Patent Grant
11840685
The contents of the electronic sequence listing (292057.xml; Size: 388,026 bytes; and Date of Creation: Dec. 15, 2022) is herein incorporated by reference in its entirety.
Genome editing is a type of genetic engineering in which DNA is inserted, deleted or replaced in the genome of a living organism using engineered nucleases (molecular scissors). Utilizing genome editing tools to genetically manipulate the genome of cells and living organism has broad applications in life sciences researches, biotechnology/agricultural technology development and most importantly pharmaceutical/clinical innovations. For example, genome editing can be used to correct the driver mutations underlying genetic diseases and leading to complete cure of these diseases in living organisms. Genome editing can also be used to engineer the genome of crops, increasing the yield of crops and conferring crops resistance to environmental contamination or pathogen infection. In addition, microbial genome transformation through accurate genome editing is of great significance in the development of renewable bio-energy.
CRISPR/Cas (Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein) system has been the most powerful genomic editing tool since its conception for its unparalleled editing efficiency, convenience and the potential applications in living organisms. Directed by a guide RNA (gRNA), the Cas nuclease can generate DNA double strand breaks (DSBs) at the targeted genomic sites in various cells (both cell lines and cells from living organisms). These DSBs are then repaired by the endogenous DNA repair system, which could be utilized to perform desired genome editing.
In general, two major DNA repair pathways can be activated by DSBs, non-homologous end joining (NHEJ) and homology-directed repair (HDR). NHEJ can introduce random insertions/deletions (indels) in the genomic DNA region around the DSBs, leading to open reading frame (ORF) shift and ultimately gene inactivation. In contrast, when HDR is triggered, the genomic DNA sequence at the target site can be replaced by the sequence of the exogenous donor DNA template through a homologous recombination mechanism, which can result in the correction of genetic mutation. However, the practical efficiency of HDR-mediated gene correction is low (normally <5%) because the occurrence of homologous recombination is both cell type-specific and cell cycle-dependent and NHEJ is triggered more frequently than HDR is. The relatively low efficiency of HDR therefore limited the translation of CRISPR/Cas genome editing tools in the field of precision gene therapy (diseases-driven gene correction).
Base editors (BE), which integrate the CRISPR/Cas system with the APOBEC (apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like) AID (activation-induced cytidine deaminase) family, was recently developed that greatly enhanced the efficiency of CRISPR/Cas-meditated gene correction. Through the fusion with the Cas9 nickase (nCas9) or a catalytically dead Cpf1 (dCpf1 also known as dCas12a), the cytosine (C) deamination activity of APOBEC/AID family members can be purposely directed to the target bases in the genome and to catalyze C to Thymine (T) substitutions at these bases.
However, as APOBEC/AID family members can induce C-to-T base substitution mutations in single-stranded DNA (ssDNA) regions, the specificity of the current base editing system is compromised, thereby limiting the applications, for instance, using BEs to restore the T-to-C mutation that result in human diseases for therapeutic purposes. Hence, creating novel BEs that can specifically edit cytosines in target region but not cause C-to-T mutations in other ssDNA regions is desirable. Such novel BEs will enable us to perform more specific base editing in various living organisms. Importantly, the high specificity of such BEs will promote the potential clinical translation, particularly in the gene therapies that involve restoring disease-related T-to-C mutations.
The present disclosure, in some embodiments, provides base editors useful for genome editing that cause reduced or even no off-target mutations common to current base editors. In certain embodiments, a nucleobase deaminase inhibitor is cleavably fused to a nucleobase deaminase involved for genome editing. In the presence of the nucleobase deaminase inhibitor, the nucleobase deaminase is unable to (is less able to) react with a nucleotide molecule. At a target editing location, the nucleobase deaminase inhibitor can be cleaved releasing a fully active nucleobase deaminase that can then carry out the editing as desired.
Accordingly, in one embodiment, provided is a fusion protein comprising: a first fragment comprising a nucleobase deaminase or a catalytic domain thereof, a second fragment comprising a nucleobase deaminase inhibitor, and a protease cleavage site between the first fragment and the second fragment.
In some embodiments, the nucleobase deaminase is an adenosine deaminase. In some embodiments, the adenosine deaminase is selected from the group consisting of tRNA-specific adenosine deaminase (TadA), adenosine deaminase tRNA specific 1 (ADAT1), adenosine deaminase tRