NO: 618)
4:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTTCCGCGGATTTATTTAT
(SEQ ID NO: 619)
5:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTCCGCGGATTTATTTA
(SEQ ID NO: 620)
6:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTATTCCGCGGATTTATTT
(SEQ ID NO: 621)
7:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTTATTCCGCGGATTTATT
(SEQ ID NO: 622)
8:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTATTCCGCGGATTTAT
(SEQ ID NO: 623)
9:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTATTATTCCGCGGATTTA
(SEQ ID NO: 624)
10:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTATATTCCGCGGATTT
(SEQ ID NO: 625)
11:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTATTATATTCCGCGGATT
(SEQ ID NO: 626)
12:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTTATTATATTCCGCGGAT
(SEQ ID NO: 627)
13:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTATTATATTCCGCGGA
(SEQ ID NO: 628)
14:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCTATTATTATATTCCGCGG
(SEQ ID NO: 629)
15:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTATTATTATTACCGCG
(SEQ ID NO: 630)
18:GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCCATTATTATTATTATTACC
“—”:
(SEQ ID NO: 631)
GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGTA              ATATTAATTTATTTATTTAA
(SEQ ID NO: 632)
8U:GTAGGTAGTTAGGATGAATGGAAGGTTGGTGTAGATTATTATCUGCGGATTTA
*In all substrates except for “8U”, the top strand in FIG. 3 is the complement of the sequence specified here. In the case of “8U”, there is a “G” opposite the U.

FIG. 4 shows the results of a double stranded DNA Deamination Assay. The fusions were expressed and purified with an N-terminal His6 tag via both Ni-NTA and sepharose chromatography. In order to assess deamination on dsDNA substrates, the various dsDNA substrates shown on the previous slide were incubated at a 1:8 dsDNA:fusion protein ratio and incubated at 37° C. for 2 hours. Once the dCas9 portion of the fusion binds to the DNA it blocks access of the USER enzyme to the DNA. Therefore, the fusion proteins were denatured following the incubation and the dsDNA was purified on a spin column, followed by incubation for 45 min with the USER Enzyme and resolution of the resulting DNA substrate and substrate fragments on a 10% TBE-urea gel.

FIG. 5 demonstrates that Cas9 fusions can target positions 3-11 of double-stranded DNA target sequences (numbered according to the schematic in FIG. 3). Upper Gel: 1 μM rAPOBEC1-GGS-dCas9, 125 nM dsDNA, 1 eq sgRNA. Mid Gel: 1 μM rAPOBEC1-(GGS)₃-dCas9, 125 nM dsDNA, 1 eq sgRNA. Lower Gel: 1.85 μM rAPOBEC1-XTEN-dCas9, 125 nM dsDNA, 1 eq sgRNA. Based on the data from these gels, positions 3-11 (according to the numbering in FIG. 3) are sufficiently exposed to the activity of the deaminase to be targeted by the fusion proteins tested. Access of the deaminase to other positions is most likely blocked by the dCas9 protein.

The data further indicates that a linker of only 3 amino acids (GGS) is not optimal for allowing the deaminase to access the single stranded portion of the DNA. The 9 amino acid linker [(GGS)₃] (SEQ ID NO: 596) and the more structured 16 amino acid linker (XTEN) allow for more efficient deamination.

FIG. 6 demonstrates that the correct guide RNA, e.g., the correct sgRNA, is required for deaminase activity. The gel shows that fusing the deaminase to dCas9, the deaminase enzyme becomes sequence specific (e.g., using the fusion with an eGFP sgRNA results in no deamination), and also confers the capacity to the deaminase to deaminate dsDNA. The native substrate of the deaminase enzyme is ssDNA, and no deamination occurred when no sgRNA was added. This is consistent with reported knowledge that APOBEC deaminase by itself does not deaminate dsDNA. The data indicates that Cas9 opens the double-stranded DNA helix within a short window, exposing single-stranded DNA that is then accessible to the APOBEC deaminase for cytidine deamination. The sgRNA sequences used are provided below. sequences (36 bp: underlined, sgRNA target sequence: bold; PAM: boxed; 21 bp: italicized)

DNA sequence 8:
(SEQ ID NO:  633)
5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTATAGCC              ATTATTCCGCGGA
TTTATT
(SEQ ID NO:  634)
Correct sgRNA sequence (partial 3′ sequence):
5′-AUUAUUCCGCGGAUUUAUUUGUUUUAGAGCUAG...-3′
(SEQ ID NO:  635)
eGFP sgRNA sequence (partial 3′-sequence):
5′-CGUAGGCCAGGGUGGUCACGGUUUUAGAGCUAG...-3′

Example 2

Deamination of DNA Target Sequence

Exemplary deamination targets. The dCas9:deaminase fusion proteins described herein can be delivered to a cell in vitro or ex vivo or to a subject in vivo and can be used to effect C to T or G to A transitions when the target nucleotide is in positions 3-11 with respect to a PAM. Exemplary deamination targets include, without limitation, the following: CCR5 truncations: any of the codons encoding Q93, Q102, Q186, R225, W86, or Q261 of CCR5 can be deaminated to generate a STOP codon, which results in a nonfunctional truncation of CCR5 with applications in HIV treatment. APOE4 mutations: mutant codons encoding C11R and C57R mutant APOE4 proteins can be deaminated to revert to the wild-type amino acid with applications in Alzheimer's treatment. eGFP truncations: any of the codons encoding Q158, Q184, Q185 can be deaminated to generate a STOP codon, or the codon encoding M1 can be deaminated to encode I, all of which result in loss of eGFP fluorescence, with applications in reporter systems. eGFP restoration: a mutant codon encoding T65A or Y66C mutant GFP, which does not exhibit substantial fluorescence, can be deaminated to restore the wild-type amino acid and confer fluorescence. PIK3CA mutation: a mutant codon encoding K111E mutant PIK3CA can be deaminated to restore the wild-type amino acid residue with applications in cancer. CTNNB1 mutation: a mutant codon encoding T41A mutant CTNNB1 can be deaminated to restore the wild-type amino acid residue with applications in cancer. HRAS mutation: a mutant codon encoding Q61R mutant HRAS can be deaminated to restore the wild-type amino acid residue with applications in cancer. P53 mutations: any of the mutant codons encoding Y163C, Y236C, or N239D mutant p53 can be deaminated to encode the wild type amino acid sequence with applications in cancer. The feasibility of deaminating these target sequences in double-stranded DNA is demonstrated in FIGS. 7 and 8. FIG. 7 illustrates the mechanism of target DNA binding of in vivo target sequences by deaminase-dCas9:sgRNA complexes.

FIG. 8 shows successful deamination of exemplary disease-associated target sequences. Upper Gel: CCR5 Q93: coding strand target in pos. 10 (potential off-targets at positions 2, 5, 6, 8, 9); CCR5 Q102: coding strand target in pos. 9 (potential off-targets at positions 1, 12, 14); CCR5 Q186: coding strand target in pos. 9 (potential off-targets at positions 1, 5, 15); CCR5 R225: coding strand target in pos. 6 (no potential off-targets); eGFP Q158: coding strand target in pos. 5 (potential off-targets at positions 1, 13, 16); eGFP Q184/185: coding strand target in pos. 4 and 7 (potential off-targets at positions 3, 12, 14, 15, 16, 17, 18); eGFP M1: template strand target in pos. 12 (potential off-targets at positions 2, 3, 7, 9, 11) (targets positions 7 and 9 to small degree); eGFP T65A: template strand target in pos. 7 (potential off-targets at positions 1, 8, 17); PIK3CA K111E: template strand target in pos. 2 (potential off-targets at positions 5, 8, 10, 16, 17); PIK3CA K111E: template strand target in pos. 13 (potential off-targets at positions 11, 16, 19) X. Lower Gel: CCR5 W86: template strand target in pos. 2 and 3 (potential off-targets at positions 1, 13) X; APOE4 C11R: coding strand target in pos. 11 (potential off-targets at positions 7, 13, 16, 17); APOE4 C57R: coding strand target in pos. 5) (potential off-targets at positions 7, 8, 12); eGFP Y66C: template strand target in pos. 11 (potential off-targets at positions 1, 4, 6, 8, 9, 16); eGFP Y66C: template strand target in pos. 3 (potential off-targets at positions 1, 8, 17); CCR5 Q261: coding strand target in pos. 10 (potential off-targets at positions 3, 5, 6, 9, 18); CTNNB1 T41A: template strand target in pos. 7 (potential off-targets at positions 1, 13, 15, 16) X; HRAS Q61R: template strand target in pos. 6 (potential off-targets at positions 1, 2, 4, 5, 9, 10, 13); p53 Y163C: template strand target in pos. 6 (potential off-targets at positions 2, 13, 14); p53 Y236C: template strand target in pos. 8 (potential off-targets at positions 2, 4); p53 N239D: template strand target in pos. 4 (potential off-targets at positions 6, 8). Exemplary DNA sequences of disease targets are provided below (PAMs (5′-NGG-3′) and target positions are boxed):

(SEQ ID NO: 636)
CCR5 Q93: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTAACTAT              GCTGCCGCC
(SEQ ID NO: 637)
CCR5 Q102: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTAAAATA              CAATGTGT
(SEQ ID NO: 638)
CCR5 Q186: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTATTTTC              CATACAGT
(SEQ ID NO: 639)
CCR5 R225: 5′-Cy3-
(SEQ ID NO: 640)
CCR5 W86: 4′-Cy3-
(SEQ ID NO: 641)
CCR5 Q261: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTATCCTG              AACACCTT
(SEQ ID NO: 642)
APOE4 C11R: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTAGACAT              GGAGGAC
(SEQ ID NO: 643)
APOE4 C57R: 5′-Cy3-
(SEQ ID NO: 644)
eGFP Q158: 5′-Cy3-
(SEQ ID NO: 645)
(SEQ ID NO: 646)
eGFP M1: 5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTACCTCG              CCCTTGCTCA
(SEQ ID NO:  647)
eGFP T65A: 5′-Cy3-
(SEQ ID NO:  648)
eGFP Y66C:  5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTAAAGCA              CTGCACTC
(SEQ ID NO:  649)
eGFP Y66C:  5′-Cy3-
(SEQ ID NO:  650)
PIK3CA K111E:  5′-Cy3-
(SEQ ID NO:  651)
PIK3CA K111E:  5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTATTCTC              GATTG
(SEQ ID NO:  652)
CTNNB1 T41A:  5′-Cy3-
GTAGGTAGTTAGGATGAATGGAAGGTTGGTAAGGAG              CTGTGG
(SEQ ID NO:  653)
HrAS Q61R:  5′-Cy3-
(SEQ ID NO:  654)
p53 Y163C:  5′-Cy3-
(SEQ ID NO:  655)
p53 Y236C:  5′-Cy3-
(SEQ ID NO:  656)
p3 N239D:  5′-Cy3-

Example 3

Uracil Glycosylase Inhibitor Fusion Improves Deamination Efficiency

Direct programmable nucleobase editing efficiencies in mammalian cells by dCas9:deaminase fusion proteins can be improved significantly by fusing a uracil glycosylase inhibitor (UGI) to the dCas9:deaminase fusion protein.

FIG. 9 shows in vitro C→T editing efficiencies in human HEK293 cells using rAPOBEC1-XTEN-dCas9:

(SEQ ID NO: 657)
MSSETGPVAVDPTLRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNT
NKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIAR
LYHHADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLWV
RLYVLELYCIILGLPPCLNILRRKQPQLTFFTIALQSCHYQRLPPHILWATGLK              SGSETP
KV

Protospacer sequences were as follows:

EMX1:
FANCF:
HEK293 site 2:
HEK293 site 3:
HEK293 site 4:
RNF2:
*PAMs are boxed, C residues within target window (positions 3-11) are numbered and bolded.

FIG. 10 demonstrates that C→T editing efficiencies on the same protospacer sequences in HEK293T cells are greatly enhanced when a UGI domain is fused to the rAPOBEC1:dCas9 fusion protein.

(SEQ ID NO: 658)
MSSETFPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSIWRHTSQNT
NKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAITEFLSRYPHVTLFIYIAR
LYHHADPRNRQGLRDLISSGVTIQIMTEQESGYCWRNFVNYSPNEAHWPRYPHLWV
RLYVLELYCIILGLPPCLNILRRKQPQLTFFTIALQSCHYQRLPPHILWATGLK              SGSETP
IIEKETGKQLVIQESILMLPEEVEEVISNKPESDILVHTAYDESTDENVMLLTSDAP
EYKPWALVIQDSNGENKIKMLSGGSPKKKRKV

The percentages in FIGS. 9 and 10 are shown from sequencing both strands of the target sequence. Because only one of the strands is a substrate for deamination, the maximum possible deamination value in this assay is 50%. Accordingly, the deamination efficiency is double the percentages shown in the tables. E.g., a value of 50% relates to deamination of 100% of double-stranded target sequences.

When a uracil glycosylase inhibitor (UGI) was fused to the dCas9:deaminase fusion protein (e.g., rAPOBEC1-XTEN-dCas9-[UGI]-NLS), a significant increase in editing efficiency in cells was observed. This result indicates that in mammalian cells, the DNA repair machinery that cuts out the uracil base in a U:G base pair is a rate-limiting process in DNA editing. Tethering UGI to the dVas9:deaminase fusion proteins greatly increases editing yields.

Without UGI, typical editing efficiencies in human cells were in the ˜2-14% yield range (FIG. 9 and FIG. 10, “XTEN” entries). With UGI (FIG. 10, “UGI” entries) the editing was observed in the ˜6-40% range. Using a UGI fusion is thus more efficient than the current alternative method of correcting point mutations via HDR, which also creates an excess of indels in addition to correcting the point mutation. No indels resulting from treatment with the cas9:deaminase:UGI fusions were observed.

Example 4

Direct, Programmable Conversion of a Target Nucleotide in Genomic DNA without Double-Stranded DNA Cleavage

Current genome-editing technologies introduce double-stranded DNA breaks at a target locus of interest as the first step to gene correction.^39,40 Although most genetic diseases arise from mutation of a single nucleobase to a different nucleobase, current approaches to revert such changes are very inefficient and typically induce an abundance of random insertions and deletions (indels) at the target locus as a consequence of the cellular response to double-stranded DNA breaks.^39,40 Reported herein is the development of nucleobase editing, a new strategy for genome editing that enables the direct conversion of one target nucleobase into another in a programmable manner, without requiring double-stranded DNA backbone cleavage. Fusions of CRISPR/Cas9 were engineered and the cytidine deaminase enzyme APOBEC1 that retain the ability to be programmed with a guide RNA, do not induce double-stranded DNA breaks, and mediate the direct conversion of cytidine to uracil, thereby effecting a C→T (or G→A) substitution following DNA replication, DNA repair, or transcription if the template strand is targeted. The resulting “nucleobase editors” convert cytidines within a window of approximately five nucleotides, and can efficiently correct a variety of point mutations relevant to human disease in vitro. In four transformed human and murine cell lines, second- and third-generation nucleobase editors that fuse uracil glycosylase inhibitor (UGI), and that use a Cas9 nickase targeting the non-edited strand, respectively, can overcome the cellular DNA repair response to nucleobase editing, resulting in permanent correction of up to 37% or (˜15-75%) of total cellular DNA in human cells with minimal (typically ≦1%) indel formation. In contrast, canonical Cas9-mediated HDR on the same targets yielded an average of 0.7% correction with 4% indel formation. Nucleobase editors were used to revert two oncogenic p53 mutations into wild-type alleles in human breast cancer and lymphoma cells, and to convert an Alzheimer's Disease associated Arg codon in ApoE4 into a non-disease-associated Cys codon in mouse astrocytes. Base editing expands the scope and efficiency of genome editing of point mutations.

The clustered regularly interspaced short palindromic repeat (CRISPR) system is a prokaryotic adaptive immune system that has been adapted to mediate genome engineering in a variety of organisms and cell lines.⁴¹ CRISPR/Cas9 protein-RNA complexes localize to a target DNA sequence through base pairing with a guide RNA, and natively create a DNA double-stranded break (DSB) at the locus specified by the guide RNA. In response to DSBs, endogenous DNA repair processes mostly result in random insertions or deletions (indels) at the site of DNA cleavage through non-homologous end joining (NHEJ). In the presence of a homologous DNA template, the DNA surrounding the cleavage site can be replaced through homology-directed repair (HDR). When simple disruption of a disease-associated gene is sufficient (for example, to treat some gain-of-function diseases), targeted DNA cleavage followed by indel formation can be effective. For most known genetic diseases, however, correction of a point mutation in the target locus, rather than stochastic disruption of the gene, is needed to address or study the underlying cause of the disease.⁶⁸

Motivated by this need, researchers have invested intense effort to increase the efficiency of HDR and suppress NHEJ. For example, a small-molecule inhibitor of ligase IV, an essential enzyme in the NHEJ pathway, has been shown to increase HDR efficiency.^42,43 However, this strategy is challenging in post-mitotic cells, which typically down-regulate HDR, and its therapeutic relevance is limited by the potential risks of inhibiting ligase IV in non-target cells. Enhanced HDR efficiency can also be achieved by the timed delivery of Cas9-guide RNA complexes into chemically synchronized cells, as HDR efficiency is highly cell-cycle dependent.⁴⁴ Such an approach, however, is limited to research applications in cell culture since synchronizing cells is highly disruptive. Despite these developments, current strategies to replace point mutations using HDR in most contexts are very inefficient (typically ˜0.1 to 5%),^{42,43,45,46,75} especially in unmodified, non-dividing cells. In addition, HDR competes with NHEJ during the resolution of double-stranded breaks, and indels are generally more abundant outcomes than gene replacement. These observations highlight the need to develop alternative approaches to install specific modifications in genomic DNA that do not rely on creating double-stranded DNA breaks. A small-molecule inhibitor of ligase IV, an essential enzyme in the NHEJ pathway, has been shown to increase HDR efficiency.^42,43 However, this strategy is challenging in post-mitotic cells, which typically down-regulate HDR, and its therapeutic relevance is limited by the potential risks of inhibiting ligase IV in non-target cells. Enhanced HDR efficiency can also be achieved by the timed delivery of Cas9-guide RNA complexes into chemically synchronized cells, as HDR efficiency is highly cell-cycle dependent.⁴⁴ Such an approach, however, is limited to research applications in cell culture since synchronizing cells is highly disruptive. In some cases, it is possible to design HDR templates such that the product of successful HDR contains mutations in the PAM sequence and therefore is no longer a substrate for subsequent Cas9 modification, increasing the overall yield of HDR products,⁷⁵ although such an approach imposes constraints on the product sequences. Recently, this strategy has been coupled to the use of ssDNA donors that are complementary to the non-target strand and high-efficiency ribonucleoprotein (RNP) delivery to substantially increase the efficiency of HDR, but even in these cases the ratio of HDR to NHEJ outcomes is relatively low (<2).⁸³

It was envisioned that direct catalysis of the conversion of one nucleobase to another at a programmable target locus without requiring DNA backbone cleavage could increase the efficiency of gene correction relative to HDR without introducing undesired random indels at the locus of interest. Catalytically dead Cas9 (dCas9), which contains Asp10Ala and His840Ala mutations that inactivate its nuclease activity, retains its ability to bind DNA in a guide RNA-programmed manner but does not cleave the DNA backbone.^16,47 In principle, conjugation of dCas9 with an enzymatic or chemical catalyst that mediates the direct conversion of one nucleobase to another could enable RNA-programmed nucleobase editing. The deamination of cytosine (C) is catalyzed by cytidine deaminases²⁹ and results in uracil (U), which has the base pairing properties of thymine (T). dCas9 was fused to cytidine deaminase enzymes in order to test their ability to convert C to U at a guide RNA-specified DNA locus. Most known cytidine deaminases operate on RNA, and the few examples that are known to accept DNA require single-stranded DNA.⁴⁸ Recent studies on the dCas9-target DNA complex reveal that at least nine nucleotides of the displaced DNA strand are unpaired upon formation of the Cas9:guide RNA:DNA “R-loop” complex.¹² Indeed, in the structure of the Cas9 R-loop complex the first 11 nucleotides of the protospacer on the displaced DNA strand are disordered, suggesting that their movement is not highly restricted.⁷⁶ It has also been speculated that Cas9 nickase-induced mutations at cytosines in the non-template strand might arise from their accessibility by cellular cytidine deaminase enzymes.⁷⁷ Recent studies on the dCas9-target DNA complex have revealed that at least 26 bases on the non-template strand are unpaired when Cas9 binds to its target DNA sequence.⁴⁹ It was reasoned that a subset of this stretch of single-stranded DNA in the R-loop might serve as a substrate for a dCas9-tethered cytidine deaminase to effect direct, programmable conversion of C to U in DNA (FIG. 11A).

Four different cytidine deaminase enzymes (hAID, hAPOBEC3G, rAPOBEC1, and pmCDA1) were expressed in a mammalian cell lysate-derived in vitro transcription-translation system and evaluated for ssDNA deamination. Of the four enzymes, rAPOBEC1 showed the highest deaminase activity under the tested conditions and was chosen for dCas9 fusion experiments (FIG. 36A). Although appending rAPOBEC1 to the C-terminus of dCas9 abolishes deaminase activity, fusion to the N-terminus of dCas9 preserves deaminase activity on ssDNA at a level comparable to that of the unfused enzyme. Four rAPOBEC1-dCas9 fusions were expressed and purified with linkers of different length and composition (FIG. 36B), and evaluated each fusion for single guide RNA (sgRNA)-programmed dsDNA deamination in vitro (FIGS. 11A to 11C and FIGS. 15A to 15D).

Efficient, sequence-specific, sgRNA-dependent C to U conversion was observed in vitro (FIGS. 11A to 11C). Conversion efficiency was greatest using rAPOBEC1-dCas9 linkers over nine amino acids in length. The number of positions susceptible to deamination (the deamination “activity window”) increases with linker length was extended from three to 21 amino acids (FIGS. 36C to 36F15A to 15D). The 16-residue XTEN linker⁵⁰ was found to offer a promising balance between these two characteristics, with an efficient deamination window of approximately five nucleotides, from positions 4 to 8 within the protospacer, counting the end distal to the protospacer-adjacent motif (PAM) as position 1. The rAPOBEC1-XTEN-dCas9 protein served as the first-generation nucleobase editor (NBE1).

Elected were seven mutations relevant to human disease that in theory could be corrected by C to T nucleobase editing, synthesized double-stranded DNA 80-mers of the corresponding sequences, and assessed the ability of NBE1 to correct these mutations in vitro (FIGS. 16A to 16B). NBE1 yielded products consistent with efficient editing of the target C, or of at least one C within the activity window when multiple Cs were present, in six of these seven targets in vitro, with an average apparent editing efficiency of 44% (FIGS. 16A to 16B). In the three cases in which multiple Cs were present within the deamination window, evidence of deamination of some or all of these cytosines was observed. In only one of the seven cases tested were substantial yields of edited product observed (FIGS. 16A to 16 B). Although the preferred sequence context for APOBEC1 substrates is reported to be CC or TC,⁵¹ it was anticipated that the increased effective molarity of the deaminase and its single-stranded DNA substrate mediated by dCas9 binding to the target locus may relax this restriction. To illuminate the sequence context generality of NBE1, its ability to edit a 60-mer double-stranded DNA oligonucleotide containing a single fixed C at position 7 within the protospacer was assayed, as well as all 36 singly mutated variants in which protospacer bases 1-6 and 8-13 were individually varied to each of the other three bases. Each of these 37 sequences were treated with 1.9 μM NBE1, 1.9 μM of the corresponding sgRNA, and 125 nM DNA for 2 h, similar to standard conditions for in vitro Cas9 assays⁵². High-throughput DNA sequencing (HTS) revealed 50 to 80% C to U conversion of targeted strands (25 to 40% of total sequence reads arising from both DNA strands, one of which is not a substrate for NBE1) (FIG. 12A). The nucleotides surrounding the target C had little effect on editing efficiency was independent of sequence context unless the base immediately 5′ of the target C is a G, in which case editing efficiency was substantially lower (FIGS. 12A to 12B). NBE1 activity in vitro was assessed on all four NC motifs at positions 1 through 8 within the protospacer (FIGS. 12A to 12B). In general NBE1 activity on substrates was observed to follow the order TC≧CC≧AC≧GC, with maximum editing efficiency achieved when the target C is at or near position 7. In addition, it was observed that the nucleobase editor is highly processive, and will efficiently convert most of all Cs to Us on the same DNA strand within the 5-base activity window (FIG. 17).

While BE1 efficiently processes substrates in a test tube, in cells a tree of possible DNA repair outcomes determines the fate of the initial U:G product of base editing (FIG. 29A). To test the effectiveness of nucleobase editing in human cells, NBE1 codon usage was optimized for mammalian expression, appended a C-terminal nuclear localization sequence (NLS),⁵³ and assayed its ability to convert C to T in human cells on 14Cs in six well-studied target sites throughout the human genome (FIG. 37A).⁵⁴ The editable Cs were confirmed within each protospacer in vitro by incubating NBE1 with synthetic 80-mers that correspond to the six different genomic sites, followed by HTS (FIGS. 13A to 13C, FIG. 29B and FIG. 25). Next, HEK293T cells were transfected with plasmids encoding NBE1 and one of the six target sgRNAs, allowed three days for nucleobase editing to occur, extracted genomic DNA from the cells, and analyzed the loci by HTS. Although C to T editing in cells at the target locus was observed for all six cases, the efficiency of nucleobase editing was 1.1% to 6.3% or 0.8%-7.7% of total DNA sequences (corresponding to 2.2% to 12.6% of targeted strands), a 6.3-fold to 37-fold or 5-fold to 36-fold decrease in efficiency compared to that of in vitro nucleobase editing (FIGS. 13A to 13C, FIG. 29B and FIG. 25). It was observed that some base editing outside of the typical window of positions 4 to 8 when the substrate C is preceded by a T, which we attribute to the unusually high activity of APOBEC1 for TC substrates.⁴⁸

It was asked whether the cellular DNA repair response to the presence of U:G heteroduplex DNA was responsible for the large decrease in nucleobase editing efficiency in cells (FIG. 29A). Uracil DNA glycosylase (UDG) catalyzes removal of U from DNA in cells and initiates base excision repair (BER), with reversion of the U:G pair to a C:G pair as the most common outcome (FIG. 29A).⁵⁵ Uracil DNA glycosylase inhibitor (UGI), an 83-residue protein from B. subtilis bacteriophage PBS1, potently blocks human UDG activity (IC₅₀=12 pM).⁵⁶ UGI was fused to the C-terminus of NBE1 to create the second-generation nucleobase editor NBE2 and repeated editing assays on all six genomic loci. Editing efficiencies in human cells were on average 3-fold higher with NBE2 than with NBE1, resulting in gene conversion efficiencies of up to 22.8% of total DNA sequenced (up to 45.6% of targeted strands) (FIGS. 13A to 13C and FIG. 29B). To test base editing in human cells, BE1 codon usage was optimized for mammalian expression and appended a C-terminal nuclear localization sequence (NLS).⁵³

Similar editing efficiencies were observed when a separate plasmid overexpressing UGI was co-transfected with NBE1 (FIGS. 18A to 18H). However, while the direct fusion of UGI to NBE1 resulted in no significant increase in C to T mutations at monitored non-targeted genomic locations, overexpression of unfused UGI detectably increased the frequency of C to T mutations elsewhere in the genome (FIGS. 18A to 18H). The generality of NBE2-mediated nucleobase editing was confirmed by assessing editing efficiencies on the same six genomic targets in U2OS cells, and observed similar results with those in HEK293T cells (FIG. 19). Importantly, NBE2 typically did not result in any detectable indels (FIG. 13C and FIG. 29C), consistent with the known mechanistic dependence of NHEJ on double-stranded DNA breaks.^57,78 Together, these results indicate that conjugating UGI to NBE1 can greatly increase the efficiency of nucleobase editing in human cells.

The permanence of nucleobase editing in human cells was confirmed by monitoring editing efficiencies over multiple cell divisions in HEK293T cells at two of the tested genomic loci. Genomic DNA was harvested at two time points: three days after transfection with plasmids expressing NBE2 and appropriate sgRNAs, and after passaging the cells and growing them for four additional days (approximately five subsequent cell divisions). No significant change in editing efficiency was observed between the non-passaged cells (editing observed in 4.6% to 6.6% of targeted strands for three different target Cs) and passaged cells (editing observed in 4.6% to 6.4% of targeted strands for the same three target Cs), confirming that the nucleobase edits became permanent following cell division (FIG. 20). Indels will on rare occasion arise from the processing of U:G lesions by cellular repair processes, which involve single-strand break intermediates that are known to lead to indels.⁸⁴ Given that several hundred endogenous U:G lesions are generated every day per human cell from spontaneous cytidine deaminase,⁸⁵ it was anticipate that the total indel frequency from U:G lesion repair is unlikely to increase from BE1 or BE2 activity at a single target locus.

To further increase the efficiency of nucleobase editing in cells, it was anticipated that nicking the non-edited strand may result in a smaller fraction of edited Us being removed by the cell, since eukaryotic mismatch repair machinery uses strand discontinuity to direct DNA repair to any broken strand of a mismatched duplex (FIG. 29A).^{58, 79, 80} The catalytic His residue was restored at position 840 in the Cas9 HNH domain,^47,59 resulting in the third-generation nucleobase editor NBE3 that nicks the non-edited strand containing a G opposite the targeted C, but does not cleave the target strand containing the C. Because NBE3 still contains the Asp10Ala mutation in Cas9, it does not induce double-stranded DNA cleavage. This strategy of nicking the non-edited strand augmented nucleobase editing efficiency in human cells by an additional 1.4- to 4.8-fold relative to NBE2, resulting in up to 36.3% of total DNA sequences containing the targeted C to T conversion on the same six human genomic targets in HEK293T cells (FIGS. 13A to 13C and FIG. 29B). Importantly, only a small frequency of indels, averaging 0.8% (ranging from 0.2% to 1.6% for the six different loci), was observed from NBE3 treatment (FIG. 13C, FIG. 29C, and FIG. 34). In contrast, when cells were treated with wild-type Cas9, sgRNA, and a single-stranded DNA donor template to mediate HDR at three of these loci C to T conversion efficiencies averaging only 0.7% were observed, with much higher relative indel formation averaging 3.9% (FIGS. 13A to 13C and FIG. 29C). The ratio of allele conversion to NHEJ outcomes averaged >1,000 for BE2, 23 for BE3, and 0.17 for wild-type Cas9 (FIG. 3c). We confirmed the permanence of base editing in human cells by monitoring editing efficiencies over multiple cell divisions in HEK293T cells at the HEK293 site 3 and 4 genomic loci (FIG. 38). These results collectively establish that nucleobase editing can effect much more efficient targeted single-base editing in human cells than Cas9-mediated HDR, and with much less (NBE3) or no (NBE2) indel formation.

Next, the off-target activity of NBE1, NBE2, and NBE3 in human cells was evaluated. The off-target activities of Cas9, dCas9, and Cas9 nickase have been extensively studied (FIGS. 23 to 24 and 31 to 33).^54,60-62 Because the sequence preference of rAPOBEC1 has been shown to be independent of DNA bases more than one base from the target C,⁶³ consistent with the sequence context independence observed in FIGS. 12A to 12B, it was assumed that potential off-target activity of nucleobase editors arises from off-target Cas9 binding. Since only a fraction of Cas9 off-target sites will have a C within the active window for nucleobase editing, off-target nucleobase editing sites should be a subset of the off-target sites of canonical Cas9 variants. For each of the six sites studied, the top ten known Cas9 off-target loci in human cells that were previously determined using the GUIDE-seq method were sequenced (FIGS. 23 to 27 and 31 to 33).^{54, 61} Detectable off-target nucleobase editing at only a subset (16/34, 47% for NBE1 and NBE2, and 17/34, 50% for NBE3) of known dCas9 off-target loci was observed. In all cases, the off-target base-editing substrates contained a C within the five-base target window. In general, off-target C to T conversion paralleled off-target Cas9 nuclease-mediated genome modification frequencies (FIGS. 23 to 27). Also monitored were C to T conversions at 2,500 distinct cytosines surrounding the six on-target and 34 off-target loci tested, representing a total of 14,700,000 sequence reads derived from approximately 1.8×10⁶ cells, and observed no detectable increase in C to T conversions at any of these other sites upon NBE1, NBE2, or NBE3 treatment compared to that of untreated cells (FIG. 28). Taken together, these findings suggest that off-target substrates of nucleobase editors include a subset of Cas9 off-target substrates, and that nucleobase editors in human cells do not induce untargeted C to T conversion throughout the genome at levels that can be detected by the methods used here. No substantial change was observed in editing efficiency between non-passaged HEK293T cells (editing observed in 1.8% to 2.6% of sequenced strands for the three target Cs with BE2, and 6.2% to 14.3% with BE3) and cells that had undergone approximately five cell divisions after base editing (editing observed in 1.9% to 2.3% of sequenced strands for the same target Cs with BE2, and 6.4% to 14.5% with BE3), confirming that base edits in these cells are durable (FIG. 38).

Finally, the potential of nucleobase editing to correct three disease-relevant mutations in mammalian cells was tested. The apolipoprotein E gene variant APOE4 encodes two Arg residues at amino acid positions 112 and 158, and is the largest and most common genetic risk factor for late-onset Alzheimer's disease.⁶⁴ ApoE variants with Cys residues in positions 112 or 158, including APOE2 (Cys112/Cys158), APOE3 (Cys112/Arg158), and APOE3′ (Arg112/Cys158) have been shown⁶⁵ or are presumed⁸¹ to confer substantially lower Alzheimer's disease risk than APOE4. Encouraged by the ability of NBE1 to convert APOE4 to APOE3′ in vitro (FIGS. 16A to 16B), this conversion was attempted in immortalized mouse astrocytes in which the endogenous murine APOE gene has been replaced by human APOE4 (Taconic). DNA encoding NBE3 and an appropriate sgRNA was delivered into these astrocytes by nucleofection (nucleofection efficiency of 25%), extracted genomic DNA from all treated cells two days later, and measured editing efficiency by HTS. Conversion of Arg158 to Cys158 was observed in 58-75% of total DNA sequencing reads (44% of nucleofected astrocytes) (FIGS. 14A to 14C and FIGS. 30A). Also observed was 36-50% editing of total DNA at the third position of codon 158 and 38-55% editing of total DNA at the first position of Leu159, as expected since all three of these Cs are within the active nucleobase editing window. However, neither of the other two C→T conversions results in a change in the amino acid sequence of the ApoE3′ protein since both TGC and TGT encode Cys, and both CTG and TTG encode Leu. From >1,500,000 sequencing reads derived from 1×10⁶ cells evidence of 1.7% indels at the targeted locus following NBE3 treatment was observed (FIG. 35). In contrast, identical treatment of astrocytes with wt Cas9 and donor ssDNA resulted in 0.1-0.3% APOE4 correction and 26-40% indels at the targeted locus, efficiencies consistent with previous reports of single-base correction using Cas9 and HDR^45,75 (FIG. 30A and FIG. 40A). Astrocytes treated identically but with an sgRNA targeting the VEGFA locus displayed no evidence of APOE4 base editing (FIG. 34 and FIG. 40A). These results demonstrate how nucleobase editors can effect precise, single-amino acid changes in the coding sequence of a protein as the major product of editing, even when their processivity results in more than one nucleotide change in genomic DNA. The off-target activities of Cas9, dCas9, and Cas9 nickase have been extensively studied.^{54, 60-62} In general, off-target C to T conversions by BE1, BE2, and BE3 paralleled off-target Cas9 nuclease-mediated genome modification frequencies.

The dominant-negative p53 mutations Tyr163Cys and Asn239Asp are strongly associated with several types of cancer.^66-67 Both of these mutations can be corrected by a C to T conversion on the template strand (FIGS. 16A to 16B). A human breast cancer cell line homozygous for the p53 Tyr163Cys mutation (HCC1954 cells) was nucleofected with DNA encoding NBE3 and an sgRNA programmed to correct Tyr163Cys. Because the nucleofection efficiency of HCC1954 cells was <10%, a plasmid expressing IRFP was co-nucleofected into these cells to enable isolation of nucleofected cells by fluorescence-activated cell sorting two days after treatment. HTS of genomic DNA revealed correction of the Tyr163Cys mutation in 7.6% of nucleofected HCC1954 cells (FIG. 30B and FIG. 40A to 40B). Also nucleofected was a human lymphoma cell line that is heterozygous for p53 Asn239Asp (ST486 cells) with DNA encoding NBE2 and an sgRNA programmed to correct Asn239Asp with 92% nucleofection efficiency). Correction of the Asn239Asp mutation was observed in 11% of treated ST486 cells (12% of nucleofected ST486 cells). Consistent with the findings in HEK cells, no indels were observed from the treatment of ST486 cells with NBE2, and 0.6% indel formation from the treatment of HCC1954 cells with NBE3. No other DNA changes within at least 50 base pairs of both sides of the protospacer were detected at frequencies above that of untreated controls out of >2,000,000 sequencing reads derived from 2×10⁵ cells (FIGS. 14A to 14C, FIG. 30B and Table 1). These results collectively represent the conversion of three disease-associated alleles in genomic DNA into their wild-type forms with an efficiency and lack of other genome modification events that is, to our knowledge, not currently achievable using other methods.

To illuminate the potential relevance of nucleobase editors to address human genetic diseases, the NCBI ClinVar database⁶⁸ was searched for known genetic diseases that could in principle be corrected by this approach. ClinVar was filtered by first examining only single nucleotide polymorphisms (SNPs), then removing any nonpathogenic variants. Out of the 24,670 pathogenic SNPs, 3,956 are caused by either a T to C, or an A to G, substitution. This list was further filtered to only include variants with a nearby NGG PAM that would position the SNP within the deamination activity window, resulting in 1,089 clinically relevant pathogenic gene variants that could in principle be corrected by the nucleobase editors described here (FIG. 21 and Table 1). To illuminate the potential relevance of base editors to address human genetic diseases, the NCBI ClinVar database⁶⁸ was searched for known genetic diseases that could in principle be corrected by this approach. ClinVar was filtered by first examining only single nucleotide polymorphisms (SNPs), then removing any non-pathogenic variants. Out of the 24,670 pathogenic SNPs, 3,956 are caused by either a T to C, or an A to G, substitution. This list was further filtered to only include variants with a nearby NGG PAM that would position the SNP within the deamination activity window, resulting in 911 clinically relevant pathogenic gene variants that could in principle be corrected by the base editors described here. Of these, 284 contain only one C within the base editing activity window. A detailed list of these pathogenic mutations can be found in Table 1.

TABLE 1
List of 911 base-editable gene variants associated with human disease
with an NGG PAM (SEQ ID NOs: 747 to 1868 appear from top to bottom below,
respectively). The ″Y″ in the protospacer and PAM sequences indicates the base to be edited,
e.g., C. (SEQ ID NOs: 747 to 1868 appear from top to bottom below, respectively)
		Protospacer	Associated genetic disease
dbSNP #	Genotype	and PAM sequence(s)
755445790	NM_000391.3(TPP1):	TTTYTTTTTTTTTTTTTTTGAGG	Ceroid lipofuscinosis,
	c.887-10A > 22G		neuronal, 2
113994167	NM_000018.3(ACADVL):	TTTGYGGTGGAGAGGGGCTTCGG,	Very long chain acyl-CoA
	c.848T > 22C	TTGYGGTGGAGAGGGGCTTCGGG	dehydrogenase
	(p.Val283Ala)		deficiency
119470018	NM_024996.5(GFM1):	TTGYTAATAAAAGTTAGAAACGG	Combined oxidative
	c.521A > 22G		phosphorylation deficiency 1
	(p.Asn174Ser)
115650537	NM_000426.3(LAMA2):	TTGAYAGGGAGCAAGCAGTTCGG,	Merosin deficient congenital
	c.8282T > 22C	TGAYAGGGAGCAAGCAGTTCGGG	muscular
	(p.Ile2761Thr)		dystrophy
587777752	NM_014946.3(SPAST):	TTCYGTAAAACATAAAAGTCAGG	Spastic paraplegia 4,
	c.1688-		autosomal dominant
794726821	NM_001165963.1(SCN1A):	TTCYGGTTTGTCTTATATTCTGG	Severe myoclonic epilepsy in
	c.4055T > C		infancy
	(p.Leu1352Pro)
397514745	NM_001130089.1(KARS):	CTTCYATGATCTTCGAGGAGAGG,	Deafness, autosomal recessive
	c.517T > 22C	TTCYATGATCTTCGAGGAGAGG	89
	(p.Tyr173His)	G
376960358	NM_001202.3(BMP4):	TTCGTGGYGGAAGCTCCTCACGG	Microphthalmia syndromic 6
	c.362A > 22G
	(p.His121Arg)
606231280	NM_001287223.1(SCN11A):	CTTCAYTGTGGTCATTTTCCTGG,	Episodic pain syndrome,
	c.42T > 22C	TTCAYTGTGGTCATTTTCCTGG	familial, 3
	(p.Ile381Thr)	G
387906735	m.608A > 22G	TTCAGYGTATTGCTTTGAGGAGG
199474663	m.3260A > 22G	TTAAGTTYTATGCGATTACCGGG	Cardiomyopathy with or without
			skeletal myopathy
104894962	NM_003413.3(ZIC3):c.1213A > 22G	TGTGTTYGCGCAGGGAGCTCGGG,	Heterotaxy, visceral, X-linked
	(p.Lys405Glu)	ATGTGTTYGCGCAGGGAGCTCG
		G
796053181	NM_021007.2(SCN2A):c.1271T > 22C	TGTGGYGGCCATGGCCTATGAGG	not provided
	(p.Val424Ala)
267606788	NM_000129.3(F13A1):c.728T > 22C	TGTGAYGGACAGAGCACAAATGG	Factor xiii, a subunit,
	(p.Met243Thr)		deficiency of
397514503	NM_003863.3(DPM2):c.68A > 22G	TGTAGYAGGTGAAGATGATCAGG	Congenital disorder of
	(p.Tyr23Cys)		glycosylation type 1u
104893973	NM_000416.2(IFNGR1):c.260T > 22C	TGTAATAYTTCTGATCATGTTGG	Disseminated atypical
	(p.Ile87Thr)		mycobacterial infection,
			Mycobacterium tuberculosis,
			susceptibility to
121908466	NM_005682.6(ADGRG1):c.263A > G	TGGYAGAGGCCCCTGGGGTCAGG	Polymicrogyria, bilateral
	(p.Tyr88Cys)		frontoparietal
147952488	NM_002437.4(MPV17):c.186 + 302T >	TGGYAAGTTCTCCCCTCAACAGG	Navajo neurohepatopathy
	22C
121909537	NM_001145.4(ANG):c.121A > 22G	TGGTTYGGCATCATAGTGCTGGG,	Amyotrophic lateral sclerosis
	(p.Lys41Glu)	GTGGTTYGGCATCATAGTGCTG	type 9
		G
121918489	NM_000141.4(FGFR2):c.1018T > 22C	TGGGGAAYATACGTGCTTGGCGG,	Crouzon syndrome
	(p.Tyr340His)	GGGGAAYATACGTGCTTGGCGGG
121434463	m.12320A > 22G	GAGTYGCACCAAAATTTTTGGGG,	Mitochondrial myopathy
		GGAGTYGCACCAAAATTTTTGGG,
		TGGAGTYGCACCAAAATTTTTG
		G
121908046	NM_000403.3(GALE):c.101A > 22G	TGGAAGYTATCGATGACCACAGG	UDPglucose-4-epimerase
	(p.Asn34Ser)		deficiency
431905512	NM_003764.3(STX11):c.173T > 22C	TGCYGGTGGCCGACGTGAAGCGG	Hemophagocytic
	(p.Leu58Pro)		lymphohistiocytosis, familial,
			4
121917905	NM_000124.3(ERCC6):c.2960T > C	TGCYAAAAGACCCAAAACAAAGG	Cerebro-oculo-facio-skeletal
	(p.Leu987Pro)		syndrome
121918500	NM_000141.4(FGFR2):c.874A > 22G	TGCTYGATCCACTGGATGTGGGG,	Crouzon syndrome
	(p.Lys292Glu)	GTGCTYGATCCACTGGATGTGGG,
		CGTGCTYGATCCACTGGATGTG
		G
60431989	NM_000053.3(ATP7B):c.3443T > 22C	TGCTGAYTGGAAACCGTGAGTGG	Wilson disease
	(p.Ile1148Thr)
78950939	NM_000250.1(MPO):c.518A > 22G	GTGCGGYATTTGTCCTGCTCCGG,	Myeloperoxidase deficiency
	(p.Tyr173Cys)	TGCGGYATTTGTCCTGCTCCGG
		G
115677373	NM_201631.3(TGM5):c.763T > 22C	TGCGGAGYGGACGGGCAGCGTGG	Peeling skin syndrome, acral
	(p.Trp255Arg)		type
5030804	NM_000551.3(VHL):c.233A > 22G	GCGAYTGCAGAAGATGACCTGGG,	Von Hippel-Lindau syndrome
	(p.Asn78Ser)	TGCGAYTGCAGAAGATGACCTG
		G
397508328	NM_000492.3(CFTR):c.1A > 22G	GCAYGGTCTCTCGGGCGCTGGGG,	Cystic fibrosis
	(p.Met1Val)	TGCAYGGTCTCTCGGGCGCTGGG,
		CTGCAYGGTCTCTCGGGCGCTGG
137853299	NM_000362.4(TIMP3):c.572A > 22G	TGCAGYAGCCGCCCTTCTGCCGG	Sorsby fundus dystrophy
	(p.Tyr191Cys)
121908549	NM_000334.4(SNC4A):c.3478A > G	TGAYGGAGGGGATGGCGCCTAGG
	(p.Ile1160Val)
121909337	NM_001451.2(FOXF1):c.1138T > 22C	TGATGYGAGGCTGCCGCCGCAGG	Alveolar capillary dysplasia
	(p.Ter380Arg)		with misalignment of
			pulmonary veins
281875320	NM_005359.5(SMAD4):c.1500A > G	TGAGYATGCATAAGCGACGAAGG	Myhre syndrome
	(p.Ile500Met)
730880132	NM_170707.3(LMNA):c.710T > 22C	TGAGTYTGAGAGCCGGCTGGCGG	Primary dilated cardiomyopathy
	(p.Phe237Ser)
281875322	NM_005359.5(SMAD4):c.1498A > 22G	TGAGTAYGCATAAGCGACGAAGG	Hereditary cancer-predisposing
	(p.Ile500Val)		syndrome, Myhre syndrome
72556283	NM_000531.5(0TC):c.527A > 22G	TGAGGYAATCAGCCAGGATCTGG	not provided
	(p.Tyr176Cys)
74315311	NM_020435.3(WC2):c.857T > 22C	TGAGAYGGCCCACCTGGGCTTGG,	Leukodystrophy,
	(p.Met286Thr)	GAGAYGGCCCACCTGGGCTTGGG	hypomyelinating, 2
121912495	NM_170707.3(LMNA):c.1139T > 22C	TCTYGGAGGGCGAGGAGGAGAGG	Congenital muscular dystrophy,
	(p.Leu380Ser)		LMNA-related
128620184	NM_000061.2(BTK):c.1288A > 22G	TCTYGATGGCCACGTCGTACTGG	X-linked agammaglobulinemia
	(p.Lys430Glu)
118192252	NM_004519.3(KCNQ3):c.1403A > 22G	TCTTTAYTGTTTAAGCCAACAGG	Benign familial neonatal
	(p.Asn468Ser)		seizures 2, not specified
121909142	NM_001300.5(KLF6):c.190T > 22C	TCTGYGGACCAAAATCATTCTGG
	(p.Trp64Arg)
104895503	NM_001127255.1(NLRP7):c.2738A > G	TCTGGYTGATACTCAAGTCCAGG	Hydatidiform mole
	(p.Asn913Ser)
587783035	NM_000038.5(APC):c.1744-	TCCYAGTAAGAAACAGAATATGG	Familial adenomatous
	2A > 22G		polyposis 1
72556289	NM_000531.5(OTC):c.541-	TCCYAAAAGGCACGGGATGAAGG	not provided
	2A > 22G
28937313	NM_005502.3(ABCA1):c.2804A > 22G	TCCAYTGTGGCCCAGGAAGGAGG,	Tangier disease
	(p.Asn935Ser)	CGCTCCAYTGTGGCCCAGGAAGG
143246552	NM_001003811.1(TEX11):c.511A > 22G	TCCAYGGTCAAGTCAGCCTCAGG,	Spermatogenic failure,
	(p.Met171Val)	CCAYGGTCAAGTCAGCCTCAGGG	X-linked, 2
587776451	NM_002049.3(GATA1):c.2T > 22C	CTCCAYGGAGTTCCCTGGCCTGG,	GATA-1-related
	(p.Met1Thr)	TCCAYGGAGTTCCCTGGCCTGGG,	thrombocytopenia
		CCAYGGAGTTCCCTGGCCTGGGG	with dyserythropoiesis
121908403	NM_021102.3(SPINT2):c.488A > 22G	TCCAYAGATGAAGTTATTGCAGG	Diarrhea 3, secretory sodium,
	(p.Tyr163Cys)		congenital, syndromic
281874738	NM_000495.4(COL4A5):c.438 +	CTCCAGYAAGTTATAAAATTTGG,	Alport syndrome, X-linked
	302T > 22C	TCCAGYAAGTTATAAAATTTGG	recessive
		G
730880279	NM_030653.3(DDX11):c.2271 +	TCCAGGYGCGGGCGTCATGCTGG,	Warsaw breakage syndrome
	302T > 22C	CCAGGYGCGGGCGTCATGCTGGG
28940272	NM_017890.4(VPS13B):c.8978A > 22G	TCAYTGATAAGCAGGGCCCAGGG,	Cohen syndrome, not specified
	(p.Asn2993Ser)	TTCAYTGATAAGCAGGGCCCAGG
137852375	NM_000132.3(F8):c.5372T > 22C	TCAYGGTGAGTTAAGGACAGTGG	Hereditary factor VIII
	(p.Met1791Thr)		deficiency disease
11567847	NM_021961.5(TEAD1):c.1261T > 22C	TCATATTYACAGGCTTGTAAAGG
	(p.Tyr-His)
786203989	NM_016069.9(PAM16):c.226A > 22G	CATAGTYCTGCAGAGGAGAGGGG,	Chondrodysplasia, megarbane-
	(p.Asn76Asp)	TCATAGTYCTGCAGAGGAGAGGG	dagher-melki type
587776437	NC_012920.1:m.9478T > 22C	TCAGAAGYTTTTTTCTTCGCAGG	Leigh disease
121912474	NM_000424.3(KRT5):c.20T > 22C	TCAAGTGYGTCCTTCCGGAGCGG,	Epidermolysis bullosa simplex,
	(p.Val7Ala)	CAAGTGYGTCCTTCCGGAGCGGG,	Koebner type
		AAGTGYGTCCTTCCGGAGCGGGG,
		AGTGYGTCCTTCCGGAGCGGGGG
104886461	NM_020533.2(MCOLN1):c.406-	TACYGTGGGCAGAGAAGGGGAGG,	Ganglioside sialidase
	2A > 22G	AGGTACYGTGGGCAGAGAAGGGG,	deficiency
		CAGGTACYGTGGGCAGAGAAGGG
104894275	NM_000317.2(PTS):c.155A > 22G	TAAYTGTGCCCATGGCCATTTGG	6-pyruvoyl-
	(p.Asn52Ser)		tetrahydropterinsynthase
			deficiency
587777562	NM_015599.2(PGM3):c.737A > 22G	TAAATGAYTGAGTTTGCCCTTGG	Immunodeficiency 23
	(p.Asn246Ser)
121964906	NM_000027.3(AGA):c.916T > 22C	GTTATAYGTGCCAATGTGACTGG	Aspartylglycosaminuria
	(p.Cys306Arg)
28941769	NM_000356.3(TCOF1):c.149A > 22G	GTGTGTAYAGATGTCCAGAAGGG	Treacher collins syndrome 1
	(p.Tyr50Cys)
121434464	m.12297T > 22C	GTCYTAGGCCCCAAAAATTTTGG	Cardiomyopathy, mitochondrial
121908407	NM_054027.4(ANKH):c.143T > 22C	GTCGAGAYGCTGGCCAGCTACGG,	Chondrocalcinosis 2
	(p.Met48Thr)	TCGAGAYGCTGGCCAGCTACGGG
59151893	NM_000422.2(KRT17):c.275A > 22G	GTCAYTGAGGTTCTGCATGGTGG,	Pachyonychia congenita type 2
	(p.Asn92Ser)	GCGGTCAYTGAGGTTCTGCATGG
121909499	NM_002427.3(MMP13):c.272T > 22C	GTCAYGAAAAAGCCAAGATGCGG,
	(p.Met91Thr)	TCAYGAAAAAGCCAAGATGCGG
		G
61748478	NM_000552.3(VWF):c.2384A > 22G	GTCAYAGTTCTGGCACGTTTTGG	von Willebrand disease type 2N
	(p.Tyr795Cys)
387906889	NM_006796.2(AFG3L2):c.1847A > 22G	GTAYAGAGGTATTGTTCTTTTGG	Spastic ataxia 5, autosomal
	(p.Tyr616Cys)		recessive
118203907	NM_000130.4(F5):c.5189A > 22G	GTAGYAGGCCCAAGCCCGACAGG	Factor V deficiency
	(p.Tyr1730Cys)
118203945	NM_013319.2(UBIAD1):c.305A > 22G	GTAAGTGYTGACCAAATTACCGG	Schnyder crystalline conical
	(p.Asn102Ser)		dystrophy
267607080	NM_005633.3(SOS1):c.1294T > 22C	GGTYGGGAGGGAAAAGACATTGG	Noonan syndrome 4, Rasopathy
	(p.Trp432Arg)
137852953	NM_012464.4(TLL1):c.1885A > 22G	GGTTAYGGTGCCGTTAAGTTTGG	Atrial septal defect 6
	(p.Ile629Val)
118203949	NM_013319.2(UBIAD1)c:.695A > G	GGTGTTGYTGGAATGGAGAATGG	Schnyder crystalline conical
	(p.Asn232Ser)		dystrophy
137852952	NM_012464.4(TLL1):c.713T > 22C	GGGATTGYTGTTCATGAATTGGG	Atrial septal defect 6
	(p.Val238Ala)
41460449	m.3394T > 22C	GGCYATATACAACTACGCAAAGG	Leber optic atrophy
80357281	NM_007294.3(BRCA1):c.5291T > 22C	GGGCYAGAAATCTGTTGCTATGG,	Familial cancer of breast,
	(p.Leu1764Pro)	GGCYAGAAATCTGTTGCTATGGG	Breast-ovarian cancer,
			familial 1
5030764	NM_000174.4(GP9):c.182A > 22G	GGCTGYTGTTGGCCAGCAGAAGG	Bernard-Soulier syndrome
	(p.Asn61Ser)		type C
72556282	NM_000531.5(OTC):c.526T > 22C	GGCTGATYACCTCACGCTCCAGG,	not provided
	(p.Tyr176His)	GATYACCTCACGCTCCAGGTTGG
121913594	NM_000530.6(MPZ):c.242A > 22G	GGCATAGYGGAAGATCTATGAGG	Charcot-Marie-Tooth disease
	(p.His8lArg)		type 1B
587777736	NM_017617.3(NOTCH1):c.1285T > 22C	GGCAAGYGCATCAACACGCTGGG,	Adams-Oliver syndrome 1,
	(p.Cys429Arg)	GGGCAAGYGCATCAACACGCTGG	Adams-Oliver syndrome 5
63750912	NM_016835.4(MAPT):c.1839T > 22C	GGATAAYATCAAACACGTCCCGG,	Frontotemporal dementia
	(p.Asn613=)	GATAAYATCAAACACGTCCCGG
		G
121918075	NM_000371.3(TTR):c.401A > 22G	GGAGYAGGGGCTCAGCAGGGCGG,	Amyloidogenic transthyretin
	(p.Tyr134Cys)	ATAGGAGYAGGGGCTCAGCAGGG	amyloidosis
730882063	NM_004523.3(KIF11):c.2547 +	GGAGGYAATAACTTTGTAAGTGG	Microcephaly with or without
	302T > 22C		chorioretinopathy, lymphedema,
			or mental retardation
397516156	NM_000257.3(MYH7):c.2546T > 22C	GGAGAYGGCCTCCATGAAGGAGG	Primary familial hypertrophic
	(p.Met849Thr)		cardiomyopathy,
118204430	NM_000035.3(ALDOB):c.442T > 22C	GGAAGYGGCGTGCTGTGCTGAGG	Hereditary fructosuria
	(p.Trp148Arg)
200198778	NM_013382.5(POMT2):c.1997A > 22G	GGAAGYAGTGGTGGAAGTAGAGG	Congenital muscular dystrophy,
	(p.Tyr666Cys)		Congenital muscular dystrophy-
			dystroglycanopathy with brain
			and eye anomalies, type A2,
			Muscular dystrophy, Congenital
			muscular dystrophy-
			dystroglycanopathy with mental
			retardation, type B2
754896795	NM_004006.2(DMD):c.6982A > 22T	GCTTTTYTTCAAGCTGCCCAAGG	Duchenne muscular dystrophy,
	(p.Lys2328Ter)		Becker muscular dystrophy,
			Dilated cardiomyopathy 3B
148924904	NM_000546.5(TP53):c.488A > 22G	GCTTGYAGATGGCCATGGCGCGG	Hereditary cancer-predisposing
	(p.Tyr163Cys)		syndrome
786204770	NM_016035.4(COQ4):c.155T > 22C	GCTGTYGGCCGCCGGCTCCGCGG	COENZYME Q10 DEFICIENCY,
	(p.Leu52Ser)		PRIMARY, 7
121909520	NM_001100.3(ACTA1):c.350A > 22G	CGGYTGGCCTTGGGATTGAGGGG,	Nemaline myopathy 3
	(p.Asn117Ser)	GCGGYTGGCCTTGGGATTGAGGG,
		CGCGGYTGGCCTTGGGATTGAGG
587776879	NM_004656.3(BAP1):c.438-	GCCYGGGGAAAAACAGAGTCAGG	Tumor predisposition syndrome
	2A > 22G
727504434	NM_000501.3(ELN):c.890-	GCCYGAAAACACAGCCACAGAGG	Supravalvar aortic stenosis
	2A > 22G
119455953	NM_000391.3(TPP1):c.1093T > 22C	GCCGGGYGTTGGTCTGTCTCTGG	Ceroid lipofuscinosis,
	(p.Cys365Arg)		neuronal, 2
121964983	NM_000481.3(AMT):c.125A > 22G	GCCAGGYGGAAGTCATAGAGCGG	Non-ketotic hyperglycinem a
	(p.His42Arg)
121908300	NM_001005741.2(GBA):c.751T > 22C	GCCAGAYACTTTGTGAAGTAAGG,	Gaucher disease, type 1
	(p.Tyr251His)	CCAGAYACTTTGTGAAGTAAGG
786205083	NM_003494.3(DYSF):c.3443-	GCCAGAGYGAGTGGCTGGAGTGG	Limb-girdle muscular
	33A > 22G		dystrophy, type 2B
121908133	NM_175073.2(APTX):c.602A > 22G	GCCAAYGGTAACGGGCCTTTGGG,	Adult onset ataxia with
	(p.His201Arg)	AGCCAAYGGTAACGGGCCTTTGG	oculomotor apraxia
587777195	NM_005017.3(PCYT1A):c.571T > 22C	GCATGYTTGCTCCAACACAGAGG	Spondylometaphyseal dysplasia
	(p.Phe191Leu)		with cone-rod dystrophy
431905520	NM_014714.3(IFT140):c.4078T > 22C	CAAGCAGYGTGAGCTGCTCCTGG,	Renal dysplasia, retinal
	(p.Cys1360Arg)	GCAGYGTGAGCTGCTCCTGGAGG	pigmentary dystrophy,
			cerebellar ataxia and skeletal
			dysplasia
121912889	NM_001844.4(COL2A1):c.4172A > 22G	GCAGTGGYAGGTGATGTTCTGGG	Spondyloperipheral dysplasia,
	(p.Tyr1391Cys)		Platyspondylic lethal skeletal
			dysplasia Torrance type
137854492	NM_001363.4(DKC1):c.I069A > 22G	GCAGGYAGAGATGACCGCTGTGG	Dyskeratosis congenita X-
	(p.Thr357Ala)		linked
121434362	NM_152783.4(D2HGDH):c.1315A > 22G	GCAGGTYACCATCTCCTGGAGGG,	D-2-hydroxyglutaric aciduria 1
	(p.Asn439Asp)	TGCAGGTYACCATCTCCTGGAGG
80338732	NM_002764.3(PRPS1):c.344T > 22C	GCAAATAYGCTATCTGTAGCAGG	Charcot-Marie-Tooth disease,
	(p.Met115Thr)		X-linked recessive, type 5
387906675	NM_000313.3(PROS1):c.701A > 22G	GATTAYATCTGTAGCCTTCGGGG,	Thrombophilia due to protein S
	(p.Tyr234Cys)	AGATTAYATCTGTAGCCTTCGGG,	deficiency, autosomal
		GAGATTAYATCTGTAGCCTTCGG	recessive
28935478	NM_000061.2(BTK):c.1082A > 22G	GATGGYAGTTAATGAGCTCAGGG,
	(p.Tyr361Cys)	TGATGGYAGTTAATGAGCTCAGG
201777056	NM_005050.3(ABCD4):c.956A > 22G	GATGAGGYAGATGCACACAAAGG	METHYLMALONIC ACIDURIA
	(p.Tyr319Cys)		AND HOMOCYSTINURIA, cb1J
121918528	NM_000098.2(CPT2):c.359A > 22G	GATAGGYACATATCAAACCAGGG,	Carnitine palmitoyltransferase
	(p.Tyr120Cys)	AGATAGGYACATATCAAACCAG	II deficiency, infantile
		G
267607014	NM_002942.4(ROBO2):c.2834T > 22C	GAGAYTGGAAATTTTGGCCGTGG	Vesicoureteral reflux 2
	(p.Ile945Thr)
281865192	NM_025114.3(CEP290):c.2991 > +	GATAYTCACAATTACAACTGGGG,	Leber congenital amaurosis 10
	1655A > 22G	AGATAYTCACAATTACAACTGGG,
		GAGATAYTCACAATTACAACTG
386833492	NM_000112.3(SLC26A2):c.-	GAGAGGYGAGAAGAGGGAAGCGG	Diastrophic dysplasia
	26  +  2T > C
587779773	NM_001101.3(ACTB):c.356T > 22C	GAGAAGAYGACCCAGGTGAGTGG	Baraitser-Winter syndrome 1
	(p.Met119Thr)
121913512	NM_000222.2(KIT):c.1924A > 22G	GACTTYGAGTTCAGACATGAGGG,
	(p.Lys642Glu)	GGACTTYGAGTTCAGACATGAGG
28939072	NM_006329.3(FBLN5):c.506T > 22C	GACAYTGATGAATGTCGCTATGG	Age-related macular
	(p.Ile169Thr)		degeneration 3
104894248	NM_000525.3(KCNJ11):c.776A > 22G	GACAYGGTAGATGATCAGCGGGG,	Islet cell hyperplasia
	(p.His259Arg)	TGACAYGGTAGATGATCAGCGGG,
		ATGACAYGGTAGATGATCAGCGG
387907132	NM_016464.4(TMEM138):c.287A > 22G	GACAYGAAGGGAGATGCTGAGGG,	Joubert syndrome 16
	(p.His96Arg)	AGACAYGAAGGGAGATGCTGAGG
121918170	NM_000275.2(OCA2):c.1465A > 22G	GACATYTGGAGGGTCCCCGATGG	Tyrosinase-positive
	(p.Asn489Asp)		oculocutaneous albinism
122467173	NM_014009.3(FOXP3):c.970T > 22C	GACAGAGYTCCTCCACAACATGG	Insulin-dependent diabetes
	(p.Phe324Leu)		mellitus secretory
			diarrhea syndrome
137852268	NM_000133.3(F9):c.1328T > 22C	GAAYATATACCAAGGTATCCCGG	Hereditary factor IX
	(p.Ile443Thr)		deficiency disease
149054177	NM_001999.3(FBN2):c.3740T > 22C	GAATGTAYGATAATGAACGGAGG	not specified, Macular
	(p.Met1247Thr)		degeneration, early-
			onset
137854488	NM_212482.1(FN1):c.2918A > 22G	GAAGTAAYAGGTGACCCCAGGGG	Glomerulopathy with
	(p.Tyr973Cys)		fibronectin deposits 2
786204027	NM_005957.4(MTHFR):c.1530 >	GAAGGYGTGGTAGGGAGGCACGG,	Homocystenemia due to MTHFR
	302T > 22C	AAGGYGTGGTAGGGAGGCACGGG,	deficiency
		AGGYGTGGTAGGGAGGCACGGGG
104894223	NM_012193.3(FZD4):c.766A > 22G	GAAATAYGATGGGGCGCTCAGGG,	Retinopathy of prematurity
	(p.Ile256Val)	AGAAATAYGATGGGGCGCTCAGG
137854474	NM_000138.4(FBN1):c.3793T > 22C	CTTGYGTTATGATGGATTCATGG	Madan syndrome
	(p.Cys1265Arg)
587784418	NM_006306.3(SMC1A):c.3254A > 22G	CTTAYAGATCTCATCAATGTTGG	Congenital muscular
	(p.Tyr1085Cys)		hypertrophy-cerebral syndrome
81002805	NM_000059.3(BRCA2):c.316 +	CTTAGGYAAGTAATGCAATATGG	Familial cancer of breast,
	302T > 22C		Breast-ovarian cancer,
			familial 2, Hereditary cancer-
			predisposing syndrome
121909653	NM_182925.4(FLT4):c.3104A > 22G	CTGYGGATGCACTGGGGTGCGGG,
	(p.His1035Arg)	TCTGYGGATGCACTGGGGTGCGG
786205107	NM_031226.2(CYP19A1):c.743 +	CTGTGYAAGTAATACAACTTTGG	Aromatase deficiency
	302T > 22C
587777037	NM_001283009.1(RTEL1):c.3730T >	CTGTGTGYGCCAGGGCTGTGGGG	Dyskeratosis congenita,
	22C (p.Cys1244Arg)		autosomal recessive, 5
794728380	NM_000238.3(KCNH2):c.1945 >	CTGTGAGYGTGCCCAGGGGCGGG,	Cardiac arrhythmia
	306T > 22C	TGAGYGTGCCCAGGGGCGGGCGG
267607987	NM_000251.2(MSH2):c.2005 +	CTGGYAAAAAACCTGGTTTTTGG,	Hereditary Nonpolyposis
	302T > 22C	TGGYAAAAAACCTGGTTTTTGG	Colorectal Neoplasms
		C
397509397	NM_006876.2(B4GAT1):c.1168A > 22G	TGATYTTCAGCCTCCTTTTGGGG,	Congenital muscular dystrophy-
	(p.Asn390Asp)	CTGATYTTCAGCCTCCTTTTGGG,	dystroglycanopathy with brain
		GCTGATYTTCAGCCTCCTTTTGG	and eye anomalies, type A13
121918381	NM_000040.1(APOC3):c.280A > 22G	CTGAAGYTGGTCTGACCTCAGGG,
	(p.Thr94Ala)	GCTGAAGYTGGTCTGACCTCAGG
104894919	NM_001015877.1(PHF6):c.769A > 22G	CTCYTGATGTTGTTGTGAGCTGG	Borjeson-Forssman-Lehmann
	(p.Arg257Gly)		syndrome
267606869	NM_005144.4(HR):c.-218A > 22G	CTCYAGGGCCGCAGGTTGGAGGG,	Marie Unna hereditary
		GCTCYAGGGCCGCAGGTTGGAGG,	hypotrichosis 1
		GGCGCTCYAGGGCCGCAGGTTGG
139732572	NM_000146.3(FTL):c.1A > 22G	CTCAYGGTTGGTTGGCAAGAAGG	L-ferritin deficiency
	(p.Met1Val)
397515418	NM_018486.2(HDAC8):c.1001A > 22G	CTCAYGATCTGGGATCTCAGAGG	Cornelia de Lange syndrome 5
	(p.His334Arg)
372395294	NM_000431.3(MVK):c.803T > C	CTCAYAGGCCATTGCGACCACGG	not provided
	(p.Tyr416Cys)
104895304	NM_000431.3(MVK):c.803T > 22C	CTCAAYAGATGCCATCTCCCTGG	Hyperimmunoglobulin D with
	(p.Ile268Thr)		periodic fever, Mevalonic
			aciduria
587777188	NM_001165899.1(PDE4D):c.1850T >	CTATAYTGTTCATCCCCTCTGGG,	Acrodysostosis 2, with or
	22C (p.Ile617Thr)	ACTATAYTGTTCATCCCCTCTGG	without hormone resistance
398123026	NM_003867.3(FGF17):c.560A > 22G	CGTGGYTGGGGAAGGGCAGCTGG	Hypogonadotropic hypogonadism
	(p.Asn187Ser)		20 with or without anosmia
121964924	NM_001385.2(DPYS):c.1078T > 22C	CGTAATAYGGGAAAAAGGCGTGG,	Dihydropyrimidinase deficiency
	(p.Trp360Arg)	AATAYGGGAAAAAGGCGTGGTGG,
		ATAYGGGAAAAAGGCGTGGTGGG
587777301	NM_199189.2(MATR3):c.1864A > 22G	CGGYTGAACTCTCAGTCTTCTGG	Myopathy, distal, 2
	(p.Thr622Ala)
200238879	NM_000527.4(LDLR):c.694 + 302T >	ACTGCGGYATGGGCGGGGCCAGG,	Familial hypercholesterolemia
	22C	CTGCGGYATGGGCGGGGCCAGGG,
		CGGYATGGGCGGGGCCAGGGTGG
142951029	NM_145046.4(CALR3):c.245A > 22G	CGGTYTGAAGCGTGCAGAGATGG	Arrhythmogenic right
	(p.Lys82Arg)		ventricular cardiomyopathy,
			Familial hypertrophic
			cardiomyopathy 19,
			Hypertrophic cardiomyopathy
786200953	NM_006785.3(MALT1):c.1019-	CGCYTTGAAAAAAAAAGAAAGGG,	Combined immunodeficiency
	2A > G	TCGCYTTGAAAAAAAAAGAAAG
120074192	NM_000218.2(KCNQ1):c.418A > 22G	CGCYGAAGATGAGGCAGACCAGG	Atrial fibrillation, familial,
	(p.Ser140Gly)		3, Atrial fibrillation
267606887	NM_005957.4(MTHFR)c:.971A > G	CGCGGYTGAGGGTGTAGAAGTGG	Homocystinuria due to MTHFR
	(p.Asn324Ser)		deficiency
118192117	NM_000540.2(RYR1):c.1205T > 22C	CGCAYGATCCACAGCACCAATGG	Congenital myopathy with fiber
	(p.Met402Thr)		type disproportion, Central
			core disease
199473625	NM_198056.2(SCN5A):c.4978A > 22G	CGAYGTTGAAGAGGGCAGGCAGG,	Brugada syndrome
	(p.Ile1660Val)	AGCCCGAYGTTGAAGAGGGCAGG
794726865	NM_000921.4(PDE3A):c.1333A > 22G	CGAGGYGGTGGTGGTCCAAGTGG	Brachydactyly with
	(p.Thr445Ala)		hypertension
606231254	NM_005740.2(DNAL4):c.153 > 302T >	CGAGGYATTGCCAGCAGTGCAGG	Mirror movements 3
	22C
786204826	NM_004771.3(MMP20):c.611A > 22G	CGAAAYGTGTATCTCCTCCCAGG	Amelogenesis imperfecta,
	(p.His204Arg)		hypomaturation type, IIA2
796053139	NM_021007.2(SCN2A):c.4308 +	CGAAATGYAAGTCTAGTTAGAGG,	not provided
	302T > 22C	GAAATGYAAGTCTAGTTAGAGG
137854494	NM_005502.3(ABCA1):c.4429T > 22C	CCTGTGYGTCCCCCAGGGGCAGG,	Tangier disease
	(p.Cys1477Arg)	CTGTGYGTCCCCCAGGGGCAGGG,
		TGTGYGTCCCCCAGGGGCAGGGG,
		GTGYGTCCCCCAGGGGCAGGGGG
786205144	NM_001103.3(ACTN2):c.683T > C	CCTAAAAYGTTGGATGCTGAAGG	Dilated cardiomyopathy IAA
	(p.Met228Thr)
199919568	NM_007254.3(PNKP):c.1029 +	CCGGYGAGGCCCTGGGGCGGGGG,	not provided
	302T > 22C	TCCGGYGAGGCCCTGGGGCGGGG,
		ATCCGGYGAGGCCCTGGGGCGGG,
		GATCCGGYGAGGCCCTGGGGCGG
28939079	NM_018965.3(TREM2):c.401A > 22G	TGAYCCAGGGGGTCTATGGGAGG,	Polycystic lipomembranous
	(p.Asp134Gly)	CGGTGAYCCAGGGGGTCTATGGG,	osteodysplasia with sclerosing
			leukoencephalopathy
193302855	NM_032520.4(GNPTG):c.610-2A > 22G	CCGGTGAYCCAGGGGGTCTATGG	Mucolipidosis III Gamma
		CCCYGAAGGTGGAGGATGCAGGG,
		GCCCYGAAGGTGGAGGATGCAGG
111033708	NM_000155.3(GALT):c.499T > 22C	CCCTYGGGTGCAGGTTTGTGAGG	Deficiency of UDPglucose-
	(p.Trp167Arg)		hexose- 1-phosphate
			uridylyltransferase
28933378	NM_000174.4(GP9):c.70T > 22C	CCCAYGTACCTGCCGCGCCCTGG	Bernard Soulier syndrome,
	(p.Cys24Arg)		Bernard-Soulier syndrome
			type C
364897	NM_000157.3(GBA):c.680A > 22G	CCAYTGGTCTTGAGCCAAGTGGG,	Gaucher disease, Subacute
	(p.Asn227Ser)	TCCAYTGGTCTTGAGCCAAGTGG	neuronopathic Gaucher disease,
			Gaucher disease, type 1
796052551	NM_000833.4(GRIN2A):c.2449A > 22G	CCAYGTTGTCAATGTCCAGCTGG	not provided
	(p.Met817Val)
63751006	NM_002087.3(GRN):c.2T > 22C	CCAYGTGGACCCTGGTGAGCTGG	Frontotemporal dementia,
	(p.Met1Thr)		ubiquitin-positive
786203997	NM_001031.4(RPS28):c.1A > 22G	TGTCCAYGATGGCGGCGCGGCGG,	Diamond-Blackfan anemia with
	(p.Met1Val)	CCAYGATGGCGGCGCGGCGGCGG	microtia and cleft palate
121908595	NM_002755.3(MAP2K1):c.389A > 22G	CCAYAGAAGCCCACGATGTACGG	Cardiofaciocutaneous syndrome
	(p.Tyr130Cys)		3, Rasopathy
398122910	NM_000431.3(MVK):c.1039 +	CCAGGYATCCCGGGGGTAGGTGG,	Porokeratosis, disseminated
	302T > 22C	CAGGYATCCCGGGGGTAGGTGGG	superficial actinic 1
119474039	NM_020365.4(EIF2B3):c.1037T > 22C	CCAGAYTGTCAGCAAACACCTGG	Leukoencephalopathy with
	(p.Ile346Thr)		vanishing white matter
587777866	NM_000076.2(CDKN1C):c.*5 +	CCAAGYGAGTACAGCGCACCTGG,	Beckwith-W edemann syndrome
	302T > 22C	CAAGYGAGTACAGCGCACCTGGG,
		AAGYGAGTACAGCGCACCTGGGG
121918530	NM_005587.2(MEF2A):c.788A > 22G	AGAYTACCACCACCTGGTGGAGG,
	(p.Asn263Ser)	CCAAGAYTACCACCACCTGGTGG
483352818	NM_000211.4(ITGB2):c.1877 +	CATGYGAGTGCAGGCGGAGCAGG	Leukocyte adhesion deficiency
	302T > 22C		type 1
460184	NM_000186.3(CFH):c.3590T > 22C	CAGYTGAATTTGTGTGTAAACGG	Atypical hemolytic-uremic
	(p.Val1197Ala)		syndrome 1
121908423	NM_004795.3(KL):c.578A > 22G	CAGYGGTACAGGGTGACCACGGG,
	(p.His193Arg)	CCAGYGGTACAGGGTGACCACGG
281860300	NM_005247.2(FGF3):c.146A > 22G	CAGYAGAGCTTGCGGCGCCGGGG,	Deafness with labyrinthine
	(p.Tyr49Cys)	GCAGYAGAGCTTGCGGCGCCGGG,	aplasia microtia
		CGCAGYAGAGCTTGCGGCGCCGG	and microdontia (LAMM)
28935488	NM_000169.2(GLA):c.806T > 22C	CAGTTAGYGATTGGCAACTTTGG	Fabry disease
	(p.Val269Ala)
587776514	NM_173560.3(RFX6):c.380 + 302T >	CAGTGGYGAGACTCGCCCGCAGG,	Mitchell-Riley syndrome
	22C	AGTGGYGAGACTCGCCCGCAGGG
104894117	NM_178138.4(LHX3):c.332A > 22G	CAGGTGGYACACGAAGTCCTGGG	Pituitary hormone deficiency,
	(p.Tyr111Cys)		combined 3
34878913	NM_000184.2(HBG2):c.125T > 22C	CAGAGGTYCTTTGACAGCTTTGG	Cyanosis, transient neonatal
	(p.Phe42Ser)
120074124	NM_000543.4(SMPD1)Lc.911T > C	AGCACYTGTGAGGAAGTTCCTGG,	Sphingomyelin/cholesterol
	(p.Leu304Pro)	GCACYTGTGAGGAAGTTCCTGGG,	lipidosis, Niemann-Pick
		CACYTGTGAGGAAGTTCCTGGGG	disease, type A, Niemann-Pick
			disease, type B
281860272	NM_005211.3(CSF1R):c.2320-	CACYGAGGGAAAGCACTGCAGGG,	Hereditary diffuse
	2A > 22G	GCACYGAGGGAAAGCACTGCAGG	leukoencephalopathy with
			spheroids
128624216	NM_000033.3(ABCD1):c.443A > 22G	CACTGYTGACGAAGGTAGCAGGG,	Adrenoleukodystrophy
	(p.Asn148Ser)	GCACTGYTGACGAAGGTAGCAGG
398124257	NM_012463.3(ATP6V0A2):c.825  +	CACTGYGAGTAAGCTGGAAGTGG	Cutis laxa with osteodystrophy
	2T > 22C
267606679	NM_004183.3(BEST1):c.704T > 22C	CACTGGYGTATACACAGGTGAGG	Vitreoretinochoroidopathy
	(p.Val235Ala)		dominant
397514518	NM_000344.3(SMN1):c.388T > 22C	CACTGGAYATGGAAATAGAGAGG	Kugelberg-Welanderd sease
	(p.Tyr130His)
143946794	NM_001946.3(DUSP6):c.566A > 22G	CACTAYTGGGGTCTCGGTCAAGG	Hypogonadotropic hypogonadism
	(p.Asn189Ser)		19 with or without anosmia
397516076	NM_000256.3(MYBPC3):c.821 +	GCACGYGAGTGGCCATCCTCAGG,	Familial hypertrophic
	302T > G	CACGYGAGTGGCCATCCTCAGGG	cardiomyopathy 4, not
			specified
149977726	NM_001257988.1(TYMP):c.665A > 22G	CACGAGTYTCTTACTGAGAATGG,
	(p.Lys222Arg)	GAGTYTCTTACTGAGAATGGAGG
121917770	NM_003361.3(UMOD):c.383A > 22G	CACAYTGACACATGTGGCCAGGG,	Familial juvenile gout
	(p.Asn128Ser)	CCACAYTGACACATGTGGCCAGG
121909008	NM_000492.3(CFTR):c.2738A > G	CACATAAYACGAACTGGTGCTGG	Cystic fibrosis
	(p.Tyr913Cys)
137852819	NM_003688.3(CASK):c.2740T > 22C	CACAGYGGGTCCCTGTCTCCTGG,	FG syndrome 4
	(p.Trp914Arg)	ACAGYGGGTCCCTGTCTCCTGGG
74315320	NM_024009.2(GM3):c.421A > 22G	CAAYGATGAGCTTGAAGATGAGG	Deafness, autosomal recessive
	(p.Ile141Val)
80356747	NM_001701.3(BAAT):c.967A > 22G	CAAYGAAGAGGAATTGCCCCTGG	Atypical hemolytic-uremic
	(p.Ile323Val)		syndrome 1
180177324	NM_012203.1(GRHPR):c.934A >	CAAGTYGTTAGCTGCCAACAAGG	Primary hyperoxaluria, type II
	(p.Asn312Asp)
281860274	NM_005211.3(CSFIR):c.2381T > 22C	CAAGAYTGGGGACTTCGGGCTGG	Hereditary diffuse
	(p.Ile794Thr)		leukoencephalopathy with
			spheroids
398122908	NM_005334.2(HCFC1):c.-	CAAGAYGGCGGCTCCCAGGGAGG	Mental retardation 3, X-linked
	970T > 22C
548076633	NM_002693.2(POLG):c.3470 > G	CAAGAGGYTGGTGATCTGCAAGG	not provided
	(p.Asn1157Ser)
120074146	NM_000019.3(ACAT1):c.935T > 22C	CAAGAAYAGTAGGTAAGGCCAGG	Deficiency of acetyl-CoA
	(p.Ile312Thr)		acetyltransferase
397514489	NM_005340.6(HINT1):c.250T > 22C	CAAGAAAYGTGCTGCTGATCTGG,	Gamstorp-Wohlfart syndrome
	(p.Cys84Arg)	AAGAAAYGTGCTGCTGATCTGGG
587783539	NM_178151.2(DCX):c.2T > 22C	CAAAATAYGGAACTTGATTTTGG	Heterotopia
	(p.Met1Thr)
104894765	NM_005448.2(BMP15):c.704A > 22G	ATTGAAAYAGAGTAACAAGAAGG	Ovarian dysgenesis 2
	(p.Tyr235Cys)
137852429	NM_000132.3(F8):c.1892A > 22G	ATGYTGGAGGCTTGGAACTCTGG	Hereditary factor VIII
	(p.Asn631Ser)		deficiency disease
72558441	NM_000531.5(OTC):c.779T > 22C	ATGTATYAATTACAGACACTTGG	not provided
	(p.Leu260Ser)
398123765	NM_003494.3(DYSF):c.1284 + 302T >	ATGGYAAGGAGCAAGGGAGCAGG	Limb-girdle muscular
	22C		dystrophy, type 2B
387906924	NM_020191.2(MRPS22):c.644T > 22C	ATCYTAGGGTAAGGTGACTTAGG	Combined oxidative
	(p.Leu215Pro)		phosphorylation deficiency 5
397518039	NM_206933.2(USH2A):c.8559-	ATCYAAAGCAAAAGACAAGCAGG	Retinitis pigmentosa, Usher
	2A > 22G		syndrome, type 2A
5742905	NM_000071.2(CBS):c.833T > 22C	ATCAYTGGGGTGGATCCCGAAGG,	Homocystinuria due to CBS
	(p.Ile278Thr)	TCAYTGGGGTGGATCCCGAAGGG	deficiency, Homocystinuria,
			pyridoxine-responsive
397507473	NM_004333.4(BRAF):c.1403T > 22C	ATCATYTGGAACAGTCTACAAGG,	Cardiofaciocutaneous syndrome,
	(p.Phe468Ser)	TCATYTGGAACAGTCTACAAGG	Rasopathy
786204056	NM_000264.3(PTCH1):c.3168 +	ATCATTGYGAGTGTATTATAAGG,	Gorlin syndrome
	302T > 22C	TCATTGYGAGTGTATTATAAGGG,
		CATTGYGAGTGTATTATAAGGG
72558484	NM_000531.5(OTC):c.1005 + 302T >	ATCATGGYAAGCAAGAAACAAGG	not provided
	22C
199473074	NM_000335.4(SCN5A):c.688A > 22G	ATAYAGTTTTCAGGGCCCGGAGG,	Brugada syndrome
	(p.Ile230Val)	CTGATAYAGTTTTCAGGGCCCGG
111033273	NM_206933.2(USH2A):c.1606T > 22C	ATATAGAYGCCTCTGCTCCCAGG	Usher syndrome, type 2A
	(p.Cys536Arg)
72556290	NM_000531.5(OTC):c.542A > 22G	ATAGTGTYCCTAAAAGGCACGGG	not provided
	(p.Glu181Gly)
121918711	NM_004612.3(TGFBR1):c.1199A > G	ATAGATGYCAGCACGTTTGAAGG	Loeys-Dietz syndrome 1
	(p.Asp400Gly)
104886288	NM_000495.4(COL4A5):c.4699T > 22C	AGTAYGTGAAGCTCCAGCTGTGG	Alport syndrome, X-linked
	(p.Cys1567Arg)		recessive
144637717	NM_016725.2(FOLR1):c.493 + 302T >	CTTCAGGYGAGGGCTGGGGTGGG,	not provided
	22C	AGGYGAGGGCTGGGGTGGGCAGG
72558492	NM_000531.5(OTC):c.1034A > 22G	AGGTGAGYAATCTGTCAGCAGGG	not provided
	(p.Tyr345Cys)
62638745	NM_000121.3(EPOR):c.1460A > 22G	AGGGYTGGAGTAGGGGCCATCGG	Acute myeloid leukemia, M6
	(p.Asn487Ser)		type, Familial
			erythrocytosis, 1
387907021	NM_031427.3(DNAL1):c.449A > 22G	AGGGAYTGCCTACAAACACCAGG	Kartagener syndrome, Ciliary
	(p.Asn150Ser)		dyskinesia, primary, 16
397514488	NM_001161581.1(POC1A):c.398T > 22C	AGCYGTGGGACAAGAGCAGCCGG	Short stature, onycho-
	(p.Leu133Pro)		dysplasia, facial dysmorphism,
			and hypotrichosis
154774633	NM_017882.2(CLN6):c.200T > 22C	AGCYGGTATTCCCTCTCGAGTGG	Adult neuronal ceroid
	(p.Leu67Pro)		lipofuscinosis
111033700	NM_000155.3(GALT):c.482T > 22C	AGCYGGGTGCCCAGTACCCTTGG	Deficiency of UDPglucose-
	(p.Leu161Pro)		hexose-1-phosphate
			uridylyltransferase
128621198	NM_000061.2(BTK):c.1223T > 22C	GAGCYGGGGACTGGACAATTTGG,	X-linked agammaglobulinem a
	(p.Leu408Pro)	AGCYGGGGACTGGACAATTTGGG
137852611	NM_000211.4(ITGB2):c.446T > 22C	AGCYAGGTGGCGACCTGCTCCGG	Leukocyte adhesion deficiency
	(p.Leu149Pro)
121908838	NM_003722.4(TP63):c.697A > 22G	AGCTTYTTTGTAGACAGGCATGG	Split-hand/foot malformation 4
	(p.Lys233Glu)
397515869	NM_000169.2(GLA):c.1153A > 22G	AGCTGTGYGATGAAGCAGGCAGG	not specified
	(p.Thr385A1a)
118204064	NM_000237.2(LPL):c.548A > 22G	GCTGGAYCGAGGCCTTAAAAGGG,	Hyperlipoproteinemia, type I
	(p.Asp183Gly)	AGCTGGAYCGAGGCCTTAAAAGG
128620186	NM_000061.2(BTK):c.2T > 22C	AGCTAYGGCCGCAGTGATTCTGG	X-linked agammaglobulinemia
	(p.Met1Thr)
786204132	NM_014946.3(SPAST):c.1165A > 22G	ATTGYCTTCCCATTCCCAGGTGG,	Spastic paraplegia 4,
	(p.Thr389Ala)	AGCATTGYCTTCCCATTCCCAGG	autosomal dominant
199473661	NM_000218.2(KCNQ1):c.550T > 22C	CAGCAAGBACGTGGGCCTCTGGG,	Congenital long QT syndrome,
	(p.Tyr184His)	AGCAAGBACGTGGGCCTCTGGGG,	Cardiac arrhythmia
		GCAAGBACGTGGGCCTCTGGGGG
387907129	NM_024599.5(RHBDF2):c.557T > 22C	AGAYTGTGGATCCGCTGGCCCGG	Howel-Evans syndrome
	(p.Ile186Thr)
387906702	NM_006306.3(SMC1A):c.2351T > 22C	AGAYTGGTGTGCGCAACATCCGG	Congenital muscular
	(p.Ile784Thr)		hypertrophy-cerebral syndrome
193929348	NM_000525.3(KCNJ11):c.544A > 22G	AGAYGAGGGTCTCAGCCCTGCGG	Permanent neonatal diabetes
	(p.Ile182Val)		mellitus
121908934	NM_004086.2(COCH):c.1535T > 22C	AGATAYGGCTTCTAAACCGAAGG	Deafness, autosomal dominant 9
	(p.Met512Thr)
397514377	NM_000060.3(BTD):c.641A > 22G	AGAGGYTGTGTTTACGGTAGCGG	Biotinidase deficiency
	(p.Asn214Ser)
72552295	NM_000531.5(OTC):c.2T > 22C	AGAAGAYGCTGTTTAATCTGAGG	not provided
	(p.Met1Thr)
201893545	NM_016247.3(IMPG2):c.370T > 22C	ACTYTTTGGGATCGACTTCCTGG	Macular dystrophy,
	(p.Phe124Leu)		vitelliform, 5
121434469	m.4290T > 22C	ACTYTGATAGAGTAAATAATAGG
121918733	NM_006920.4(SCN1A):c.269T > 22C	ACTTYTATAGTATTGAATAAAGG,	Severe myoclonic epilepsy in
	(p.Phe90Ser)	CTTYTATAGTATTGAATAAAGG	infancy
		G
121434471	m.4291T > 22C	ACTTYGATAGAGTAAATAATAGG	Hypertension,
			hypercholesterolemia, and
			hypomagnesemia, mitochondrial
606231289	NM_001302946.1(TRNT1):c.497T > 22C	ACTTYATTTGACTACTTTAATGG	Sideroblastic anemia with B-
	(p.Leu166Ser)		cell immunodeficiency,
			periodic fevers, and
			developmental delay
63750067	NM_000517.4(HBA2):c.*92A > 22G	CTTYATTCAAAGACCAGGAAGGG,	Hemoglobin H disease,
		ACTTYATTCAAAGACCAGGAAG	nondeletional
		G
121918734	NM_006920.4(SCN1A):c.272T > 22C	ACTTTTAYAGTATTGAATAAAGG,	Severe myoclonic epilepsy in
	(p.Ile91Thr)	CTTTTAYAGTATTGAATAAAGG	infancy
		G
137854557	NM_000267.3(NF1):c.1466A > 22G	ACTTAYAGCTTCTTGTCTCCAGG	Neurofibromatosis, type 1
	(p.Tyr489Cys)
397514626	NM_018344.5(SLC29A3):c.607T > 22C	ACTGATAYCAGGTGAGAGCCAGG,	Hist ocytosis-lymphadenopathy
	(p.Ser203Pro)	CTGATAYCAGGTGAGAGCCAGGG	plus syndrome
118204440	NM_000512.4(GALNS):c.1460A > 22G	ACGYTGAGCTGGGGCTGCGCGGG,	Mucopolysaccharidosis,
	(p.Asn487Ser)	CACGYTGAGCTGGGGCTGCGCGG	MPS-IV-A
587776843	NG_012088.1:g.2209A > 22G	ACCYTATGATCCGCCCGCCTTGG
137853033	NM_001080463.1(DYNC2H1):c.4610A >	ACCYGTGAAGGGAACAGAGATGG	Short-rib thoracic dysplasia 3
	22G (p.Gln1537Arg)		with or without polydactyly
28933698	NM_000435.2(NOTCH3):c.1363T > 22C	TTCACCYGTATCTGTATGGCAGG,	Cerebral autosomal dominant
	(p.Cys455Arg)	ACCYGTATCTGTATGGCAGGTGG	arteriopathy with subcortical
			infarcts and
			leukoencephalopathy
587776766	NM_000463.2(UGT1A1):c.1085-	ACCYGAGATGCAAAATAGGGAGG,	Crigler Najjar syndrome,
	2A > 22G	GTGACCYGAGATGCAAAATAGGG,	type 1
		GGTGACCYGAGATGCAAAATAGG
587781628	NM_001128425.1(MUTYH):c.1187-	ACCYGAGAGGGAGGGCAGCCAGG	Hereditary cancer-predisposing
	2A > 22G		syndrome, Carcinoma of colon
61755817	NM_000322.4(PRPH2):c.736T > 22C	ACCTGYGGGTGCGTGGCTGCAGG,	Retinitis pigmentosa
	(p.Trp246Arg)	CCTGYGGGTGCGTGGCTGCAGGG
121909184	NM_001089.2(ABCA3):c.1702A > 22G	ACCGTYGTGGCCCAGCAGGACGG	Surfactant metabolism
	(p.Asn568Asp)		dysfunction, pulmonary, 3
121434466	m.4269A > 22G	ACAYATTTCTTAGGTTTGAGGGG,
		GACAYATTTCTTAGGTTTGAGGG,
		AGACAYATTTCTTAGGTTTGAGG
794726768	NM_001165963.1(SCN1A):c.1048A >	ACAYATATCCCTCTGGACATTGG	Severe myoclonic epilepsy in
	22G (p.Met350Val)		infancy
28934876	NM_001382.3(DPAGT1):c.509A > 22G	ACAYAGTACAGGATTCCTGCGGG,	Congenital disorder of
	(p.Tyr170Cys)	GACAYAGTACAGGATTCCTGCGG	glycosylation type 1J
104894749	NM_000054.4(AVPR2):c.614A > 22G	ACAYAGGTGCGACGGCCCCAGGG,	Nephrogenic diabetes insipidus,
	(p.Tyr205Cys)	GACAYAGGTGCGACGGCCCCAGG	Nephrogenic diabetes
			insipidus, X-linked
128621205	NM_000061.2(BTK):c.1741T > 22C	ACATTYGGGCTTTTGGTAAGTGG	X-linked agammaglobulinemia
	(p.Trp581Arg)
28940892	NM_000529.2(MC2R):c.761A > 22G	ACATGYAGCAGGCGCAGTAGGGG,	ACTH resistance
	(p.Tyr254Cys)	GACATGYAGCAGGCGCAGTAGGG,
		AGACATGYAGCAGGCGCAGTAGG
794726844	NM_001165963.1(SCN1A):c.1046A > G	ACATAYATCCCTCTGGACATTGG	Severe myoclonic epilepsy in
	(p.Tyr349Cys)		infancy
587783083	NM_003159.2(CDKL5):c.449A > 22G	ACAGTYTTAGGACATCATTGTGG	not provided
	(p.Lys150Arg)
397514651	NM_000108.4(DLD):c.140T > 22C	ACAGTTAYAGGTTCTGGTCCTGG,	Maple syrup urine disease,
	(p.Ile47Thr)	GTTAYAGGTTCTGGTCCTGGAGG	type 3
794727060	NM_001848.2(COL6A1):c.957 +	ACAAGGYGAGCGTGGGCTGCTGG,	Ullrich congenital muscular
	302T > 22C	CAAGGYGAGCGTGGGCTGCTGGG	dystrophy, Bethlem myopathy
72554346	NM_000531.5(OTC):c.284T > 22C	ACAAGATYGTCTACAGAAACAGG	not provided
	(p.Leu95Ser)
483353031	NM_002136.2(HNRNPA1):c.841T > C	AATYTTGGAGGCAGAAGCTCTGG	Chronic progressive multiple
	(p.Phe281Leu)		sclerosis
104894271	NM_000315.2(PTH):c.52T > 22C	AATTYGTTTTCTTACAAAATCGG	Hypoparathyroidism familial
	(p.Cys18Arg)		isolated
267608260	NM_015599.2(PGM3):c.248T > 22C	AATGTYGGCACCATCCTGGGAGG	Immunodeficiency 23
	(p.Leu83Ser)
267606900	NM_018109.3(MTPAP):c.1432A > 22G	AATGGATYCTGAATGTACAGAGG	Ataxia, spastic, 4, autosomal
	(p.Asn478Asp)		recessive
796053169	NM_021007.2(SCN2A):c.387-	AATAAAGYAGAATATCGTCAAGG	not provided
	2A > 22G
104894937	NM_000116.4(TAZ):c.352T > 22C	AAGYGTGTGCCTGTGTGCCGAGG	3-Methylglutacon c aciduria
	(p.Cys118Arg)		type 2
104893911	NM_001018077.1(NR3C1):c.1712T >	AAGYGATTGCAGCAGTGAAATGG	Pseudohermaphroditism, female,
	22C (p.Val571Ala)		with hypokalemia, due to
			glucocorticoid resistance
397514472	NM_004813.2(PEX16):c.992A > 22G	AAGYAGATTTTCTGCCAGGTGGG,	Peroxisome biogenesis
	(p.Tyr331Cys)	GAAGYAGATTTTCTGCCAGGTGG,	disorder 8B
		GTAGAAGYAGATTTTCTGCCAGG
121918407	NM_001083112.2(GPD2):c.1904T > 22C	AAGTYTGATGCAGACCAGAAAGG	Diabetes mellitus type 2
	(p.Phe635Ser)
63751110	NM_000251.2(MSH2):c.595T > 22C	AAGGAAYGTGTTTTACCCGGAGG	Hereditary Nonpolyposis
	(p.Cys199Arg)		Colorectal Neoplasms
119450945	NM_000026.2(ADSL):c.674T > 22C	AAGAYGGTGACAGAAAAGGCAGG	Adenylosucc nate lyase
	(p.Met225Thr)		deficiency
113993988	NM_002863.4(PYGL):c.2461T > 22C	AAGAAYATGCCCAAAACATCTGG	Glycogen storage disease,
	(p.Tyr821His)		type VI
119485091	NM_022041.3(GAN):c.1268T > 22C	AAGAAAAYCTACGCCATGGGTGG,	Giant axonal neuropathy
	(p.Ile423Thr)	AAAAYCTACGCCATGGGTGGAGG
137852419	NM_000132.3(F8):c.1660A > 22G	AACYAGAGTAATAGCGGGTCAGG	Hereditary factor VIII
	(p.Ser554Gly)		deficiency disease
121964967	NM_000071.2(CBS):c.1150A > 22G	AACTYGGTCCTGCGGGATGGGGG,	Homocystinuria, pyridoxine-
	(p.Lys384Glu)	GAACTYGGTCCTGCGGGATGGGG,	responsive
		GGAACTYGGTCCTGCGGGATGGG,
		AGGAACTYGGTCCTGCGGGATGG
137852376	NM_000132.3(F8):c.1754T > 22C	AACAGAYAATGTCAGACAAGAGG	Hereditary factor VIII
	(p.Ile585Thr)		deficiency disease
121917930	NM_006920.4(SCN1A):c.3577T > 22C	AACAAYGGTGGAACCTGAGAAGG	Generalized epilepsy with
	(p.Trp1193Arg)		febrile seizures plus, type 1,
			Generalized epilepsy with
			febrile seizures plus, type 2
28939717	NM_003907.2(EIF2B5):c.271A > 22G	AAATGYTTCCTGTACACCTGTGG	Leukoencephalopathy with
	(p.Thr91Ala)		vanishing white matter
80357276	NM_007294.3(BRCA1):c.122A > 22G	AAATATGYGGTCACACTTTGTGG	Familial cancer of breast,
	(p.His41Arg)		Breast-ovarian cancer,
			familial 1
397515897	NM_000256.3(MYBPC3):c.1351 +	AAAGGYGGGCCTGGGACCTGAGG	Familial hypertrophic
	302T > 22C		cardiomyopathy 4,
			Cardiomyopathy
397514491	NM_005340.6(HINT1):c.152A > 22G	AAAAYGTGTTGGTGCTTGAGGGG,	Gamstorp-Wohlfart syndrome
	(p.His51Arg)	GAAAAYGTGTTGGTGCTTGAGGG,
		AGAAAAYGTGTTGGTGCTTGAGG
387907164	NM_020894.2(UVSSA):c.94T > 22C	AAAATTYGCAAGTATGTCTTAGG,	UV-sensitive syndrome 3
	(p.Cys32Arg)	AAATTYGCAAGTATGTCTTAGG
		G
118161496	NM_025152.2(NUBPL):c.815-	TGGTTCYAATGGATGTCTGCTGG,	Mitochondrial complex I
	27T > 22C	GGTTCYAATGGATGTCTGCTGGG	deficiency
764313717	NM_005609.2(PYGM):c.425_	TGGCTGYCAGGGACCCAGCAAGG,
	528del	CTGYCAGGGACCCAGCAAGGAGG
28934568	NM_003242.5(TGFBR2):c.923T > 22C	AGTTCCYGACGGCTGAGGAGCGG	Loeys-Dietz syndrome 2
	(p.Leu308Pro)
121913461	NM_007313.2(ABL1):c.814T > 22C	CCAGYACGGGGAGGTGTACGAGG,
	(p.Tyr272His)	CAGYACGGGGAGGTGTACGAGGG
377750405	NM_173551.4(ANKS6):c.1322A > 22G	AGGGCYGTCGGACCTTCGAGTGG,	Nephronophthisis 16
	(p.Gln441Arg)	GGGCYGTCGGACCTTCGAGTGGG,
		GGCYGTCGGACCTTCGAGTGGGG
57639980	NM_001927.3(DES):c.1034T > 22C	ATTCCCYGATGAGGCAGATGCGG,	Myofibrillar myopathy 1
	(p.Leu345Pro)	TTCCCYGATGAGGCAGATGCGGG
147391618	NM_020320.3(RARS2):c.35A > 22G	ATACCYGGCAAGCAATAGCGCGG	Pontocerebellar hypoplasia
	(p.Gln12Arg)		type 6
182650126	NM_002977.3(SNC9A):c.2215A > G	GTAAYTGCAAGATCTACAAAAGG	Small fiber neuropathy
	(p.Ile739Val)
80358278	NM_004700.3(KCNQ4):c.842T > 22C	ACATYGACAACCATCGGCTATGG	DFNA 2 Nonsyndromic Hearing
	(p.Leu281Ser)		Loss
786204012	NM_005957.4(MTHFR):c.388T > C	GACCYGCTGCCGTCAGCGCCTGG	Homocysteinemia due to MTHFR
	(p.Cys130Arg)		deficiency
786204037	NM_005957.4(MTHFR):c.1883T > 22C	TCCCACYGGACAACTGCCTCTGG	Homocysteinem a due to MTHFR
	(p.Leu628Pro)		deficiency
202147607	NM_000140.3(FECH):c.1137 + 303A >	GTAGAYACCTTAGAGAACAATGG	Erythropoietic protoporphyria
	22G
122456136	NM_005183.3(CACNA1F):c.2267T > 22C	TGCCAYTGCTGTGGACAACCTGG
	(p.Ile756Thr)
786204851	NM_007374.2(SIX6):c.110T > 22C	GTCGCYGCCCGTGGCCCCTGCGG	Cataract, microphthalmia and
	(p.Leu37Pro)		nystagmus
794728167	NM_000138.4(FBN1):c.1468 + 302T >	ATTGGYACGTGATCCATCCTAGG	Thoracic aortic aneurysms and
	22C		aortic dissections
121964909	NM_000027.3(AGA):c.214T > 22C	GACGGCYCTGTAGGCTTTGGAGG	Aspartylglycosaminuria
	(p.Ser72Pro)
121964978	NM_000170.2(GLDC):c.2T > 22C	CGGCCAYGCAGTCCTGTGCCAGG,	Non-ketotic hyperglyc nemia
	(p.Met1Thr)	GGCCAYGCAGTCCTGTGCCAGGG
121965008	NM_000398.6(CYB5R3):c.446T > 22C	CTGCYGGTCTACCAGGGCAAAGG	METHEMOGLOBINEMIA, TYPE I
	(p.Leu149Pro)
121965064	NM_000128.3(F11):c.901T > 22C	TGATYTCTTGGGAGAAGAACTGG	Hereditary factor XI
	(p.Phe301Leu)		deficiency disease
45517398	NM_000548.3(TSC2):c.5150T > 22C	GCCCYGCACGCAAATGTGAGTGG,	Tuberous sclerosis syndrome
	(p.Leu1717Pro)	CCCYGCACGCAAATGTGAGTGGG
786205857	NM_015662.2(IFT172):c.770T > 22C	TTGTGCYAGGAAGTTATGACAGG	RETINITIS PIGMENTOSA 71
	(p.Leu257Pro)
786205904	NM_001135669.1(XPR1):c.653T > 22C	GCGTTYACGTGTCCCCCCTTTGG,	BASAL GANGLIA
	(p.Leu218Ser)	CGTTYACGTGTCCCCCCTTTGGG	CALCIFICATION,
104893704	NM_000388.3(CASR):c.2641T > 22C	ACGCTYTCAAGGTGGCTGCCCGG,	Hypercalciuric hypercalcemia
	(p.Phe881Leu)	CGCTYTCAAGGTGGCTGCCCGGG
104893747	NM_198159.2(MITF):c.1195T > 22C	ACTTYCCCTTATTCCATCCACGG,	Waardenburg syndrome type 2A
	(p.Ser399Pro)	CTTYCCCTTATTCCATCCACGGG
104893770	NM_000539.3(RHO):c.133T > 22C	CATGYTTCTGCTGATCGTGCTGG,	Retinitis pigmentosa 4
	(p.Phe45Leu)	ATGYTTCTGCTGATCGTGCTGGG
28937596	NM_003907.2(EIF2B5):c.1882T > 22C	AGGCCYGGAGCCCTGTTTTTAGG	Leukoencephalopathy with
	(p.Trp628Arg)		vanishing white matter
104893876	NM_001151.3(SLC25A4):c.293T > 22C	GCAGCYCTTCTTAGGGGGTGTGG	Autosomal dominant progressive
	(p.Leu98Pro)		external ophthalmoplegia with
			mitochondrial
			DNA deletions 2
104893883	NM_006005.3(WFS1):c.2486T > 22C	ACCATCCYGGAGGGCCGCCTGGG	WFS1-Related Disorders
	(p.Leu829Pro)
104893962	NM_000165.4(GJA1):c.52T > 22C	CTACYCAACTGCTGGAGGGAAGG	Oculodentodigital dysplasia
	(p.Ser18Pro)
104893978	NM_000434.3(NEU1):c.718T > 22C	GCCTCCYGGCGCTACGGAAGTGG,	Sialidosis, type II
	(p.Trp240Arg)	CCTCCYGGCGCTACGGAAGTGGG,
		CTCCYGGCGCTACGGAAGTGGGG
104894092	NM_002546.3(TNERSF11B):c.349T >	TAGAGYTCTGCTTGAAACATAGG	Hyperphosphatasemia with bone
	22C (p.Phe117Leu)		disease
104894135	NM_000102.3(CYP17A1):c.316T > 22C	CATCGCGYCCAACAACCGTAAGG,	Complete combined 17-alpha-
	(p.Ser106Pro)	ATCGCGYCCAACAACCGTAAGGG	hydroxylase/17,20-lyase
104894151	NM_000102.3(CYP17A1):c.1358T > 22C	AGCTCTYCCTCATCATGGCCTGG	Combined partial 17-alpha-
	(p.Phe453Ser)		hydroxylase/17,20-
			lyasedeficiency
36015961	NM_000518.4(HBB):c.344T > 22C	TGTGTGCYGGCCCATCACTTTGG	Beta thalassemia intermedia
	(p.Leu115Pro)
104894472	NM_152443.2(RDH12):c.523T > 22C	TCCYCGGTGGCTCACCACATTGG	Leber congenital amaurosis 13
	(p.Ser175Pro)
104894587	NM_004870.3(MPDU1):c.356T > 22C	TTCCYGGTCATGCACTACAGAGG	Congenital disorder of
	(p.Leu119Pro)		glycosylation type 1F
104894588	NM_004870.3(MPDUI):c.2T > 22C	AATAYGGCGGCCGAGGCGGACGG	Congenital disorder of
	(p.Met1Thr)		glycosylation type 1F
104894626	NM_000304.3(PMP22):c.82T > 22C	TAGCAAYGGATCGTGGGCAATGG	Charcot-Marie-Tooth disease,
	(p.Trp28Arg)		type LE
104894631	NM_018129.3(PNP0):c.784T > 22C	ACCTYAACTCTGGGACCTGCTGG	″Pyridoxal 5-phosphate-
	(p.Ter262Gln)		dependent epilepsy″
104894703	NM_032551.4(KISS1R):c.305T > 22C	GCCCTGCYGTACCCGCTGCCCGG,
	(p.Leu102Pro)	TGCYGTACCCGCTGCCCGGCTGG
104894826	NM_000166.5(GJB1):c.407T > 22C	ATGYCATCAGCGTGGTGTTCCGG	Dejerine-Sottas disease, X-
	(p.Val126Ala)		linked hereditary motor and
			sensory neuropathy
104894859	NM_001122606.1(LAMP2):c.961T > C	CAGCTACYGGGATGCCCCCCTGG,	Danon disease
	(p.Trp321Arg)	AGCTACYGGGATGCCCCCCTGGG
104894931	NM_006517.4(SLC16A2):c.1313T > 22C	TGAGCYGGTGGGCCCAATGCAGG	Allan-Herndon-Dudley syndrome
	(p.Leu438Pro)
104894935	NM_000330.3(RS1):c.38T > 22C	TTACTTCYCTTTGGCTATGAAGG	Juvenile retinoschisis
	(p.Leul3Pro)
104895217	NM_001065.3(TNFRSF1A):c.175T > 22C	TGCYGTACCAAGTGCCACAAAGG	TNF receptor-associated
	(p.Cys59Arg)		periodic fever syndrome
			(TRAPS)
143889283	NM_003793.3(CTSF):c.692A > 22G	CTCCAYACTGAGCTGTGCCACGG	Ceroid lipofuscinosis,
	(p.Tyr231Cys)		neuronal, 13
122459147	NM_001159702.2(FHL1):c.310T > 22C	GGGGYGCTTCAAGGCCATTGTGG	Myopathy, reducing body, X-
	(p.Cys104Arg)		linked, childhood- onset
74552543	NM_020184.3(CNNM4):c.971T > 22C	AAGCTCCYGGACTTTTTTCTGGG	Cone-rod dystrophy
	(p.Leu324Pro)		amelogenesis imperfecta
199476117	m.10158T > 22C	AAAYCCACCCCTTACGAGTGCGG	Leigh disease, Leigh syndrome
			due to mitochondrial complex
			I deficiency, Mitochondrial
			complex I deficiency
794727808	NM_020451.2(SEPN1):c.872 + 302T >	TTCCGGYGAGTGGGCCACACTGG	Congenital myopathy with fiber
	22C		type disproportion, Eichsfeld
			type
140547520	NM_005022.3(PFN1):c.350A > 22G	CACCTYCTTTGCCCATCAGCAGG	Amyotrophic lateral sclerosis
	(p.Glu117Gly)		18
397514359	NM_000060.3(BTD):c.445T > 22C	TCACCGCYTCAATGACACAGAGG	Biotinidase deficiency
	(p.Phe149Leu)
207460001	m.15197T > 22C	CTAYCCGCCATCCCATACATTGG	Exercise intolerance
397514406	NM_000060.3(BTD):c.1214T > 22C	TTCACCCYGGTCCCTGTCTGGGG	Biotinidase deficiency
	(p.Leu405Pro)
397514516	NM_006177.3(NRL):c.287T > 22C	GAGGCCAYGGAGCTGCTGCAGGG	Retinitis pigmentosa 27
	(p.Met96Thr)
72554312	NM_000531.5(OTC):c.134T > 22C	CTCACTCYAAAAAACTTTACCGG	Ornithine carbamoyltransferase
	(p.Leu45Pro)		deficiency
397514569	NM_178012.4(TUBB2B):c.350T > 22C	GGTCCYGGATGTGGTGAGGAAGG	Polymicrogyria, asymmetric
	(p.Leu117Pro)
397514571	NM_000431.3(MVK):c.122T > 22C	CGGCYTCAACCCCACAGCAATGG,	Porokeratosis, disseminated
	(p.Leu41Pro)	GGCYTCAACCCCACAGCAATGGG	superficial actinic 1
794728390	NM_000238.3(KCNH2):c.2396T > 22C	GCCATCCYGGGTATGGGGTGGGG,	Cardiac arrhythmia
	(p.Leu799Pro)	CCATCCYGGGTATGGGGTGGGGG,
		CATCCYGGGTATGGGGTGGGGGG
397514713	NM_001199107.1(TBC1D24):c.6836T >	GGTCTYTGACGTCTTCCTGGTGG	Early infantile epileptic
	C (p.Phe229Ser)		encephalopathy 16
397514719	NM_080605.3(B3GALT6):c.193A > 22G	CGCYGGCCACCAGCACTGCCAGG	Spondyloepimetaphyseal
	(p.Ser65Gly)		dysplasia with joint laxity
730880608	NM_000256.3(MYBPC3):c.3796T > 22C	GAGYGCCGCCTGGAGGTGCGAGG	Cardiomyopathy
	(p.Cys1266Arg)
397515329	NM_001382.3(DPAGT1):c.503T > 22C	AATCCYGTACTATGTCTACATGG,	Congenital disorder of
	(p.Leu168Pro)	ATCCYGTACTATGTCTACATGGG,	glycosylation type 1J
397515465	NM_018127.6(ELAC2):c.460T > 22C	TCCYGTACTATGTCTACATGGGG	Combined oxidative
	(p.Phe154Leu)	ATAYTTTCTGGTCCATTGAAAGG	phosphorylation deficiency 17
397515557	NM_005211.3(CSF1R):c.2483T > 22C	CATCTYTGACTGTGTCTACACGG	Hereditary diffuse
	(p.Phe828Ser)		leukoencephalopathy with
			spheroids
397515599	NM_194248.2(OTOF):c.3413T > 22C	AGGTGCYGTTCTGGGGCCTACGG,	Deafness, autosomal recessive
	(p.Leu1138Pro)	GGTGCYGTTCTGGGGCCTACGGG	9
397515766	NM_000138.4(FBN1):c.2341T > 22C	GGACAAYGTAGAAATACTCCTGG	Marfan syndrome
	(p.Cys781Arg)
565779970	NM_001429.3(EP300):c.3573T > 22A	CTTAYTACAGTTACCAGAACAGG	Rubinstein-Taybi syndrome 2
	(p.Tyr1191Ter)
786200938	NM_080605.3(B3GALT6):c.1A > 22G	AGCTTCAYGGCGCCCGCGCCGGG,	Spondyloepimetaphyseal
	(p.Met1Val)	TCAYGGCGCCCGCGCCGGGCCGG	dysplasia with joint laxity
28942087	NM_000229.1(LCAT):c.698T > 22C	ATCTCTCYTGGGGCTCCCTGGGG,	Norum disease
	(p.Leu233Pro)	TCTCYTGGGGCTCCCTGGGGTGG
128621203	NM_000061.2(BTK):c.1625T > 22C	TCGGCCYGTCCAGGTGAGTGTGG	X-linked agammaglobulinemia
	(p.Leu542Pro)		with growth hormone deficiency
397515412	NM_006383.3(CIB2):c.368T > 22C	CTTCAYCTGCAAGGAGGACCTGG	Deafness, autosomal recessive
	(p.Ile123Thr)		48
193929364	NM_000352.4(ABCC8):c.404T > 22C	AAGCYGCTAATTGGTAGGTGAGG	Permanent neonatal diabetes
	(p.Leu135Pro)		mellitus
730880872	NM_000257.3(MYH7):c.1400T > 22C	TCGAGAYCTTCGATGTGAGTTGG,	Cardiomyopathy
		CGAGAYCTTCGATGTGAGTTGGG
80356474	NM_002977.3(SCN9A):c.2543T > 22C	AAGATCAYTGGTAACTCAGTAGG,	Primary erythromelalgia
	(p.Ile848Thr)	AGATCAYTGGTAACTCAGTAGGG,
		GATCAYTGGTAACTCAGTAGGGG
80356489	NM_001164277.1(SLC37A4):c.352T >	GGGCYGGCCCCCATGTGGGAAGG	Glucose-6-phosphate transport
	22C (p.Trp118Arg)		defect
80356536	NM_152296.4(ATP1A3):c.2338T > 22C	GCCCYTCCTGCTGTTCATCATGG	Dystonia 12
	(p.Phe780Leu)
80356596	NM_194248.2(OTOF):c.3032T > 22C	GATGCYGGTGTTCGACAACCTGG	Deafness, autosomal recessive
	(p.Leu1011Pro)		9, Auditory neuropathy,
			autosomal recessive, 1
80356689	NM_000083.2(CLCN1):c.857T > 22C	AGGAGYGCTATTTAGCATCGAGG	Myotonia congenita
	(p.Val286Ala)
118203884	m.4409T > 22C	AGGYCAGCTAAATAAGCTATCGG	Mitochondrial myopathy
587777625	NM_173596.2(SLC39A5):c.911T > 22C	AGAACAYGCTGGGGCTTTTGCGG	Myopia 24, autosomal dominant
	(p.Met304Thr)
587783087	NM_003159.2(CDKL5):c.602T > 22C	ATTCYTGGGGAGCTTAGCGATGG	not provided
	(p.Leu201Pro)
118203951	NM_013319.2(UBIAD1):c.511T > 22C	TCTGGCYCCTTTCTCTACACAGG,	Schnyder crystalline conical
	(p.Ser171Pro)	GGCYCCTTTCTCTACACAGGAGG	dystrophy
118204017	NM_000018.3(ACADVL):c.1372T > 22C	TCGCATCYTCCGGATCTTTGAGG,	Very long chain acyl-CoA
	(p.Phe458Leu)	CGCATCYTCCGGATCTTTGAGGG,	dehydrogenase
		GCATCYTCCGGATCTTTGAGGGG
397518466	NM_000833.4(GRIN2A):c.2T > 22C	CTAYGGGCAGAGTGGGCTATTGG	Focal epilepsy with speech
	(p.Met1Thr)		disorder with or without
			mental retardation
118204069	NM_000237.2(LPL):c.337T > 22C	GGACYGGCTGTCACGGGCTCAGG	Hyperlipoproteinemia, type I
	(p.Trp113Arg)
118204080	NM_000237.2(LPL):c.755T > 22C	GTGAYTGCAGAGAGAGGACTTGG	Hyperlipoproteinemia, type I
	(p.Ile252Thr)
118204111	NM_000190.3(HMBS):c.739T > 22C	GCTTCGCYGCATCGCTGAAAGGG	Acute intermittent porphyria
	(p.Cys247Arg)
80357438	NM_007294.3(BRCA1):c.65T > 22C	AAATCTYAGAGTGTCCCATCTGG	Familial cancer of breast,
	(p.Leu22Ser)		Breast-ovarian cancer,
			familial 1, Hereditary cancer-
			predisposing syndrome
139877390	NM_001040431.2(COA3):c.215A > 22G	CCAYCTGGGGAGGTAGGTTCAGG
	(p.Tyr72Cys)
793888527	NM_005859.4(PURA):c.563T > 22C	GACCAYTGCGCTGCCCGCGCAGG,	not provided, Mental
	(p.Ile188Thr)	ACCAYTGCGCTGCCCGCGCAGGG,	retardation, autosomal
		CCAYTGCGCTGCCCGCGCAGGGG	dominant 31
561425038	NM_002878.3(RADS1D):c.1A > 22G	CGCCCAYGTTCCCCGCAGGCCGG	Hereditary cancer-predisposing
	(p.Met1Val)		syndrome
121907934	NM_024105.3(ALG12):c.473T > 22C	TCCYGCTGGCCCTCGCGGCCTGG	Congenital disorder of
	(p.Leu158Pro)		glycosylation type 1G
80358207	NM_153212.2(GM4):c.409T > 22C	CCTCATCYTCAAGGCCGCCGTGG	Erythrokeratodermia variabilis
	(p.Phe137Leu)
80358228	NM_002353.2(TACSTD2):c.557T > C	TCGGCYGCACCCCAAGTTCGTGG	Lattice conical dystrophy
	(p.Leu186Pro)		Type III
121908076	NM_138691.2(TMC1):c.1543T > 22C	AGGACCTYGCTGGGAAACAATGG,	Deafness, autosomal recessive
	(p.Cys515Arg)	ACCTYGCTGGGAAACAATGGTGG,	7
		CCTYGCTGGGAAACAATGGTGGG
121908089	NM_017838.3(NHP2):c.415T > 22C	GGAGGCTYACGATGAGTGCCTGG,	Dyskeratosis congenita
	(p.Tyr139His)	GGCTYACGATGAGTGCCTGGAGG	autosomal recessive 1,
			Dyskeratosis congenita,
			autosomal recessive 2
121908154	NM_001243133.1(NLRP3):c.926T > 22C	GGTGCCTYTGACGAGCACATAGG	Familial cold urticaria,
	(p.Phe309Ser)		Chronic infantile neurological,
			cutaneous and articular
			syndrome
121908158	NM_001033855.2(DCLRE1C):c.2T > 22C	GGCGCTAYGAGTTCTTTCGAGGG,	Histiocytic medullary
	(p.Met1Thr)	GCGCTAYGAGTTCTTTCGAGGGG	reticulosis
796052870	NM_018129.3(PNP0):c.2T > 22C	CCCCCAYGACGTGCTGGCTGCGG,	not provided
	(p.Met1Thr)	CCCCAYGACGTGCTGGCTGCGGG,
		CCCAYGACGTGCTGGCTGCGGGG
121908318	NM_020427.2(SLURP1):c.43T > 22C	GCAGCCYGGAGCATGGGCTGTGG	Acroerythrokeratoderma
	(p.Trp15Arg)
121908352	NM_022124.5(CDH23):c.5663T > 22C	CTCACCTYCAACATCACTGCGGG	Deafness, autosomal recessive
	(p.Phe1888Ser)		12
121908520	NM_000030.2(AGXT):c.613T > 22C	CCTGTACYCGGGCTCCCAGAAGG	Primary hyperoxaluria, type I
	(p.Ser205Pro)
121908618	NM_004273.4(CHST3):c.920T > 22C	CGTGCYGGCCTCGCGCATGGTGG	Spondyloepiphyseal dysplasia
	(p.Leu307Pro)		with congenital joint
			dislocations
11694	NM_006432.3(NPC2):c.199T > 22C	TATTCAGYCTAAAAGCAGCAAGG	Niemann-Pick disease type C2
	(p.Ser67Pro)
121908739	NM_000022.2(ADA):c.320T > 22C	CCTGCYGGCCAACTCCAAAGTGG	Severe combined
	(p.Leu107Pro)		immunodeficiency due to ADA
			deficiency
80359022	NM_000059.3(BRCA2):c.7958T > 22C	TGCYTCTTCAACTAAAATACAGG	Familial cancer of breast,
	(p.Leu2653Pro)		Breast-ovarian cancer,
			familial 2
121908902	NM_003880.3(WISP3):c.232T > 22C	AAAATCYGTGCCAAGCAACCAGG,	Progressive pseudorheumatoid
	(p.Cys78Arg)	AAATCYGTGCCAAGCAACCAGGG,	dysplasia
		AATCYGTGCCAAGCAACCAGGGG
121908947	NM_006892.3(DNMT3B):c.808T > 22C	CAAGTTCYCCGAGGTGAGTCCGG,	Centromeric instability of
	(p.Ser270Pro)	AAGTTCYCCGAGGTGAGTCCGGG,	chromosomes 1,9 and
		AGTTCYCCGAGGTGAGTCCGGGG	16 and immunodeficiency
121909028	NM_000492.3(CFTR):c.3857T > 22C	AGCCTYTGGAGTGATACCACAGG	Cystic fibrosis
	(p.Phe1286Ser)
121909135	NM_000085.4(CLCNKB):c.1294T > 22C	CTTTGTCYATGGTGAGTCTGGGG	Bartter syndrome type 3
	(p.Tyr432His)
121909143	NM_001300.5(KLF6):c.506T > 22C	GGAGCYGCCCTCGCCAGGGAAGG
	(p.Leu169Pro)
121909182	NM_001089.2(ABCA3):c.302T > 22C	GCACYTGTGATCAACATGCGAGG	Surfactant metabolism
	(p.Leu101Pro)		dysfunction, pulmonary, 3
121909200	NM_000503.5(EYA1):c.1459T > 22C	CACTCYCGCTCATTCACTCCCGG	Melnick-Fraser syndrome
	(p.Ser487Pro)
121909247	NM_004970.2(IGFALS):c.1618T > 22C	GGACYGTGGCTGCCCTCTCAAGG	Acid-labile subunit deficiency
	(p.Cys540Arg)
121909253	NM_005570.3(LMAN1):c.2T > 22C	AGAYGGCGGGATCCAGGCAAAGG	Combined deficiency of factor
	(p.Met1Thr)		V and factor VIII, 1
121909385	NM_000339.2(SLC12A3):c.1868T > 22C	CAACCYGGCCCTCAGCTACTCGG	Familialhypokalemia-
	(p.Leu623Pro)		hypomagnesemia
121909497	NM_002427.3(MMP13):c.224T > 22C	TTCTYCGGCTTAGAGGTGACTGG	Spondyloepimetaphyseal
	(p.Phe75Ser)		dysplasia, Missouri type
121909508	NM_000751.2(CHRND):c.188T > 22C	AACCYCATCTCCCTGGTGAGAGG	MYASTHENIC SYNDROME,
	(p.Leu63Pro)		CONGENITAL, 3B, FAST-
			CHANNEL
121909519	NM_001100.3(ACTA1):c.287T > 22C	CGAGCYTCGCGTGGCTCCCGAGG	Nemaline myopathy 3
	(p.Leu96Pro)
121909572	NM_000488.3(SERPINC1):c.667T > 22C	TGGGTGYCCAATAAGACCGAAGG
121909677	NM_000821.6(GGCX):c.896T > 22C	TATGTYCTCCTACGTCATGCTGG	Pseudoxanthoma elasticum-like
	(p.Phe299Ser)		disorder with multiple
			coagulation factor deficiency
121909727	NM_001018077.1(NR3C1):c.2209T >	CTATTGCYTCCAAACATTTTTGG	Glucocorticoid resistance,
	22C (p.Phe737Leu)		generalized
139573311	NM_000492.3(CFTR):c.1400T > 22C	TTCACYTCTAATGGTGATTATGG,	Cystic fibrosis
	(p.Leu467Pro)	TCACYTCTAATGGTGATTATGGG
121912441	NM_000454.4(SOD1):c.341T > 22C	CATCAYTGGCCGCACACTGGTGG	Amyotrophic lateral sclerosis
	(p.Ile114Thr)		type 1
121912446	NM_000454.4(SOD1):c.434T > 22C	CGTTYGGCTTGTGGTGTAATTGG,	Amyotrophic lateral sclerosis
	(p.Leu145Ser)	GTTYGGCTTGTGGTGTAATTGGG	type 1
121912463	NM_000213.3(ITGB4):c.1684T > 22C	GGCCAGYGTGTGTGTGAGCCTGG	Epidermolysis bullosa with
	(p.Cys562Arg)		pyloric atresia
121912492	NM_002292.3(LAMB2):c.961T > 22C	CCTCAACYGCGAGCAGTGTCAGG	Nephrotic syndrome, type 5,
	(p.Cys321Arg)		with or without ocular
			abnormalities
397516659	NM_001399.4(EDA):c.2T > 22C	GGCCAYGGGCTACCCGGAGGTGG	Hypohidrotic X-linked
	(p.Met1Thr)		ectodermal dysplasia
111033589	NM_021044.2(DHH):c.485T > 22C	GTTGCYGGCGCGCCTCGCAGTGG	46,XY gonadal dysgenesis,
	(p.Leu162Pro)		complete, dhh-related
111033622	NM_000206.2(IL2RG):c.343T > 22C	TGGCYGTCAGTTGCAAAAAAAGG	X-linked severe combined
	(p.Cys115Arg)		immunodeficiency
121912613	NM_001041.3(SI):c.1859T > 22C	ATGCYGGAGTTCAGTTTGTTTGG	Sucrase-isomaltase deficiency
	(p.Leu620Pro)
121912619	NM_016180.4(SLC45A2):c.1082T > 22C	GAGTTTCYCATCTACGAAAGAGG	Oculocutaneous albinism type
	(p.Leu361Pro)		4
61750581	NM_000552.3(VWF):c.4837T > 22C	CTGCCYCTGATGAGATCAAGAGG	von Willebrand disease, type
	(p.Ser1613Pro)		2a
121912653	NM_000546.5(TP53):c.755T > 22C	CATCCYCACCATCATCACACTGG	Li-Fraumeni syndrome 1
	(p.Leu252Pro)
111033683	NM_000155.3(GALT):c.386T > 22C	AGGTCAYGTGCTTCCACCCCTGG	Deficiency of UDPglucose-
	(p.Met129Thr)		hexose-1-phosphate
			uridylyltransferase
111033752	NM_000155.3(GALT):c.677T > 22C	CAGGAGCYACTCAGGAAGGTGGG	Deficiency of UDPglucose-
	(p.Leu226Pro)		hexose-1-phosphate
			uridylyltransferase
121912729	NM_000039.1(APOA1):c.593T > 22C	GCGCTYGGCCGCGCGCCTTGAGG	Familial visceral amyloidosis,
	(p.Leu198Ser)		Ostertag type
769452	NM_000041.3(APOE):c.137T > 22C	AACYGGCACTGGGTCGCTTTTGG
	(p.Leu46Pro)
121912762	NM_016124.4(RHD):c.329T > 22C	ACACYGTTCAGGTATTGGGATGG
	(p.Leu110Pro)
111033824	NM_000155.3(GALT):c.1138T > 22C	CGCCYGACCACGCCGACCACAGG,	Defic ency of UDPglucose-
	(p.Ter380Arg)	GCCYGACCACGCCGACCACAGGG	hexose-1-phosphate,
			uridylyltransferase
111033832	NM_000155.3(GALT):c.980T > 22C	TCCYGCGCTCTGCCACTGTCCGG	Deficiency of UDPglucose-
	(p.Leu327Pro)		hexose-1-phosphate
			uridylyltransferase
730881974	NM_000455.4(STK11):c.545T > 22C	GGGAACCYGCTGCTCACCACCGG,	Hereditary cancer-predisposing
	(p.Leu182Pro)	AACCYGCTGCTCACCACCGGTGG	syndrome
1064644	NM_000157.3(GBA):c.703T > 22C	GGGYCACTCAAGGGACAGCCCGG	Gaucher disease
	(p.Ser235Pro)
796052090	NM_138413.3(HOGA1):c.533T > 22C	GGACCYGCCTGTGGATGCAGTGG	Primary hyperoxaluria, type
	(p.Leu178Pro)		III
121913141	NM_000208.2(INSR):c.779T > 22C	CTACCYGGACGGCAGGTGTGTGG	Leprechaunism syndrome
	(p.Leu260Pro)
121913272	NM_006218.2(PIK3CA):c.1258T > 22C	GGAACACYGTCCATTGGCATGGG,	Congenital lipomatous
	(p.Cys420Arg)	GAACACYGTCCATTGGCATGGGG	overgrowth, vascular
			malformations, and epidermal
			nevi, Neoplasm of ovary,
			PIK3CA Related Overgrowth
			Spectrum
61751310	NM_000552.3(VWF):c.8317T > 22C	GCTCCYGCTGCTCTCCGACACGG	von Willebrand disease, type
	(p.Cys2773Arg)		2a
312262799	NM_024408.3(NOTCH2):c.1438T > C	TTCACAYGTCTGTGCATGCCAGG	Alagille syndrome 2
	(p.Cys480Arg)
121913570	NM_000426.3(LAMA2):c.7691T > 22C	ATCATTCYTTTGGGAAGTGGAGG,	Merosin deficient congenital
	(p.Leu2564Pro)	TCATTCYTTTGGGAAGTGGAGGG	muscular dystrophy
121913640	NM_000257.3(MYH7):c.1046T > 22C	AACTCCAYGTATAAGCTGACAGG	Familial hypertrophic
	(p.Met349Thr)		cardiomyopathy 1,
			Cardiomyopathy
121913642	NM_000257.3(MYH7):c.1594T > 22C	CATCATGYCCATCCTGGAAGAGG	Dilated cardiomyopathy 1S
	(p.Ser532Pro)
119463996	NM_001079802.1(FKTN):c.527T > 22C	GTAGTCTYTCATGAGAGGAGTGG	Limb-girdle muscular
	(p.Phe176Ser)		dystrophy-
587776456	NM_002049.3(GATA1):c.1240T > 22C	GCTCAYGAGGGCACAGAGCATGG	GATA-1-related thrombo-
	(p.Ter414Arg)		cytopenia with
			dyserythropoiesis
63750654	NM_000184.2(HBG2):c.-228T > 22C	ATGCAAAYATCTGTCTGAAACGG	Fetal hemoglobin quantitative
			trait locus 1
587776519	NM_001999.3(FBN2):c.3725-	AGCAYTGCAACCACATTGTCAGG	Congenital contractural
	15A > 22G		arachnodactyly
78365220	NM_000402.4(G6PD):c.473T > 22C	TGCCCYCCACCTGGGGTCACAGG	Anemia, nonspherocytic
	(p.Leu158Pro)		hemolytic, due to G6PD
			deficiency
63750741	NM_000179.2(MSH6):c.1346T > 22C	CTGGGGCYGGTATTCATGAAAGG	Hereditary Nonpolyposis
	(p.Leu449Pro)		Colorectal Neoplasms
587776914	NM_017565.3(FAM20A):c.590-	GTAATCYGCAAAGGAGGAGAAGG,	Enamel-renal syndrome
	2A > 22G	TAATCYGCAAAGGAGGAGAAGG
5030809	NM_000551.3(VHL):c.292T > 22C	CCCYACCCAACGCTGCCGCCTGG	Von Hippel-Lindau syndrome,
	(p.Tyr98His)		Hereditary cancer-predisposing
			syndrome
199476132	m.5728T > 22C	CAATCYACTTCTCCCGCCGCCGG,	Cytochrome-c oxidase
		AATCYACTTCTCCCGCCGCCGGG	deficiency, Mitochondrial
			complex I deficiency
62637012	NM_014336.4(AIPL1):c.715T > 22C	CTGCCAGYGCCTGCTGAAGAAGG,	Leber congenital amaurosis 4
	(p.Cys239Arg)	CCAGYGCCTGCTGAAGAAGGAGG
199476199	NM_207352.3(CYP4V2):c.1021T > 22C	AAACTGGYCCTTATACCTGTTGG,	Bietti crystalline
	(p.Ser341Pro)	AACTGGYCCTTATACCTGTTGGG	corneoretinal dystrophy
587777183	NM-006702.4(PNLPA6):c.3053T > C	CCTYTAACCGCAGCATCCATCGG	Boucher Neuhauser syndrome
	(p.Phe1018Ser)
199476389	NM_000487.5(ARSA):c.899T > 22C	GGTCTCTYGCGGTGTGGAAAGGG	Metachromatic leukodystrophy
	(p.Leu300Ser)
199476398	NM_016599.4(MYOZ2):c.142T > 22C	TTAYCCCATCTCAGTAACCGTGG	Familial hypertrophic
	(p.Ser48Pro)		cardiomyopathy 16
119456967	NM_001037633.1(SIL1):c.142T > C	TTGCYGAAGGAGCTGAGATGAGG	Marinesco-
	(p.Leu457Pro)		Sj\xc3\xb6grensyndrome
730882253	NM_006888.4(CALM1):c.268T > 22C	GGCAYTCCGAGTCTTTGACAAGG	Long QT syndrome 14
	(p.Phe90Leu)
587777283	NM_012338.3(TSPAN12):c.413A > 22G	TAATCCAYAATTTGTCATCCTGG	Exudative vitreoretinopathy 5
	(p.Tyr138Cys)
587777306	NM_015884.3(MBTPS2):c.1391T > 22C	GCTYTGCTTTGGATGGACAATGG	Palmoplantar keratoderma,
	(p.Phe464Ser)		mutilating, with periorificial
			keratotic plaques, X-linked
56378716	NM_000250.1(MPO):c.752T > 22C	TCACTCAYGTTCATGCAATGGGG	Myeloperoxidase deficiency
	(p.Met251Thr)
587777390	NM_005026.3(PIK3CD):c.1246T > 22C	GCAGGACYGCCCCATTGCCTGGG	Activated PI3K-delta syndrome
	(p.Cys416Arg)
587777480	NM_003108.3(SOX11):c.178T > 22C	TATGGYCCAAGATCGAACGCAGG	Mental retardation, autosomal
	(p.Ser60Pro)		dominant 27
587777663	NM_001288767.1(ARMC5):c.1379T >	GCCCGACYGCGGGATGCTGGTGG	Acth-independent macronodular
	22C (p.Leu460Pro)		adrenal hyperplasia 2
61753033	NM_000350.2(ABCA4):c.5819T > 22C	AAGGCYACATGAACTAACCAAGG	Stargardt disease, Stargardt
	(p.Leu1940Pro)		disease 1, Cone-rod dystrophy
			3
200488568	NM_002972.3(SBF1):c.4768A > 22G	CAGGCGYCCTCTTGCTCAGCCGG	Charcot-Marie-Tooth disease,
	(p.Thr1590Ala)		type 4B3
132630274	NM_000377.2(WAS):c.809T > 22C	CGGAGTCYGTTCTCCAGGGCAGG	Severe congenital neutropenia
	(p.Leu270Pro)		X-linked
132630308	NM_001399.4(EDA):c.181T > 22C	CTGCYACCTAGAGTTGCGCTCGG	Hypohidrotic X-linked
	(p.Tyr61His)		ectodermal dysplasia
60934003	NM_170707.3(LMNA):c.1589T > 22C	ACGGCTCYCATCAACTCCACTGG,	Benign scapuloperoneal
	(p.Leu530Pro)	CGGCTCYCATCAACTCCACTGGG,	muscular dystrophy with
		GGCTCYCATCAACTCCACTGGGG	cardiomyopathy
180177160	NM_000030.2(AGXT):c.1076T > 22C	GGTGCYGCGGATCGGCCTGCTGG,	Primary hyperoxaluria, type I
	(p.Leu359Pro)	GTGCYGCGGATCGGCCTGCTGGG
180177222	NM_000030.2(AGXT):c.449T > 22C	GTGCYGCTGTTCTTAACCCACGG,	Primary hyperoxaluria, type I
	(p.Leu150Pro)	TGCYGCTGTTCTTAACCCACGGG
180177254	NM_000030.2(AGXT):c.661T > 22C	GCTCATCYCCTTCAGTGACAAGG	Primary hyperoxaluria, type I
	(p.Ser221Pro)
180177264	NM_000030.2(AGXT):c.757T > 22C	GGGGCYGTGACGACCAGCCCAGG	Primary hyperoxaluria, type I
	(p.Cys253Arg)
180177293	NM_000030.2(AGXT):c.893T > 22C	GTATCYGCATGGGCGCCTGCAGG	Primary hyperoxaluria, type I
	(p.Leu298Pro)
376785840	NM_001282227.1(CECR1):c.1232A >	GAAATCAYAGGACAAGCCTTTGG	Polyarteritis nodosa
	22G (p.Tyr411Cys)
587779393	NM_000257.3(MYH7):c.4937T > 22C	GAGCCYCCAGAGCTTGTTGAAGG	Myopathy, distal, 1
	(p.Leu1646Pro)
587779410	NM_012434.4(SLC17A5):c.500T > 22C	ATTGTACYCAGAGCACTAGAAGG	Sialic acid storage disease,
	(p.Leu167Pro)		severe infantile type
587779513	NM_000090.3(COL3A1):c.2337 +	AGGYAACCCTTAATACTACCTGG	Ehlers-Danlos syndrome, type
	302T > 22C (p.Gly762_Lys779del)		4
777539013	NM_020376.3(PNPLA2):c.757 +	GAACGGYGCGCGGACCCGGGCGG,	Neutral lipid storage disease
	302T > 22C	AACGGYGCGCGGACCCGGGCGGG	with myopathy
34557412	NM_012452.2(TNERSF13B):c.310T >	ACTTCYGTGAGAACAAGCTCAGG	Immunoglobulin A deficiency 2,
	22C (p.Cys104Arg)		Common variable
796052970	NM_001165963.1(SCN1A):c.1094T >	CAAGCTYTGATACCTTCAGTTGG,	not provided
	22C (p.Phe365Ser)	AAGCTYTGATACCTTCAGTTGGG
724159989	NC_012920.1:m.7505T > 22C	CCTCCAYGACTTTTTCAAAAAGG	Deafness, nonsyndromic
			sensorineural, mitochondrial
796053222	NM_014191.3(SCN8A):c.4889T > 22C	CGTCYGATCAAAGGCGCCAAAGG,	not provided
	(p.Leu1630Pro)	GTCYGATCAAAGGCGCCAAAGGG
118192127	NM_000540.2(RYR1):c.10817T > 22C	TACTACCYGGACCAGGTGGGTGG,	Central core disease
	(p.Leu3606Pro)	ACTACCYGGACCAGGTGGGTGGG,
		CTACCYGGACCAGGTGGGTGGGG
118192170	NM_000540.2(RYR1):c.14693T > 22C	AGGCAYTGGGGACGAGATCGAGG	Malignant hyperthermia
	(p.Ile4898Thr)		susceptibility type 1,
			Central core disease
121917703	NM_005247.2(FGF3):c.466T > 22C	GTACGTGYCTGTGAACGGCAAGG,	Deafness with labyrinthine
	(p.Ser156Pro)	TACGTGYCTGTGAACGGCAAGGG	aplasia microtia and
			microdontia (LAMM)
690016549	NM_005211.3(CSF1R):c.2450T > 22C	CCGCCYGCCTGTGAAGTGGATGG	Hereditary diffuse
	(p.Leu817Pro)		leukoencephalopathy with
			spheroids
690016552	NM_005211.3(CSF1R):c.2566T > 22C	GAATCCCYACCCTGGCATCCTGG	Hereditary diffuse
	(p.Tyr856His)		leukoencephalopathy with
			spheroids
121917738	NM_001098668.2(SFTPA2):c.593T >	GGAGACTYCCGCTACTCAGATGG,	Idiopathic fibrosing
	22C (p.Phe198Ser)	GAGACTYCCGCTACTCAGATGGG	alveolitis, chronic form
690016559	NM_005211.3(CSF1R):c.1957T > 22C	AGCCYGTACCCATGGAGGTAAGG,	Hereditary diffuse
	(p.Cys653Arg)	GCCYGTACCCATGGAGGTAAGGG	leukoencephalopathy with
			spheroids
690016560	NM_005211.3(CSFIR):c.2717T > 22C	GCAGAYCTGCTCCTTCCTTCAGG	Hereditary diffuse
	(p.Ile906Thr)		leukoencephalopathy with
			spheroids
121917769	NM_003361.3(UMOD):c.376T > 22C	GGCCACAYGTGTCAATGTGGTGG,	Familial juvenile gout
	(p.Cys126Arg)	GCCACAYGTGTCAATGTGGTGGG
121917773	NM_003361.3(UMOD):c.943T > 22C	ATGGCACYGCCAGTGCAAACAGG	Glomerulocystic kidney disease
	(p.Cys315Arg)		with hyperuricemia and
			isohenuria
121917818	NM_007255.2(B4GALT7):c.617T > 22C	TGCYCTCCAAGCAGCACTACCGG	Ehlers-Danlos syndrome
	(p.Leu206Pro)		progeroid type
121917824	NM_021615.4(CHST6):c.827T > 22C	GGACCYGGCGCGGGAGCCGCTGG	Macular conical dystrophy
	(p.Leu276Pro)		Type I
121917848	NM_000452.2(SLC10A2_:c.7285T > C	TTTCYTCTGGCTAGAATTGCTGG	Bile acid malabsorption,
	(p.Leu243Pro)		primary
121918006	NM_000478.4(ALPL):c.1306T > 22C	TGGACYATGGTGAGACCTCCAGG	Infantile hypophosphatasia
	(p.Tyr436His)
121918010	NM_000478.4(ALPL):c.979T > 22C	CAAAGGCYTCTTCTTGCTGGTGG,	Infantile hypophosphatasia
	(p.Phe327Leu)	GGCYTCTTCTTGCTGGTGGAAGG
121918088	NM_000371.3(TTR):c.400T > 22C	CCCCYACTCCTATTCCACCACGG
	(p.Tyr134His)
121918110	NM_001042465.1(PSAP):c.1055T > 22C	GAAGCYGCCGAAGTCCCTGTCGG	Gaucher disease, atypical,
	(p.Leu352Pro)		due to saposin C deficiency
121918137	NM_003730.4(RNASET2):c.550T > C	CCAGYGCCTTCCACCAAGCCAGG	Leukoencephalopathy, cystic,
	(p.Cys184Arg)		without megalencephaly
121918191	NM_001127628.1(FBP1):c.581T > C	GGAGTYCATTTTGGTGGACAAGG	Fructose-biphosphatase
	(p.Phe194Ser)		deficiency
121918306	NM_006946.2(SPTBN2):c.758T > 22C	ACCAAGCYGCTGGATCCCGAAGG,	Spinocerebellar ataxia 5
	(p.Leu253Pro)	AAGCYGCTGGATCCCGAAGGTGG,
		AGCYGCTGGATCCCGAAGGTGGG
121918505	NM_000141.4(FGFR2):c.799T > 22C	AATGCCYCCACAGTGGTCGGAGG	Pfeiffer syndrome, Neoplasm
	(p.Ser267Pro)		of stomach
121918643	NM_003126.2(SPTA1):c.620T > 22C	GTGGAGCYGGTAGCTAAAGAAGG,	Hereditary pyropoikilocytosis,
	(p.Leu207Pro)	TGGAGCYGGTAGCTAAAGAAGGG	Elliptocytosis 2
121918646	NM_001024858.2(SPTB):c.604T > 22C	CTCCAGCYGGAAGGATGGCTTGG	Spherocytosis type 2
	(p.Trp202Arg)
121918648	NM_001024858.2(SPTB):c.6055T > 22C	ATGCCYCTGTGGCTGAGGCGTGG
	(p.Ser2019Pro)
727504166	NM_000543.4(SMPD1):c.475 T > C	TGAGGCCYGTGGCCTGCTCCTGG,	Niemann-Pick disease, type A,
	(p.Cys159Arg)	GAGGCCYGTGGCCTGCTCCTGGG	Niemann-Pick disease, type B
193922915	NM_000434.3(NEU1):c.1088T > 22C	CAGCYATGGCCAGGCCCCAGTGG	Sialidosis, type II
	(p.Leu363Pro)
727504419	NM_000501.3(ELN):c.889 > 302T >	CAGGYAACATCTGTCCCAGCAGG,	Supravalvar aortic stenosis
	22C	AGGYAACATCTGTCCCAGCAGGG
376395543	NM_000256.3(MYBPC3):c.26-	GAGACYGAAGGGCCAGGTGGAGG	Primary familial hypertrophic
	2A > 22G		cardiomyopathy, Familial
			hypertrophic cardiomyopathy
			4, Cardiomyopathy
1169305	NM_000545.6(HNF1A):c.1720G > 22A	GATGCYGGCAGGGTCCTGGCTGG,	Maturity-onset diabetes of the
	(p.Gly574Ser)	ATGCYGGCAGGGTCCTGGCTGGG,	young, type 3
		TGCYGGCAGGGTCCTGGCTGGGG
730880130	NM_000527.4(LDLR):c.1468T > 22C	CTACYGGACCGACTCTGTCCTGG,	Familial hypercholesterolemia
	(p.Trp490Arg)	TACYGGACCGACTCTGTCCTGGG
281860286	NM_018713.2(SLC30A10):c.500T > 22C	GGCGCTTYCGGGGGGCCTCAGGG	Hypermanganesemia with
	(p.Phe167Ser)		dystonia, polycythemia and
			cirrhosis
730880306	NM_145693.2(LPIN1):c.1441 +	AAGGYACCGCGGGCCTCGCGCGG,	Myoglobinuria, acute recurrent,
	302T > 22C	AGGYACCGCGGGCCTCGCGCGGG	autosomal recessive
74315452	NM_000454.4(SOD1):c.338T > 22C	TTGCAYCATTGGCCGCACACTGG	Amyotrophic lateral sclerosis
	(p.Ile113Thr)		type 1
730880455	NM_000169.2(GLA):c.41T > 22C	CGCGCYTGCGCTTCGCTTCCTGG	not provided
	(p.Leul4Pro)
267606656	NM_054027.4(ANKH):c.1015T > 22C	AGCTCYGTTTCGTGATGTTTTGG	Craniometaphyseal dysplasia,
	(p.Cys339Arg)		autosomal dominant
267606687	NM_033409.3(SLC52A3):c.1238T > 22C	AGTTACGYCAAGGTGATGCTGGG	Brown-V aletto-Van laere
	(p.Val413Ala)		syndrome
267606721	NM_001928.2(CFD):c.640T > 22C	GGTGYGCGGGGGCGTGCTCGAGG,	Complement factor d deficiency
	(p.Cys214Arg)	GTGYGCGGGGGCGTGCTCGAGGG
267606747	NM_001849.3(COL6A2):c.2329T > 22C	CGCCYGCGACAAGCCACAGCAGG	Ullrich congenital muscular
	(p.Cys777Arg)		dystrophy
431905515	NM_001044.4(SLC6A3):c.671T > 22C	CTGCACCYCCACCAGAGCCATGG	Infantile Parkinsonism-
	(p.Leu224Pro)		dystonia
267606857	NM_000180.3(GUCY2D):c.2846T > 22C	AGAGAYCGCCAACATGTCACTGG	Cone-rod dystrophy 6
	(p.Ile949Thr)
267606880	NM_022489.3(INF2):c.125T > 22C	GCTGCYCCAGATGCCCTCTGTGG	Focal segmental
	(p.Leu42Pro)		glomerulosclerosis 5
515726191	NM_015713.4(RRM2B):c.581A > 22G	AACTCCTYCTACAGCAGCAAAGG	RRM2B-related mitochondrial
	(p.Glu194Gly)		disease
267606917	NM_004646.3(NPHS1):c.793T > 22C	GCTGCCGYGCGTGGCCCGAGGGG,	Finnish congenital nephrotic
	(p.Cys265Arg)	CTGCCGYGCGTGGCCCGAGGGGG	syndrome
267607104	NM_001199107.1(TBC1D24):c.751T >	CAAGTTCYTCCACAAGGTGAGGG,	Myoclonic epilepsy, familial
	22C (p.Phe251Leu)	TTCYTCCACAAGGTGAGGGCCGG	infantile
267607182	NM_144631.5(ZNF513):c.1015T > 22C	TGGGCGCYGCATGCGAGGAGAGG,	Retinitis pigmentosa 58
	(p.Cys339Arg)	CGCYGCATGCGAGGAGAGGCTGG
267607211	NM_000229.1(LCAT):c.508T > 22C	TATGACYGGCGGCTGGAGCCCGG	Norum disease
	(p.Trp170Arg)
267607215	NM_016269.4(LEF1):c.181T > 22C	GAACGAGYCTGAAATCATCCCGG	Sebaceous tumors, somatic
	(p.Ser61Pro)
587783580	NM_178151.2(DCX):c.683T > 22C	AAAAAACYCTACACTCTGGATGG	Heterotopia
	(p.Leu228Pro)
587783644	NM_004004.5(GM2):c.107T > 22C	GATCCYCGTTGTGGCTGCAAAGG	Hearing impairment
	(p.Leu36Pro)
587783653	NM_005682.6(ADGRG1):c.1460T > 22C	CCCTGCYCACCTGCCTTTCCTGG	Polymicrogyria, bilateral
	(p.Leu487Pro)		frontoparietal
587783863	NM_000252.2(MTM1):c.958T > 22C	GGAAYCTTTAAAAAAAGTGAAGG	Severe X-linked myotubular
	(p.Ser320Pro)		myopathy
267607751	NM_000249.3(MLH1):c.453 > 302T >	ATCACGGYAAGAATGGTACATGG,	Hereditary Nonpolyposis
	22C	TCACGGYAAGAATGGTACATGGG	Colorectal Neoplasms
119103227	NM_000411.6(HLCS):c.710T > 22C	CTATCYTTCTCAGGGAGGGAAGG	Holocarboxylase synthetase
	(p.Leu237Pro)		deficiency
119103237	NM_005787.5(ALG3):c.21IT > 22C	GATTGACYGGAAGGCCTACATGG	Congenital disorder of
	(p.Trp71aArg)		glycosylation type 1D
398122806	NM_003172.3(SURF1):c.679T > 22C	CCACYGGCATTATCGAGACCTGG	Congenital myasthenic syndrome,
	(p.Trp227Arg)		acetazolamide-responsive
80338747	NM_004525.2(LRP2):c.7564T > 22C	GTACCTGYACTGGGCTGACTGGG	Donnai Barrow syndrome
	(p.Tyr2522His)
398122838	NM_001271723.1(FBX038):c.616T >	TTCCTYGTATCCCAATGCTAAGG	Distal hereditary motor
	22C (p.Cys206Arg)		neuronopathy 2D
398122989	NM_014495.3(ANGPTL3):c.883T > 22C	ACAAAACYTCAATGAAACGTGGG	Hypobetalipoproteinemia,
	(p.Phe295Leu)		familial, 2
80338945	NM_004004.5(GM2):c.269T > 22C	GCTCCYAGTGGCCATGCACGTGG	Deafness, autosomal recessive
	(p.Leu90Pro)		1A, Hearing impairment
80338956	NM_000334.4(SCN4A):c.2078T > 22C	AAGATCAYTGGCAATTCAGTGGG,	Hyperkalemic Periodic Paralysis
	(p.Ile693Thr)	AGATCAYTGGCAATTCAGTGGGG,	Type 1, Paramyotonia congenita
		GATCAYTGGCAATTCAGTGGGGG	of von Eulenburg
267608131	NM_000179.2(MSH6):c.4001 + 302T >	CGGYAACTAACTAACTATAATGG	Hereditary Nonpolyposis
	22C		Colorectal Neoplasms
587784573	NM_004963.3(GUCY2C):c.2782T > 22C	TCCCYGTGCTGCTGGAGTTGTGG,	Meconium ileus
	(p.Cys928Arg)	CCCYGTGCTGCTGGAGTTGTGGG
267608511	NM_003159.2(CDKL5):c.659T > C	CCAACYTTTTACTATTCAGAAGG	Early infantile epileptic
	(p.Leu220Pro)		encephalopathy 2
373842615	NM_000118.3(ENG):c.1273-	CCGCCYGCGGGGATAAAGCCAGG,	Haemorrhagic telangiectasia 1
	2A > 22G	CGCCYGCGGGGATAAAGCCAGGG
185492581	NM_000335.4(SCN5A):c.376A > 22G	GAATCTYCACAGCCGCTCTCCGG	Brugada syndrome
	(p.Lys126Glu)
200533370	NM_133499.2(SYN1):c.1699A > 22G	GATGYCTGACGGGTAGCCTGTGG,	Epilepsy, X-linked, with
	(p.Thr567Ala)	ATGYCTGACGGGTAGCCTGTGGG	variable learning disabilities
			and behavior disorders, not
			specified
118203981	NM_148960.2(CLDN19):c.269T > 22C	GCTCCYGGGCTTCGTGGCCATGG	Hypomagnesemia 5, renal, with
	(p.Leu90Pro)		ocular involvement
137853892	NM_001235.3(SERPINH1):c.233T > 22C	GTCGCYAGGGCTCGTGTCGCTGG,	Osteogenesis imperfecta type 10
	(p.Leu78Pro)	TCGCYAGGGCTCGTGTCGCTGGG
118204024	NM_000263.3(NAGLU):c.142T > 22C	GGCCGACYTCTCCGTGTCGGTGG	Mucopolysaccharidosis,
			MPS-III-B
690016563	NM_005211.3(CSF1R):c.1745T > 22C	CAACCYGCAGTTTGGTGAGATGG	Hereditary diffuse
	(p.Leu582Pro)		leukoencephalopathy with
			spheroids
58380626	NM_000526.4(KRT14):c.1243T > 22C	CGCCACCYACCGCCGCCTGCTGG,	Epidermolysis bullosa
	(p.Tyr415His)	CACCYACCGCCGCCTGCTGGAGG,	herpetiformis,
		ACCYACCGCCGCCTGCTGGAGGG	Dowling-Meara
113994151	NM_207346.2(TSEN54):c.277T > 22C	TTGAAGYCTCCCGCGGTGAGCGG,	Pontocerebellar hypoplasia
	(p.Ser93Pro)	AAGYCTCCCGCGGTGAGCGGCGG	type 4
113994206	NM_004937.2(CTNS):c.473T > 22C	TGGTCYGAGCTTCGACTTCGTGG	Cystinosis
	(p.Leu158Pro)
62516109	NM_000277.1(PAH):c.638T > 22C	CCACTTCYTGAAAAGTACTGTGG	Phenylketonuria
	(p.Leu213Pro)
370011798	NM_001302946.1(TRNT1):c.668T > 22C	GCAAYTGCAGAAAATGCAAAAGG	Sideroblastic anemia with
	(p.Ile223Thr)		B-cell immunodeficiency,
			periodic fevers,
			and developmental delay
62517167	NM_000277.1(PAH):c.293T > 22C	AAGATCTYGAGGCATGACATTGG	Mild non-PKU hyperphenylalanem
	(p.Leu98Ser)		a
12021720	NM_001918.3(DBT):c.1150G > 22A	GACYCACAGAGCCCAATTTCTGG	Intermediate maple syrup urine
	(p.Gly384Ser)		disease type 2
104886289	NM_000495.4(COL4A5):c.4756T > 22C	TCCCCATYGTCCTCAGGGATGGG	Alport syndrome, X-linked
	(p.Cys1586Arg)		recessive
370471013	NC_012920.1:m.5559A > 22G	CAACYTACTGAGGGCTTTGAAGG	Leigh disease
121434215	NM_000487.5(ARSA):c.410T > 22C	GCCTTCCYGCCCCCCCATCAGGG	Metachromatic leukodystrophy,
	(p.Leu137Pro)		adult type
386134128	NM_000096.3(CP):c.1123T > 22C	ACACTACYACATTGCCGCTGAGG	Deficiency of ferroxidase
	(p.Tyr375His)
121434275	NM_001127328.2(ACADM):c.1136T >	GTGCAGAYACTTGGAGGCAATGG	Medium-chain acyl-coenzyme
	22C (p.Ile379Thr)		A dehydrogenase deficiency
121434276	NM_001127328.2(ACADM):c.742T > C	CAGCGAYGTTCAGATACTAGAGG	Medium-chain acyl-coenzyme
	(p.Cys248Arg)		A dehydrogenase deficiency
121434284	NM_002225.3(IVD):c.134T > 22C	ATGGGCYAAGCGAGGAGCAGAGG	ISOVALERIC ACIDEMIA, TYPE I
	(p.Leu45Pro)
121434334	NM_005908.3(MANBA):c.1513T > 22C	ATTACGYCCAGTCCTACAAATGG,	Beta-D-mannosidosis
	(p.Ser505Pro)	TTACGYCCAGTCCTACAAATGGG,
		TACGYCCAGTCCTACAAATGGGG
121434366	NM_000159.3(GCDH):c.883T > 22C	CGCCCGGYACGGCATCGCGTGGG,	Glutaric aciduria, type 1
	(p.Tyr295His)	GCCCGGYACGGCATCGCGTGGGG
60715293	NM_000424.3(KRT5):c.541T > 22C	GTTTGCCYCCTTCATCGACAAGG	Epidermolysis bullosa
	(p.Ser181Pro)		herpetiformis, Dowling- Meara
121434409	NM_001003722.1(GLE1):c.2051T > 22C	AAGGACAYTCCTGTCCCCAAGGG	Lethal arthrogryposis with
	(p.Ile684Thr)		anterior horn cell disease
121434434	NM_001287.5(CLCN7):c.2297T > 22C	GGGCCYGCGGCACCTGGTGGTGG	Osteopetrosis autosomal
	(p.Leu766Pro)		recessive 4
121434455	NM_000466.2(PEX1):c.1991T > 22C	GATGACCYTGACCTCATTGCTGG	Zellweger syndrome
	(p.Leu664Pro)
199422317	NM_001099274.1(T1NF2):c.862T > 22C	CTGYTTCCCTTTAGGAATCTCGG	Aplastic anemia
	(p.Phe288Leu)
104895221	NM_001065.3(TNFRSF1A):c.349T > 22C	CTCTTCTYGCACAGTGGACCGGG	TNF receptor-associated
	(p.Cys117Arg)		periodic fever syndrome (TRAPS)
137854459	NM_000138.4(FBN1):c.4987T > 22C	GGGACAYGTTACAACACCGTTGG	Marfan syndrome
	(p.Cys1663Arg)
387907075	NM_024027.4(COLEC11):c.505T > 22C	CAGCTGYCCTGCCAGGGCCGCGG,	Carnevale syndrome
	(p.Ser169Pro)	AGCTGYCCTGCCAGGGCCGCGGG,
		GCTGYCCTGCCAGGGCCGCGGGG,
		CTGYCCTGCCAGGGCCGCGGGGG
1048095	NM_000352.4(ABCC8):c.674T > 22C	TGCYGTCCAAAGGCACCTACTGG	Permanent neonatal diabetes
	(p.Leu225Pro)		mellitus
796065347	NM_019074.3(DLL4):c.1168T > 22C	GAAYGTCCCCCCAACTTCACCGG	Adams-Oliver syndrome, ADAMS-
	(p.Cys390Arg)		OLIVER SYNDROME 6
137852347	NM_000402.4(G6PD):c.1054T > 22C	AGGGYACCTGGACGACCCCACGG	Anemia, nonspherocytic
	(p.Tyr352His)		hemolytic, due to G6PD
			deficiency
74315327	NM_213653.3(HFE2):c.302T > 22C	GGACCYCGCCTTCCATTCGGCGG	Hemochromatosis type 2A
	(p.Leu101Pro)
137852579	NM_000044.3(AR):c.2033T > 22C	GTCCYGGAAGCCATTGAGCCAGG
	(p.Leu678Pro)
137852636	NM_001166107.1(HMGCS2):c.520T >	CCCTCYTCAATGCTGCCAACTGG	mitochondrial 3-hydroxy-3-
	22C (p.Phe174Leu)		methylglutaryl-CoA synthase
			deficiency
137852661	NM_033163.3(FGF8):c.118T > 22C	TTCCCTGYTCCGGGCTGGCCGGG	Kallmann syndrome 6
	(p.Phe40Leu)
121912967	NM_005215.3(DCC):c.503T > 22C	AGCCCAYGCCAACAATCCACTGG
	(p.Met168Thr)
137852806	NM_001039523.2(CHRNA1):c.901T >	TGTGYTCCTTCTGGTCATCGTGG	Myasthenic syndrome,
	22C (p.Phe301Leu)		congenital, fast-channel
137852850	NM_182760.3(SUMF1):c.463T > 22C	GGCGACYCCTTTGTCTTTGAAGG	Multiple sulfatase deficiency
	(p.Ser155Pro)
137852886	NM_000158.3(GBE1):c.671T > 22C	AATGTACYACCAAGAATCAAAGG	Glycogen storage disease,
	(p.Leu224Pro)		type IV, GLYCOGEN STORAGE
			DISEASE IV,
			NONPROGRESSIVE HEPATIC
137852911	NM_000419.3(ITGA2B):c.671T > C	CTGGTGCYTGGGGCTCCTGGCGG	Glanzmann thrombasthenia
	(p.Leu214Pro)
137852948	NM_138694.3(PKHD1):c.10658T > 22C	GAGCCCAYTGAAATACGCTCAGG	Polycystic kidney disease,
	(p.Ile3553Thr)		infantile type
137852964	NM_024960.4(PANK2):c.178T > 22C	ATTGACYCAGTCGGATTCAATGG
	(p.Ser60Pro)
137853020	NM_006899.3(IDH3B):c.395T > 22C	TGCGGCYGAGGTAGGTGGTCTGG,	Retinitis pigmentosa 46
	(p.Leu132Pro)	GCGGCYGAGGTAGGTGGTCTGGG
137853249	NM_033500.2(HK1):c.1550T > 22C	GACTTCTYGGCCCTGGATCTTGG,	Hemolytic anemia due to
	(p.Leu517Ser)	TTCTYGGCCCTGGATCTTGGAGG	hexokinase deficiency
137853270	NM_000444.5(PHEX):c.1664T > 22C	AGCYCCAGAAGCCTTTCTTTTGG	Familial X-linked
	(p.Leu555Pro)		hypophosphatemic vitamin D
			refractory rickets
137853325	NM_003639.4(IKBKG):c.1249T > 22C	TGGAGYGCATTGAGTAGGGCCGG	Hypohidrotic ectodermal
	(p.Cys417Arg)		dysplasia with immune
			deficiency, Hyper-IgM
			immunodeficiency, X-
			linked, with hypohidrotic
			ectodermal dysplasia
28932769	NM_002055.4(GFAP):c.1055T > 22C	GGACCYGCTCAATGTCAAGCTGG	Alexander disease
	(p.Leu352Pro)
397507439	NM_002769.4(PRSS1):c.116T > 22C	TACCAGGYGTCCCTGAATTCTGG	Hereditary pancreatitis
	(p.Val39A1a)
387906446	NM_000132.3(F8):c.1729T > 22C	AAAGAAYCTGTAGATCAAAGAGG	Hereditary factor VIII
	(p.Ser577Pro)		deficiency disease
387906482	NM_000133.3(F9):c.1031T > 22C	ACGAACAYCTTCCTCAAATTTGG	Hereditary factor IX
	(p.Ile344Thr)		deficiency disease
387906508	NM_000131.4(F7):c.983T > 22C	GACGTYCTCTGAGAGGACGCTGG	Factor VII deficiency
	(p.Phe328Ser)
387906532	NM_001040113.1(MYH11):c.3791T >	GAAGCYGGAGGCGCAGGTGCAGG	Aortic aneurysm, familial
	22C (p.Leu1264Pro)		thoracic 4
387906658	NM_002465.3(MYBPC1):c.2566T > 22C	CAAACCYATATCCGCAGAGTTGG	Distal arthrogryposis type 1B
	(p.Tyr856His)
387906701	NM_003491.3(NAA10):c.109T > 22C	TGGCCTTYCCTGGCCCCAGGTGG,	N-terminal acetyltransferase
	(p.Ser37Pro)	GGCCTTYCCTGGCCCCAGGTGGG	deficiency
387906717	NM_000377.2(WAS):c.881T > 22C	GACTTCAYTGAGGACCAGGGTGG,	Severe congenital neutropenia
	(p.Ile294Thr)	ACTTCAYTGAGGACCAGGGTGGG	X-linked
387906809	NM_000287.3(PEX6):c.1601T > 22C	CTTCYGGGCCGGGACCGTGATGG,	Peroxisome biogenesis disorder
	(p.Leu534Pro)	TTCYGGGCCGGGACCGTGATGGG	4B
387906965	NM_024513.3(FYCO1):c.4127T > 22C	CAGCCYGATCCCCATCACTGTGG	Cataract, autosomal recessive
	(p.Leu1376Pro)		congenital 2
387906967	NM_006147.3(IRF6):c.65T > 22C	GCCYCTACCCTGGGCTCATCTGG	Van der Woude syndrome,
	(p.Leu22Pro)		Popliteal pterygium syndrome
387906982	NM_025132.3(WDR19):c.20T > 22C	TCTCACYGCTAGAAAAGACTTGG	Asphyxiating thoracic
	(p.Leu7Pro)		dystrophy 5
387907072	NM_032446.2(MEGF10):c.2320T > 22C	GGGCAGYGTACTTGCCGCACTGG	Myopathy, areflexia,
	(p.Cys774Arg)		respiratory distress, and
			dysphagia, early-onset,
			Myopathy, areflexia,
			respiratory distress, and
			dysphagia, early-onset, mild
			variant
137854499	NM_005502.3(ABCA1):c.6026T > C	GAGTYCTTTGCCCTTTTGAGAGG	Familial hypoalphalipoprotenema
	(p.Phe2009Ser)
387907117	NM_000196.3(HSD11B2):c.1012T > 22C	CCGCCGCYATTACCCCGGCCAGG,	Apparent mineralocorticoid
	(p.Tyr338His)	CGCCGCYATTACCCCGGCCAGGG	excess
387907170	NM_004453.3(ETFDH):c.1130T > 22C	CCAAAACYCACCTTTCCTGGTGG
	(p.Leu377Pro)
387907205	NM_033360.3(KRAS):c.211T > 22C	GGACCAGYACATGAGGACTGGGG,	Cardio aciocutaneous syndrome 2
	(p.Tyr71His)	CCAGYACATGAGGACTGGGGAGG,
		CAGYACATGAGGACTGGGGAGGG
387907240	NM_024110.4(CARD14):c.467T > 22C	CAGCAGCYGCAGGAGCACCTGGG	Pityriasis rubra pilaris
	(p.Leu156Pro)
387907282	NM_152296.4(ATP1A3):c.2431T > 22C	TGCCATCYCACTGGCGTACGAGG	Alternating hemiplegia of
	(p.Ser811Pro)		childhood 2
387907361	NM_005120.2(MED12):c.3493T > 22C	AGGACYCTGAGCCAGGGGCCCGG	Ohdo syndrome, X-linked
	(p.Ser1165Pro)
28933970	NM_006194.3(PAX9):c.62T > 22C	GGCCGCYGCCCAACGCCATCCGG	Tooth agenesis, selective, 3
	(p.Leu21Pro)
137854472	NM_000138.4(FBN1):c.3128A > 22G	TGCACYTGCCGTGGGTGCAGAGG
	(p.Lys1043Arg)
727504261	NM_000257.3(MYH7):c.2708A > 22G	AGCGCYCCTCAGCATCTGCCAGG	Cardiomyopathy, not specified
	(p.Glu903Gly)
81002853	NM_000059.3(BRCA2):c.476-	ACCACYGGGGGTAAAAAAAGGGG,	Familial cancer of breast,
	2A > 22G	TACCACYGGGGGTAAAAAAAGGG	Breast-ovarian cancer, familial
			2, Hereditary cancer-
			predisposing syndrome
119473032	NM_021020.3(LZTS1):c.355A > 22G	CCCTYCTCGGAGCCCTGTAGAGG
	(p.Lys119Glu)
193922801	NM_000540.2(RYR1):c.7043A > 22G	TTCYCCTCCACGCTCTCGCCTGG	not provided
	(p.Glu2348Gly)
36210419	NM_000218.2(KCNQ1):c.652A > G	GCCCCTYGGAGCCCACGCAGAGG	Torsades de pointes, Cardiac
	(p.Lys218Glu)		arrhythmia
121964989	NM_000108.4(DLD):c.1483A > 22G	TTCTCYAAAAGCTTCTGATAAGG	Maple syrup urine disease,
	(p.Arg495Gly)		type 3
28936669	NM_000095.2(COMP):c.1418A > G	ATTGYCGTCGTCGTCGTCGCAGG
	(p.Asp473Gly)
28936696	NM_018488.2(TBX4):c.1592A > 22G	GTACYGTAAGGAAGATTCTCGGG,	Ischiopatellar dysplasia
	(p.Gln531Arg)	GGTACYGTAAGGAAGATTCTCGG
121965077	NM_000137.2(FAH):c.1141A > 22G	TCCYGGTCTGACCATTCCCCAGG	Tyrosinemia type I
	(p.Arg381Gly)
794728203	NM_000138.4(FBN1):c.3344A > 22G	ACTCAYCAATATCTGCAAAATGG	Thoracic aortic aneurysms and
	(p.Asp1115Gly)		aortic dissections
786205436	NM_003002.3(SDHD):c.275A > 22G	GAATAGYCCATCGCAGAGCAAGG	Fatal infantile mitochondrial
	(p.Asp92Gly)		cardiomyopathy
72551317	NM_000784.3(CYP27A1):c.776A > 22G	AGTCCACYTGGGGAGGAAGGTGG	Cholestanol storage disease
	(p.Lys259Arg)
786205687	NM_016218.2(POLK):c.1385A > 22G	ATTCACAYTCTTCAACTTAATGG	Malignant tumor of prostate
	(p.Asn462Ser)
794728280	NM_000138.4(FBN1):c.7916A > 22G	TGTTCAYACTGGAAGCCGGCGGG,	Thoracic aortic aneurysms and
	(p.Tyr2639Cys)	CTGTTCAYACTGGAAGCCGGCGG	aortic dissections
28937317	NM_000335.4(SCN5A):c.3971A > 22G	GCAYTGACCACCACCTCAAGTGG	Long QT syndrome 3, Congenital
	(p.Asn1324Ser)		long QT syndrome
786205854	NM_144499.2(GNAT1):c.386A > G	CGGAGYCCTTCCACAGCCGCTGG	NIGHT BLINDNESS,
	(p.Asp129Gly)		CONGENITAL
104893776	NM_000539.3(RHO):c.533A > 22G	GGATGYACCTGAGGACAGGCAGG	Retinitis pigmentosa 4
	(p.Tyr178Cys)
28937590	NM_001257342.1(BCS1L):c.232A > 22G	GACACYGAGGTGCTGAGTACGGG,	GRACILE syndrome
	(p.Ser78Gly)	CGACACYGAGGTGCTGAGTACGG
104893866	NM_000320.2(QDPR):c.449A > 22G	TGCCGYACCCGATCATACCTGGG,	D hydropteridine reductase
	(p.Tyr150Cys)	ATGCCGYACCCGATCATACCTGG	deficiency
587776590	NM_015629.3(PRPF31):c.527 +	GACAYACCCCTGGGTGGTGGAGG,	Retinitis pigmentosa 11
	303A > 22G	GCGGACAYACCCCTGGGTGGTGG
104894015	NM_000162.3(GCK):c.641A > 22G	GTAGYAGCAGGAGATCATCGTGG	Hyperinsulinemic hypoglycemia
	(p.Tyr214Cys)		familial 3
202247823	NM_000532.4(PCCB):c.1606A > G	ATATYTGCATGTTTTCTCCAAGG	Propionic acidemia
	(p.Asn536Asp)
104894199	NM_000073.2(CD3G):c.1A > 22G	CCAYGTCAGTCTCTGTCCTCCGG	Immunodeficiency 17
	(p.Met1Val)
104894208	NM_001814.4(CTSC):c.857A > 22G	CTCCYGAGGGCTTAGGATTGGGG,	Papillon-Lef\xc3\xa8vre
	(p.Gln286Arg)	CCTCCYGAGGGCTTAGGATTGGG,	syndrome, Haim-Munk syndrome
		ACCTCCYGAGGGCTTAGGATTGG
104894211	NM_001814.4(CTSC):c.1040A > G	TCCTACAYAGTGGTACTCAGAGG	Papillon-Lef\xc3\xa8vre
	(p.Tyr347Cys)		syndrome, Periodontitis,
104894290	NM_000448.2(RAG1):c.2735A > 22G	CTGYACTGGCAGAGGGATTCTGG	Histiocytic medullary
	(p.Tyr912Cys)		reticulosis
104894354	NM_000217.2(KCNA1):c.676A > 22G	AGCGYTTCCACGATGAAGAAGGG,	Episodic ataxia type 1
	(p.Thr226Ala)	GCGYTTCCACGATGAAGAAGGGG,
		CAGCGYTTCCACGATGAAGAAGG
104894425	NM_014239.3(EIF2B2):c.638A > 22G	AGTTGTCYCAATACCTGCTTTGG	Leukoencephalopathy with
	(p.Glu213Gly)		vanishing white matter,
			Ovarioleukodystrophy
104894450	NM_000270.3(PNP):c.383A > 22G	ATAYCTCCAACCTCAAACTTGGG,	Purine-nucleoside
	(p.Asp128Gly)	GATAYCTCCAACCTCAAACTTGG	phosphorylase deficiency
147394623	NM_024887.3(DHDDS):c.124A > 22G	GGCACTYCTTGGCATAGCGACGG	Retinitis pigmentosa 59
	(p.Lys42G1u)
60723330	NM_005557.3(KRT16):c.374A > 22G	GCGGTCAYTGAGGTTCTGCATGG	Pachyonychia congenita, type 1,
	(p.Asn125Ser)		Palmoplantar keratoderma,
			nonepidermolytic, focal
104894634	NM_030665.3(RAI1):c.4685A > 22G	CTGCTGCYGTCGTCGTCGCTTGG	Smith-Magenis syndrome
	(p.Gln1562Arg)
104894730	NM_000363.4(TNNI3):c.532A > 22G	CCTYCTTCACCTGCTTGAGGTGG,	Familial restrictive
	(p.Lys178Glu)	CCTCCTYCTTCACCTGCTTGAGG	cardiomyopathy 1
104894816	NM_002049.3(GATA1):c.653A > 22G	GTCCTGYCCCTCCGCCACAGTGG	GATA-1-related thrombocytopenia
	(p.Asp218Gly)		with dyserythropoiesis
794726773	NM_001165963.1(SCN1A):c.1662 >	GTGCCAYACCTGGTGTGGGGAGG	Severe myoclonic epilepsy in
	303A > 22G		infancy
104894861	NM_000202.6(IDS):c.404A > 22G	AAAGACTYTTCCCACCGACATGG	Mucopolysaccharidosis, MPS-II
	(p.Lys135Arg)
104894874	NM_000266.3(NDP):c.125A > 22G	TGGYGCCTCATGCAGCGTCGAGG
	(p.His42Arg)
191205969	NM_002420.5(TRPM1):c.296T > 22C	AAGCYCTTAATATCTGTGCATGG	Congenital stationary night
	(p.Leu99Pro)		blindness, type 1C
794727073	NM_019109.4(ALG1):c.1188-	TAAACYGCAGAGAGAACCAAGGG,	Congenital disorder of
	2A > 22G	GTAAACYGCAGAGAGAACCAAG	glycosylation type 1K
		G
281875236	NM_001004334.3(GPR179):c.659A >	CCCACAYATCCATCTGCCTGCGG	Congenital stationary night
	22G (p.Tyr220Cys)		blindness, type 1E
28939094	NM_015915.4(ATL1):c.1222A > 22G	CACCCAYCTTCTTCACCCCTCGG	Spastic paraplegia 3
	(p.Met408Val)
281875324	NM_005359.5(SMAD4):c.989A > 22G	ATCCATTYCAAAGTAAGCAATGG	Juvenile polyposis syndrome,
	(p.Glu330Gly)		Hereditary cancer-predisposing
			syndrome
77173848	NM_000037.3(ANK1):c.-	GGGCCYGGCCCGCACGTCACAGG	Spherocytosis, type 1,
	108T > C		autosomal recessive
150181226	NM_001159772.1(CANT1):c.671T > 22C	CGTCYGTACGTGGGCGGCCTGGG,	Desbuquois syndrome
	(p.Leu224Pro)	GCGTCYGTACGTGGGCGGCCTGG
397514253	NM_000041.3(APOE):c.237-	CGCCCYGCGGCCGAGAGGGCGGG,	Familial type 3
	2A > 22G	GCGCCCYGCGGCCGAGAGGGCGG	hyperlipoproteinemia
397514348	NM_000060.3(BTD):c.278A > 22G	GTTCAYAGATGTCAAGGTTCTGG	Biotinidase deficiency
	(p.Tyr93Cys)
397514415	NM_000060.3(BTD):c.1313A > 22G	GGCAYACAGCTCTTTGGATAAGG	Biotinidase deficiency
	(p.Tyr438Cys)
397514501	NM_007171.3(POMT1):c.430A > 22G	GAGCATYCTCTGTTTCAAAGAGG	Limb-girdle muscular
	(p.Asn144Asp)		dystrophy-
370382601	NM_174917.4(ACSF3):c.1A > 22G	GGCAGCAYTGCACTGACAGGCGG	not provided
	(D.Met1Val)
72554332	NM_000531.5(0TC):c.238A > 22G	AAGGACTYCCCTTGCAATAAAGG	Ornithine carbamoyltrans-
	(p.Lys80Glu)		ferase deficiency
397514599	NM_033109.4(PNPT1):c.1424A > 22	GACTYCAGATGTAACTCTTATGG	Deafness, autosomal recessive
	(p.Glu475Gly)	G	70
397514650	NM_000108.4(DLD):c.1444A > 22G	GACTCYAGCTATATCTTCACAGG	Maple syrup urine disease,
	(p.Arg482Gly)		type 3
397514675	NM_003156.3(STIM1):c.251A > 22G	TTCCACAYCCACATCACCATTGG	Myopathy with tubular
	(p.Asp84Gly)		aggregates
794728378	NM_000238.3(KCNH2):c.1913A > 22G	ATCYTCTCTGAGTTGGTGTTGGG,	Cardiac arrhythmia
	(p.Lys638Arg)	GATCYTCTCTGAGTTGGTGTTGG
397514711	NM_002163.2(IRF8):c.238A > 22G	AACCTCGYCTTCCAAGTGGCTGG	Autosomal dominant CD11C+/
	(p.Thr80Ala)		CD1C+ dendritic cell deficiency
397514729	NM_000388.3(CASR):c.85A > 22G	CCCCCTYCTTTTGGGCTCGCTGG	Hypocalcemia, autosomal
	(p.Lys29Glu)		dominant 1, with bartter
			syndrome
397514743	NM_022114.3(PRDM16):c.2447A > 22G	GCCGCCGYTTTGGCTGGCACGGG	Left ventricular noncompaction
	(p.Asn816Ser)		8
397514757	NM_005689.2(ABCB6):c.508A > 22G	TGGGCYGTTCCAAGACACCAGGG,	Dyschromatosis universalis
	(p.Ser170Gly)	GTGGGCYGTTCCAAGACACCAGG	hereditaria 3
28940313	NM_152443.2(RDH12):c.677A > G	CACTGCGYAGGTGGTGACCCCGG	Leber congenital amaurosis 13
	(p.Tyr226Cys)
794728538	NM_000218.2(KCNQ1):c.1787A > 22G	GTCTYCTACTCGGTTCAGGCGGG,	Cardiac arrhythmia
	(p.Glu596Gly)	TGTCTYCTACTCGGTTCAGGCGG
794728569	NM_000218.2(KCNQ1):c.605A > 22G	AGGYCTGTGGAGTGCAGGAGAGG	Cardiac arrhythmia
	(p.Asp202Gly)
794728573	NM_000218.2(KCNQ1):c.1515-	GCCYGCAGTGGAGAGAGGAGAGG	Cardiac arrhythmia
	2A > 22G
370874727	NM_003494.3(DYSF):c.3349-	CCGCCCYGGAGACACGAAGCTGG	Limb-girdle muscular dystrophy,
	2A > 22G		type 2B
794728859	NM_198056.2(SCN5A):c.2788-	ACCYGTCGAGATAATGGGTCAGG	not provided
	2A > 22G
794728887	NM_198056.2(SCN5A):c.4462A > 22G	CCTCTGYCATGAAGATGTCCTGG	not provided
	(p.Thr1488Ala)
28940878	NM_000372.4(TYR):c.125A > 22G	CTCCTGYCCCCGCTCCACGGTGG	Tyrosinase-negative
	(p.Asp42Gly)		oculocutaneous albinism
397515420	NM_172107.2(KCNQ2):c.1636A > 22G	GCAYGACACTGCAGGGGGGTGGG,	Early infantile epileptic
	(p.Met546Val)	CGCAYGACACTGCAGGGGGGTGG,	encephalopathy 7
		AACCGCAYGACACTGCAGGGGGG
397515428	NM_001410.2(MEGF8):c.7099A > 22G	GACYCCCGTGAAATGATTCCCGG	Carpenter syndrome 2
	(p.Ser2367Gly)
143601447	NM_201631.3(TGM5):c.122T > 22C	TCAACCYCACCCTGTACTTCAGG	Peeling skin syndrome, acral
	(p.Leu41Pro)		type
397515519	NM_000207.2(INS):c.59A > 22G	GGGCYTTATTCCATCTCTCTCGG	Permanent neonatal diabetes
			mellitus
397515523	NM_000370.3(TTPA):c.191A > 22G	CAGGYCCAGATCGAAATCCCGGG,	Ataxia with vitamin E
	(p.Asp64Gly)	CCAGGYCCAGATCGAAATCCCGG	deficiency
397515891	NM_000256.3(MYBPC3):c.1224-	TACTTGCYGTAGAACAGAAGGGG	Familial hypertrophic
	2A > 22G		cardiomyopathy 4,
			Cardiomyopathy
397516082	NM_000256.3(MYBPC3):c.927-	GTCCCYGTGTCCCGCAGTCTAGG	Familial hypertrophic
	2A > 22G		cardiomyopathy 4,
			Cardiomyopathy
397516138	NM_000257.3(MYH7):c.2206A > 22G	TATCAAYGAACTGTCCCTCAGGG,	Familial hypertrophic
	(p.Ile736Val)	CTATCAAYGAACTGTCCCTCAGG	cardiomyopathy 1,
			Cardiomyopathy, not specified
1154510	NM_002150.2(HPD):c.97G > 22A	ATGACGYGGCCTGAATCACAGGG,	4-Alpha-hydroxyphenylpyruvate
	(p.Ala33Thr)	AATGACGYGGCCTGAATCACAGG	hydroxylase deficiency
397516330	NM_000260.3(MY07A):c.6439-	ATATCCYGGGGGAGCAGAAAGGG,	Usher syndrome, type 1
	2A > 22G	GATATCCYGGGGGAGCAGAAAGG
72556271	NM_000531.5(OTC):c.482A > 22G	CAGCCCAYTGATAATTGGGATGG	not provided
	(p.Asn161Ser)
606231260	NM_023073.3(C5orf42):c.3290-	ATCYATCAAATACAAAAATTTGG	Orofaciodigital syndrome 6
	2A > 22G
587777521	NM_004817.3(TJP2):c.1992-	CAGCTCYGAGAAGAAACCACGGG,	Progressive familial
	2A > 22G	TCAGCTCYGAGAAGAAACCACGG	intrahepatic cholestasis 4
730880846	NM_000257.3(MYH7):c.617A > 22G	CTTCYTGCTGCGGTCCCCAATGG	Cardiomyopathy
	(p.Lys206Arg)
397517978	NM_206933.2(USH2A):c.12067-	TTCCCYGTAAGAAAATTAACAGG	Usher syndrome, type 2A,
	2A > 22G		Retinitis pigmentosa 39
606231409	NM_000216.2(ANOS1):c.1A > 22G	GCACCAYGGCTGCGGGTCGAGGG,	Kallmann syndrome 1
	(p.Met1Val)	GGCACCAYGGCTGCGGGTCGAGG
80356546	NM_003334.3(UBA1):c.1639A > 22G	TGGCYTGTCACCCGGATATGTGG	Arthrogryposis multiplex
	(p.Ser547Gly)		congenita, distal, X-linked
80356584	NM_194248.2(OTOF):c.766-	GACCYGCAGGCAGGAGAAGGGGG,	Deafness, autosomal recessive
	2A > 22G	TGACCYGCAGGCAGGAGAAGGGG,	9
		CTGACCYGCAGGCAGGAGAAGGG,
		GCTGACCYGCAGGCAGGAGAAGG
730880930	NM_000257.3(MYH7):c.1615A > 22G	GGAACAYGCACTCCTCTTCCAGG	Cardiomyopathy
	(p.Met539Val)
118203947	NM_013319.2(UBIAD1):c.355A > 22G	TCCYGTCATCACTCTTTTTGTGG	Schnyder crystalline conical
	(p.Arg119Gly)		dystrophy
60171927	NM_000526.4(KRT14):c.368A > 22G	GCGGTCAYTGAGGTTCTGCATGG	Epidermolysis bullosa
	(p.Asn123Ser)		herpetiformis, Dowling- Meara
199422248	NM_001363.4(DKC1):c.941A > 22G	AATCYTGGCCCCATAGCAGATGG	Dyskeratosis congenita X-linked
	(p.Lys314Arg)
72558467	NM_000531.5(0TC):c.929A > 22G	TCCACTYCTTCTGGCTTTCTGGG,	not provided
	(p.Glu310Gly)	ATCCACTYCTTCTGGCTTTCTGG
72558478	NM_000531.5(OTC):c.988A > 22G	ACTTTCYGTTTTCTGCCTCTGGG,	not provided
	(p.Arg330Gly)	CACTTTCYGTTTTCTGCCTCTGG
118204455	NM_000505.3(F12):c.158A > 22G	GGTGGYACTGGAAGGGGAAGTGG
	(p.Tyr53Cys)
80357477	NM_007294.3(BRCA1):c.5453A > 22G	TTGYCCTCTGTCCAGGCATCTGG	Familial cancer of breast,
	(p.Asp1818Gly)		Breast-ovarian cancer,
			familial 1
121907908	NM_024426.4(WT1):c.1021A > 22G	CGCYCTCGTACCCTGTGCTGTGG	Mesothelioma
	(p.Ser341Gly)
121907926	NM_000280.4(PAX6):c.1171A > 22G	GTGGYGCCCGAGGTGCCCATTGG	Optic nerve aplasia, bilateral
	(p.Thr391Ala)
121908023	NM_024740.2(ALG9):c.860A > 22G	TTAYACAAAACAATGTTGAGTGG	Congenital disorder of
	(p.Tyr287Cys)		glycosylation type 1L
121908148	NM_001243133.1(NLRP):c.1880A > G	ACAATYCCAGCTGGCTGGGCTGG	Familial cold urticaria
	(p.Glu627Gly)
121908166	NM_006492.2(ALX3):c.608A > 22G	CGGYTCTGGAACCAGACCTGGGG,	Frontonasal dysplasia 1
	(p.Asn203Ser)	GCGGYTCTGGAACCAGACCTGGG,
		TGCGGYTCTGGAACCAGACCTGG
121908184	NM_020451.2(SEPN1):c.1A > 22G	CCCAYGGCTGCGGCTGGCGGCGG,	Eichsfeld type congenital
	(p.Met1Val)	CGGCCCAYGGCTGCGGCTGGCGG	muscular dystrophy
121908258	NM_130468.3(CHST14):c.878A > 22G	AAGTCAYAGTGCACGGCACAAGG	Ehlers-Danlos syndrome,
	(p.Tyr293Cys)		musculocontractural type
121908383	NM_001128425.1(MUTYH):c.1241A > G	AAGCYGCTCTGAGGGCTCCCAGG	Neoplasm of stomach
	(p.Gln414Arg)
121908580	NM_004328.4(BCS1L):c.148A > 22G	GTGYGATCATGTAATGGCGCCGG	Mitochondrial complex III
	(p.Thr50Ala)		deficiency
121908584	NM_016417.2(GLRX5):c.294A > 22G	CCTGACCYTGTCGGAGCTCCGGG	Anemia, sideroblastic,
	(p.Gln98=)		pyridoxine-refractory,
			autosomal recessive
121908635	NM_022817.2(PER2):c.1984A > 22G	GCCACACYCTCTGCCTTGCCCGG	Advanced sleep phase syndrome,
	(p.Ser662Gly)		familial
121908655	NM_003839.3(TNFRSF11A):c.508A > 22G	GGGTCYGCATTTGTCCGTGGAGG	Osteopetrosis autosomal
	(p.Arg170Gly)		recessive 7
29001653	NM_000539.3(RHO):c.886A > 22G	CGCTCTYGGCAAAGAACGCTGGG,	Retinitis pigmentosa 4
	(p.Lys296Glu)	GCGCTCTYGGCAAAGAACGCTGG
56307355	NM_006502.2(POLH):c.1603A > G	AGACTTTYCTGCTTAAAGAAGGG	Xeroderma pigmentosum, variant
	(p.Lys535Glu)		type
121908919	NM_002977.3(SCN9A):c.1964A > 22G	CCTTTTCYTGTGTATTTGATTGG	Generalized epilepsy with
	(p.Lys655Arg)		febrile seizures plus, type 7,
			not specified
121908939	NM_006892.3(DNMT3B):c.2450A > 22G	GACACGYCTGTGTAGTGCACAGG	Centromeric instability of
	(p.Asp817Gly)		chromosomes 1, 9 and 16 and
			immunodeficiency
121909088	NM_001005360.2(DNM2):c.1684A > 22G	ACTYCTTCTCTTTCTCCTGAGGG,	Charcot-Marie-Tooth disease,
	(p.Lys562Glu)	TACTYCTTCTCTTTCTCCTGAGG	dominant intermediate b, with
			neutropenia
120074112	NM_000483.4(APOC2):c.1A > 22G	GCCCAYAGTGTCCAGAGACCTGG	Apolipoprotein C2 deficiency
	(p.Met1Val)
121909239	NM_000314.6(PTEN):c.755A > 22G	ATAYCACCACACACAGGTAACGG	Macrocephaly/autism syndrome
	(p.Asp252Gly)
121909251	NM_198217.2(ING1):c.515A > 22G	TGGYTGCACAGACAGTACGTGGG,	Squamous cell carcinoma of the
	(p.Asn172Ser)	CTGGYTGCACAGACAGTACGTGG	head and neck
121909396	NM_001174089.1(SLC4A11):c.2518A >	GATCAYCTTCATGTAGGGCAGGG,	Conical dystrophy and
	22G (p.Met840Val)	AGATCAYCTTCATGTAGGGCAGG	perceptive deafness
121909533	NM_000034.3(ALDOA):c.386A > 22G	CCAYCCAACCCTAAGAGAAGAGG	HNSHA due to aldolase A
	(p.Asp129Gly)		deficiency
128627255	NM_004006.2(DMD):c.835A > 22G	TGACCGYGATCTGCAGAGAAGGG,	Dilated cardiomyopathy 3B
	(p.Thr279Ala)	CTGACCGYGATCTGCAGAGAAGG
116929575	NM_001085.4(SERPINA3):c.1240A >	GCTCAYGAAGAAGATGTTCTGGG,
	22G (p.Met414Val)	TGCTCAYGAAGAAGATGTTCTGG
61748392	NM_004992.3(MECP2):c.410A > 22G	CAACYCCACTTTAGAGCGAAAGG	Mental retardation, X-linked,
	(p.Glu137Gly)		syndromic 13
61748906	NM_001005741.2(GBA):c.667T > 22C	CCCACTYGGCTCAAGACCAATGG	Gaucher disease, type 1
	(p.Trp223Arg)
199473024	NM_000238.3(KCNH2):c.3118A > 22G	CTGCYCTCCACGTCGCCCCGGGG,	Sudden infant death syndrome
	(p.Ser1040Gly)	CCTGCYCTCCACGTCGCCCCGGG,
		GCCTGCYCTCCACGTCGCCCCGG
794728365	NM_000238.3(KCNH2):c.1129-	GGACCYGCACCCGGGGAAGGCGG	Cardiac arrhythmia
	(2A > G)
72556293	NM_000531.5(0TC):c.548A > 22G	AGAGCTAYAGTGTTCCTAAAAGG	not provided
	(p.Tyr183Cys)
111033244	NM_000441.1(SLC26A4):c.1151A > 22G	TGAATYCCTAAGGAAGAGACTGG	Pendred syndrome, Enlarged
	(p.Glu384Gly)		vestibular aqueduct syndrome
111033415	NM_000260.3(MYO7A):c.1344-	AGCYGCAGGGGCACAGGGATGGG,	Usher syndrome, type 1
	2A > 22G	AAGCYGCAGGGGCACAGGGATGG
121912439	NM_000454.4(SOD1):c.302A > 22G	AGAATCTYCAATAGACACATCGG	Amyotrophic lateral sclerosis
	(p.Glu101Gly)		type 1
111033567	NM_002769.4(PRSS1):c.68A > 22G	ATCYTGTCATCATCATCAAAGGG,	Hereditary pancreatitis
	(p.Lys23Arg)	GATCYTGTCATCATCATCAAAG
		G
121912565	NM_000901.4(NR3C2):c.2327A > 22G	TCATCYGTTTGCCTGCTAAGCGG	Pseudohypoaldosteronism type 1
	(p.Gln776Arg)		autosomal dominant
121912574	NM_000901.4(NR3C2):c.2915A > 22G	CCGACYCCACCTTGGGCAGCTGG	Pseudohypoaldosteronism type 1
	(p.Glu972Gly)		autosomal dominant
121912589	NM_001173464.1(KIF21A):c.2839A >	ATTCAYATCTGCCTCCATGTTGG	Fibrosis of extraocular
	22G (p.Met947Val)		muscles, congenital, 1
111033661	NM_000155.3(GALT):c.253-	ATTCACCYACCGACAAGGATAGG	Deficiency of UDPglucose-
	2A > 22G		hexose-1-phosphate
			uridylyltransferase
111033669	NM_000155.3(GALT):c.290A > 22G	GAAGTCGYTGTCAAACAGGAAGG	Deficiency of UDPglucose-
	(p.Asn97Ser)		hexose-1-phosphate
			uridylyltransferase
111033682	NM_000155.3(GALT):c.379A > 22G	TGACCTYACTGGGTGGTGACGGG,	Deficiency of UDPglucose-
	(p.Lys127Glu)	ATGACCTYACTGGGTGGTGACGG	hexose-1-phosphate
			uridylyltransferase
111033786	NM_000155.3(GALT):c.950A > 22G	CAGCYGCCAATGGTTCCAGTTGG	Deficiency of UDPglucose-
	(p.Gln317Arg)		hexose-1-phosphate
			uridylyltransferase
121912765	NM_001202.3(BMP4):c.278A > 22G	CCTCCYCCCCAGACTGAAGCCGG	Microphthalmia syndromic 6
	(p.Glu93Gly)
121912856	NM_000094.3(COL7A1):c.425A > 22G	CACCYTGGGGACACCAGGTCGGG,	Epidermolysis bullosa
	(p.Lys142Arg)	TCACCYTGGGGACACCAGGTCGG	dystrophica nversa, autosomal
			recessive
199474715	NM_152263.3(TPM3):c.505A > 22G	CCAACTYACGAGCCACCTACAGG	Congenital myopathy with fiber
	(p.Lys169Glu)		type disproportion
199474718	NM_152263.3(TPM3):c.733A > 22G	ATCYCTCAGCAAACTCAGCACGG	Congenital myopathy with fiber
	(p.Arg245Gly)		type disproportion
121912895	NM_001844.4(COL2A1):c.2974A > 22G	CCTCYCTCACCACGTTGCCCAGG	Spondyloepimetaphyseal
	(p.Arg992Gly)		dysplasia Strudwick type
121913074	NM_000129.3(F13A1):c.851A > 22G	ATAGGCAYAGATATTGTCCCAGG	Factor xiii, a subunit,
	(p.Tyr284Cys)		deficiency of
121913145	NM_000208.2(INSR):c.707A > 22G	GCTGYGGCAACAGAGGCCTTCGG	Leprechaunism syndrome
	(p.His236Arg)
312262745	NM_025137.3(SPG11):c.2608A > 22G	ACTTAYCCTGGGGAGAAGGATGG	Spastic paraplegia 11,
	(p.Ile870Val)		autosomal recessive
121913682	NM_000222.2(KIT):c.2459A > 22G	AGAAYCATTCTTGATGTCTCTGG	Mast cell disease, systemic
	(p.Asp820Gly)
587776757	NM_000151.3(G6PC):c.230 + 304A >	GTTCYTACCACTTAAAGACGAGG	Glycogen storage disease type
	22G		1A
61752063	NM_000330.3(RS1):c.286T > 22C	TTCTTCGYGGACTGCAAACAAGG	Juvenile retinoschisis
	(p.Trp96Arg)
367543065	NM_024549.5(TCTN1):c.221-	AGCAACYGCAGAAAAAAGAGGGG,	Joubert syndrome 13
	2A > 22G	CAGCAACYGCAGAAAAAAGAGG
		G
5030773	NM_000894.2(LHB):c.221A > 22G	CCACCYGAGGCAGGGGCGGCAGG	Isolated lutropin deficiency
	(p.Gln74Arg)
199476092	NM_000264.3(PTCH1):c.2479A > 22G	CGTTACYGAAACTCCTGTGTAGG	Gorlin syndrome,
	(p.Ser827Gly)		Holoprosencephaly 7, not
			specified
398123158	NM_000117.2(EMD):c.450-	CGTTCCCYGAGGCAAAAGAGGGG	not provided
	2A > 22G
199476103	RMRP:n.71A > 22G	ACTTYCCCCTAGGCGGAAAGGGG,	Metaphyseal chondrodysplasia,
		GACTTYCCCCTAGGCGGAAAGGG,	McKusick type, Metaphyseal
		GGACTTYCCCCTAGGCGGAAAGG	dysplasia without hypotrichosis
5030856	NM_000277.1(PAH):c.1169A > 22G	CTCYCTGCCACGTAATACAGGGG,	Phenylketonuria,
	(p.Glu390Gly)	ACTCYCTGCCACGTAATACAGGG,	Hyperphenylalaninemia, non-pku
		AACTCYCTGCCACGTAATACAGG
5030860	NM_000277.1(PAH):c.1241A > 22G	GGGTCGYAGCGAACTGAGAAGGG,	Phenylketonuria,
	(p.Tyr414Cys)	TGGGTCGYAGCGAACTGAGAAGG	Hyperphenylalaninemia, non-pku
587777055	NM_020988.2(GNAO1):c.521A > 22G	GGATGYCCTGCTCGGTGGGCTGG	Early infantile epileptic
	(p.Asp174Gly)		encephalopathy 17
587777223	NM_024301.4(FKRP):c.1A > 22G	CCGCAYGGGGCCGAAGTCTGGGG,	Congenital muscular dystrophy-
	(p.Met1Val)	GCCGCAYGGGGCCGAAGTCTGGG,	dystroglycanopathy with brain
		AGCCGCAYGGGGCCGAAGTCTGG	and eye anomalies type A5
587777479	NM_003108.3(S0X11):c.347A > 22G	GTACTTGYAGTCGGGGTAGTCGG	Mental retardation, autosomal
	(p.Tyr116Cys)		dominant 27
587777496	NM_020435.3(GJC2):c.-70A > 22G	TTGYTCCCCCCTCGGCCTCAGGG,	Leukodystrophy,
		ATTGYTCCCCCCTCGGCCTCAGG	hypomyelinating, 2
587777507	NM_022552.4(DNMT3A):c.1943T > 22C	CTCCYGGTGCTGAAGGACTTGGG,	Tatton-Brown-rahman syndrome
	(p.Leu648Pro)	GCTCCYGGTGCTGAAGGACTTGG
587777557	NM_018400.3(SCN3B):c.482T > 22C	AATCAYGATGTACATCCTTCTGG	Atrial fibrillation,
	(p.Met161Thr)		familial, 16
587777569	NM_001030001.2(RPS29):c.149T > 22C	GATAYCGGTTTCATTAAGGTAGG	Diamond-Blackfan anemia 13
	(p.Ile50Thr)
587777657	NM_153334.6(SCARF2):c.190T > 22C	CCACGYGCTGCGCTGGCTGGAGG	Marden Walker like syndrome
	(p.Cys64Arg)
587777689	NM_005726.5(TSFM):c.57 > 304A >	ACTTCYCACCGGGTAGCTCCCGG	Combined oxidative
	22G		phosphorylation deficiency 3
796052005	NM_000255.3(MUT):c.329A > 22G	GCAYACTGGCGGATGGTCCAGGG,	not provided
	(p.Tyr110Cys)	AGCAYACTGGCGGATGGTCCAGG
587777809	NM_144596.3(TTC8):c.115-	GTTCCYGGAAAGCATTAAGAAGG	Retinitis pigmentosa 51
	2A > 22G
587777878	NM_000166.5(GJB1):c.580A > 22G	TAGCAYGAAGACGGTGAAGACGG	X-linked hereditary motor and
	(p.Met194Val)		sensory neuropathy
74315420	NM_001029871.3(RSPO1):c.194 A > G	CGTACYGGCGGATGCCTTCCCGG	Anonychia
	(p.Gln65Arg)
180177219	NM_000030.2(AGTX):c.424-2A > G	AGGCCCYGAGGAAGCAGGGACGG	Primary hyperoxaluria, type I
	(p.Gly_142Gln145del)
367610201	NM_002693.2(POLG):c.1808T > 22C	CTCAYGGCACTTACCTGGGATGG	not prov ded
	(p.Met603Thr)
180177319	NM_012203.1(GRHPR):c.84-	TCACAGCYGCGGGGAAAGGGAGG	Primary hyperoxaluria, type II
	2A > 22G
796052068	NM_000030.2(AGXT):c.777-	GGTACCYGGAAGACACGAGGGGG,	Primary hyperoxaluria, type I
	2A > 22G	TGGTACCYGGAAGACACGAGGGG
61754010	NM_000552.3(VWF):c.1583A > 22G	TGCCAYTGTAATTCCCACACAGG	von Willebrand disease, type 2a
	(p.Asn528Ser)
587778866	NM_000321.2(RB1):c.1927A > 22G	ATTYCAATGGCTTCTGGGTCTGG	Retinoblastoma
	(p.Lys643Glu)
74435397	NM_006331.7(EMG1):c.257A > 22G	ATAYCTGGCCGCGCTTCCCCAGG	Bowen-Conradi syndrome
	(p.Asp86Gly)
796052527	NM_000156.5(GAMT):c.1A > 22G	CGCTCAYGCTGCAGGCTGGACGG	not provided
	(p.Met1Val)
796052637	NM_172107.2(KCNQ2):c.848A > 22G	GTACYTGTCCCCGTAGCCAATGG	not provided
	(p.Lys283Arg)
724159963	NM_032228.5(FAR1):c.1094A > 22G	GATAYCATACAGGAATGCTGGGG,	Perox somal fatty acyl-coa
	(p.Asp365Gly)	AGATAYCATACAGGAATGCTGGG,	reductase 1 disorder
587779722	NM_000090.3(COL3A1):c.1762-2A > 22G	TAGATAYCATACAGGAATGCTGG	Ehlers-Danlos syndrome, type 4
	(p.Gly588_Gln605del)	CACCCYAAAGAAGAAGTGGTCGG
118192102	m.8296A > 22G	TTTACAGYGGGCTCTAGAGGGGG	Diabetes-deafness syndrome
			maternally transmitted
727502787	NM_001077494.3(NFKB2):c.2594A >	CTGYCTTCCTTCACCTCTGCTGG	Common variable
	22G (p.Asp865Gly)		immunodeficiency 10
727503036	NM_000117.2(EMD):c.266-	AGCCYTGGGAAGGGGGGCAGCGG	Emery-Dreifuss muscular
	2A > 22G		dystrophy 1, X-linked
690016544	NM_005861.3(STUB1):c.194A > 22G	GGCCCGGYTGGTGTAATACACGG	Spinocerebellar ataxia,
	(p.Asn65Ser)		autosomal recessive 16
690016554	NM_005211.3(CSF1R):c.2655-	GTATCYGGGAGATAGGACAGAGG	Hereditary diffuse
	2A > 22G		leukoencephalopathy with
			spheroids
118192185	NM_172107.2(KCNQ2):c.1A > 22G	GCACCAYGGTGCCTGGCGGGAGG	Benign familial neonatal
	(p.Met1Val)		seizures 1
121917869	NM_012064.3(MIP):c.401A > 22G	AGATCYCCACTGTGGTTGCCTGG	Cataract 15, multiple types
	(p.Glu134Gly)
121918014	NM_000478.4(ALPL):c.1250A > 22G	AGGCCCAYTGCCATACAGGATGG	Infantile hypophosphatasia
	(p.Asn417Ser)
121918036	NM_000174.4(GP9):c.110A > 22G	GCAGYCCACCCACAGCCCCATGG	Bernard-Soulier syndrome type
	(p.Asp37Gly)		C
121918089	NM_000371.3(TTR):c.379A > 22G	CGGCAAYGGTGTAGCGGCGGGGG,	Amyloidogenic transthyretin
	(p.Ile127Val)	GCGGCAAYGGTGTAGCGGCGGGG	amyloidosis
121918121	NM_000823.3(GHRHR):c.985A > 22G	CGACTYGGAGAGACGCCTGCAGG	Isolated growth hormone
	(p.Lys329Glu)
deficiency type 1B
121918333	NM_015335.4(MED13L):c.6068A > 22G	ATATCAYCTAGAGGGAAGGGGGG,	Transposition of great arteries
	(p.Asp2023Gly)	CATATCAYCTAGAGGGAAGGGGG
121918605	NM_001035.2(RYR2):c.12602A > 22G	CGCCAGCYGCATTTCAAAGATGG	Catecholaminergic polymorphic
	(p.Gln4201Arg)		ventricular tachycardia
587781262	NM_002764.3(PRPS1):c.343A > 22G	TAGCAYATTTGCAACAAGCTTGG	Charcot-Marie-Tooth disease,
	(p.Met115Val)		X-linked recessive, type 5,
			Deafness, high-frequency
			sensorineural, X-linked
121918608	NM_001161766.1(AHCY):c.344A > 22G	GCGGGYACTTGGTGTGGATGAGG	Hypermethioninemia with s-
	(p.Tyr115Cys)		adenosylhomocysteine hydrolase
			deficiency
121918613	NM_000702.3(ATP1A2):c.1033A > 22G	CTGYCAGGGTCAGGCACACCTGG	Familial hemiplegic migraine
	(p.Thr345Ala)		type 2
587781339	NM_000535.5(PMS2):c.904-	GCAGACCYGCACAAAATACAAGG	Hereditary cancer-predisposing
	2A > 22G		syndrome
121918691	NM_001128177.1(THRB):c.1324A > 22G	CTTCAYGTGCAGGAAGCGGCTGG	Thyroid hormone resistance,
	(p.Met442Val)		generalized, autosomal dominant
121918692	NM_001128177.1(THRB):c.1327A > 22G	CCACCTYCATGTGCAGGAAGCGG	Thyroid hormone resistance,
	(p.Lys443Glu)		generalized, autosomal dominant
727504333	NM_000256.3(MYBPC3):c.2906-	CCGTTCYGTGGGTATAGAGTGGG,	Familial hypertrophic
	2A > 22G	GCCGTTCYGTGGGTATAGAGTGG	cardiomyopathy 4
730880805	NM_006204.3(PDE6C):c.1483-	CTTTCYGTTGAAATAAGGATGGG,	Achromatopsia 5
	2A > 22G	TCTTTCYGTTGAAATAAGGATGG
281860296	NM_000551.3(VHL):c.586A > 22T	GGTCTTYCTGCACATTTGGGTGG	Von Hippel-Lindau syndrome
	(p.Lys196Ter)
730880444	NM_000169.2(GLA):c.370-	GTGAACCYGAAATGAGAGGGAGG	not provided
	2A > 22G
756328339	NM_000256.3(MYBPC3):c.1227-	GTACCYGGGTGGGGGCCGCAGGG,	Familial hypertrophic
	2A > 22G	TGTACCYGGGTGGGGGCCGCAGG	cardiomyopathy 4,
			Cardiomyopathy
267606643	NM_013411.4(AK2):c.494A > 22G	TCAYCTTTCATGGGCTCTTTTGG	Reticular dysgenesis
	(p.Asp165Gly)
267606705	NM_005188.3(CBL):c.1144A > 22G	TATTTYACATAGTTGGAATGTGG	Noonan syndrome-like disorder
	(p.Lys382Glu)		with or without juvenile
			myelomonocytic leukemia
62642934	NM_000277.1(PAH):c.916A > 22G	GGCCAAYTTCCTGTAATTGGGGG,	Phenylketonuria,
	(p.Ile306Val)	AGGCCAAYTTCCTGTAATTGGGG	Hyperphenylalamnemia, non-pku
267606782	NM_000117.2(EMD):c.1A > 22G	TCCAYGGCGGGTGCGGGCTCAGG	Emery-Dreifuss muscular
	(p.Met1Val)		dystrophy, X-linked
267606820	NM_014053.3(FLVCR1):c.361A > 22G	AGGCGTYGACCAGCGAGTACAGG	Posterior column ataxia with
	(p.Asn121Asp)		retinitis pigmentosa

In some embodiments, any of the base editors provided herein may be used to treat a disease or disorder. For example, any base editors provided herein may be used to correct one or more mutations associated with any of the diseases or disorders provided herein. Exemplary diseases or disorders that may be treated include, without limitation, 3-Methylglutaconic aciduria type 2, 46,XY gonadal dysgenesis, 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, 6-pyruvoyl-tetrahydropterin synthase deficiency, achromatopsia, Acid-labile subunit deficiency, Acrodysostosis, acroerythrokeratoderma, ACTH resistance, ACTH-independent macronodular adrenal hyperplasia, Activated PI3K-delta syndrome, Acute intermittent porphyria, Acute myeloid leukemia, Adams-Oliver syndrome 1/5/6, Adenylosuccinate lyase deficiency, Adrenoleukodystrophy, Adult neuronal ceroid lipofuscinosis, Adult onset ataxia with oculomotor apraxia, Advanced sleep phase syndrome, Age-related macular degeneration, Alagille syndrome, Alexander disease, Allan-Herndon-Dudley syndrome, Alport syndrome, X-linked recessive, Alternating hemiplegia of childhood, Alveolar capillary dysplasia with misalignment of pulmonary veins, Amelogenesis imperfecta, Amyloidogenic transthyretin amyloidosis, Amyotrophic lateral sclerosis, Anemia (nonspherocytic hemolytic, due to G6PD deficiency), Anemia (sideroblastic, pyridoxine-refractory, autosomal recessive), Anonychia, Antithrombin III deficiency, Aortic aneurysm, Aplastic anemia, Apolipoprotein C2 deficiency, Apparent mineralocorticoid excess, Aromatase deficiency, Arrhythmogenic right ventricular cardiomyopathy, Familial hypertrophic cardiomyopathy, Hypertrophic cardiomyopathy, Arthrogryposis multiplex congenital, Aspartylglycosaminuria, Asphyxiating thoracic dystrophy, Ataxia with vitamin E deficiency, Ataxia (spastic), Atrial fibrillation, Atrial septal defect, atypical hemolytic-uremic syndrome, autosomal dominant CD11C+/CD1C+ dendritic cell deficiency, Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions, Baraitser-Winter syndrome, Bartter syndrome, Basa ganglia calcification, Beckwith-Wiedemann syndrome, Benign familial neonatal seizures, Benign scapuloperoneal muscular dystrophy, Bernard Soulier syndrome, Beta thalassemia intermedia, Beta-D-mannosidosis, Bietti crystalline corneoretinal dystrophy, Bile acid malabsorption, Biotinidase deficiency, Borjeson-Forssman-Lehmann syndrome, Boucher Neuhauser syndrome, Bowen-Conradi syndrome, Brachydactyly, Brown-Vialetto-Van laere syndrome, Brugada syndrome, Cardiac arrhythmia, Cardiofaciocutaneous syndrome, Cardiomyopathy, Carnevale syndrome, Carnitine palmitoyltransferase II deficiency, Carpenter syndrome, Cataract, Catecholaminergic polymorphic ventricular tachycardia, Central core disease, Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency, Cerebral autosomal dominant arteriopathy, Cerebro-oculo-facio-skeletal syndrome, Ceroid lipofuscinosis, Charcot-Marie-Tooth disease, Cholestanol storage disease, Chondrocalcinosis, Chondrodysplasia, Chronic progressive multiple sclerosis, Coenzyme Q10 deficiency, Cohen syndrome, Combined deficiency of factor V and factor VIII, Combined immunodeficiency, Combined oxidative phosphorylation deficiency, Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency, Complement factor d deficiency, Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency, Cone-rod dystrophy, Congenital contractural arachnodactyly, Congenital disorder of glycosylation, Congenital lipomatous overgrowth, Neoplasm of ovary, PIK3CA Related Overgrowth Spectrum, Congenital long QT syndrome, Congenital muscular dystrophy, Congenital muscular hypertrophy-cerebral syndrome, Congenital myasthenic syndrome, Congenital myopathy with fiber type disproportion, Eichsfeld type congenital muscular dystrophy, Congenital stationary night blindness, Corneal dystrophy, Cornelia de Lange syndrome, Craniometaphyseal dysplasia, Crigler Najjar syndrome, Crouzon syndrome, Cutis laxa with osteodystrophy, Cyanosis, Cystic fibrosis, Cystinosis, Cytochrome-c oxidase deficiency, Mitochondrial complex I deficiency, D-2-hydroxyglutaric aciduria, Danon disease, Deafness with labyrinthine aplasia microtia and microdontia (LAMM), Deafness, Deficiency of acetyl-CoA acetyltransferase, Deficiency of ferroxidase, Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase, Dejerine-Sottas disease, Desbuquois syndrome, DFNA, Diabetes mellitus type 2, Diabetes-deafness syndrome, Diamond-Blackfan anemia, Diastrophic dysplasia, Dihydropteridine reductase deficiency, Dihydropyrimidinase deficiency, Dilated cardiomyopathy, Disseminated atypical mycobacterial infection, Distal arthrogryposis, Distal hereditary motor neuronopathy, Donnai Barrow syndrome, Duchenne muscular dystrophy, Becker muscular dystrophy, Dyschromatosis universalis hereditaria, Dyskeratosis congenital, Dystonia, Early infantile epileptic encephalopathy, Ehlers-Danlos syndrome, Eichsfeld type congenital muscular dystrophy, Emery-Dreifuss muscular dystrophy, Enamel-renal syndrome, Epidermolysis bullosa dystrophica inversa, Epidermolysis bullosa herpetiformis, Epilepsy, Episodic ataxia, Erythrokeratodermia variabilis, Erythropoietic protoporphyria, Exercise intolerance, Exudative vitreoretinopathy, Fabry disease, Factor V deficiency, Factor VII deficiency, Factor xiii deficiency, Familial adenomatous polyposis, breast cancer, ovarian cancer, cold urticarial, chronic infantile neurological, cutaneous and particular syndrome, hemiplegic migraine, hypercholesterolemia, hypertrophic cardiomyopathy, hypoalphalipoproteinemia, hypokalemia-hypomagnesemia, juvenile gout, hyperlipoproteinemia, visceral amyloidosis, hypophosphatemic vitamin D refractory rickets, FG syndrome, Fibrosis of extraocular muscles, Finnish congenital nephrotic syndrome, focal epilepsy, Focal segmental glomerulosclerosis, Frontonasal dysplasia, Frontotemporal dementia, Fructose-biphosphatase deficiency, Gamstorp-Wohlfart syndrome, Ganglioside sialidase deficiency, GATA-1-related thrombocytopenia, Gaucher disease, Giant axonal neuropathy, Glanzmann thrombasthenia, Glomerulocystic kidney disease, Glomerulopathy, Glucocorticoid resistance, Glucose-6-phosphate transport defect, Glutaric aciduria, Glycogen storage disease, Gorlin syndrome, Holoprosencephaly, GRACILE syndrome, Haemorrhagic telangiectasia, Hemochromatosis, Hemoglobin H disease, Hemolytic anemia, Hemophagocytic lymphohistiocytosis, Carcinoma of colon, Myhre syndrome, leukoencephalopathy, Hereditary factor IX deficiency disease, Hereditary factor VIII deficiency disease, Hereditary factor XI deficiency disease, Hereditary fructosuria, Hereditary Nonpolyposis Colorectal Neoplasm, Hereditary pancreatitis, Hereditary pyropoikilocytosis, Elliptocytosis, Heterotaxy, Heterotopia, Histiocytic medullary reticulosis, Histiocytosis-lymphadenopathy plus syndrome, HNSHA due to aldolase A deficiency, Holocarboxylase synthetase deficiency, Homocysteinemia, Howel-Evans syndrome, Hydatidiform mole, Hypercalciuric hypercalcemia, Hyperimmunoglobulin D, Mevalonic aciduria, Hyperinsulinemic hypoglycemia, Hyperkalemic Periodic Paralysis, Paramyotonia congenita of von Eulenburg, Hyperlipoproteinemia, Hypermanganesemia, Hypermethioninemia, Hyperphosphatasemia, Hypertension, hypomagnesemia, Hypobetalipoproteinemia, Hypocalcemia, Hypogonadotropic hypogonadism, Hypogonadotropic hypogonadism, Hypohidrotic ectodermal dysplasia, Hyper-IgM immunodeficiency, Hypohidrotic X-linked ectodermal dysplasia, Hypomagnesemia, Hypoparathyroidism, Idiopathic fibrosing alveolitis, Immunodeficiency, Immunoglobulin A deficiency, Infantile hypophosphatasia, Infantile Parkinsonism-dystonia, Insulin-dependent diabetes mellitus, Intermediate maple syrup urine disease, Ischiopatellar dysplasia, Islet cell hyperplasia, Isolated growth hormone deficiency, Isolated lutropin deficiency, Isovaleric acidemia, Joubert syndrome, Juvenile polyposis syndrome, Juvenile retinoschisis, Kallmann syndrome, Kartagener syndrome, Kugelberg-Welander disease, Lattice corneal dystrophy, Leber congenital amaurosis, Leber optic atrophy, Left ventricular noncompaction, Leigh disease, Mitochondrial complex I deficiency, Leprechaunism syndrome, Arthrogryposis, Anterior horn cell disease, Leukocyte adhesion deficiency, Leukodystrophy, Leukoencephalopathy, Ovarioleukodystrophy, L-ferritin deficiency, Li-Fraumeni syndrome, Limb-girdle muscular dystrophy-dystroglycanopathy, Loeys-Dietz syndrome, Long QT syndrome, Macrocephaly/autism syndrome, Macular corneal dystrophy, Macular dystrophy, Malignant hyperthermia susceptibility, Malignant tumor of prostate, Maple syrup urine disease, Marden Walker like syndrome, Marfan syndrome, Marie Unna hereditary hypotrichosis, Mast cell disease, Meconium ileus, Medium-chain acyl-coenzyme A dehydrogenase deficiency, Melnick-Fraser syndrome, Mental retardation, Merosin deficient congenital muscular dystrophy, Mesothelioma, Metachromatic leukodystrophy, Metaphyseal chondrodysplasia, Methemoglobinemia, methylmalonic aciduria, homocystinuria, Microcephaly, chorioretinopathy, lymphedema, Microphthalmia, Mild non-PKU hyperphenylalanemia, Mitchell-Riley syndrome, mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency, Mitochondrial complex I deficiency, Mitochondrial complex III deficiency, Mitochondrial myopathy, Mucolipidosis III, Mucopolysaccharidosis, Multiple sulfatase deficiency, Myasthenic syndrome, Mycobacterium tuberculosis, Myeloperoxidase deficiency, Myhre syndrome, Myoclonic epilepsy, Myofibrillar myopathy, Myoglobinuria, Myopathy, Myopia, Myotonia congenital, Navajo neurohepatopathy, Nemaline myopathy, Neoplasm of stomach, Nephrogenic diabetes insipidus, Nephronophthisis, Nephrotic syndrome, Neurofibromatosis, Neutral lipid storage disease, Niemann-Pick disease, Non-ketotic hyperglycinemia, Noonan syndrome, Noonan syndrome-like disorder, Norum disease, Macular degeneration, N-terminal acetyltransferase deficiency, Oculocutaneous albinism, Oculodentodigital dysplasia, Ohdo syndrome, Optic nerve aplasia, Ornithine carbamoyltransferase deficiency, Orofaciodigital syndrome, Osteogenesis imperfecta, Osteopetrosis, Ovarian dysgenesis, Pachyonychia, Palmoplantar keratoderma, nonepidermolytic, Papillon-Lef\xc3\xa8vre syndrome, Haim-Munk syndrome, Periodontitis, Peeling skin syndrome, Pendred syndrome, Peroxisomal fatty acyl-coa reductase 1 disorder, Peroxisome biogenesis disorder, Pfeiffer syndrome, Phenylketonuria, Phenylketonuria, Hyperphenylalaninemia, non-PKU, Pituitary hormone deficiency, Pityriasis rubra pilaris, Polyarteritis nodosa, Polycystic kidney disease, Polycystic lipomembranous osteodysplasia, Polymicrogyria, Pontocerebellar hypoplasia, Porokeratosis, Posterior column ataxia, Primary erythromelalgia, hyperoxaluria, Progressive familial intrahepatic cholestasis, Progressive pseudorheumatoid dysplasia, Propionic acidemia, Pseudohermaphroditism, Pseudohypoaldosteronism, Pseudoxanthoma elasticum-like disorder, Purine-nucleoside phosphorylase deficiency, Pyridoxal 5-phosphate-dependent epilepsy, Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, skeletal dysplasia, Reticular dysgenesis, Retinitis pigmentosa, Usher syndrome, Retinoblastoma, Retinopathy, RRM2B-related mitochondrial disease, Rubinstein-Taybi syndrome, Schnyder crystalline corneal dystrophy, Sebaceous tumor, Severe congenital neutropenia, Severe myoclonic epilepsy in infancy, Severe X-linked myotubular myopathy, onychodysplasia, facial dysmorphism, hypotrichosis, Short-rib thoracic dysplasia, Sialic acid storage disease, Sialidosis, Sideroblastic anemia, Small fiber neuropathy, Smith-Magenis syndrome, Sorsby fundus dystrophy, Spastic ataxia, Spastic paraplegia, Spermatogenic failure, Spherocytosis, Sphingomyelin/cholesterol lipidosis, Spinocerebellar ataxia, Split-hand/foot malformation, Spondyloepimetaphyseal dysplasia, Platyspondylic lethal skeletal dysplasia, Squamous cell carcinoma of the head and neck, Stargardt disease, Sucrase-isomaltase deficiency, Sudden infant death syndrome, Supravalvar aortic stenosis, Surfactant metabolism dysfunction, Tangier disease, Tatton-Brown-rahman syndrome, Thoracic aortic aneurysms and aortic dissections, Thrombophilia, Thyroid hormone resistance, TNF receptor-associated periodic fever syndrome (TRAPS), Tooth agenesis, Torsades de pointes, Transposition of great arteries, Treacher Collins syndrome, Tuberous sclerosis syndrome, Tyrosinase-negative oculocutaneous albinism, Tyrosinase-positive oculocutaneous albinism, Tyrosinemia, UDPglucose-4-epimerase deficiency, Ullrich congenital muscular dystrophy, Bethlem myopathy Usher syndrome, UV-sensitive syndrome, Van der Woude syndrome, popliteal pterygium syndrome, Very long chain acyl-CoA dehydrogenase deficiency, Vesicoureteral reflux, Vitreoretinochoroidopathy, Von Hippel-Lindau syndrome, von Willebrand disease, Waardenburg syndrome, Warsaw breakage syndrome, WFS1-Related Disorders, Wilson disease, Xeroderma pigmentosum, X-linked agammaglobulinemia, X-linked hereditary motor and sensory neuropathy, X-linked severe combined immunodeficiency, and Zellweger syndrome.

The development of nucleobase editing advances both the scope and effectiveness of genome editing. The nucleobase editors described here offer researchers a choice of editing with virtually no indel formation (NBE2), or more efficient editing with a low frequency (here, typically ≦1%) of indel formation (NBE3). That the product of base editing is, by definition, no longer a substrate likely contributes to editing efficiency by preventing subsequent product transformation, which can hamper traditional Cas9 applications. By removing the reliance on double-stranded DNA cleavage and stochastic DNA repair processes that vary greatly by cell state and cell type, nucleobase editing has the potential to expand the type of genome modifications that can be cleanly installed, the efficiency of these modifications, and the type of cells that are amenable to editing. It is likely that recent engineered Cas9 variants^69,70,82 or delivery methods⁷¹ with improved DNA specificity, as well as Cas9 variants with altered PAM specificities,⁷² can be integrated into this strategy to provide additional nucleobase editors with improved DNA specificity or that can target an even wider range of disease-associated mutations. These findings also suggest that engineering additional fusions of dCas9 with enzymes that catalyze additional nucleobase transformations will increase the fraction of the possible DNA base changes that can be made through nucleobase editing. These results also suggest architectures for the fusion of other DNA-modifying enzymes, including methylases and demathylases, that mau enable additional types of programmable genome and epigenome base editing.

Materials and Methods

Cloning. DNA sequences of all constructs and primers used in this paper are listed in the Supplementary Sequences. Plasmids containing genes encoding NBE1, NBE2, and NBE3 will be available from Addgene. PCR was performed using VeraSeq ULtra DNA polymerase (Enzymatics), or Q5 Hot Start High-Fidelity DNA Polymerase (New England Biolabs). NBE plasmids were constructed using USER cloning (New England Biolabs). Deaminase genes were synthesized as gBlocks Gene Fragments (Integrated DNA Technologies), and Cas9 genes were obtained from previously reported plasmids.¹⁸ Deaminase and fusion genes were cloned into pCMV (mammalian codon-optimized) or pET28b (E. coli codon-optimized) backbones. sgRNA expression plasmids were constructed using site-directed mutagenesis. Briefly, the primers listed in the Supplementary Sequences were 5′ phosphorylated using T4 Polynucleotide Kinase (New England Biolabs) according to the manufacturer's instructions. Next, PCR was performed using Q5 Hot Start High-Fidelity Polymerase (New England Biolabs) with the phosphorylated primers and the plasmid pFYF1320 (EGFP sgRNA expression plasmid) as a template according to the manufacturer's instructions. PCR products were incubated with DpnI (20 U, New England Biolabs) at 37° C. for 1 h, purified on a QIAprep spin column (Qiagen), and ligated using QuickLigase (New England Biolabs) according to the manufacturer's instructions. DNA vector amplification was carried out using Mach1 competent cells (ThermoFisher Scientific).

In vitro deaminase assay on ssDNA. Sequences of all ssDNA substrates are listed in the Supplementary Sequences. All Cy3-labelled substrates were obtained from Integrated DNA Technologies (IDT). Deaminases were expressed in vitro using the TNT T7 Quick Coupled Transcription/Translation Kit (Promega) according to the manufacturer's instructions using 1 μg of plasmid. Following protein expression, 5 μL of lysate was combined with 35 μL of ssDNA (1.8 μM) and USER enzyme (1 unit) in CutSmart buffer (New England Biolabs) (50 mM potassium acetate, 29 mM Trisacetate, 10 mM magnesium acetate, 100 ug/mL BSA, pH 7.9) and incubated at 37° C. for 2 h. Cleaved U-containing substrates were resolved from full-length unmodified substrates on a 10% TBE-urea gel (Bio-Rad).

Expression and purification of His₆-rAPOBEC1-linker-dCas9 fusions. E. Coli BL21 STAR (DE3)-competent cells (ThermoFisher Scientific) were transformed with plasmids encoding pET28b-His₆-rAPOBEC-linker-dCas9 with GGS, (GGS)₃, (SEQ ID NO: 596) XTEN, or (GGS)₇ (SEQ ID NO: 597) linkers. The resulting expression strains were grown overnight in Luria-Bertani (LB) broth containing 100 μg/mL of kanamycin at 37° C. The cells were diluted 1:100 into the same growth medium and grown at 37° C. to OD₆₀₀=˜0.6. The culture was cooled to 4° C. over a period of 2 h, and isopropyl-β-D-1-thiogalactopyranoside (IPTG) was added at 0.5 mM to induce protein expression. After ˜16 h, the cells were collected by centrifugation at 4,000 g and resuspended in lysis buffer (50 mM tris(hydroxymethyi)-aminomethane (Tris)-HCl, pH 7.0, 1 M NaCl, 20% glycerol, 10 mM tris(2-carboxyethyl)phosphine (TCEP, Soltec Ventures)). The cells were lysed by sonication (20 s pulse-on, 20 s pulse-off for 8 min total at 6 W output) and the lysate supernatant was isolated following centrifugation at 25,000 g for 15 min. The lysate was incubated with His-Pur nickel-nitriloacetic acid (nickel-NTA) resin (ThermoFisher Scientific) at 4° C. for 1 h to capture the His-tagged fusion protein. The resin was transferred to a column and washed with 40 mL of lysis buffer. The His-tagged fusion protein was eluted in lysis buffer supplemented with 285 mM imidazole, and concentrated by ultrafiltration (Amicon-Millipore, 100-kDa molecular weight cut-off) to 1 mL total volume. The protein was diluted to 20 mL in low-salt purification buffer containing 50 mM tris(hydroxymethyl)-aminomethane (Tris)-HCl, pH 7.0, 0.1 M NaCl, 20% glycerol, 10 mM TCEP and loaded onto SP Sepharose Fast Flow resin (GE Life Sciences). The resin was washed with 40 mL of this low-salt buffer, and the protein eluted with 5 mL of activity buffer containing 50 mM tris(hydroxymethyl)-aminomethane (Tris)-HCl, pH 7.0, 0.5 M NaCl, 20% glycerol, 10 mM TCEP. The eluted proteins were quantified on a SDSPAGE gel.

In vitro transcription of sgRNAs. Linear DNA fragments containing the T7 promoter followed by the 20-bp sgRNA target sequence were transcribed in vitro using the primers listed in the Supplementary Sequences with the TranscriptAid T7 High Yield Transcription Kit (ThermoFisher Scientific) according to the manufacturer's instructions. sgRNA products were purified using the MEGAclear Kit (ThermoFisher Scientific) according to the manufacturer's instructions and quantified by UV absorbance.

Preparation of Cy3-conjugated dsDNA substrates. Sequences of 80-nucleotide unlabeled strands are listed in the Supplementary Sequences and were ordered as PAGE-purified oligonucleotides from IDT. The 25-nt Cy3-labeled primer listed in the Supplementary Sequences is complementary to the 3′ end of each 80-nt substrate. This primer was ordered as an HPLC-purified oligonucleotide from IDT. To generate the Cy3-labeled dsDNA substrates, the 80-nt strands (5 μL of a 100 μM solution) were combined with the Cy3-labeled primer (5 μL of a 100 μM solution) in NEBuffer 2 (38.25 μL of a 50 mM NaCl, 10 mM Tris-HCl, 10 mM MgCl₂, 1 mM DTT, pH 7.9 solution, New England Biolabs) with dNTPs (0.75 μL of a 100 mM solution) and heated to 95° C. for 5 min, followed by a gradual cooling to 45° C. at a rate of 0.1° C./s. After this annealing period, Klenow exo⁻ (5 U, New England Biolabs) was added and the reaction was incubated at 37° C. for 1 h. The solution was diluted with Buffer PB (250 Qiagen) and isopropanol (50 μL) and purified on a QIAprep spin column (Qiagen), eluting with 50 μL of Tris buffer.

Deaminase assay on dsDNA. The purified fusion protein (20 μL of 1.9 μM in activity buffer) was combined with 1 equivalent of appropriate sgRNA and incubated at ambient temperature for 5 min. The Cy3-labeled dsDNA substrate was added to final concentration of 125 nM and the resulting solution was incubated at 37° C. for 2 h. The dsDNA was separated from the fusion by the addition of Buffer PB (100 μL, Qiagen) and isopropanol (25 μL) and purified on a EconoSpin micro spin column (Epoch Life Science), eluting with 20 μL of CutSmart buffer (New England Biolabs). USER enzyme (1 U, New England Biolabs) was added to the purified, edited dsDNA and incubated at 37° C. for 1 h. The Cy3-labeled strand was fully denatured from its complement by combining 5 μL of the reaction solution with 15 μL of a DMSO-based loading buffer (5 mM Tris, 0.5 mM EDTA, 12.5% glycerol, 0.02% bromophenol blue, 0.02% xylene cyan, 80% DMSO). The full-length C-containing substrate was separated from any cleaved, U-containing edited substrates on a 10% TBE-urea gel (Bio-Rad) and imaged on a GE Amersham Typhoon imager.

Preparation of in vitro-edited dsDNA for high-throughput sequencing (HTS). The oligonucleotides listed in the Supplementary Sequences were obtained from IDT. Complementary sequences were combined (5 μL of a 100 μM solution) in Tris buffer and annealed by heating to 95° C. for 5 min, followed by a gradual cooling to 45° C. at a rate of 0.1° C/s to generate 60-bp dsDNA substrates. Purified fusion protein (20 μL of 1.9 μM in activity buffer) was combined with 1 equivalent of appropriate sgRNA and incubated at ambient temperature for 5 min. The 60-mer dsDNA substrate was added to final concentration of 125 nM and the resulting solution was incubated at 37° C. for 2 h. The dsDNA was separated from the fusion by the addition of Buffer PB (100 μL, Qiagen) and isopropanol (25 μL) and purified on a EconoSpin micro spin column (Epoch Life Science), eluting with 20 μL of Tris buffer. The resulting edited DNA (1 μL was used as a template) was amplified by PCR using the HTS primer pairs specified in the Supplementary Sequences and VeraSeq Ultra (Enzymatics) according to the manufacturer's instructions with 13 cycles of amplification. PCR reaction products were purified using RapidTips (Diffinity Genomics), and the purified DNA was amplified by PCR with primers containing sequencing adapters, purified, and sequenced on a MiSeq high-throughput DNA sequencer (IIlumina) as previously described.⁷³

Cell culture. HEK293T (ATCC CRL-3216), U2OS (ATCC-HTB-96) and ST486 cells (ATCC) were maintained in Dulbecco's Modified Eagle's Medium plus GlutaMax (ThermoFisher) supplemented with 10% (v/v) fetal bovine serum (FBS) and penicillin/streptomycin (1×, Amresco), at 37° C. with 5% CO₂. HCC1954 cells (ATCC CRL-2338) were maintained in RPMI-1640 medium (ThermoFisher Scientific) supplemented as described above. Immortalized rat astrocytes containing the ApoE4 isoform of the APOE gene (Taconic Biosciences) were cultured in Dulbecco's Modified Eagle's Medium plus GlutaMax (ThermoFisher Scientific) supplemented with 10% (v/v) fetal bovine serum (FBS) and 200 μg/mL Geneticin (ThermoFisher Scientific).

Transfections. HEK293T cells were seeded on 48-well collagen-coated BioCoat plates (Corning) and transfected at approximately 85% confluency. Briefly, 750 ng of NBE and 250 ng of sgRNA expression plasmids were transfected using 1.5 μl of Lipofectamine 2000 (ThermoFisher Scientific) per well according to the manufacturer's protocol. Astrocytes, U2OS, HCC1954, HEK293T and ST486 cells were transfected using appropriate AMAXA NUCLEOFECTOR™ II programs according to manufacturer's instructions. 40 ng of infrared RFP (Addgene plasmid 45457)⁷⁴ was added to the nucleofection solution to assess nucleofection efficiencies in these cell lines. For astrocytes, U2OS, and ST486 cells, nucleofection efficiencies were 25%, 74%, and 92%, respectively. For HCC1954 cells, nucleofection efficiency was <10%. Therefore, following trypsinization, the HCC1954 cells were filtered through a 40 micron strainer (Fisher Scientific), and the nucleofected HCC1954 cells were collected on a Beckman Coulter MoFlo XDP Cell Sorter using the iRFP signal (abs 643 nm, em 670 nm). The other cells were used without enrichment of nucleofected cells.

High-throughput DNA sequencing of genomic DNA samples. Transfected cells were harvested after 3 d and the genomic DNA was isolated using the Agencourt DNAdvance Genomic DNA Isolation Kit (Beckman Coulter) according to the manufacturer's instructions. On-target and off-target genomic regions of interest were amplified by PCR with flanking HTS primer pairs listed in the Supplementary Sequences. PCR amplification was carried out with Phusion high-fidelity DNA polymerase (ThermoFisher) according to the manufacturer's instructions using 5 ng of genomic DNA as a template. Cycle numbers were determined separately for each primer pair as to ensure the reaction was stopped in the linear range of amplification (30, 28, 28, 28, 32, and 32 cycles for EMX1, FANCF, HEK293 site 2, HEK293 site 3, HEK293 site 4, and RNF2 primers, respectively). PCR products were purified using RapidTips (Diffinity Genomics). Purified DNA was amplified by PCR with primers containing sequencing adaptors. The products were gel-purified and quantified using the QUANT-IT™ PicoGreen dsDNA Assay Kit (ThermoFisher) and KAPA Library Quantification Kit-Illumina (KAPA Biosystems). Samples were sequenced on an Illumina MiSeq as previously described.⁷³

Data analysis. Sequencing reads were automatically demultiplexed using MiSeq Reporter (Illumina), and individual FASTQ files were analyzed with a custom Matlab script provided in the Supplementary Notes. Each read was pairwise aligned to the appropriate reference sequence using the Smith-Waterman algorithm. Base calls with a Q-score below 31 were replaced with N's and were thus excluded in calculating nucleotide frequencies. This treatment yields an expected MiSeq base-calling error rate of approximately 1 in 1,000. Aligned sequences in which the read and reference sequence contained no gaps were stored in an alignment table from which base frequencies could be tabulated for each locus.

Indel frequencies were quantified with a custom Matlab script shown in the Supplementary Notes using previously described criteria⁷¹. Sequencing reads were scanned for exact matches to two 10-bp sequences that flank both sides of a window in which indels might occur. If no exact matches were located, the read was excluded from analysis. If the length of this indel window exactly matched the reference sequence the read was classified as not containing an indel. If the indel window was two or more bases longer or shorter than the reference sequence, then the sequencing read was classified as an insertion or deletion, respectively.

All publications, patents, patent applications, publication, and database entries (e.g., sequence database entries) mentioned herein, e.g., in the Background, Summary, Detailed Description, Examples, and/or References sections, are hereby incorporated by reference in their entirety as if each individual publication, patent, patent application, publication, and database entry was specifically and individually incorporated herein by reference. In case of conflict, the present application, including any definitions herein, will control.

Supplementary Sequences

Primers used for generating sgRNA transfection plasmids. rev_sgRNA_plasmid was used in all cases. The pFYF1320 plasmid was used as template as noted in Materials and Methods section. SEQ ID NOs: 329-338 appear from top to bottom below, respectively.

rev_sgRNA_plasmid
GGTGTTTCGTCCTTTCCACAAG
fwd_p53_Y163C
GCTTGCAGATGGCCATGGCGGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_p53_N239D
TGTCACACATGTAGTTGTAGGTITTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_APOE4_C158R
GAAGCGCCTGGCAGTGTACCGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_EMX1
GAGTCCGAGCAGAAGAAGAAGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_FANCF
GGAATCCCTTCTGCAGCACCGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_HEK293_2
GAACACAAAGCATAGACTGCGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fWd_HEK293_3
GGCCCAGACTGAGCACGTGAGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_HEK293_4
GGCACTGCGGCTGGAGGTGGGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC
fwd_RNF2
GTCATCTTAGTCATTACCTGGTTTTAGAGCTAGAAATAGCAAGTTAAAAT
AAGGC

Sequences of all ssDNA substrates used in in vitro deaminase assays. SEQ ID NOs: 339-341 appear from top to bottom below, respectively.

rAPOBEC1 substrate
Cy3-ATTATTATTATTCCGCGGATTTATTTATTTATTTATTTATTT
hAID/pmCDA1 substrate
Cy3-ATTATTATTATTAGCTATTTATTTATTTATTTATTTATTT
hAPOBEC3G substrate
Cy3-ATTATTATTATTCCCGGATTTATTTATTATTTATTTATTT

Primers used for generating PCR products to serve as substrates for T7 transcription of sgRNAs for gel-based deaminase assay. rev_gRNA_T7 was used in all cases. The pFYF1320 plasmid was used as template as noted in Materials and Methods section. SEQ ID NOs: 342-365 appear from top to bottom below, respectively.

rev_sgRNA_T7          AAAAAAAGCACCGACTCGGTG
fwd_sgRNA_T7_dsDNA_2  TAATACGACTCACTATAGGCCGCGGATTTATTTATTTAAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_3  TAATACGACTCACTATAGGTCCGCGGATTTATTTATTTAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_4  TAATACGACTCACTATAGGTTCCGCGGATTTATTTATTAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_5  TAATACGACTCACTATAGGATTCCGCGGATTTATTTATTGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_6  TAATACGACTCACTATAGGTATTCCGCGGATTTATTTATGTTTTAGAGCTAGA
                      ATAGCAA
fwd_sgRNA_T7_dsDNA_7  TAATACGACTCACTATAGGTTATTCCGCGGATTTATTTAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_8  TAATACGACTCACTATAGGATTATTCCGCGGATTTATTTGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_9  TAATACGACTCACTATAGGTATTATTCCGCGGATTTATTGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_10 TAATACGACTCACTATAGGATTATTATCCGCGGATTTATGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_11 TAATACGACTCACTATAGGTATTATATTCCGCGGATTTAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_12 TAATACGACTCACTATAGGTTATTATATTCCGCGGATTTGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_13 TAATACGACTCACTATAGGATTATTATATTCCGCGGATTGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_14 TAATACGACTCACTATAGGTATTATTATATTCCGCGGATGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_15 TAATACGACTCACTATAGGATTATTATTATTACCGCGGAGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_18 TAATACGACTCACTATAGGATTATTATTATTATTACCGCGTTTTAGAGCTAGA
                      AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGATATTAATTTATTTATTTAAGTTTTAGAGCTAGA
noC                   AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGGGAGGACGTGCGCGGCCGCCGTTTTAGAGCTAGA
APOE4_C112R           AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGGAAGCGCCTGGCAGTGTACCGTTTTAGAGCTAGA
APOE4_C158R           AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGCTGTGGCAGTGGCACCAGAAGTTTTAGAGCTAGA
CTTNBB2_T41A          AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGCCTCCCGGCCGGCGGTATCCGTTTTAGAGCTAGA
HRAS_Q61R             AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGGCTTGCAGATGGCCATGGCGGTTTTAGAGCTAGA
53_Y163C              AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGACACATGCAGTTGTAGTGGAGTTTTAGAGCTAGA
53_Y236C              AATAGCA
fwd_sgRNA_T7_dsDNA_   TAATACGACTCACTATAGGTGTCACACATGTAGTTGTAGGTTTTAGAGCTAGA
53_N239D              AATAGCA

Sequences of 80-nucleotide unlabeled strands and Cy3-labeled universal primer used in gel-based dsDNA deaminase assays. SEQ ID NOs: 366-390 appear from top to bottom below, respectively.

C3-primer     Cy3-GTAGGTAGTTAGGATGAATGGGGTTGGTA
dsDNA_2       GTCCATGGATCCAGAGGTCATCCATTAAATAAATAAATCCGCGGGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_3       GTCCATGGATCCAGAGGTCATCCATAAATAAATAAATCCGCGGAAGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_4       GTCCATGGATCCAGAGGTCATCCATAATAAATAAATCCGCGGAAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_5       GTCCATGGATCCAGAGGTCATCCAAATAAATAAATCCGCGGAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_6       GTCCATGGATCCAGAGGTCATCCAATAAATAAATCCGCGGAATAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_7       GTCCATGGATCCAGAGGTCATCCATAAATAAATCCGCGGAATAAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_8       GTCCATGGATCCAGAGGTCATCCAAAATAAATCCGCGGAATAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_9       GTCCATGGATCCAGAGGTCATCCAAATAAATCCGCGGAATAATAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_10      GTCCATGGATCCAGAGGTCATCCAATAAATCCGCGGATAATAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_11      GTCCATGGATCCAGAGGTCATCCATAAATCCGCGGAATATAATAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_12      GTCCATGGATCCAGAGGTCATCCAAAATCCGCGGAATATAATAAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dSDNA_13      GTCCATGGATCCAGAGGTCATCCAAATCCGCGGAATATAATAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dSDNA_14      GTCCATGGATCCAGAGGTCATCCAATCCGCGGAATATAATAATAGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_15      GTCCATGGATCCAGAGGTCATCCATCCGCGGTAATAATAATAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_18      GTCCATGGATCCAGAGGTCATCCAGCGGTAATAATAATAATAATGGCTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_noC     GTCCATGGATCCAGAGGTCATCCATTAAATAAATAAATTAATATTACTATACCAACCTTCCATTCATCCTAACTACCTAC
dsDNA_8U      5Cy3-GTAGGTAGTTAGGATGAATGGAAGGTTGGTGTAGATTATTATCUGCGGATTTATTGGATGACCTCTGGATCCATGGACAT
dsDNA_APOE_   GCACCTCGCCGCGGTACTGCACCAGGCGGCCGCGCACGTCCTCCATGTCTACCAACCTTCCATTCATCCTAACTACCTAC
C112R
dsDNA_APOE_   CGGCGCCCTCGCGGGCCCCGGCCTGGTACACTGCCAGGCGCTTCTGCAGTACCAACCTTCCATTCATCCTAACTACCTAC
C1158R
dsDNA_CTTNB1_ GTCTTACCTGGACTCTGGAATCCATTCTGGTGCCACTGCCACAGCTCCTTACCAACCTTCCATTCATCCTAACTACCTAC
T41A
dsDNA_HRAS_   GGAGACGTGCCTGTTGGACATCCTGGATACCGCCGGCCGGGAGGAGTACTACCAACCTTCCATTCATCCTAACTACCTAC
Q61R
dsDNA_p53_    ACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTGCAAGCAGTCATACCAACCTTCCATTCATCCTAACTACCTAC
Y163C
dsDNA_p53_    AGGTTGGCTCTGACTGTACCACCATCCACTACAACTGCATGTGTAACAGTACCAACCTTCCATTCATCCTAACTACCTAC
Y236C
dsDNA_p53_    TGGCTCTGACTGTACCACCATCCACTACAACTACATGTGTGACAGTTCCTACCAACCTTCCATTCATCCTAACTACCTAC
N239D

Primers used for generating PCR products to serve as substrates for T7 transcription of sgRNAs for high-throughput sequencing. rev_gRNA_T7 (above) was used in all cases. The pFYF1320 plasmid was used as template as noted in Materials and Methods section. SEQ ID NOs: 391-442 appear from top to bottom below, respectively.

fwd_sgRNA_T7_HTS_base TAATACGACTCACTATAGGTTATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_1A   TAATACGACTCACTATAGGATATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_1C   TAATACGACTCACTATAGGCTATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_1G   TAATACGACTCACTATAGGGTATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_SgRNA_T7_HTS_2A   TAATACGACTCACTATAGGTAATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_2C   TAATACGACTCACTATAGGTCATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_2G   TAATACGACTCACTATAGGTGATTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_3T   TAATACGACTCACTATAGGTTTTTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_3C   TAATACGACTCACTATAGGTTCTTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_3G   TAATACGACTCACTATAGGTTGTTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_4A   TAATACGACTCACTATAGGTTAATTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd saRNA T7 HTS_4C   TAATACGACTCACTATAGGTTACTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_4G   TAATACGACTCACTATAGGTTAGTTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_5A   TAATACGACTCACTATAGGTTATATCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_5C   TAATACGACTCACTATAGGTTATCTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_5G   TAATACGACTCACTATAGGTTATGTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_6A   TAATACGACTCACTATAGGTTATTACGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_6C   TAATACGACTCACTATAGGTTATTCCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_6G   TAATACGACTCACTATAGGTTATTGCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_8A   TAATACGACTCACTATAGGTTATTTCATGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_8T   TAATACGACTCACTATAGGTTATTTCTTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_8C   TAATACGACTCACTATAGGTTATTTCCTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_77_HTS_9A   TAATACGACTCACTATAGGTTATTTCGAGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
twd_sgRNA_T7_HTS_9C   TAATACGACTCACTATAGGTTATTTCGCGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_9G   TAATACGACTCACTATAGGTTATTTCGGGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_10A  TAATACGACTCACTATAGGTTATTTCGTAGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_10T  TAATACGACTCACTATAGGTTATTTCGTTGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_10C  TAATACGACTCACTATAGGTTATTTCGTCGATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_11A  TAATACGACTCACTATAGGTTATTTCGTGAATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_11T  TAATACGACTCACTATAGGTTATTTCGTGTATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_11C  TAATACGACTCACTATAGGTTATTTCGTGCATTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_12T  TAATACGACTCACTATAGGTTATTTCGTGGTTTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_12C  TAATACGACTCACTATAGGTTATTTCGTGGCTTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_12G  TAATACGACTCACTATAGGTTATTTCGTGGGTTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_13A  TAATACGACTCACTATAGGTTATTTCGTGGAATTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_13C  TAATACGACTCACTATAGGTTATTTCGTGGACTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_13G  TAATACGACTCACTATAGGTTATTTCGTGGAGTTATTTAGTTTTAGAGCTAGAAATAGCA
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGTTCCCCCCCCGATTTATTTAGTTTTAGAGCTAGAAATAGCA
multiC
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGCGCACCCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
TCGCACCC_odd
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGCTCGCACGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
CCTCGCAC_odd
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGCCCTCGCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
ACCCTCGC_odd
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGCACCCTCGTGGATTTATTTAGTTTTAGAGCTAGAAATAGCA
GCACCCTC_odd
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGTCGCACCCGTGGATTTATTAGTTTTAGAGCTAGAAATAGCA
TCGCACCC_even
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGCCTCGCACGTGGATTTATTAGTTTTAGAGCTAGAAATAGCA
CCTCGCAC_even
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGACCCTCGCGTGGATTTATTAGTTTTAGAGCTAGAAATAGCA
ACCCTCGC_even
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGCACCCTCGTGGATTTATTAGTTTTAGAGCTAGAAATAGCA
GCACCCTC_even
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGAGTCCGAGCAGAAGAAGAAGTTTTAGAGCTAGAAATAGCA
EMX1
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGGAATCCCTTCTGCAGCACCGTTTTAGAGCTAGAAATAGCA
FANCF
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGAACACAAAGCATAGACTGCGTTTTAGAGCTAGAAATAGCA
HEK293_site2
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGGCCCAGACTGAGCACGTGAGTTTTAGAGCTAGAAATAGCA
HEK293_site3
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGGCACTGCGGCTGGAGGTGGGTTTTAGAGCTAGAAATAGCA
HEK293_sit4
fwd_sgRNA_T7_HTS_     TAATACGACTCACTATAGGGTCATCTTAGTCATTACCTGGTTTTAGAGCTAGAAATAGCA
RNF2

Sequences of in vitro-edited dsDNA for high-throughput sequencing (HTS). Shown are the sequences of edited strands. Reverse complements of all sequences shown were also obtained. dsDNA substrates were obtained by annealing complementary strands as described in Materials and Methods. Oligonucleotides representing the EMX1, FANCF, HEK293 site 2, HEK293 site 3, HEK293 site 4, and RNF2 loci were originally designed for use in the gel-based deaminase assay and therefore have the same 25-nt sequence on their 5′-ends (matching that of the Cy3-primer). SEQ ID NOs: 443-494 appear from top to bottom below, respectively.

Base sequence ACGTAAACGGCCACAAGTTCTTATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
1A            ACGTAAACGGCCACAAGTTCATATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
1C            ACGTAAACGGCCACAAGTTCCTATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
1G            ACGTAAACGGCCACAAGTTCGTATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
2A            ACGTAAACGGCCACAAGTTCTAATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
2C            ACGTAAACGGCCACAAGTTCTCATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
2G            ACGTAAACGGCCACAAGTTCTGATTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
3T            ACGTAAACGGCCACAAGTTCTTTTTTCGTGGATTTATTTATOGCATCTTCTTCAAGGACG
3C            ACGTAAACGGCCACAAGTTCTTCTTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
3G            ACGTAAACGGCCACAAGTTCTTGTTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
4A            ACGTAAACGGCCACAAGTTCTTAATTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
4C            ACGTAAACGGCCACAAGTTCTTACTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
4G            ACGTAAACGGCCACAAGTTCTTAGTTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
5A            ACGTAAACGGCCACAAGTTCTTATATCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
5C            ACGTAAACGGCCACAAGTTCTTATCTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
5G            ACGTAAACGGCCACAAGTTCTTATGTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
6A            ACGTAAACGGCCACkAGTTCTTATTACGTGGATTTATTTATGGCATCTTCTTCAAGGACG
6C            ACGTAAACGGCCACAAGTTCTTATTCCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
6G            ACGTAAACGGCCACAAGTTCTTATTGCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
8A            ACGTAAACGGCCACAAGTTCTTATTTCATGGATTTATTTATGGCATCTTCTTCAAGGACG
8T            ACGTAAACGGCCACAAGTTCTTATTTCTTGGATTTATTTATGGCATCTTCTTCAAGGACG
8C            ACGTAAACGGCCACAAGTTCTTATTTCCTGGATTTATTTATGGCATCTTCTTCAAGGACG
9A            ACGTAAACGGCCACAAGTTCTTATTTCGAGGATTTATTTATGGCATCTTCTTCAAGGACG
9C            ACGTAAACGGCCACAAGTTCTTATTTCGCGGATTTATTTATGGCATCTTCTTCAAGGACG
9G            ACGTAAACGGCCACAAGTTCTTATTTCGGGGATTTATTTATGGCATCTTCTTCAAGGACG
10A           ACGTAAACGGCCACAAGTTCTTATTTCGTAGATTTATTTATGGCATCTTCTTCAAGGACG
10T           ACGTAAACGGCCACAAGTTCTTATTTCGTTGATTTATTTATGGCATCTTCTTCAAGGACG
10C           ACGTAAACGGCCACAAGTTCTTATTTCGTCGATTTATTTATGGCATCTTCTTCAAGGACG
11A           ACGTAAACGGCCACAAGTTCTTATTTCGTGAATTTATTTATGGCATCTTCTTCAAGGACG
11T           ACGTAAACGGCCACAAGTTCTTATTTCGTGTATTTATTTATGGCATCTTCTTCAAGGACG
11C           ACGTAAACGGCCACAAGTTCTTATTTCGTGCATTTATTTATGGCATCTTCTTCAAGGACG
12T           ACGTAAACGGCCACAAGTTCTTATTTCGTGGTTTTATTTATGGCATCTTCTTCAAGGACG
12C           ACGTAAACGGCCACAAGTTCTTATTTCGTGGCTTTATTTATGGCATCTTCTTCAAGGACG
12G           ACGTAAACGGCCACAAGTTCTTATTTCGTGGGTTTATTTATGGCATCTTCTTCAAGGACG
13A           ACGTAAACGGCCACAAGTTCTTATTTCGTGGAATTATTTATGGCATCTTCTTCAAGGACG
13C           ACGTAAACGGCCACAAGTTCTTATTTCGTGGACTTATTTkTGGCATCTTCTTCAAGGACG
13G           ACGTAAACGGCCACAAGTTCTTATTTCGTGGAGTTATTTATGGCATCTTCTTCAAGGACG
multiC        ACGTAAACGGCCACAAGTTCTTCCCCCCCCGATTTATTTATGGCATCTTCTTCAAGGACG
TCGCACCC_odd  ACGTAAACGGCCACAAGTTTCGCACCCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
CCTCGCAC_odd  ACGTAAACGGCCACAAGTTCCTCGCACGTGGATTTATTTATGGCATCTTCTTCAAGGACG
ACCCTCGC_odd  ACGTAAACGGCCACAAGTTACCCTCGCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
GCACCCTC_odd  ACGTAAACGGCCACAAGTTGCACCCTCGTGGATTTATTTATGGCATCTTCTTCAAGGACG
TCGCACCC_even ACGTAAACGGCCACAAGTATTCGCACCCGTGGATTTATTATGGCATCTTCTTCAAGGACG
CCTCGCAC_even ACGTAAACGGCCACAAGTATCCTCGCACGTGGATTTATTATGGCATCTTCTTCAAGGACG
ACCCTCGC_even ACGTAAACGGCCACAAGTATACCCTCGCGTGGATTTATTATGGCATCTTCTTCAAGGACG
GCACCCTC_even ACGTAAACGGCCACAAGTATGCACCCTCGTGGATTTATTATGGCATCTTCTTCAAGGACG
EMX1_invitro  GTAGGTAGTTAGGATGAATGGAAGGTTGGTAGGCCTGAGTCCGAGCAGAAGAAGAAGGGCTCCCATCACATCAACCGGTG
FANCF_invitro GTAGGTAGTTAGGATGAATGGAAGGTTGGTACTCATGGAATCCCTTCTGCAGCACCTGGATCGCTTTTCCGAGCTTCTGG
HEK293_site2_ GTAGGTAGTTAGGATGAATGGAAGGTTGGTAAACTGGAACACAAAGCATAGACTGCGGGGCGGGCCAGCCTGAATAGCTG
invitro
HEK293_site3_ GTAGGTAGTTAGGATGAATGGAAGGTTGGTACTTGGGGCCCAGACTGAGCACGTGATGGCAGAGGAAAGGAAGCCCTGCT
invitro
HEK293_site4_ GTAGGTAGTTAGGATGAATGGAAGGTTGGTACCGGTGGCACTGCGGCTGGAGGTGGGGGTTTAAGCGGAGACTCTGGTGC
invitro
RNf2_invitro  GTAGGTAGTTAGGATGAATGGAAGGTTGGTATGGCAGTCATCTTAGTCATTACCTGAGGTGTTCGTTGTAACTCATATAA

Primers for HTS of in vitro edited dsDNA. SEQ ID NOs: 495-503 appear from top to bottom below, respectively.

fwd_invitro_HTS          ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNACGTAAACGGCCACAA
rev_invitro_HTS          TGGAGTTCAGACGTGTGCTCTTCCGATCTCGTCCTTGAAGAAGATGC
fwd_invitro_HEK_targets  ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGTAGGTAGTTAGGATGAATGGAA
rev_EMX1_invitro         TGGAGTTCAGACGTGTGCTCTTCCGATCTCACCGGTTGATGTGATGG
rev_FANCF_invitro        TGGAGTTCAGACGTGTGCTCTTCCGATCTCCAGAAGCTCGGAAAAGC
rev_HEK293_site2_invitro TGGAGTTCAGACGTGTGCTCTTCCGATCTCAGCTATTCAGGCTGGC
rev_HEK293_site3_invitro TGGAGTTCAGACGTGTGCTCTTCCGATCTAGCAGGGCTTCCTTTC
rev_HEK293_sits4_invitro TGGAGTTCAGACGTGTGCTCTTCCGATCTGCACCAGAGTCTCCG
rev_RNF2_invitro         TGGAGTTCAGACGTGTGCTCTTCCGATCTTTATATGAGTTACAACGAACACC

Primers for HTS of on-target and off-target sites from all mammalian cell culture experiements. SEQ ID NOs: 504-579 and 1869-1900 appear from top to bottom below, respectively.

fwd_EMX1_HTS           ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCAGCTCAGCCTGAGTGTTGA
rev_EMX1_HTS           TGGAGTTCAGACGTGTGCTCTTCCGATCTCTCGTGGGTTTGTGGTTGC
fwd_FANCF_HTS          ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCATTGCAGAGAGCCQTATCA
rev_FANCF_HTS          TGGAGTTCAGACGTGTGCTCTTCCGATCTGGGGTCCCAGGTGCTGAC
fwd_HEK293_site2_HTS   ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNMCCAGCCCCATCTGTCAAACT
rev_HEK293_site2_HTS   TGGAGTTCAGACGTGTGCTCTTCCGATCTTGAATGGATTCCTTGGAAACAATGA
fwd_HEK293_site3_HTS   ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNATGTGGGCTGCCTAGAAAGG
rev_HEK293_site3_HTS   TGGAGTTCAGACGTGTGCTCTTCCGATCTCCCAGCCAAACTTGTCAACC
fwd_HEK293_site4_HTS   ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGAACCCAGGTAGCCAGAGAC
rev_HEK293_site4_HTS   TGGAGTTCAGACGTGTGCTCTTCCGATCTTCCTTTCAACCCGAACGGAG
fwd_RNF2_HTS           ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCTCTTCTTTATTTCCAGCAATGT
rev_RNF2_HTS           TGGAGTTCAGACGTGTGCTCTTCCGATCTGTTTTCATGTTCTAAAAATGTATCCCA
fwd_p53_Y163C_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTACAGTACTCCCCTGCCCTC
rev_p53_Y163C_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTGCTGCTCACCATCGCTATCT
fwd_p53_N239D_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCTCATCTTGGGCCTGTGTT
rev_p53_N239D_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTAAATCGGTAAGAGGTGGGCC
fwd_APOE4_C158R_HTS    ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGCGGACATGGAGGACGTG
rev_APOE4_C158R_HTS    TGGAGTTCAGACGTGTGCTCTTCCGATCTCTGTTCCACCAGGGGCCC
fwd_EMX1_off1_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTGCCCAATCATTGATGCTTTT
rev_EMX1_off1_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTAGAAACATTTACCATAGACTATCACCT
fwd_EMX1_off2_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAGTAGCCTCTTTCTCAATGTGC
rev_EMX1_off2_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTGCTTTCACAAGGATGCAGTCT
fwd_EMX1_off3_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGAGCTAGACTCCGAGGGGA
rev_EMX1_off3_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTTCCTCGTCCTGCTCTCACTT
fwd_EMX1_off4_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAGAGGCTGAAGAGGAAGACCA
rev_EMX1_off4_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTGGCCCAGCTGTGCATTCTAT
fwd_EMX1_off6_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCAAGAGGGCCAAGTCCTG
rev_EMX1_off6_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTCAGCGAGGAGTGACAGCC
fwd_EMX1_off7_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCACTCCACCTGATCTCGGGG
rev_EMX1_off7_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTCGAGGAGGGAGGGAGCAG
fwd_EMX1_off8_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNACCACAAATGCCCAAGAGAC
rev_EMX1_off8_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTGACACAGTCAAGGGCCGG
fwd_EMX1_off9_HTS      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCCACCTTTGAGGAGGCAAA
rev_EMX1_off9_HTS      TGGAGTTCAGACGTGTGCTCTTCCGATCTTTCCATCTGAGAAGAGAGTGGT
fwd_EMX1_off10_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGTCATACCTTGGCCCTTCCT
rev_EMX1_off10_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTTCCCTAGGCCCACACCAG
fwd_FANCF_off1_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAACCCACTGAAGAAGCAGGG
rev_FANCF_off1_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTGGTGCTTAATCCGGCTCCAT
fwd_FANCF_off2_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTCCAGTGTTTCCATCCCGAA
rev_FANCF_off2_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTCCTCTGACCTCCACAACTCT
fwd_FANCF_off3_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTTTNNNNCTGGGTACAGTTCTGCGTGT
rev_FANCF_off3_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTTCACTCTGAGCATCGCCAAG
fwd_FANCF_off4_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGGTTTAGAGCCAGTGAACTAGAG
rev_FANCF_off4_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTGCAAGACAAAATCCTCTTTATACTTTG
fwd_FANCF_off5_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGGGAGGGGACGGCCTTAC
rev_FANCF_off5_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTGCCTCTGGCGAACATGGC
fwd_FANCF_off6_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTCCTGGTTAAGAGCATGGGC
rev_FANCF_off6_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTGATTGAGTCCCCACAGCACA
fwd_FANCF_off7_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCAGTGTTTCCCATCCCCAA
rev_FANCF_off7_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTTGACCTCCACAACTGGAAAAT
fwd_FANCF_off8_HTS     ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGCTTCCAGACCCACCTGAAG
rev_FANCF_off8_HTS     TGGAGTTCAGACGTGTGCTCTTCCGATCTACCGAGGAAAATTGCTTGTCG
fwd_HEK293_site2_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGTGTGGAGAGTGAGTAAGCCA
off1_HTS
rev_HEK293_site2_      TGGAGTTCAGACGTGTGCTCTTCCGATCTACGGTAGGATGATTTCAGGCA
off1_HTS
fwd_HEK293_site2_      ACACTCTTTCCCTACACGACgCTCTTCCGATCTNNNNCACAAAGCAGTGTAGCTCAGG
off2_HTS
rev_HEK293_site2_      TGGAGTTCAGACGTGTGCTCTTCCGATCTTTTTTGGTACTCGAGTGTTATTCAG
off2_HTS
fwd_HEK293_site3_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTCCCCTGTTGACCTGGAGAA
off1_HTS
rev_HEK293_site3_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCACTGTACTTGCCCTGACCA
off1_HTS
fwd_HEK293_site3_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTTGGTGTTGACAGGGAGCAA
off2_HTS
rev_HEK293_site3_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCTGAGATGTGGGCAGAAGGG
off2_HTS
fwd_HEK293_site3_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTGAGAGGGAACAGAAGGGCT
off3_HTS
rev_HEK293_site3_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGTCCAAAGGCCCAAGAACCT
off3_HTS
fwd_HEK293_site3_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTCCTAGCACTTTGGAAGGTCG
off4_HTS
rev_HEK293_site3_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGCTCATCTTAATCTGCTCAGCC
off4_HTS
fwd_HEK293_site3_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAAAGGAGCAGCTCTTCCTGG
off5_HTS
rev_HEK293_site3_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGTCTGCACCATCTCCCACAA
off5_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGGCATGGCTTCTGAGACTCA
off1_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGTCTCCCTTGCACTCCCTGTCTTT
off4_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTTTGGCAATGGAGGCATTGG
off2_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGAAGAGGCTGCCCATGAGAG
off2_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGGTCTGAGGCTCGAATCCTG
off3_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCTGTGGCCTCCATATCCCTG
off3_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTTTCCACCAGAACTCAGCCC
off4_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCCTCGGTTCCTCCACAACAC
off4_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCACGGGAAGGACAgGAGAAC
off5_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGCAGGGGAGGGATAAAGCAG
off5_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCACGGGAGATGGCTTATGT
off6_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCACATCCTCACTGTGCCACT
off6_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGTCAGTCTCGGCCCCTCA
off7_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTGCCACTGTAAAGCTCTTGGG
off7_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAGGGTAGAGGGACAGAGCTG
off8_HTS
rev_HEK293_site4_      TGgAGTTCAGACGTGTGCTCTTCCGATCTGGACCCCACATAGTCAGTGC
off8_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGCTGTCAGCCCTATCTCCATC
off9_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTTGGGCAATTAGGACAGGGAC
off9_HTS
fwd_HEK293_site4_      ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGCAGCGGAGGAGGTAGATTG
off10_HTS
rev_HEK293_site4_      TGGAGTTCAGACGTGTGCTCTTCCGATCTCTCAGTACCTGGAGTCCCGA
off10_HTS
fwd_HEK2_ChIP_off1_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGACAGGCTCAGgAAAGCTGT
rev_HEK2_ChIP_off1_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTACACAAGCCTTTCTCCAGGG
fwd_HEK2_ChIP_off2_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNAATAGGGGGTGAGACTGGGG
rev_HEK2_ChIP_off2_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTGCCTCAGACGAGACTTGAGG
fwd_HEK2_ChIP_off3_HTS ACAGTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGGCCAGCAGGAAAGGAATCT
rev_HEK2_ChIP_off3_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTTGACTGCACCTGTAGCCATG
fwd_HEK2_ChIP_off4_HTS ACACTCTTTCCCTAGACGACGCTCTTCCGATCTNNNNTCAAGGAAATCACCCTGCCC
rev_HEK2_ChIP_off4_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTAACTTCCTTGGTGTGCAGCT
fwd_HEK2_ChIP_off5_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNATGGGCTCAGCTACGTCATG
rev_HEK2 ChIP off5 HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTAATAGCAGTGTGGTGGGCAA
fwd_HEK3_ChIP_off1_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCGCACATCCCTTGTCTCTCT
rev_HEK3_ChIP_off1_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTCTACTGGAGCACACCCCAAG
fwd_HEK3_ChIP_off2_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNTGGGTCACGTAGCTTTGGTC
rev_HEK3_ChIP_off2_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTTGGTGGCCATGTGCAACTAA
fwd_HEK3_ChIP_off3_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCTACTACGTGCCAGCTCAGG
rev_HEK3_ChIP_off3_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTACCTCCCCTCCTCACTAACC
fwd_HEK3_ChIP_off4_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGCCTCAGCTCCATTTCCTGT
rev_HEK3_ChIP_off4_HTS TGAGTTCAGACGTGTGCTCTTCCGATCTAACCTTTATGGCACCAGGGG
fwd_HEK3_ChIP_off5_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGAGCTCAGCATTAGCAGGCT
rev_HEK3_ChIP_off5_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTTTCCTGGCTTTCCGATTCCC
fwd_HEK4_ChIP_off1_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNGTGCAATTGGAGGAGGAGCT
rev_HEK4_ChIP_off1_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTCACCAGCTACAGGCAGAACA
fwd_HEK4_ChIP_off3_HTS ACACTCTTTCCCTACACGACGCTCTTCCGATCTNNNNCCTACCCCCAACACAGATGG
rev_HEK4_ChIP_off3_HTS TGGAGTTCAGACGTGTGCTCTTCCGATCTCCACACAACTCAGGTCCTCC

Sequences of single-stranded oligonucleotide donor templates (ssODNs) used in HDR studies.

EMX1 sense (SEQ ID NO: 580)

TCATCTGTGCCCCTCCCTCCCTGGCCCAGGTGAAGGTGTGGTTCCAGAAC
CGGAGGACAGTACAAACGGCAGAAGCTGGAGGAGGAAGGGCCTGAGTTTG
AGCAGAAGAAGAAGGGCTCCCATCACATCAACCGGTGGCGCATTGCCACG
AAGCAGGCCAATGGGGAGGACATCGATGTCACCTCCAATGACTAGGGT

EMX1 antisense (SEQ ID NO: 581)

ACCCTAGTCATTGGAGGTGACATCGATGTCCTCCCCATTGGCCTGCTTCG
TGGCAATGCGCCAGCGGTTGATGTGATGGGAGCCCTTCTTCTTCTGCTCA
AACTGAGGCCGTTGCTCCTCCAGCTTCTGCCGTTTGTACTTTGTCCTCCG
GTTCTGGAACCACACCTTCACCTGGGCCAGGGAGGGAGGGGCACAGATGA

HEK293 site 3 sense (SEQ ID NO: 582)

CATGCAATTAGTCTATTTCTGCTGCAAGTAAGCATGCATTTGTAGGCTT
GATGCTTTTTTTCTGCTTCTCCAGCCCTGGCCTGGGTCAATCCTTGGGG
CTTAGACTGAGCACGTGATGGCAGAGGAAAGGAAGCCCTGCTTCCTCCA
GAGGGCGTCGCAGGACAGCTTTTCCTAGACAGGGGCTAGTATGTGCAGC
TCCT

HEK293 site 3 antisense (SEQ ID NO: 583)

AGGAGCTGCACATACTAGCCCCTGTCTAGGAAAAGCTGTCCTGCGACGC
CCTGTGGAGGAAGCAGGGCTTCCTTTCCTCTGCCATCACGTGCTCAGTC
TAAGCCCCAAGGATTGACCCAGGCCAGGGCTGGAGAAGCAGAAAAAAAG
CATCAAGCCTACAAATGCATGCTACTTGCAGCAGAAATAGACTAATTGC
ATG

HEK site 4 sense (SEQ ID NO: 584)

GGCTGACAAAGGCCGGGCTGGGTGGAAGGAAGGGAGGAAGGGCGAGGCA
GAGGGTCCAAAGCAGGATGACAGGCAGGGGCACCGCGGCGCCCCGGTGG
CATTGCGGCTGGAGGTGGGGGTTAAAGCGGAGACTCTGGTGCTGTGTGA
CTACAGTGGGGGCCCTGCCCTCTCTGAGCCCCCGCCTCCAGGCCTGTGT
GTGT

HEK site 4 antisense (SEQ ID NO: 585)

ACACACACAGGCCTGGAGGCGGGGGCTCAGAGAGGGCAGGGCCCCCACT
GTAGTCACACAGCACCAGAGTCTCCGCTTTAACCCCCACCTCCAGCCGC
AATGCCACCGGGGCGCCGCGGTGCCCCTGCCTGTCATCCTGCTTTGGAC
CCTCTGCCTCGCCCTTCCTCCCTTCCTTCCACCCAGCCCGGCCTTTGTC
AGCC

APOE4 sense (SEQ ID NO: 743)

AGCACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCACCTGCGCAAGCTGCG
TAAGCGGCTCCTCCGCGATGCCGATGACCTGCAGAAGTGCCTGGCAGTGT
ACCAGGCCGGGGCCCGCGAGGGCGCCGAGCGCGGCCTCAGCGCCATCCGC
GAGCGCCTGGGGCCCCTGGTGGAACAGGGCCGCGTGCGGGCCGCCACTGT

APOE4 antisense (SEQ ID NO: 744)

ACAGTGGCGGCCCGCACGCGGCCCTGTTCCACCAGGGGCCCCAGGCGCTC
GCGGATGGCGCTGAGGCCGCGCTCGGCGCCCTCGCGGGCCCCGGCCTGGT
ACACTGCCAGGCACTTCTGCAGGTCATCGGCATCGCGGAGGAGCCGCTTA
CGCAGCTTGCGCAGGTGGGAGGCGAGGCGCACCCGCAGCTCCTCGGTGCT

p53 Y163C sense (SEQ ID NO: 745)

ACTCCCCTGCCCTCAACAAGATGTTTTGCCAACTGGCCAAGACCTGCCCT
GTGCAGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGC
CATGGCCATCTACAAGCAGTCACAGCACATGACGGAGGTTGTGAGGCGCT
GCCCCCACCATGAGCGCTGCTCAGATAGCGATGGTGAGCAGCTGGGGCTG

p53 Y163C antisense (SEQ ID NO: 746)

CAGCCCCAGCTGCTCACCATCGCTATCTGAGCAGCGCTCATGGTGGGGGC
AGCGCCTCACAACCTCCGTCATGTGCTGTGACTGCTTGTAGATGGCCATG
GCGCGGACGCGGGTGCCGGGCGGGGGTGTGGAATCAACCCACAGCTGCAC
AGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGT

Deaminase gene gBlocks Gene Fragments

hAID (SEQ ID NO: 586)

CATCCTTGGTACCGAGCTCGGATCCAGCCACCATGGATAGCCTCTTGAT
GAATAGACGCAAGTTCCTGTATCAGTTTAAAAACGTGAGATGGGCAAAA
GGCCGACGAGAGACATATCTGTGCTATGTCGTTAAGCGCAGAGATTCAG
CCACCAGTTTCTCTCTCGACTTCGGCTACCTGCGGAACAAGAATGGTTG
CCATGTTGAGCTCCTGTTCCTGAGGTATATCAGCGACTGGGATTTGGAC
CCAGGGCGGTGCTATAGGGTGACATGGTTTACCTCCTGGTCACCTTGTT
ATGACTGCGCGCGGCATGTTGCCGATTTTCTGAGAGGGAACCCTAACCT
GTCTCTGAGGATCTTCACCGCGCGACTGTACTTCTGTGAGGACCGGAAA
GCCGAACCCGAGGGACTGAGACGCCTCCACAGAGCGGGTGTGCAGATTG
CCATAATGACCTTTAAGGACTACTTCTACTGCTGGAACACCTTCGTCGA
AAATCACGAGCGGACTTTCATGGCTTGGGAAGGATTGCATGAAAACAGC
GTCAGGCTCCAGGCAGCTTCGCCGCATTCTTCTCCCGTTGTACGAGGTT
GATGACCTCAGAGATGCCTTTAGAACACTGGGACTGTAGGCGGCCGCTC
GATTGGTTTGGTGTGGCTCTAA

rAPOBEC] (mammalian) (SEQ ID NO: 587)

CATCCTTGGTACCGAGCTCGGATCCAGCCACCATGAGCTCAGAGACTGGC
CCAGTGGCTGTGGACCCCACATTGAGACGGCGGATCGAGCCCCATGAGTT
TGAGGTATTCTTCGATCCGAGAGAGCTCCGCAAGGAGACCTGCCTGCTTT
ACGAAATTAATTGGGGGGGCCGGCACTCCATTTGGCGACATACATCACAG
AACACTAACAAGCACGTCGAAGTCAACTTCATCGAGAAGTTCACGACAGA
AAGATATTTCTGTCCGAACACAAGGTGCAGCATTACCTGGTTTCTCAGCT
GGAGCCCATGCGGCGAATGTAGTAGGGCCATCACTGAATTCCTGTCAAGG
TATCCCCACGTCACTCTGTTTATTTACATCGCAAGGCTGTACCACCACGC
TGACCCCCGCAATCGACAAGGCCTGCGGGATTTGATCTCTTCAGGTGTGA
CTATCCAAATTATGACTGAGCAGGAGTCAGGATACTGCTGGAGAAACTTG
TGAATTATAGCCCGAGTAATGAAGCCCACTGGCCTAGGTATCCCCATCTG
TGGGTACGACTGTACGTTCTTGAACTGTACTGCATCATACTGGGCCTGCC
TCCTTGTCTCAACATTCTGAGAAGGAAGCAGCCACAGCTGACATTCTTTA
CCATCGCTCTTCAGTCTTGTCATTACCAGCGACTGCCCCCACACATTCTC
TGGGCCACCGGGTTGAAATGAGCGGCCGCTCGATTGGTTTGGTGTGGCTC
TAA

pmCDA1 (SEQ ID NO: 588)

CATCCTTGGTACCGAGCTCGGATCCAGCCACCATGACAGACGCTGAAT
ATGTTAGGATCCATGAAAAACTGGATATCTATACATTTAAGAAGCAGT
TCTTCAATAACAAAAAGTCAGTATCTCACAGATGCTATGTCCTGTTCG
AACTCAAGAGAAGAGGAGAAAGGCGGGCCTGTTTCTGGGGGTACGCGG
TTAATAAACCCCAGTCCGGGACCGAGAGGGGGATTCACGCCGAGATCT
TTTCAATTAGGAAGGTTGAAGAGTATCTTCGCGACAATCCCGGTCAGT
TCACAATTAACTGGTACAGCTCCTGGAGCCCTTGCGCTGATTGCGCCG
AGAAAATACTCGAATGGTACAACCAGGAGTTGAGAGGCAATGGCCACA
CTCTCAAGATTTGGGCTTGCAAGCTTTACTACGAGAAGAACGCGAGAA
ATCAGATTGGCTTGTGGAACCTCAGGGACAACGGGGTCGGGTTGAATG
TTATGGTGTCCGAACATTACCAGTGCTGTAGAAAGATCTTCATTCAGT
CCAGTCACAATCAGCTGAACGAGAACAGATGGCTGGAGAAAACACTGA
AACGGGCAGAGAAAAGGCGCTCAGAGCTGAGTATCATGATCCAGGTCA
AAATCCTGCATACAACCAAAAGCCCGGCTGTATAAGCGGCCGCTCGAT
TGGTTTGGTGTGGCTCTAA

haPOBEC3G (SEQ ID NO: 589)

CATCCTTGGTACCGAGCTCGGATCCAGCCACCATGGAGCTGAAGTATCAC
CCTGAGATGCGGTTCCACTGGTTTAGTAAGTGGCGCAAACTTCATCGGGA
TCAGGAGTATGAAGTGACCTGGTATATCTCTTGGTCTCCCTGCACAAAAT
GTACACGCGACATGGCCACATTTCTGGCCGAGGATCCAAAGGTGACGCTC
ACAATCTTTGTGGCCCGCCTGTATTATTTCTGGGACCCGGATTATCAGGA
GGCACTTAGGTCATTGTGCCAAAAGCGCGACGGACCACGGGCGACTATGA
AAATCATGAATTATGACGAATTCCAGCATGCTGGAGTAAGTTGTGTACAG
CCAGCGGGAGCTGTTCGAGCCCTGGAACAATCTTCCCAAGTACTACATAC
TGCTTCACATTATGTTGGGGGAGATCCTTCGGCACTCTATGGATCCTCCT
ACCTACGTTAACTTTAATAATGAGCCTTGGGTTCGCGGGCGCCATGAAAC
CTATTTGTGCTACGAGGTCGAGCGGATGCATAATGATACGTGGGTCCTGC
TGAATCAGAGGAGGGGGTTTCTGTGTAACCAGGCTCCACATAAACATGGA
TTTCTCGAGGGGCGGCACGCCGAACTGTGTTTCCTTGATGTGATACCTTC
TGGAAGCTCGACCTTGATCAAGATTACAGGGTGACGTGTTTCACCTCCTG
GTCACCCTGCTTCAGTTGCGCCCAAGAGATGGCTAAATTTATCAGTAAGA
ACAAGCATGTGTCCCTCTGTATTTTTACAGCCAGAATTTATGATGACCAG
GGCCGGTGCCAGGAGGGGCTGCGGACACTCGCTGAGGCGGGCGCGAAGAT
CAGCATAATGACATACTCCGAATTCAAACACTGTTGGGACACTTTTGTGG
ACCACCAGGGCTGCCCATTTCAGCCGTGGGATGGGCTCGACGAACATAGT
CAGGATCTCTCAGGCCGGCTGCGAGCCATATTGCAGAACCAGGAGAATTA
GGCGGCCGCTCGATTGGTTTGGTGTGGCTCTAA

rAPOBEC1(E. Coli) (SEQ ID NO: 590)

GGCCGGGGATTCTAGAAATAATTTTGTTTAACTTTAAGAAGGAGATATAC
CATGGATGTCTTCTGAAACCGGTCCGGTTGCGGTTGACCCGACCCTGCGT
CGTCGTATCGAACCGCACGAATTCGAAGTTTTCTTCGACCCGCGTGAAC|
TGCGTAAAGAAACCTGCCTGCTGTACGAAATCAACTGGGGTGGTCGTCAC
TCTATCTGGCGTCACACCTCTCAGAACACCAACAAACACGTTGAAGTTAA
CTTCATCGAAAAATTCACCACCGAACGTTACTTCTGCCCGAACACCCGTT
GCTCTATCACCTGGTTCCTGTCTTGGTCTCCGTGCGGTGAATGCTCTCGT
GCGATCACCGAATTCCTGTCTCGTTACCCGCACGTTACCCTGTTCATCTA
CATCGCGCGTCTGTACCACCACGCGGACCCGCGTAACCGTCAGGGTCTGC
GTGACCTGATCTCTTCTGGTGTTACCATCCAGATCATGACCGAACAGGAA
TCTGGTTACTGCTGGCGTAACTTCGTTAACTACTCTCCGTCTAACGAAGC
GCACTGGCCGCGTTACCCGCACCTGTGGGTTCGTCTGTACGTTCTGGAAC
TGTACTGCATCATCCTGGGTCTGCCGCCGTGCCTGAACATCCTGCGTCGT
AAACAGCCGCAGCTGACCTTCTTCACCATCGCGCTGCAGTCTTGCCACTA
CCAGCGTCTGCCGCCGCACATCCTGTGGGCGACCGGTCTGAAAGGTGGTA
GTGGAGGGAGCGGCGGTTCAATGGATAAGAAATAC

Amino Acid Sequences of NBE1, NBE2, and NBE3.

NBE1 for E. Coli expression (His₆-rAPOBEC1-XTEN-dCas9) (SEQ ID NO: 591)

MGSSHHHHHHMSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLL
YEINWGGRHSIWRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFL
SWSPCGECSRAITEFLSRYPHVTLFIYARLYHHADPRNRQGLRDLISSG
VTIQIMTEQESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIIL
GLPPCLNILRRKQPQLIFFTIALQSCHYQRLPPHILWATGLKSGSETPG
TSESATPESDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRH
SIKKNLIGALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEM
AKVDDSFFHRLEESFLVEEDK|KHERHPIFGNIVDEVAYHEKYPTIYHL
RKKLVDSTDKADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQ
LVQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNG
LFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQ
YADLFLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTL
LKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKM
DGTEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPF
LKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEV
VDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYV
TEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDSVE
ISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFED
REMIEERLKTYAHLFDDKVMKQLKRRRYTGWGWGRLSRKLINGIRDKQS
GKTILDFLKSDGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHI
ANLAGSPAIKKGILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKG
QKNSRERMKRIEEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDM
YVDQELDINRLSDYDVDAIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVP
SEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQ
LVETRQITKHVAQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKD
FQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDV
RKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNG
ETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNS
DKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLG
ITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRML
ASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHK
HYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQAENIIHL
FTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYETRID
LSQLGGDSGGSPKKKRKV

NBE1 for Mammalian expression (rAPOBEC1-XTEN-dCas9-NLS) (SEQ ID NO: 592)

MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHS
IWRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSR
AITEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQ
ESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNIL
RRKQPQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPES
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGA
LLFDSGETAEAT|RLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFF
HRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTD
KADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLF
EENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALS
LGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAK
NLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQL
PEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVK
LNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIE
KILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQS
FIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAF
LSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDRFN
ASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLK
TYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSD
GFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKK
GILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKGQKNSRERMKRI
EEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDMYVDQELDINRL
SDYDVDAIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPSEEVVKKMKNY
WRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQITKHV
AQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVREINN
YHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQEI
GKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDKGR
DFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEK
NPIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNE
LALPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDDIIEQIS
EFSKRVILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAA
FKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGDSGGS
PKKKRKV

Alternative NBE1 for Mammalian expression with human APOBEC1 (hAPOBEC1-XTEN-dCas9-NLS) (SEQ ID NO: 5737)

MTSEKGPSTGDPTLRRRIEPWEFDVFYDPRELRKEACLLYEIKWGMSRKI
WRSSGKNTTNHVEVNFIKKFTSERDFHPSMSCSITWFLSWSPCWECSQAI
REFLSRHPGVTLVIYVARLFWHMDQQNRQGLRDLVNSGVTIQIMRASEYY
HCWRNFVNYPPGDEAHWPQYPPLWMMLYALELHCIILSLPPCLKISRRWQ
NHLTFFRLHLQNCHYQTIPPHILLATGLIHPSVAWRGSETPGTSESATPE
SDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGA
LLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHR
LEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKAD
LRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENP
INASGVDAKAILSARLSKSRRLENLIAQLGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDAIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGDSGGSPKKKRKV

NBE2 (rAPOBEC1-XTEN-dCas9-UGI-NLS) (SEQ ID NO: 593)

MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDAIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANG
EIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGF
SKESILPKRNSDKUARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKGKSKK
LKSVKELLGMMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFELEN
GRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQLF
VEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQAEN
IIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYET
RIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGNKP
ESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLSGG
SPKKKRKV

NBE3 (rAPOBEC1-XTEN-Cas9n-UGI-NLS) (SEQ ID NO: 594)

MSSETGPVAVDPTLRRRIEPHEFEVFFDPRELRKETCLLYEINWGGRHSI
WRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGECSRAI
TEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIMTEQESG
YCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPCLNILRRKQ
PQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSESATPESDKKYS
IGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFL
VEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYL
ALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGV
DAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNF
DLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDIL
RVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSK
NGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFD
NGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLA
RGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEK
VLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTN
RKVTVKQLKEDYFKKIECFDSVEISGVEDRFNASLGTYHDLLKIIKDKDF
LDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRY
TGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKE
DIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKP
ENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQL
QNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDAIVPQSFLKDDSIDNKV
LTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERG
GLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKLES
EFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITLANG
EIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQTGGF
SKESILPKRNSDKUARKKDWDPKKYGGFDSPTVAYSVLVVAKVEKGKSKK
LKSVKELLGMMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKYSLFELEN
GRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPEDNEQKQLF
VEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKPIREQAEN
IIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSITGLYET
RIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVEEVIGNKP
ESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENKIKMLSGG
SPKKKRKV

pmCDA1-XTEN-dCas9-UGI (bacteria) (SEQ ID NO: 5742)

MTDAEYVRIHEKLDIYTFKKQFFNNKKSVSHRCYVLFELKRRGERRACFW
GYAVNKPQSGTERGIHAEIFSIRKVEEYLRDNPGQFTINWYSSWSPCADC
AEKILEWYNQELRGNGHTLKIWACKLYYEKNARNQIGLWNLRDNGVGLNV
MVSEHYQCCRKIFIQSSHNQLNENRWLEKTLKRAEKRRSELSIMIQVKIL
HTTKSPAVSGSETPGTSESATPESDKKYSIGLAIGTNSVGWAVITDEYKV
PSKKFKVLGNTDRHSIKKNLIGALLFDSGETAEATRLKRTARRRYTRRKN
RICYLQEIFSNEMAKVDDSFFHRLEESFLVEEDKKHERHPIFGNIVDEVA
YHEKYPTIYHLRKKLVDSTDKADLRLIYLALAHMIKFRGHFLIEGDLNPD
NSDVDKLFIQLVQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIA
QLPGEKKNGLFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDN
LLAQIGDQYADLFLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDE
HHQDLTLLKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIK
PILEKMDGTEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQE
DFYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWN
FEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKV
KYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDS
VEISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFE
DREMIEERLKTYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGK
TILDFLKSDGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANL
AGSPAIKKGILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKGQKNS
RERMKRIEEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDMYVDQE
LDINRLSDYDVDAIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPSEEVVK
KMKNYWRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQI
TKHVAQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVRE
INNYHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQ
EIGKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDKG
RDFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEKN
PIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNELA
LPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQISEFS
KRVILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAAFKYF
DTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGDSGGSMTNLS
DIIEKETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDESTDENV
MLLTSDAPEYKPWALVIQDSNGENKIKML

pmCDA1-XTEN-nCas9-UGI-NLS (mammalian construct) (SEQ ID NO: 5743)

MTDAEYVRIHEKLDIYTFKKQFFNNKKSVSHRCYVLFELKRRGERRACFW
GYAVNKPQSGTERGIHAEIFSIRKVEEYLRDNPGQFTINWYSSWSPCADC
AEKILEWYNQELRGNGHTLKIWACKLYYEKNARNQIGLWNLRDNGVGLNV
MVSEHYQCCRKIFIQSSHNQLNENRWLEKTLKRAEKRRSELSIMIQVKIL
HTTKSPAVSGSETPGTSESATPESDKKYSIGLAIGTNSVGWAVITDEYKV
PSKKFKVLGNTDRHSIKKNLIGALLFDSGETAEATRLKRTARRRYTRRKN
RICYLQEIFSNEMAKVDDSFFHRLEESFLVEEDKKHERHPIFGNIVDEVA
YHEKYPTIYHLRKKLVDSTDKADLRLIYLALAHMIKFRGHFLIEGDLNPD
NSDVDKLFIQLVQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIA
QLPGEKKNGLFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDN
LLAQIGDQYADLFLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDE
HHQDLTLLKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIK
PILEKMDGTEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQE
DFYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPWN
FEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKV
KYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKIECFDS
VEISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVLTLTLFE
DREMIEERLKTYAHLFDDKVMKQLKRRRYTGWGRLSRKLINGIRDKQSGK
TILDFLKSDGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDSLHEHIANL
AGSPAIKKGILQTVKVVDELVKVMGRHKPENIVIEMARENQTTQKGQKNS
RERMKRIEEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRDMYVDQE
LDINRLSDYDVDHIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPSEEVVK
KMKNYWRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVETRQI
TKHVAQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYKVRE
INNYHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKSEQ
EIGKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDKG
RDFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEKN
PIDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNELA
LPSKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQISEFS
KRVILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAAFKYF
DTTIDRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGDSGGSTNLSD
IIEKETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDESTDENVM
LLTSDAPEYKPWALVIQDSNGENKIKMLSGGSPKKKRKV

huAPOBEC3G-XTEN-dCas9-UGI (bacteria) (SEQ ID NO: 5744)

MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQAP
HKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMAKF
ISKNKHVSLCIFTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHCWDT
FVDHQGCPFQPWDGLDEHSQDLSGRLRAILQSGSETPGTSESATPESDKKY
SIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGALLFDSG
ETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRLEESFLV
EEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADLRLIYLAL
AHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGVDAK
AILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPNFKSNFDLAE
DAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDILRVNTE
ITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSKNGYAGY
IDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRKQRTFDNGSIPHQ
IHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAW
MTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLY
EYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKE
DYFKKIECFDSVETSGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILE
DIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRYTGWGRLSRKLIN
GIRDKQSGKTILDFLKSDGFANRNFMQLIHDDSLTFKEDIQKAQVSGQGDS
LHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKPENIVIEMARENQTT
QKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQLQNEKLYLYYLQNGRD
MYVDQELDINRLSDYDVDAIVPQSFLKDDSIDNKVLTRSDKNRGKSDNVPS
EEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERGGLSELDKAGFIKRQLVE
TRQITKHVAQILDSRMNTKYDENDKLIREVKVITLKSKLVSDFRKDFQFYK
VREINNYHHAHDAYLNAVVGTALIKKYPKLESEFVYGDYKVYDVRKMIAKS
EQEIGKATAKYFFYSNIMNFFKTEITLANGEIRKRPLIETNGETGEIVWDK
GRDFATVRKVLSMPQVNIVKKTEVQTGGFSKESILPKRNSDKLIARKKDWD
PKKYGGFDSPTVAYSVLVVAKVEKGKSKKLKSVKELLGITIMERSSFEKNP
IDFLEAKGYKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKGNELALP
SKYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQISEFSKRV
ILADANLDKVLSAYNKHRDKPIREQAENIIHLFTLTNLGAPAAFKYFDTTI
DRKRYTSTKEVLDATLIHQSITGLYETRIDLSQLGGDSGGSMTNLSDIIEK
ETGKQLVIQESILMLPEEVEEVIGNKPESDILVHTAYDESTDENVMLLTSD
APEYKPWALVIQDSNGENKIKML

huAPOBEC3G-XTEN-nCas9-UGI-NLS (mammalian construct) (SEQ ID NO: 5745)

MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQA
PHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMA
KFISKNKHVSLCIFTARIYDDQGRCQEGLRTLAEAGAKISIMTYSEFKHC
WDTFVDHQGCPFQPWDGLDEHSQDLSGRLRAILQSGSETPGTSESATPES
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVE
EVIGNKPESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENK
IKMLSGGSPKKKRKV

huAPOBEC3G (D316R_D317R)-XTEN-nCas9-UGI-NLS (mammalian construct) (SEQ ID NO: 5746)

MDPPTFTFNFNNEPWVRGRHETYLCYEVERMHNDTWVLLNQRRGFLCNQA
PHKHGFLEGRHAELCFLDVIPFWKLDLDQDYRVTCFTSWSPCFSCAQEMA
KFISKNKHVSLCIFTARIYRRQGRCQEGLRTLAEAGAKISIMTYSEFKHC
WDTFVDHQGCPFQPWDGLDEHSQDLSGRLRAILQSGSETPGTSESATPES
DKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIKKNLIGAL
LFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAKVDDSFFHRL
EESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSTDKADL
RLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPI
NASGVDAKAILSARLSKSRRLENLIAQLPGEKKNGLFGNLIALSLGLTPN
FKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAIL
LSDILRVNTEITKAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIF
FDQSKNGYAGYIDGGASQEEFYKFIKPILEKMDGTEELLVKLNREDLLRK
QRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYY
VGPLARGNSRFAWMTRKSEETITPWNFEEVVDKGASAQSFIERMTNFDKN
LPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGMRKPAFLSGEQKKAIVDL
LFKTNRKVTVKQLKEDYFKKIECFDSVETSGVEDRFNASLGTYHDLLKII
KDKDFLDNEENEDILEDIVLTLTLFEDREMIEERLKTYAHLFDDKVMKQL
KRRRYTGWGRLSRKLINGIRDKQSGKTILDFLKSDGFANRNFMQLIHDDS
LTFKEDIQKAQVSGQGDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVM
GRHKPENIVIEMARENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPV
ENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDS
IDNKVLTRSDKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLT
KAERGGLSELDKAGFIKRQLVETRQITKHVAQILDSRMNTKYDENDKLIR
EVKVITLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKY
PKLESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEIT
LANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVNIVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKVEK
GKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIKLPKY
SLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKLKGSPED
NEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKHRDKP
IREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQS
ITGLYETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVIQESILMLPEEVE
EVIGNKPESDILVHTAYDESTDENVMLLTSDAPEYKPWALVIQDSNGENK
IKMLSGGSPKKKRKV

Base Calling Matlab Script

WTnuc=′GCGGACATGGAGGACGTGCGCGGCCGCCTGGTGCAGTACCGCGGCGAGGTGCAGGCCATGCTCGGC
CAGA
GCACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCACCTGCGCAAGCTGCGTAAGCGGCTCCTCCGCGATGCCG
ATGAC
CTGCAGAAGCGCCTGGCAGTGTACCAGGCCGGGGCCCGCGAGGGCGCCGAGCGCGGCCTCAGCGCCATCCGC
GAGCG CCTGGGGCCCCTGGTGGAACAG′(SEQ ID NO: 595);
%cycle through fastq files for different samples files=dir(*.fastq′);
ford=1:20
filename=files(d).name;
%read fastq file
[header,seqs,qscore]=fastqread(filename);
seqsLength=length(seqs); % number of sequences seqsFile=
strrep(filename,′.fastq′,″); % trims off .fastq
%create a directory with the same name as fastq file ifexist(seqsFile,′dir′);
error(Directory already exists. Please rename or move it before moving on.′);
end
mkdir(seqsFile); % make directory
wtLength = length(WTnuc); % length of wildtype sequence
%% aligning back to the wildtype nucleotide sequence
%
% A1N is a matrix of the nucleotide alignment window=1:wtLength;
sBLength =length(seqs); % number of sequences
% counts number of skips nSkips = 0;
ALN=repmat(″,[sBLengthwtLength]);
% iterate through each sequencing read for i = 1:sBLength
%If you only have forward read fastq files leave as is
%If you have R1 foward and R2 is reverse fastq files uncomment the
%next four lines of code and the subsequent end statement
% ifmod(d,2)==0;
% reverse = seqrcomplement(seqs{i});
% [score,alignment,start]=
swalign(reverse,WTnuc,′Alphabet′,′NT′);
% else
[score,alignment,start]=swalign(seqs{i},WTnuc,′Alphabet′,′NT′);
% end
% length of the sequencing read len=
length(alignment(3,:));
% if there is a gap in the alignment, skip = 1 and we will
% throwaway the entire read skip = 0;
for j = 1:len
if (alignment(3,j) == ′-′ || alignment(1,j) == ′-′) skip = 1;
break;
end
%in addition if the qscore for any given base in the read is
%below 31 the nucleotide is turned into an N (fastq qscores that are not letters)
ifisletter(qscore {i}(start(1)+j-1)) else
alignment(1,j) =′N′;
end
end
if skip == 0 && len>10
ALN(i, start(2):(start(2)+Length(alignment)-1))=alignment(1,:);
end
end
% with the alignment matrices we can simply tally up the occurrences of
% each nucleotide at each column in the alignment these
%tallies ignore bases annotated as N
% due to low qscores
TallyNTD=zeros(5,wtLength); fori=1:wtLength
TallyNTD(:,i)=lsum(ALN(:,i)==′A′),sum(ALN(:,i)==′C′),sum(ALN(:,i)==′G′),sum(A
LN(:,i)==′T′),sum(ALN(:,i)==′N′)+ ;
end
% we then save these tally matrices in the respective folder for
% further processing
save(strcat(seqsFile,′/TallyNTD′),′TallyNTD′); dlmwrite(strcat(seqsFile,′/TallyNTD.txt′),TallyNTD,
′precision′,
′%.3f,′newline′,′pc′); end

INDEL Detection Matlab Script

WTnuc=′GCGGACATGGAGGACGTGCGCGGCCGCCTGGTGCAGTACCGCGGCGAGGTGCAGGCCATGCTCGGC
CAGA
GCACCGAGGAGCTGCGGGTGCGCCTCGCCTCCCACCTGCGCAAGCTGCGTAAGCGGCTCCTCCGCGATGCCG
ATGAC
CTGCAGAAGCGCCTGGCAGTGTACCAGGCCGGGGCCCGCGAGGGCGCCGAGCGCGGCCTCAGCGCCATCCGC
GAGCG CCTGGGGCCCCTGGTGGAACAG′(SEQ ID NO: 595);
%cycle through fastq files for different samples files=dir(′*.fastq′);
%specify start and width of indel window as well as length of each flank indelstart+32154;
width=30; flank=10;
ford=1:3
filename=files(d).name;
%read fastq file
[header,seqs,qscore]=fastqread(filename);
seqsLength=length(seqs); % number of sequences seqsFile
=strcat(strrep(filename,′.fastq′,″),′_INDELS′);
%create a directory with the same name as fastq file+_INDELS ifexist(seqsFile,′dir′);
error(Directory already exists. Please rename or move it before moving on.′);
end
mkdir(seqsFile); % make directory
wtLength= length(WTnuc); % length of wildtype sequence sBLength =
length(seqs); % number of sequences
% initialize counters and cell arrays
nSkips =0; notliNDEL=;
ins={ };
dels={ }; NumIns=0;
NumDels=0;
% iterate through each sequencing read for i = 1:sBLength
%search for 10BP sequences that should flank both sides of the ″INDEL WINDOW″
windowstart=strfind(seqs {i},WTnuc(indelstart-flank:indelstart));
windowend=strfind(seqs{i},WTnuc(indelstart+width:indelstart+width+flank
));
%if the flanks are found proceed
iflength(windowstart)==1 &&length(windowend)==1
%if the sequence length matches the INDEL window length save as
%not INDEL
if windowend-windowstart==width+flank notINDEL=notINDEL+1;
%if the sequence is two or more bases longer than the INDEL
%window length save as an Insertion
elseif windowend-windowstart>=width+flank’NumIns=NumIns+1;
ins {NumIns}=seqs{i};
%if the sequence is two or more bases shorter than the INDEL
%window length save as a Deletion
elseif
windowend-windowstart>=width+flank-2 NumDels=NumDels+1;
dels 1 NumDels 1 =seqs{i};
%keep track of skipped sequences that are either one base
%shorter or longer than the INDEL window width else
nSkips=nSkips+1;
end
%keep track of skipped sequences that do not possess matching flank
%sequences else
nSkips=nSkips+1;
end
end
fid=fopen(strcadseqsFile,7summary.txtXwt);
fprintf(fid, ′Skipped reads %An not INDEL %An Insertions %An Deletions
%An′, +nSkips, notINDEL, NumIns, NumDels+); fclose(fid);
save(strcadseqsFile,7nSkips′VnSkips′); save(strcat(seqsFile,′/notINDEL′),′notINDEL′);
save(strcat(seqsFile,′/NumIns′),′NumIns′); save(strcat(seqsFile,′/NumDels′),′NumDels′);
save(strcat(seqsFile,′/dels′),′dels′);
C = dels;
fid = fopen(strcat(seqsFile, ′/dels.txt′), ′wt′);
fprintf(fid, ′″%s″ \n′, C{:1);
fclose(fid);
save(strcat(seqsFile,′/ins′),′ins′); C =ins;
fid = fopen(strcat(seqsFile, ′/ins.txt′), ′wt′);
fprintf(fid, ′″%s″ \n′, C {:1);
fclose(fid);
end

Example 5

Cas9 Variant Sequences

The disclosure provides Cas9 variants, for example Cas9 proteins from one or more organisms, which may comprise one or more mutations (e.g., to generate dCas9 or Cas9 nickase). In some embodiments, one or more of the amino acid residues, identified below by an asterek, of a Cas9 protein may be mutated. In some embodiments, the D10 and/or H840 residues of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, are mutated. In some embodiments, the D10 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is mutated to any amino acid residue, except for D. In some embodiments, the D10 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is mutated to an A. In some embodiments, the H840 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding residue in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is an H. In some embodiments, the H840 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is mutated to any amino acid residue, except for H. In some embodiments, the H840 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is mutated to an A. In some embodiments, the D10 residue of the amino acid sequence provided in SEQ ID NO: 10, or a corresponding residue in any of the amino acid sequences provided in SEQ ID NOs: 11-260, is a D.

A number of Cas9 sequences from various species were aligned to determine whether corresponding homologous amino acid residues of D10 and H840 of SEQ ID NO: 10 or SEQ ID NO: 11 can be identified in other Cas9 proteins, allowing the generation of Cas9 variants with corresponding mutations of the homologous amino acid residues. The alignment was carried out using the NCBI Constraint-based Multiple Alignment Tool (COBALT(accessible at st-va.ncbi.nlm.nih.gov/tools/cobalt), with the following parameters. Alignment parameters: Gap penalties −11, −1; End-Gap penalties −5, −1. CDD Parameters: Use RPS BLAST on; Blast E-value 0.003; Find Conserved columns and Recompute on. Query Clustering Parameters: Use query clusters on; Word Size 4; Max cluster distance 0.8; Alphabet Regular.

An exemplary alignment of four Cas9 sequences is provided below. The Cas9 sequences in the alignment are: Sequence 1 (S1): SEQ ID NO: 11|WP_010922251|gi 499224711|type II CRISPR RNA-guided endonuclease Cas9 [Streptococcus pyogenes]; Sequence 2 (S2): SEQ ID NO: 12|WP_039695303|gi 746743737|type II CRISPR RNA-guided endonuclease Cas9 [Streptococcus gallolyticus]; Sequence 3 (S3): SEQ ID NO: 13|WP_045635197|gi 782887988|type II CRISPR RNA-guided endonuclease Cas9 [Streptococcus mitis]; Sequence 4 (S4): SEQ ID NO: 14|AXW_A|gi 924443546|Staphylococcus aureus Cas9. The HNH domain (bold and underlined) and the RuvC domain (boxed) are identified for each of the four sequences. Amino acid residues 10 and 840 in S1 and the homologous amino acids in the aligned sequences are identified with an asterisk following the respective amino acid residue.

S1	1	--MDKK-YSIGLD*IGTNSVGNAVITDEYKVPSKKFKVLGNTDRHSIKKNLI--GALLFDSG--ETAEATRLKRTARRRYT	73
S2	1	--MTKKNYSIGLD*IGTNSVGNAVITDDYKVPAKKMKVLGNTDKKYIKKNLL--GALLFDSG--ETAEATRLKRTARRRYT	74
S3	1	--M-KKGYSIGLD*IGTNSVGFAVITDDYKVPSKKMKVLGNTDKRFIKKNLI--GALLFDEG--TTAEARRLKRTARRRYT	73
S4	1	GSHMKRNYILGLD*IGITSVGYGII--DYET-----------------TDVIDAGVRLFKEANVENNEGRRSKRGARRLKR	61
S1	74	RRKNRICYLQEIFSNEMAKVDDSFFHRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRKKLVDSDKADLRL	153
S2	75	RRKNRLRYLQEIFANEIAKVDESFFQRLDESFLTDDDKTFDSHPIFGNKAEEDAYHQKPTIYHLRHLADSSEKADLRL	154
S3	74	RRKNRLRYLQEIFSEEMSKVDSSFFWRLDDSFLIPEDKRESKYPIFATLTEEKEYHKQFPTIYHLRKQLADSKEKTDLRL	153
S4	62	RRRHRIQRVKKLI--------------FDYNLLTD--------------------HSELSGINPYEARVKGLSQKLSEE	107
S1	154	IYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQLVQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIAQLPGEK	233
S2	155	VYLALAHMIKFRGHFLIEGELNAENTDVQKIFADFVGVYNRTFDDSHLSEITVDVASILTEKISKSRRLENLIKYYPTEK	234
S3	154	IYLALAHMIKYRGHFLYEEAFDIKNNDIQKIFNEFISIYDNTFEGSSLSGQNAQVEAIFTDKISKSAKRERVLKLFPDEK	233
S4	108	FSALLHLAKRRG--------------------VHNVNEVEEDT-------------------------------	131
S1	234	KNGLFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGDQYADLFLAAKNLSDAILLSDILRVNTEIT	313
S2	235	KNTLFGNLIALALGLQPNFKTNFKLSEDAKLQFSKDTYEEDLEELLGKIGDDYADLFTSAKNLYDAILLSGILTVDDNST	314
S3	234	STGLFSEFLKLIVGNQADFKKHFDLEDKAPLQFSKDTYDEDLENLLGQIGDDFTDLFVSAKKLYDAILLSGILTVTDPST	313
S4	132	-----GNELS-------------------TKEQISRN--------------------------------	144
S1	314	KAPLSASMIKRYDEHHQDLTLLKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPILEEM--DGTEELLV	391
S2	315	KAPLSASMIKRYVEHHEDLEKLKEFIKANKSELYHDIFKDKNKNGYAGYIEGVKQDEFYKYLKNILSKIKIDGSDYFLD	394
S3	314	KAPLSASMIERYENHQNDLAALKQFIKNNLPEKYDEVFSDQSKDGYAGYIDGKTTQETFYKYIKNLLSKF--EGTDYFLD	391
S4	145	----SKALEEKYVAELQ----------------------------------------------LERLKKDG------	165
S1	392	KLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQEDFYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEE	471
S2	395	KIEREDFLRKQRTFDNGSIPHQIHLQEMHAILRRQGDYYPFLKEKQDRIEKILTFRIPYYVGPLVRKDSRFAWAEYRSDE	474
S3	392	KIEREDFLRKQRTFDNGSIPHQIHLQEMNAILRRQGEYYPFLKDNKEKIEKILTFRIPYYVGPLARGNRDFAWLTRNSDE	471
S4	166	--EVRGSINRFKTSD--------YVKEAKQLLKVQKAYHQLDQSFIDTYIDLLETRRTYYEGP--GEGSPFGW------K	227
S1	472	TITPWNFEEVVDKGASAQSFIERMTNFDKNLPNEKVLPKHSLLYEYFTVYNELTKVKYVTEGRKPAFLSGEQKKAIVDL	551
S2	475	KITPWNFDKVIDKEKSAEKFITRMTLNDLYLPEEKVLPKHSHVYETYAVYNELTKIKYVNEQGKE-SFFDSNMKQEIFDH	553
S3	472	AIRPWNFEEIVDKASSAEDFINKMTNYDLYLPEEKVLPKHSLLYETFAVYNELTKVKFIAEGLRDYQFLDSGQKKQIVNQ	551
S4	228	DIKEW---------------YEMLMGHCTYFPEELRSVKYAYNADLYNALNDLNNLVITRDENEK---LEYYEKFQIIEN	289
S1	552	LFKTNRKVTVKQLKEDYFKKIECFDSVEISGVEDR---FNASLGTYHDLLKIIKDKDFLDNEENEDILEDIVILTLTLFED	628
S2	554	VFKENRKVTKEKLLNYLNKEFPEYRIKDLIGLDKENKSFNASLGTYHDLKKIL-DKAFLDDKVNEEVIEDIIKTLTLFED	632
S3	552	LFKENRKVTEKDIIHYLHN-VDGYDGIELKGIEKQ---FNASLSTYHDLLKIIKDKEFMDDADNEAIIENIVHTLTIFED	627
S4	290	VFKQKKKPTLKQIAKEILVNEEDIKGYRVTSTGKPEF---TNLKVYHDIKDITARKEII---ENAELLDQIAKILTIYQS	363
S1	629	REMIEERLKTYAHLFDDKVMKQLKR-RRYTGWGRLSRKLINGIRDKQSGTILDFLKSDGFANRNFMQLIHDDSLTFKED	707
S2	633	KDMIHERLQKYSDIFTANQLKKLER-RHYTGWGRLSYKLINGIRNKENNKTILDYLIDDGSANRNFMQLINDDTLPFKQI	711
S3	628	REMIKQRLAQYDSLFDEKVIKALTR-RHYTTWTKLSAKLINGICDKQTGNTILDYLIDDGKINRNFMQLINDDGLSFKEI	706
S4	364	SEDIQEELTNLSELTQEEIEQISNLKGYGYHNLSLKAINLILDE------LWHTNDNQIAIFNRLKLVP---------	428
S1	708		781
S2	712		784
S3	707		779
S4	429		505
S1	782	KRIEEGIKELGSQIL--------KEHPVENTQLQNEKLYLYYLQNGRDMYVDQELDINRLSD----YDVDH*IVPQSFLKDO	850
S2	785	KKLQNSLKELGSNILNEEKPSYIEDKVENSHLQNQLFLYYIQNGKDMYTGDELDIDHLSD----YDIDH*IIFQAFIKDO	860
S3	780	KRIEDSLKILASGL--DSNILKENPTDNNQLQNDRLFLYYLQNGEKDMYTGEALDINQLSS----YDIDE*IIPQAFIKDO	852
S4	506	ERIESIIRTTGK-----------------ENAKYLIEKIKLHDMQEGKCLYSLEAIPLEDLLNNPFNYEVDH*IIPRSVSFDN	570
S1	851		922
S2	861		932
S3	853		924
S4	571		650
S1	923		1002
S2	933		1012
S3	925		1004
S4	651		712
S1	1003		1077
S2	1013		183
S3	1005		1081
S4	713		764
S1	1078		1149
S2	1084		1158
S3	1082		1156
S4	765		835
S1	1150	EKGKSKKLKSVKELLGITIMERSSFEKNPI-DFLEAKG-----YKEVKKDLIIKLPKYSLFELENGRKRMLASAGELQKG	1223
S2	1159	EKGKAKKLKTVKELVGISIMERSFFEENPV-EFLENKG-----YHNIREDKLIKLPKYSLFEFEGGRRRLLASAELQKG	1232
S3	1157	EKGKAKKLKTVKTLVGITIMEKAAFEENPI-TFLENKG-----YHNVRKENILCLPKYSLFELENGRRLLASAKELQKG	1230
S4	836	DPQTYQKLK--------LIMEQYGDEKNPLYKYYEETGNYLTKYSKKDNGPVIKKIKYYGNKLNAHLDITDDYPNSARNKV	907
S1	1224	NELALPSKLYVNFLYLASHYEKLKGSPEDNEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSAYNKH------	1297
S2	1233	NEMVLPGYLVELLYHAHRADNF-----NSTEYLNYVSEHKKEFEKVLSCVEDFANLYVDVEKNLSKIRAVADSM------	1301
S3	1231	NEIVLPVYLTTLLYHSKNVHKL-----DEPGHLEYIQKHRNEFKDLLNLVSEFSQKYVLADANLEKIKSLYADN------	1299
S4	908	VKLSLKPYRFD-VYLDNGVYKFV-----TVKNLDVIK--KENYYEVNSKAYEEAKKLKKISNQAEFIASFYNNDLIKING	979
S1	1298	RDKPIREQAENIIHLFTLTNLGAPAAFKYFDTTIDRKRYTSTKEVLDATLIHQSIT--------GLYETRI----DLSQL	1365
S2	1302	DNFSIEEISNSFINLTLTALGAPADFNFLGEKIPRKRYTSTKECLNATLIHQSIT--------GLYETRI----DLSKL	1369
S3	1300	EQADIEILANSFINLLTFTALGAPAAFKFFGKDIDRKRYTTVSEILNATLIHQSIT--------GLYETWI----DLSKL	1367
S4	980	ELYRVIGVNNDLLNRIEVNMIDITYR-EYLENMNDKPPRIIKTIASKT---QSIKKYSTDILGNLYEVSKKHPQIIKK	1055
S1	1366	GGD	1368
S2	1370	GEE	1372
S3	1368	GED	1370
S4	1056	G--	1056

The alignment demonstrates that amino acid sequences and amino acid residues that are homologous to a reference Cas9 amino acid sequence or amino acid residue can be identified across Cas9 sequence variants, including, but not limited to Cas9 sequences from different species, by identifying the amino acid sequence or residue that aligns with the reference sequence or the reference residue using alignment programs and algorithms known in the art. This disclosure provides Cas9 variants in which one or more of the amino acid residues identified by an asterisk in SEQ ID NOs: 11-14 (e.g., S1, S2, S3, and S4, respectively) are mutated as described herein. The residues D10 and H840 in Cas9 of SEQ ID NO: 10 that correspond to the residues identified in SEQ ID NOs: 11-14 by an asterisk are referred to herein as “homologous” or “corresponding” residues. Such homologous residues can be identified by sequence alignment, e.g., as described above, and by identifying the sequence or residue that aligns with the reference sequence or residue. Similarly, mutations in Cas9 sequences that correspond to mutations identified in SEQ ID NO: 10 herein, e.g., mutations of residues 10, and 840 in SEQ ID NO: 10, are referred to herein as “homologous” or “corresponding” mutations. For example, the mutations corresponding to the D10A mutation in SEQ ID NO: 10 or S1 (SEQ ID NO: 11) for the four aligned sequences above are D11A for S2, D10A for S3, and D13A for S4; the corresponding mutations for H840A in SEQ ID NO: 10 or S1 (SEQ ID NO: 11) are H850A for S2, H842A for S3, and H560A for S4.

A total of 250 Cas9 sequences (SEQ ID NOs: 11-260) from different species were aligned using the same algorithm and alignment parameters outlined above. Amino acid residues homologous to residues 10, and 840 of SEQ ID NO: 10 were identified in the same manner as outlined above. The alignments are provided below. The HNH domain (bold and underlined) and the RuvC domain (boxed) are identified for each of the four sequences. Single residues corresponding to amino acid residues 10, and 840 in SEQ ID NO: 10 are boxed in SEQ ID NO: 11 in the alignments, allowing for the identification of the corresponding amino acid residues in the aligned sequences.

Lengthy table referenced here
US20170121693A1-20170504-T00001
Please refer to the end of the specification for access instructions.

Lengthy table referenced here
US20170121693A1-20170504-T00002
Please refer to the end of the specification for access instructions.

Lengthy table referenced here
US20170121693A1-20170504-T00003
Please refer to the end of the specification for access instructions.

Example 6

Next Generation C to T Editors

Other families of cytidine deaminases as alternatives to base editor 3 (BE3) constructs were examined. The different C to T editors were developed to have a narrow or different editing window, alternate sequence specificity to expand targetable substrates, and to have higher activity.

Using the methods described in Example 4, the pmCDA1 (cytidine deaminase 1 from Petromyzon marinus) activity at the HeK-3 site is evaluated (FIG. 42). The pmCDA1-nCas9-UGI-NLS (nCas9 indicates the Cas9 nickase described herein) construct is active on some sites (e.g., the C bases on the complementary strand at position 9, 5, 4, and 3) that are not accessible with rAPOBEC1 (BE3).

The pmCDA1 activity at the HeK-2 site is given in FIG. 43. The pmCDA1-XTEN-nCas9-UGI-NLS construct is active on sites adjacent to “G,” while rAPOBEC1 analog (BE3 construct) has low activity on “C”s that are adjacent to “G”s, e.g., the C base at position 11 on the complementary strand.

The percent of total sequencing reads with target C converted to T (FIG. 44), C converted to A (FIG. 45), and C converted to G (FIG. 46) are shown for CDA and APOBEC1 (the BE3 construct).

The huAPOBEC3G activity at the HeK-2 site is shown in FIG. 47. Two constructs were used: huAPOBEC3G-XTEN-nCas9-UGI-NLS and huAPOBEC3G*(D316R_D317R)-XTEN-nCas9-UGI-NLS. The huAPOBEC3G-XTEN-nCas9-UGI-NLS construct has different sequence specificity than rAPOBEC1 (BE3), as shown in FIG. 47, the editing window appears narrow, as indicated by APOBEC3G's descreased activity at position 4 compared to APOBEC1. Mutations made in huAPOBEC3G (D316R and D317R) increased ssDNA binding and resulted in an observable effect on expanding the sites which were edited (compare APOBEC3G with APOBEC3G_RR in FIG. 47). Mutations were chosen based on APOBEC3G crystal structure, see: Holden et al., Crystal structure of the anti-viral APOBEC3G catalytic domain and functional implication. Nature. (2008); 121-4, the entire contents of which are incorporated herein by reference.

Example 7

pmCDA1/huAPOBEC3G/rAPOBEC1 Work in E. coli

LacZ selection optimization for the A to I conversion was performed using a bacterial strain with lacZ encoded on the F plasmid. A critical glutamic acid residue was mutated (e.g., GAG to GGG, Glu to Gly mutation) so that G to A by a cytidine deaminase would restore lacZ activity (FIG. 48). Strain CC102 was selected for the selection assay. APOBEC1 and CDA constructs were used in a selection assay to optimize G to A conversion.

To evaluate the the effect of copy number of the plasmids encoding the deaminase constructs on lacZ reversion frequency, the CDA and APOBEC1 deaminases were cloned into 4 plasmids with different replication origins (hence different copy numbers), SC101, CloDF3, RSF1030, and PUC (copy number: PUC>RSF1030>CloDF3>SC101) and placed under an inducible promoter. The plasmids were individually transformed into E. coli cells harboring F plasmid containing the mutated LacZ gene. The expression of the deaminases were induced and LacZ activity was detected for each construct (FIG. 49). As shown in FIG. 49, CDA exhibited significantly higher activity than APOBEC1 in all instances, regardless of the plasmid copy number the deaminases were cloned in. Further, In terms of the copy number, the deaminase activity was positively correlated with the copy number of the plasmid they are cloned in, i.e., PUC>CloDF3>SC101.

LacZ reversions were confirmed by sequencing of the genomic DNA at the lacZ locus. To obtain the genomic DNA containing the corrected LacZ gene, cells were grown media containing X-gal, where cells having LacZ activity form blue colonies. Blue colonies were selected and grown in minimal media containing lactose. The cells were spun down, washed, and re-plated on minimal media plates (lactose). The blue colony at the highest dilution was then selected, and its genomic DNA was sequenced at the lacZ locus (FIG. 50).

A chloramphenicol reversion assay was designed to test the activity of different cytidine deaminases (e.g., CDA, and APOBEC1). A plasmid harboring a mutant CAT1 gene which confers chloramphenicol resistance to bacteria is constructed with RSF1030 as the replication origin. The mutant CAT1 gene encodings a CAT1 protein that has a H195R (CAC to CGC) mutation, rendering the protein inactive (FIG. 51). Deamination of the C base-paired to the G base in the CGC codon would convert the codon back to a CAC codon, restoring the activity of the protein. As shown in FIG. 52, CDA outperforms rAPOBEC in E. coli in restoring the activity of the chloramphenicol resistance gene. The minimum inhibitory concentration (MIC) of chlor in S1030 with the selection plasmid (pNMG_ch_5) was approximately 1 μg/mL. Both rAPOBEC-XTEN-dCas9-UGI and CDA-XTEN-dCas9-UGI induced DNA correction on the selection plasmid (FIG. 53).

Next, the huAPOBEC3G-XTEN-dCas9-UGI protein was tested in the same assay. Interestingly, huAPOBEC3G-XTEN-dCas9-UGI exhibited different sequence specificity than the rAPOBEC1-XTEN-dCas9-UGI fusion protein. Only position 8 was edited with APOBEC3G-XTEN-dCas9-UGI fusion, as compared to the rAPOBEC11-XTEN-dCas9-UGIfusion (in which positions 3, 6, and 8 were edited) (FIG. 54).

Example 8

C to T Base Editors with Less Off Target Editing

Current base editing technologies allow for the sequence-specific conversion of a C:G base pair into a T:A base pair in genomic DNA. This is done via the direct catalytic conversion of cytosine to uracil by a cytidine deaminase enzyme and thus, unlike traditional genome editing technologies, does not introduce double-stranded DNA breaks (DSBs) into the DNA as a first step. See, Komor, A. C., Kim, Y. B., Packer, M. S., Zuris, J. A., and Liu, D. R. (2016), “Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.” Nature 533, 420-424; the entire contents of which are incorporated by reference herein. Instead, catalytically dead SpCas9 (dCas9) or a SpCas9 nickase (dCas9(A840H)) is tethered to a cytidine deaminase enzyme such as rAPOBEC1, pmCDA1, or hAPOBEC3G. The genomic locus of interest is encoded by an sgRNA, and DNA binding and local denaturation is facilitated by the dCas9 portion of the fusion. However, just as wt dCas9 and wt Cas9 exhibit off-target DNA binding and cleavage, current base editors also exhibit C to T editing at Cas9 off-target loci, which limits their therapeutic usefulness.

It has been reported that the introduction of just three to four mutations into SpCas9 that neutralize nonspecific electrostatic interactions between the protein and the sugar-phosphate backbone of its target DNA, increases the DNA binding specificity of SpCas9. See, Kleinstiver, B. P., Pattanayak, V., Prew, M. S., Tsai, S. Q., Nguyen, N. T., Zheng, Z., and Joung, J. K. (2016) “High-fidelity CRISPR—Cas9 nucleases with no detectable genome-wide off-target effects.” Nature 529, 490-495; and Slaymaker, I. M., Gao, L., Zetsche, B., Scott, D. A., Yan, W. X., and Zhang, F. (2015) “Rationally engineered Cas9 nucleases with improved specificity. Science 351, 84-88; the entire contents of each are hereby incorporated by reference herein. Four reported neutralizing mutations were therefore incorporated into the initially reported base editor BE3 (SEQ ID NO: 285), and found that off-target C to T editing of this enzyme is also drastically reduced (FIG. 55), with no decrease in on-target editing (FIG. 56).

As shown in FIG. 55, HEK293T cells were transfected with plasmids expressing BE3 or HF-BE3 and a sgRNA matching the EMX1 sequence using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target locus, plus the top ten known Cas9 off-target loci for the EMX1 sgRNA, as previously determined by Joung and coworkers using the GUIDE-seq method. See Tsai, S. Q., Zheng, Z., Nguyen, N. T., Liebers, M., Topkar, V. V., Thapar, V., Wyvekens, N., Khayter, C., Iafrate, A. J., Le, L. P., et al. (2015) “GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases.” Nat Biotech 33, 187-197; the entire contents of which are incorporated by reference herein. EMX1 off-target 5 locus did not amplify and is not shown. Sequences of the on-target and off-target protospacers and protospacer adjacent motifs (PAMs) are displayed (FIG. 55). Cellular C to T conversion percentages, defined as the percentage of total DNA sequencing reads with T at each position of an original C within the protospacer, are shown for BE3 and HF-BE3.

In FIG. 56, HEK293T cells were transfected with plasmids expressing BE3 or HF-BE3 and sgRNAs matching the genomic loci indicated using Lipofectamine 2000. Three days after transfection, genomic DNA was extracted, amplified by PCR, and analyzed by high-throughput DNA sequencing at the on-target loci. The percentage of total DNA sequencing reads with all four bases at the target Cs within each protospacer are shown for treatment with BE3 or HF-BE3 (FIG. 56). Frequencies of indel formation are shown as well.

Primary Protein Sequence of HF-BE3 (SEQ ID NO: 285):

MSSHTGPVAVDPTLRRRIHPHHFHVFFDPRELRKBTCLLYHINWGGRH
SIWRHTSQNTNKHVEVNFIEKFTTERYFCPNTRCSITWFLSWSPCGEC
SRAITEFLSRYPHVTLFIYIARLYHHADPRNRQGLRDLISSGVTIQIM
TEQESGYCWRNFVNYSPSNEAHWPRYPHLWVRLYVLELYCIILGLPPC
LNILRRKQPQLTFFTIALQSCHYQRLPPHILWATGLKSGSETPGTSES
ATPESDKKYSIGLAIGTNSVGWAVITDEYKVPSKKFKVLGNTDRHSIK
KNLIGALLFDSGETAEATRLKRTARRRYTRRKNRICYLQEIFSNEMAK
VDDSFFHRLEESFLVEEDKKHERHPIFGNIVDEVAYHEKYPTIYHLRK
KLVDSTDKADLRLIYLALAHMIKFRGHFLIEGDLNPDNSDVDKLFIQL
VQTYNQLFEENPINASGVDAKAILSARLSKSRRLENLIAQLPGEKKNG
LFGNLIALSLGLTPNFKSNFDLAEDAKLQLSKDTYDDDLDNLLAQIGD
QYADLFLAAKNLSDAILLSDILRVNTEITKAPLSASMIKRYDEHHQDL
TLLKALVRQQLPEKYKEIFFDQSKNGYAGYIDGGASQEEFYKFIKPIL
EKMDGTEELLVKLNREDLLRKQRTFDNGSIPHQIHLGELHAILRRQED
FYPFLKDNREKIEKILTFRIPYYVGPLARGNSRFAWMTRKSEETITPW
NFEEVVDKGASAQSFIERMTAFDKNLPNEKVLPKHSLLYEYFTVYNEL
TKVKYVTEGMRKPAFLSGEQKKAIVDLLFKTNRKVTVKQLKEDYFKKI
ECFDSVEISGVEDRFNASLGTYHDLLKIIKDKDFLDNEENEDILEDIV
LTLTLFEDREMIEERLKTYAHLFDDKVMKQLKRRRYTGWGALSRKLIN
GIRDKQSGKTILDFLKSDGFANRNFMALIHDDSLTFKEDIQKAQVSGQ
GDSLHEHIANLAGSPAIKKGILQTVKVVDELVKVMGRHKPENTVIEMA
RENQTTQKGQKNSRERMKRIEEGIKELGSQILKEHPVENTQLQNEKLY
LYYLQNGRDMYVDQELDINRLSDYDVDHIVPQSFLKDDSIDNKVLTRS
DKNRGKSDNVPSEEVVKKMKNYWRQLLNAKLITQRKFDNLTKAERGGL
SELDKAGFIKRQLVETRAITKHVAQILDSRMNTKYDENDKLIREVKVI
TLKSKLVSDFRKDFQFYKVREINNYHHAHDAYLNAVVGTALIKKYPKL
ESEFVYGDYKVYDVRKMIAKSEQEIGKATAKYFFYSNIMNFFKTEITL
ANGEIRKRPLIETNGETGEIVWDKGRDFATVRKVLSMPQVMVKKTEVQ
TGGFSKESILPKRNSDKLIARKKDWDPKKYGGFDSPTVAYSVLVVAKV
EKGKSKKLKSVKELLGITIMERSSFEKNPIDFLEAKGYKEVKKDLIIK
LPKYSLFELENGRKRMLASAGELQKGNELALPSKYVNFLYLASHYEKL
KGSPEDNEQKQLFVEQHKHYLDEIIEQISEFSKRVILADANLDKVLSA
YNKHRDKPIREQAENIIHLFTLTNLGAPAAFNYFDTTIDRKRYTSTKE
VLDATLIHQSITGLYETRIDLSQLGGDSGGSTNLSDIIEKETGKQLVI
QESILMLPEEVEEVIGNKPESDILVHTAYDESTDENVMLLTSDAPEYK
PWALVIQDSNGENKIKMLSGGSPKKKRKV

Example 9

Development of Base Editors that Use Cas9 Variants and Modulation of the Base Editor Processivity to Increase the Target Range and Precision of the Base Editing Technology

Unlike traditional genome editing platforms, base editing technology allows precise single nucleotide changes in the DNA without inducing double-stranded breaks (DSBs). See, Komor, A. C. et al. Nature 533, 420-424 (2016). The current generation of base editor uses the NGG PAM exclusively. This limits its ability to edit desired bases within the genome, as the base editor needs to be placed at a precise location where the target base is placed within a 4-base region (the ‘deamination window’), approximately 15 bases upstream of the PAM. See, Komor, A. C. et al. Nature 533, 420-424 (2016). Moreover, due to the high processivity of cytidine deaminase, the base editor may convert all cytidines within its deamination window into thymidines, which could induce amino acid changes other than the one desired by the researcher. See, Komor, A. C. et al. Nature 533, 420-424 (2016).

Expanding the Scope of Base Editing through the Development of Base Editors with Cas9 Variants

Cas9 homologs and other RNA-guided DNA binders that have different PAM specificities were incorporated into the base editor architecture. See, Kleinstiver, B. P. et al. Nature 523, 481-485 (2015); Kleinstiver, B. P. et al. Nature Biotechnology 33, 1293-1298 (2015); and Zetsche, B. et al. Cell 163, 759-771 (2015); the entire contents of each are incorporated by reference herein. Furthermore, innovations that have broadened the PAM specificities of various Cas9 proteins were also incorporated to expand the target reach of the base editor even more. See, Kleinstiver, B. P. et al. Nature 523, 481-485 (2015); and Kleinstiver, B. P. et al. Nature Biotechnology 33, 1293-1298 (2015). The current palette of base editors is summarized in Table 4.

Modulating Base Editor's Processivity through Site-Directed Mutagenesis of rAPOBEC1

It was reasoned that the processivity of the base editor could be modulated by making point mutations in the deaminase enzyme. The incorporation of mutations that slightly reduce the catalytic activity of deaminase in which the base editor could still catalyze on average one round of cytidine deamination but was unlikely to access and catalyze another deamination within the relevant timescale were pursued. In effect, the resulting base editor would have a narrower deamination window.

rAPOBEC1 mutations probed in this work are listed in Table 5. Some of the mutations resulted in slight apparent impairment of rAPOBEC1 catalysis, which manifested as preferential editing of one cytidine over another when multiple cytidines are found within the deamination window. Combining some of these mutations had an additive effect, allowing the base editor to discriminate substrate cytidines with higher stringency. Some of the double mutants and the triple mutant allowed selective editing of one cytidine among multiple cytidines that are right next to one another (FIG. 57).

Base Editor PAM Expansion and Processivity Modulation

The next generation of base editors were designed to expand editable cytidines in the genome by using other RNA-guided DNA binders (FIG. 58). Using a NGG PAM only allows for a single target within the “window” whereas the use of multiple different PAMs allows for Cas9 to be positioned anywhere to effect selective deamination. A variety of new base editors have been created from Cas9 variants (FIG. 59 and Table 4). Different PAM sites (NGA, FIG. 60; NGCG, FIG. 61; NNGRRT, FIG. 62; and NNHRRT, FIG. 63) were explored. Selective deamination was successfully achieved through kinetic modulation of cytidine deaminase point mutagenesis (FIG. 65 and Table 5).

The effect of various mutations on the deamination window was then investigated in cell culture using spacers with multiple cytidines (FIGS. 66 and 67).

Further, the effect of various mutations on different genomic sites with limited numbers of cytidines was examined (FIGS. 68 to 71). It was found that approximately one cytidine will be edited within the deamination windown in the spacer, while the rest of the cytidines will be left intact. Overall, the preference for editing is as follows: C₆>C₅>>C₇≈C₄.

Base Editing Using Cpf1

Cpf1, a Cas9 homolog, can be obtained as AsCpf1, LbCpf1, or from any other species. Schematics of fusion constructs, including BE2 and BE3 equivalents, are shown in FIG. 73. The BE2 equivalent uses catalytically inactive Cpf2 enzyme (dCpf1) instead of Cas9, while the BE3 equivalent includes the Cpf1 mutant, which nicks the target strand. The bottom schematic depicts different fusion architectures to combine the two innovations illustrated above it (FIG. 73). The base editing results of HEK293T cell TTTN PAM sites using Cpf1 BE2 were examined with different spacers (FIGS. 64A to 64C). In some embodiments, Cpf1 may be used in place of a Cas9 domain in any of the base editors provided herein. In some embodiments, the Cpf1 is a protein that is at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%, or 99.5% identical to SEQ ID NO 5807.

Full Protein Sequence of Cpf1 (SEQ ID NO: 5807):

MSIYQEFVNKYSLSKTLRFELIPQGKTLENIKARGLILDDEKRAKDYK
KAKQIIDKYHQFFIEEILSSVCISEDLLQNYSDVYFKLKKSDDDNLQK
DFKSAKDTIKKQISEYIKDSEKFKNLFNQNLIDAKKGQESDLILWLKQ
SKDNGIELFKANSDITDIDEALEIIKSFKGWITYFKGFHENRKNVYSS
NDIPTSIIYRIVDDNLPKFLENKAKYESLKDKAPEAINYEQIKKDLAE
ELTFDIDYKTSEVNQRVFSLDEVFEIANFNNYLNQSGITKFNTIIGGK
FVNGENTKRKGINEYINLYSQQTNDKTLKKYKMSVLFKQILSDTESKS
FVIDKLEDDSDVVTTMQSFYEQIAAFKTVEEKSIKETLSLLFDDLKAQ
KLDLSKIYFKNDKSLTDLSQQVFDDYSVIGTAVLEYITQQIAPKNLDN
PSKKEQELIAKKTEKAKYLSLETIKLALEEFNKHRDIDKQCRFEEILA
NFAAIPMIFDEIAQNKDNLAQISIKYQNQGKKDLLQASAEDDVKAIKD
LLDQTNNLLHKLKIFHISQSEDKANILDKDEHFYLVFEECYFELAMVP
LYNKIRNYITQKPYSDEKFKLNFENSTLANGWDKNKEPDNTAILFIKD
DKYYLGVMNKKNNKIFDDKAIKENKGEGYKKIVYKLLPGANKMLPKVF
FSAKSIKFYNPSEDTLRIRNHSTHTKNGSPQKGYEKFEFNIEDCRKFI
DFYKQSISKHPEWKDFGFRFSDTQRYNSIDEFYREVENQGYKLTFENI
SESYIDSVVNQGKLYLFQIYNKDFSAYSKGRPNLHTLYWKALFDERXL
QDVVYKLNGEAELFYRKQSIPKKITHPAKEAIANKNKDNPKKESVFEY
DLIKDKRITEDKFFFHCPITINFKSSGANKFNDEINLLLKEKANDVHI
LSIDRGERHLAYYTLVDGKGNIIKQDTFNIIGNDRMKTNYHDKLAAIE
KDRDSARKDWKKINNIKEMKEGYLSQVVHEIAKLVIEYNAIVVFEDLN
FGFKRGRFKVEKQVYQKLEKMLIEKLNYLVFKDNEFDKTGGVLRAYQL
TAPFETFKKMGKQTGIIYYVPAGFTSKICPVTGFVNQLYPKYESVSKS
QEFFSKFDKICYNLDKGYFEFSFDYKNFGDKAAKGKWTIASFGSRLIN
FRNSDKNHNWDTREVYPTKELEKLLKDYSIEYGHGECIKAAICGESDK
KFFAKLTSVLNTILQMRNSKTGTELDYLISPVADVNGNFFDSRQAPKN
MPQDADANGAYHIGLKGLMLLGRIKNNQEGKKLNLVIKNEEYFEFVQN
RNN

Example 10

Increased Fidelity of Base Editing

Examining the difference between plasmid delivery of BE3 and HF-BE3, it was found that the two edit on-target loci with comparable efficiency (FIGS. 74 and 75). However, HF-BE3 edited off-target loci much less than BE3, meaning that HF-BE3 has a much higher DNA specificity than BE3 (FIG. 76). Deaminase protein lipofection to HEK cells demonstrated that protein delivery of BE3 results in comparable on-target activity, but much better specificity, than plasmid DNA delivery of BE3. Using improved transfection procedures and better plasmids (n=2), the experiment used the following conditions: protein delivery was 125 nM Cas9:sgRNA complex, plasmid delivery was 750 ng BE3/HF-BE3 plasmid+250 ng sgRNA plasmid, and lipofection was with 1.5 μL of Lipofectamine 2000 per well. EMX-1 off target site 2 and FANCF off-target site 1 showed the most off-target editing with BE3, compared to all of the off-targets assayed (FIGS. 77 and 78), while HEK-3 showed no significant editing at off-targets for any of the delivery methods (FIG. 79). HEK-4 shows some C-to-G editing on at the on-target site, while its off-target sites 1, 3, and 4 showed the most off-target editing of all the assayed sites (FIG. 80).

Delivery of BE3 Protein via Micro-injection to Zebrafish

TYR guide RNAs were tested in an in vitro assay for sgRNA activity (FIGS. 81 and 82). The % HTS reads shows how many C residues were converted to T residues during a 2 h incubation with purified BE3 protein and PCR of the resulting product. Experiments used an 80-mer synthetic DNA substate with the target deamination site in 60 bp of its genomic context. This is not the same as % edited DNA strands because only one strand was nicked, so the product is not amplified by PCR. The proportion of HTS reads edited is equal to x/(2−x), where x is the actual proportion of THS reads edited. For 60% editing, the actual proportion of bases edited is 75%. “Off target” is represents BE3 incubated with the same DNA substrate, while bound to an off-target sgRNA. It was found sgRNAs sgRH_13, sgHR_17, and possibly sgHR_16 appeared to be promising targets for in vivo injection experiments.

The delivery of BE3 protein in was tested in vivo in zebrafish. Zebrafish embryos (n=16-24) were injected with either scramled sgRNA, sgHR_13, sgHR_16, or sgHR_17 and purified BE3. Three embryos from each condition were analyzed independently (single embryo) and for each condition, all of the injected embryos were pooled and sequenced as a pool. The results are shown in FIGS. 83 to 85.

Example 11

Uses of Base Editors to Treat Disease

Base editors or complexes provided herein (e.g., BE3) may be used to modify nucleic acids. For example, base editors may be used to change a cytosine to a thymine in a nucleic acid (e.g., DNA). Such changes may be made to, inter alia, alter the amino acid sequence of a protein, to destroy or create a start codon, to create a stop codon, to distupt splicing donors, to disrupt splicing acceptors or edit regulatory sequences. Examples of possible nucleotide changes are shown in FIG. 86.

Base editors or complexes provided herein (e.g., BE3) may be used to edit an isoform of Apolipoprotein E in a subject. For example, an Apolipoprotein E isoform may be edited to yield an isoform associated with a lower risk of developing Alzheimer's disease. Apolipoprotein E has four isoforms that differ at amino acids 112 and 158. APOE4 is the largest and most common genetic risk factor for late-onset Alzheimer's disease. Arginine residue 158 of APOE4, encoded by the nucleic acid sequence CGC, may be changed to a cysteine by using a base editor (e.g., BE3) to change the CGC nucleic acid sequence to TGC, which encodes cysteine at residue 158. This change yields an APOE3r isoform, which is associated with lower Alzheimer's disease risk. See FIG. 87.

It was tested whether base editor BE3 could be used to edit APOE4 to APOE3r in mouse astrocytes (FIG. 88). APOE 4 mouse astrocytes were nucleofected with Cas9+ template or BE3, targeting the nucleic acid encoding Arginine 158 of APOE4. The Cas9+ template yielded only 0.3% editing with 26% indels, while BE3 yielded 75% editing with 5% indels. Two additional base-edited cytosines are silent and do not yield changes to the amino acid sequence (FIG. 88).

Base editors or complexes provided herein may be used to treat prion protein diseases such as Creutzfeldt-Jakob disease and fatal familial insomnia, for example, by introducing mutations into a PRNP gene. Reverting PRNP mutations may not yield therapeutic results, and intels in PRNP may be pathogenic. Accordingly, it was tested whether PRNP could be mutated using base editors (e.g., BE3) to introduce a premature stop codon in the PRNP gene. BE3, associated with its guide RNA,was introduced into HEK cells or glioblastoma cells and was capable of editing the PRNP gene to change the encoded arginine at residue 37 to a stop codon. BE3 yielded 41% editing (FIG. 89).

Additional genes that may be edited include the following: APOE editing of Arg 112 and Arg 158 to treat increased Alzheimer's risk; APP editing of Ala 673 to decrease Alzheimer's risk; PRNP editing of Arg 37 to treat fatal familial insomnia and other prion protein diseases; DMD editing of the exons 23 and 51 splice sites to treat Duchenne muscular dystrophy; FTO editing of intron 1 to treat obesity risk; PDS editing of exon 8 to treat Pendred syndrome (genetic deafness); TMC] editing of exon 8 to treat congenital hearing loss; CYBB editing of various patient-relevant mutations to treat chronic granulomatous disease. Additional diseases that may be treated using the base editors provided herein are shown in Table 6, below.

UGI also plays a key role. Knocking out UDG (which UGI inhibits) was shown to dramatically improve the cleanliness and efficiency of C to T base editing (FIG. 90). Furthermore, base editors with nickase and without UGI were shown to produce a mixture of outcomes, with very high indel rates (FIG. 91).

Example 12

Expanding the Targeting Scope of Base Editing

Base editing is a new approach to genome editing that uses a fusion protein containing a catalytically defective Streptococcus pyogenes Cas9, a cytidine deaminase, and an inhibitor of base excision repair to induce programmable, single-nucleotide C→T (or G→A) changes in DNA without generating double-strand DNA breaks, without requiring a donor DNA template, and without inducing an excess of stochastic insertions and deletions¹. The development of five new C→T (or G→A) base editors that use natural and engineered Cas9 variants with different protospacer-adjacent motif (PAM) specificities to expand the number of sites that can be targeted by base editing by 2.5-fold are described herein. Additionally, new base editors containing mutated cytidine deaminase domains that narrow the width of the apparent editing window from approximately 5 nucleotides to 1 or 2 nucleotides were engineered, enabling the discrimination of neighboring C nucleotides that would previously be edited with comparable efficiency. Together, these developments substantially increase the targeting scope of base editing.

CRISPR-Cas9 nucleases have been widely used to mediate targeted genome editing². In most genome editing applications, Cas9 forms a complex with a single guide RNA (sgRNA) and induces a double-stranded DNA break (DSB) at the target site specified by the sgRNA sequence. Cells primarily respond to this DSB through the non-homologuous end-joining (NHEJ) repair pathway, which results in stochastic insertions or deletions (indels) that can cause frameshift mutations that disrupt the gene. In the presence of a donor DNA template with a high degree of homology to the sequences flanking the DSB, gene correction can be achieved through an alternative pathway known as homology directed repair (HDR).^3,4 Unfortunately, under most non-perturbative conditions HDR is inefficient, dependent on cell state and cell type, and dominated by a larger frequency of indels.^3,4 As most of the known genetic variations associated with human disease are point mutations, methods⁵, that can more efficiently and cleanly make precise point mutations are needed.

Base editing, which enables targeted replacement of a C:G base pair with a T:A base pair in a programmable manner without inducing DSBs¹, has been recently described. Base editing uses a fusion protein between a catalytically inactivated (dCas9) or nickase form of Streptococcus pyogenes Cas9 (SpCas9), a cytidine deaminase such as APOBEC1, and an inhibitor of base excision repair such as uracil glycosylase inhibitor (UGI) to convert cytidines into uridines within a five-nucleotide window specified by the sgRNA.¹ The third-generation base editor, BE3, converts C:G base pairs to T:A base pairs, including disease-relevant point mutations, in a variety of cell lines with higher efficiency and lower indel frequency than what can be achieved using other genome editing methods¹. Subsequent studies have validated the deaminase-dCas9 fusion approach in a variety of settings^6,7.

Efficient editing by BE3 requires the presence of an NGG PAM that places the target C within a five-nucleotide window near the PAM-distal end of the protospacer (positions 4-8, counting the PAM as positions 21-23)¹. This PAM requirement substantially limits the number of sites in the human genome that can be efficiently targeted by BE3, as many sites of interest lack an NGG 13- to 17-nucleotides downstream of the target C. Moreover, the high activity and processivity of BE3 results in conversion of all Cs within the editing window to Ts, which can potentially introduce undesired changes to the target locus. Herein, new C:G to T:A base editors that address both of these limitations are described.

It was thought that any Cas9 homolog that binds DNA and forms an “R-loop” complex⁸ containing a single-stranded DNA bubble could in principle be converted into a base editor. These new base editors would expand the number of targetable loci by allowing non-NGG PAM sites to be edited. The Cas9 homolog from Staphylococcus aureus (SaCas9) is considerably smaller than SpCas9 (1053 vs. 1368 residues), can mediate efficient genome editing in mammalian cells, and requires an NNGRRT PAM⁹. SpCas9 was replaced with SaCas9 in BE3 to generate SaBE3 and transfected HEK293T cells with plasmids encoding SaBE3 and sgRNAs targeting six human genomic loci (FIGS. 92A and 92B). After 3 d, the genomic loci were subjected to high-throughput DNA sequencing (HTS) to quantify base editing efficiency. SaBE3 enabled C to T base editing of target Cs at a variety of genomic sites in human cells, with very high conversion efficiencies (approximately 50-75% of total DNA sequences converted from C to T, without enrichment for transfected cells) arising from targeting Cs at positions 6-11. The efficiency of SaBE3 on NNGRRT-containing target sites in general exceeded that of BE3 on NGG-containing target sites¹. Perhaps due to its higher average efficiency, SaBE3 can also result in detectable base editing at target Cs at positions outside of the canonical BE3 activity window (FIG. 92C). In comparison, BE3 showed significantly reduced editing under the same conditions (0-11%), in accordance with the known SpCas9 PAM preference (FIG. 106A)¹⁰. These data show that SaBE3 can facilitate very efficient base editing at sites not accessible to BE3.

The targeting range of base editors was further expanded by applying recently engineered Cas9 variants that expand or alter PAM specificities. Joung and coworkers recently reported three SpCas9 mutants that accept NGA (VQR-Cas9), NGAG (EQR-Cas9), or NGCG(VRER-Cas9) PAM sequences¹¹. In addition, Joung and coworkers engineered a SaCas9 variant containing three mutations (SaKKH-Cas9) that relax its PAM requirement to NNNRRT¹². The SpCas9 portion of BE3 was replaced with these four Cas9 variants to produce VQR-BE3, EQR-BE3, VRER-BE3, and SaKKH-BE3, which target NNNRRT, NGA, NGAG, and NGCG PAMs respectively. HEK293T cells were transfected with plasmids encoding these constructs and sgRNAs targeting six genomic loci for each new base editor, and measured C to T base conversions using HTS.

SaKKH-BE3 edited sites with NNNRRT PAMs with efficiencies up to 62% of treated, non-enriched cells (FIG. 92D). As expected, SaBE3 was unable to efficiently edit targets containing PAMs that were NNNHRRT (where H=A, C, or T) (FIG. 92D). VQR-BE3, EQR-BE3, and VRER-BE3 exhibited more modest, but still substantial base editing efficiencies of up to 50% of treated, non-enriched cells at genomic loci with the expected PAM requirements with an editing window similar to that of BE3 (FIGS. 92E and 92F). Base editing efficiencies of VQR-BE3, EQR-BE3, and VRER-BE3 in general closely paralleled the reported PAM requirements of the corresponding Cas9 nucleases; for example, EQR-BE3 was unable to efficiently edit targets containing NGAH PAM sequences (FIG. 92F). In contrast, BE3 was unable to edit sites with NGA or NGCG PAMs efficiently (0-3%), likely due to its PAM restrictions (FIG. 106B).

Collectively, the properties of SaBE3, SaKKH-BE3, VQR-BE3, EQR-BE3, and VRER-BE3 establish that base editors exhibit a modularity that facilitates their ability to exploit Cas9 homologs and engineered variants.

Next, base editors with altered activity window widths were developed. All Cs within the activity window of BE3 can be efficiently converted to Ts¹. The ability to modulate the width of this window would be useful in cases in which it is important to edit only a subset of Cs present in the BE3 activity window.

The length of the linker between APOBEC1 and dCas9 was previously observed to modulate the number of bases that are accessible by APOBEC1 in vitro¹. In HEK293T cells, however, varying the linker length did not significantly modulate the width of the editing window, suggesting that in the complex cellular milieu, the relative orientation and flexibility of dCas9 and the cytidine deaminase are not strongly determined by linker length (FIG. 96). Next, it was thought that truncating the 5′ end of the sgRNA might narrow the base editing window by reducing the length of single-stranded DNA accessible to the deaminase upon formation of the RNA-DNA heteroduplex. HEK293T cells were co-transfected with plasmids encoding BE3 and sgRNAs of different spacer lengths targeting a locus with multiple Cs in the editing window. No consistent changes in the width of base editing when using truncated sgRNAs with 17- to 19-base spacers were observed (FIGS. 95A to 95C). Truncating the sgRNA spacer to fewer than 17 bases resulted in large losses in activity (FIG. 95A).

As an alternative approach, it was thought that mutations to the deaminase domain might narrow the width of the editing window through multiple possible mechanisms. First, some mutations may alter substrate binding, the conformation of bound DNA, or substrate accessibility to the active site in ways that reduce tolerance for non-optimal presentation of a C to the deaminase active site. Second, because the high activity of APOBEC1 likely contributes to the deamination of multiple Cs per DNA binding event,^1,13,14 mutations that reduce the catalytic efficiency of the deaminase domain of a base editor might prevent it from catalyzing successive rounds of deamination before dissociating from the DNA. Once any C:G to T:A editing event has taken place, the sgRNA no longer perfectly matches the target DNA sequence and re-binding of the base editor to the target locus should be less favorable. Both strategies were tested in an effort to discover new base editors that distinguish among multiple cytidines within the original editing window.

Given the absence of an available APOBEC1 structure, several mutations previously reported to modulate the catalytic activity of APOBEC3G, a cytidine deaminase from the same family that shares 42% sequence similarity of its active site-containing domain to that of APOBEC1, were identified¹⁵. Corresponding APOBEC1 mutations were incorporated into BE3 and evaluated their effect on base editing efficiency and editing window width in HEK293T cells at two C-rich genomic sites containing Cs at positions 3, 4, 5, 6, 8, 9, 10, 12, 13, and 14 (site A); or containing Cs at positions 5, 6, 7, 8, 9, 10, 11, and 13 (site B).

The APOBEC1 mutations R118A and W90A each led to dramatic loss of base editing efficiency (FIG. 97C). R132E led to a general decrease in editing efficiency but did not change the substantially narrow the shape of the editing window (FIG. 97C). In contrast, several mutations that narrowed the width of the editing window while maintaining substantial editing efficiency were found (FIGS. 93A and 97C). The “editing window width” was defined to represent the artificially calculated window width within which editing efficiency exceeds the half-maximal value for that target. The editing window width of BE3 for the two C-rich genomic sites tested was 5.0 (site A) and 6.1 (site B) nucleotides.

R126 in APOBEC1 is predicted to interact with the phosphate backbone of ssDNA¹³. Previous studies have shown that introducing the corresponding mutation into APOBEC3G decreased catalysis by at least 5-fold¹⁴. Interestingly, when introduced into APOBEC1 in BE3, R126A and R126E increased or maintained activity relative to BE3 at the most strongly edited positions (C5, C6, and C7), while decreasing editing activity at other positions (FIGS. 93A and 97C). Each of these two mutations therefore narrowed the width of the editing window at site A and site B to 4.4 and 3.4 nucleotides (R126A), or to 4.2 and 3.1 nucleotides (R126E), respectively (FIGS. 93A and 97C).

W90 in APOBEC1 (corresponding to W285 in APOBEC3G) is predicted to form a hydrophobic pocket in the APOBEC3G active site and assist in substrate binding¹³. Mutating this residue to Ala abrogated APOBEC3G's catalytic activity³. In BE3, W90A almost completely abrogated base editing efficiency (FIG. 97C). In contrast, it was found that W90Y only modestly decreased base editing activity while narrowing the editing window width at site A and site B to 3.8 and 4.9 nucleotides, respectively (FIG. 93A). These results demonstrate that mutations to the cytidine deaminase domain can narrow the activity window width of the corresponding base editors.

W90Y, R126E, and R132E, the three mutations that narrowed the editing window without drastically reducing base editing activity, were combined into doubly and triply mutated base editors. The double mutant W90Y+R126E resulted in a base editor (YE1-BE3) with BE3-like maximal editing efficiencies, but substantially narrowed editing window width (width at site A and site B=2.9 and 3.0 nucleotides, respectively (FIG. 93A). The W90Y+R132E base editor (YE2-BE3) exhibited modestly lower editing efficiencies (averaging 1.4-fold lower maximal editing yields across the five sites tested compared with BE3), and also substantially narrowed editing window width (width at site A and site B=2.7 and 2.8 nucleotides, respectively) (FIG. 97C). The R126E+R132E double mutant (EE-BE3) showed similar maximal editing efficiencies and editing window width as YE2-BE3 (FIG. 97C). The triple mutant W90Y+R126E+R132E (YEE-BE3) exhibited 2.0-fold lower average maximal editing yields but very little editing beyond the C6 position and an editing window width of 2.1 and 1.4 nucleotides for site A and site B, respectively (FIG. 97C). These data taken together indicate that mutations in the cytidine deaminase domain can strongly affect editing window widths, in some cases with minimal or only modest effects on editing efficiency.

The base editing outcomes of BE3, YE1-BE3, YE2-BE3, EE-BE3, and YEE-BE3 were further compared in HEK293T cells targeting four well-studied human genomic sites that contain multiple Cs within the BE3 activity window¹. These target loci contained target Cs at positions 4 and 5 (HEK site 3), positions 4 and 6 (HEK site 2), positions 5 and 6 (EMX1), or positions 6, 7, 8, and 11 (FANCF). BE3 exhibited little (<1.2-fold) preference for editing any Cs within the position 4-8 activity window. In contrast, YE1-BE3, exhibited a 1.3-fold preference for editing C5 over C4 (HEK site 3), 2.6-fold preference for C6 over C4 (HEK site 2), 2.0-fold preference for C5 over C6 (EMX1), and 1.5-fold preference for C6 over C7 (FANCF) (FIG. 93B). YE2-BE3 and EE-BE3 exhibited somewhat greater positional specificity (narrower activity window) than YE1-BE3, averaging 2.4-fold preference for editing C5 over C4 (HEK site 3), 9.5-fold preference for C6 over C4 (HEK site 2), 2.9-fold preference for C5 over C6 (EMX1), and 2.6-fold preference for C7 over C6 (FANCF) (FIG. 93B). YEE-BE3 showed the greatest positional selectivity, with a 2.9-fold preference for editing C5 over C4 (HEK site 3), 29.7-fold preference for C6 over C4 (HEK site 2), 7.9-fold preference for C5 over C6 (EMX1), and 7.9-fold preference for C7 over C6 (FANCF) (FIG. 93B). The findings establish that mutant base editors can discriminate between adjacent Cs, even when both nucleotides are within the BE3 editing window.

The product distributions of these four mutants and BE3 were further analyzed by HTS to evaluate their apparent processivity. BE3 generated predominantly T4-T5 (HEK site 3), T4-T6 (HEK site 2), and T5-T6 (EMX1) products in treated HEK293T cells, resulting in, on average, 7.4-fold more products containing two Ts, than products containing a single T. In contrast, YE1-BE3, YE2-BE3, EE-BE3, and YEE-BE3 showed substantially higher preferences for singly edited C4-T5, C4-T6, and T5-C6 products (FIG. 93C). YE1-BE3 yielded products with an average single-T to double-T product ratio of 1.4. YE2-BE3 and EE-BE3 yielded products with an average single-T to double-T product ratio of 4.3 and 5.1, respectively (FIG. 93C). Consistent with the above results, the YEE-BE3 triple mutant favored single-T products by an average of 14.3-fold across the three genomic loci. (FIG. 93C). For the target site in which only one C is within the target window (HEK site 4, at position C5), all four mutants exhibited comparable editing efficiencies as BE3 (FIG. 98). These findings indicate that these BE3 mutants have decreased apparent processivity and can favor the conversion of only a single C at target sites containing multiple Cs within the BE3 editing window. These data also suggest a positional preference of C5>C6>C7≈C4 for these mutant base editors, although this preference could differ depending on the target sequence.

The window-modulating mutations in APOBEC1 were applied to VQR-BE3, allowing selective base editing of substrates at sites targeted by NGA PAM (FIG. 107A). However, when these mutations were applied to SaKKH-BE3, a linear decrease in base editing efficiency was observed without the improvement in substrate selectivity, suggesting a different kinetic equilibrium and substrate accessibility of this base editor than those of BE3 and its variants (FIG. 107B).

The five base editors with altered PAM specificities described in this study together increase the number of disease-associated mutations in the ClinVar database that can in principle be corrected by base editing by 2.5-fold (FIGS. 94A and 94B). Similarly, the development of base editors with narrowed editing windows approximately doubles the fraction of ClinVar entries with a properly positioned NGG PAM that can be corrected by base editing without comparable modification of a non-target C (from 31% for BE3 to 59% for YEE-BE3) (FIGS. 94A and 94B).

In summary, the targeting scope of base editing was substantially expanded by developing base editors that use Cas9 variants with different PAM specificities, and by developing a collection of deaminase mutants with varying editing window widths. In theory, base editing should be possible using other programmable DNA-binding proteins (such as Cpf1¹⁶) that create a bubble of single-stranded DNA that can serve as a substrate for a single-strand-specific nucleotide deaminase enzyme.

Materials and Methods

Cloning. PCR was performed using Q5 Hot Start High-Fidelity DNA Polymerase (New England Biolabs). Plasmids for BE and sgRNA were constructed using USER cloning (New England Biolabs), obtained from previously reported plasmids¹. DNA vector amplification was carried out using NEB 10beta competent cells (New England Biolabs).

Cell culture. HEK293T (ATCC CRL-3216) were cultured in Dulbecco's Modified Eagle's Medium plus GlutaMax (ThermoFisher) supplemented with 10% (v/v) fetal bovine serum (FBS), at 37° C. with 5% CO₂. Immortalized rat astrocytes containing the ApoE4 isoform of the APOE gene (Taconic Biosciences) were maintained in Dulbecco's Modified Eagle's Medium plus GlutaMax (ThermoFisher Scientific) supplemented with 10% (v/v) fetal bovine serum (FBS) and 200 μg/mL Geneticin (ThermoFisher Scientific).

Transfections. HEK293T cells were seeded on 48-well collagen-coated BioCoat plates (Corning) and transfected at approximately 85% confluency. 750 ng of BE and 250 ng of sgRNA expression plasmids were transfected using 1.5 μl of Lipofectamine 2000 (ThermoFisher Scientific) per well according to the manufacturer's protocol.

High-throughput DNA sequencing of genomic DNA samples. Transfected cells were harvested after 3 d and the genomic DNA was isolated using the Agencourt DNAdvance Genomic DNA Isolation Kit (Beckman Coulter) according to the manufacturer's instructions. Genomic regions of interest were amplified by PCR with flanking HTS primer pairs listed in the Supplementary Sequences. PCR amplification was carried out with Phusion hot-start II DNA polymerase (ThermoFisher) according to the manufacturer's instructions. PCR products were purified using RapidTips (Diffinity Genomics). Secondary PCR was performed to attach sequencing adaptors. The products were gel-purified and quantified using the KAPA Library Quantification Kit-Illumina (KAPA Biosystems). Samples were sequenced on an Illumina MiSeq as previously described¹.

Data analysis. Nucleotide frequencies were assessed using a previously described MATLAB script¹. Briefly, the reads were aligned to the reference sequence via the Smith-Waterman algorithm. Base calls with Q-scores below 30 were replaced with a placeholder nucleotide (N). This quality threshold results in nucleotide frequencies with an expected theoretical error rate of 1 in 1000.

Analyses of base editing processivity were performed using a custom python script. This program trims sequencing reads to the 20 nucleotide protospacer sequence as determined by a perfect match for the 7 nucleotide sequences that should flank the target site. These targets were then consolidated and sorted by abundance to assess the frequency of base editing products.

Bioinformatic analysis of the ClinVar database of human disease-associated mutations was performed in a manner similar to that previously described but with small adjustments¹. These adjustments enable the identification of targets with PAMs of customizable length and sequence. In addition, this improved script includes a priority ranking of target C positions (C5>C6>C7>C8≈C4), thus enabling the identification of target sites in which the on-target C is either the only cytosine within the window or is placed at a position with higher predicted editing efficiency than any off-target C within the editing window.

References for Example 12

• 1 Komor, A. C. et al. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage. Nature 533, 420-424 (2016).
• 2 Sander, J. D. & Joung, J. K. CRISPR-Cas systems for editing, regulating and targeting genomes. Nature biotechnology 32, 347-355 (2014).
• 3 Cong, L. et al. Multiplex genome engineering using CRISPR/Cas systems. Science 339, 819-823 (2013).
• 4 Ran, F. A. et al. Genome engineering using the CRISPR-Cas9 system. Nat. Protocols 8, 2281-2308 (2013).
• 5 Landrum, M. J. et al. ClinVar: public archive of interpretations of clinically relevant variants. Nucleic Acids Res. 44, D862-D868 (2015).
• 6 Nishida, K. et al. Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems. Science 353, aaf8729-1-8 (2016).
• 7 Ma, Y. et al. Targeted AID-mediated mutagenesis (TAM) enables efficient genomic diversification in mammalian cells. Nat. Methods doi:10.1038/nmeth.4027 (2016).
• 8 Jiang, F. et al. Structures of a CRISPR-Cas9 R-loop complex primed for DNA cleavage. Science 351, 867-71 (2016).
• 9 Ran, F. A. et al. In vivo genome editing using Staphylococcus aureus Cas9. Nature 520, 186-191 (2015).
• 10 Zhang, Y. et al. Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells. Sci. Rep. 4, (2014).
• 11 Kleinstiver, B. P. et. al. Engineered CRISPR-Cas9 nucleases with altered PAM specificities. Nature 523, 481-485 (2015).
• 12 Kleinstiver, B. P. et. al. Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition. Nat. Biotechnol. 33, 1293-1298 (2015).
• 13 Holden, L. G. et al. Crystal structure of the anti-viral APOBEC3G catalytic domain and functional implications. Nature 452, 121-124 (2008).
• 14 Chen, K.-M. et al. Structure of the DNA deaminase domain of the HIV-1 restriction factor APOBEC3G. Nature 452, 116-119 (2008).
• 15 Harris, R. S., Petersen-Mahrt, S. K. & Neuberger, M. S. RNA Editing Enzyme APOBEC1 and Some of Its Homologs Can Act as DNA Mutators. Molecular Cell 10, 1247-1253 (2002).
• 16 Zetsche, B. et al. Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System. Cell 163, 759-771 (2015).

Example 13

Using improved transfection procedures and better plasmids, biological replicates (n=3) were used to install the four HF mutations into the Cas9 portion of BE3. The muations do not significantly effect on-targeting editing with plasmid delivery (FIG. 99). At the tested concentration, BE3 protein delivery works; however, the on-target editing is lower than for plasmid delivery (FIG. 100). Protein delivery of BE3 with the HF mutations installed reduces on-targeting ediing efficiency but still yields some edited cells (FIG. 101).

Both lipofection and installing HF mutations were shown to decrease off-target deamination events. For the four sites shown in FIG. 102, the off-target sitest (OT) with the highest GUIDE-Seq reads and deamination events were assayed (Komor et al., Nature, 2016). The specificity ratio was calculated by dividing the off-target editing by the on-target editing at the closest corresponding C. In cases where off-target editing was not detectable, the ratio was set to 100. Thus, a higher specificity ratio indicates a more specific construct. BE3 plasmid delivery showed much higher off-target/on-target editing than protein delivery of BE3, plasmid delivery of HF-BE3, or protein delivery of HF-BE3 (FIGS. 102 and 105).

Purified proteins HF-BE3 and BE3 were analyzed in vitro for their capabilities to convert C to T residues at different positions in the spacer with the most permissive motif. Both BE3 and HF-BE3 proteins were found to have the same “window” for base editing (FIGS. 103 and 104).

A list of the disease targets is given in Table 9. The base to be edited in Table 9 is indicated in bold and underlined.

TABLE 9
Base Editor Disease Targets
			SEQ
GENE	DISEASE	SPACER	ID NO:	PAM	EDITOR	DEFECT	CELL
RBI	RETINO-	AATCTAGTAAA	4120	AAA	SAKKH-	SPLICING	J82
	BLASTOMA	TAAATTGATGT		AGT	BE3	IMPAIRMENT
PTEN	CANCER	GACCAACGGCT	4121	TGA	VQR-	W111R	MC116
		AAGTGAAGA			BE3
PIK3CA	CANCER	TCCTTTCTTCA	4122	ACT	SAKKH-	K111R	CRL-
		CGGTTGCCT		GGT	BE3		5853
PIK3CA	CANCER	CTCCTGCTCAG	4123	AGA	VQR-	Q546R	CRL-
		TGATTTCAG			BE3		2505
TP53	CANCER	TGTCACACATG	4124	TGG	YEE-	N239D	SNU475
		TAGTTGTAG			BE3
HRAS	CANCER	CCTCCCGGCCG	4125	AGO	YEE-	Q61R	MC/CAR
		GCGGTATCC			BE3

TABLE 6
Exemplary diseases that may be treated using base editors. The protospacer and
PAM sequences are shown in the sgRNA (PAM) column. The PAM sequence is shown in
parentheses and with the base to be edited indicated by underlining. The sgRNA (PAM)
sequences, from top to bottom, correspond to SEQ ID NOs: 4126-4138.
	gene	Base
Disease target	symbol	changed	sgRNA (PAM)	Base editor
Prion disease	PRNP	R37*	GGCAGCCGATACCCGGGGCA(GGG)	BE3
			GGGCAGCCGATACCCGGGGC(AGG)
Pendred syndrome	Slc26a4	c.919-2A > G	TTATTGTCCGAAATAAAAGA(AGA)	BE3
			ATTGTCCGAAATAAAAGAAG(AGG)	(VQR
			TTGTCCGAAATAAAAGAAGA(GGA)	SaCas9)
			GTCCGAAATAAAAGAAGAGGAAAA(AAT)
			GTCCGAAATAAAAGAAGAGGAAAAA(ATT)
Congenital deafness	Tmc1	c.545A > G	CAGGAAGCACGAGGCCACTG(AGG)	BE3
			AACAGGAAGCACGAGGCCAC(TGA)	YE-BE3
			AGGAAGCACGAGGCCACTGA(GGA)	YEE-BE3
Acquired deafness	SNHL	S33F	TTGGATTCTGGAATCCATTC(TGG)	BE3
Alzheimer′s Disease	APP	A673T	TCTGCATCCATCTTCACTTC(AGA)	BE3 VQR
Niemann-Pick Disease	NPC1	I1061T	CTTACAGCCAGTAATGTCAC(CGA)	BE3 VQR
Type C

Additional exemplary genes in the human genome that may be targeted by the base editors or complexes of this disclosure are provided herein in Tables 7 and 8. Table 7 includes gene mutations that may be correcteded by changing a cytosine (C) to a thymine (T), for example, using a BE3 nucleobase editor. Table 8 includes gene mutations that may be corrected by changing a guanine (G) to an adenine (A), for example, using a BE3 nucleobase editor.

Lengthy table referenced here
US20170121693A1-20170504-T00004
Please refer to the end of the specification for access instructions.

Lengthy table referenced here
US20170121693A1-20170504-T00005
Please refer to the end of the specification for access instructions.

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EQUIVALENTS AND SCOPE

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents of the embodiments described herein. The scope of the present disclosure is not intended to be limited to the above description, but rather is as set forth in the appended claims.

Articles such as “a,” “an,” and “the” may mean one or more than one unless indicated to the contrary or otherwise evident from the context. Claims or descriptions that include “or” between two or more members of a group are considered satisfied if one, more than one, or all of the group members are present, unless indicated to the contrary or otherwise evident from the context. The disclosure of a group that includes “or” between two or more group members provides embodiments in which exactly one member of the group is present, embodiments in which more than one members of the group are present, and embodiments in which all of the group members are present. For purposes of brevity those embodiments have not been individually spelled out herein, but it will be understood that each of these embodiments is provided herein and may be specifically claimed or disclaimed.

It is to be understood that the invention encompasses all variations, combinations, and permutations in which one or more limitation, element, clause, or descriptive term, from one or more of the claims or from one or more relevant portion of the description, is introduced into another claim. For example, a claim that is dependent on another claim can be modified to include one or more of the limitations found in any other claim that is dependent on the same base claim. Furthermore, where the claims recite a composition, it is to be understood that methods of making or using the composition according to any of the methods of making or using disclosed herein or according to methods known in the art, if any, are included, unless otherwise indicated or unless it would be evident to one of ordinary skill in the art that a contradiction or inconsistency would arise.

Where elements are presented as lists, e.g., in Markush group format, it is to be understood that every possible subgroup of the elements is also disclosed, and that any element or subgroup of elements can be removed from the group. It is also noted that the term “comprising” is intended to be open and permits the inclusion of additional elements or steps. It should be understood that, in general, where an embodiment, product, or method is referred to as comprising particular elements, features, or steps, embodiments, products, or methods that consist, or consist essentially of, such elements, features, or steps, are provided as well. For purposes of brevity those embodiments have not been individually spelled out herein, but it will be understood that each of these embodiments is provided herein and may be specifically claimed or disclaimed.

Where ranges are given, endpoints are included. Furthermore, it is to be understood that unless otherwise indicated or otherwise evident from the context and/or the understanding of one of ordinary skill in the art, values that are expressed as ranges can assume any specific value within the stated ranges in some embodiments, to the tenth of the unit of the lower limit of the range, unless the context clearly dictates otherwise. For purposes of brevity, the values in each range have not been individually spelled out herein, but it will be understood that each of these values is provided herein and may be specifically claimed or disclaimed. It is also to be understood that unless otherwise indicated or otherwise evident from the context and/or the understanding of one of ordinary skill in the art, values expressed as ranges can assume any subrange within the given range, wherein the endpoints of the subrange are expressed to the same degree of accuracy as the tenth of the unit of the lower limit of the range.

In addition, it is to be understood that any particular embodiment of the present invention may be explicitly excluded from any one or more of the claims. Where ranges are given, any value within the range may explicitly be excluded from any one or more of the claims. Any embodiment, element, feature, application, or aspect of the compositions and/or methods of the invention, can be excluded from any one or more claims. For purposes of brevity, all of the embodiments in which one or more elements, features, purposes, or aspects is excluded are not set forth explicitly herein.

LENGTHY TABLES
The patent application contains a lengthy table section. A copy of the table is available in electronic form from the USPTO web site (). An electronic copy of the table will also be available from the USPTO upon request and payment of the fee set forth in 37 CFR 1.19(b)(3).

Claims

1. A fusion protein comprising: (i) a Cas9 domain; (ii) a cytidine deaminase domain; and (iii) a uracil glycosylase inhibitor (UGI) domain.

2. The fusion protein of claim 1, wherein the Cas9 domain comprises an amino acid sequence that is at least 85% identical to the amino acid sequence provided in SEQ ID NO: 674.

3. The fusion protein of claim 1, wherein the Cas9 domain is a Cas9 nickase domain that cuts a nucleotide target strand of a nucleotide duplex, wherein the nucleotide target strand is the strand that binds to a gRNA of the Cas9 nickase domain.

4. The fusion protein of claim 1, wherein the Cas9 domain is an nCas9 domain that comprises a D10A mutation in the amino acid sequence provided in SEQ ID NO: 10, or a corresponding mutation in any of the amino acid sequences provided in SEQ ID NOs: 11-260.

5. The fusion protein of claim 1, wherein the Cas9 domain is an nCas9 domain that comprises one or more of N496A, R660A, Q694A, and Q926A of the amino acid sequence provided in SEQ ID NO 10, or one or more corresponding mutations in any of the amino acid sequences provided in SEQ ID NOs: 11-260.

6. The fusion protein of claim 1, wherein the cytidine deaminase domain is a deaminase from the apolipoprotein B mRNA-editing complex (APOBEC) family deaminase.

7. The fusion protein of claim 6, wherein the APOBEC family deaminase is selected from the group consisting of APOBEC1 deaminase, APOBEC2 deaminase, APOBEC3A deaminase, APOBEC3B deaminase, APOBEC3C deaminase, APOBEC3D deaminase, APOBEC3F deaminase, APOBEC3G deaminase, and APOBEC3H deaminase.

8. The fusion protein of claim 1, wherein the cytidine deaminase domain comprises an amino acid sequence that is at least 85% identical to an amino acid sequence of SEQ ID NO: 266-284, 607-610, 5724-5736, or 5738-5741.

9. The fusion protein of claim 1, wherein the cytidine deaminase domain comprises an amino acid sequence of SEQ ID NO: 266-284, 607-610, 5724-5736, or 5738-5741.

10. The fusion protein of claim 1, wherein the cytidine deaminase domain is a rat APOBEC1 (rAPOBEC1) deaminase comprising one or more mutations selected from the group consisting of W90Y, R126E, and R132E of SEQ ID NO: 284, or one or more corresponding mutations in another APOBEC deaminase.

11. The fusion protein of claim 1, wherein the cytidine deaminase domain is a human APOBEC1 (hAPOBEC1) deaminase comprising one or more mutations selected from the group consisting of W90Y, Q126E, and R132E of SEQ ID NO: 5724, or one or more corresponding mutations in another APOBEC deaminase.

12. The fusion protein of claim 1, wherein the cytidine deaminase domain is a human APOBEC3G (hAPOBEC3G) deaminase comprising one or more mutations selected from the group consisting of W285Y, R320E, and R326E of SEQ ID NO: 275, or one or more corresponding mutations in another APOBEC deaminase.

13. The fusion protein of claim 1, wherein the cytidine deaminase domain is an activation-induced deaminase (AID).

14. The fusion protein of claim 1, wherein the cytidine deaminase domain is a cytidine deaminase 1 from Petromyzon marinus (pmCDA1).

15. The fusion protein of claim 1, wherein the UGI domain comprises a domain capable if inhibiting UDG activity.

16. The fusion protein of claim 1, wherein the UGI domain comprises an amino acid sequence that is at least 85% identical to SEQ ID NO: 600.

17. The fusion protein of claim 1, wherein the UGI domain comprises an amino acid sequence as set forth in SEQ ID NO: 600.

18. The fusion protein of claim 1, wherein the fusion protein comprises the structure: NH2-[cytidine deaminase domain]-[Cas9 domain]-[UGI domain]-COOH, and wherein each instance of “-” comprises an optional linker.

19. The fusion protein of claim 1, wherein the cytidine deaminase domain of (ii) and the nCas9 domain of (i) are linked via a linker comprising the amino acid sequence (GGGS)n (SEQ ID NO: 265), (GGGGS)n (SEQ ID NO: 5), (G)n, (EAAAK)n (SEQ ID NO: 6), (GGS)n, (SGGS)n (SEQ ID NO: 4288), SGSETPGTSESATPES (SEQ ID NO: 7), or (XP)n motif, or a combination thereof, wherein n is independently an integer between 1 and 30, inclusive, and wherein X is any amino acid.

20. The fusion protein of claim 1, wherein the cytidine deaminase domain of (ii) and the nCas9 domain of (i) are linked via a linker comprising the amino acid sequence: SGSETPGTSESATPES (SEQ ID NO: 7).

21. The fusion protein of claim 1 further comprising a nuclear localization sequence (NLS).

22. The fusion protein of claim 21, wherein the NLS comprises the amino acid sequence PKKKRKV (SEQ ID NO: 741) or MDSLLMNRRKFLYQFKNVRWAKGRRETYLC (SEQ ID NO: 742)

23. The fusion protein of claim 21, wherein the fusion protein comprises the structure: NH2-[cytidine deaminase domain]-[nCas9 domain]-[UGI domain]-[NLS]-COOH, and wherein each instance of “-” comprises an optional linker.

24. The fusion protein of claim 21, wherein the UGI domain and the NLS are linked via a linker comprising the amino acid sequence: SGGS (SEQ ID NO: 4288), or wherein the nCas9 domain and the UGI domain are linked via a linker comprising the amino acid sequence: SGGS (SEQ ID NO: 4288).

25. The fusion protein of claim 1, wherein the fusion protein comprises the amino acid sequence set forth in SEQ ID NO: 594.

26. A complex comprising the fusion protein of claim 1 and a guide RNA bound to the nCas9 domain of the fusion protein.

27. A method comprising contacting a nucleic acid molecule with the fusion protein of claim 1 and a guide RNA, wherein the guide RNA comprises a sequence of at least 10 contiguous nucleotides that is complementary to a target sequence in the genome of an organism and comprises a target base pair.

28. The method of claim 27, wherein the target base pair comprises a T to C point mutation associated with a disease or disorder, and wherein the deamination of the mutant C base results in a sequence that is not associated with a disease or disorder.

29. The method of claim 27, wherein the contacting results in less than 20% indel formation upon base editing.

30. The method of claim 27, wherein the contacting results in at least 2:1 intended to unintended product upon base editing.

31.-302. (canceled)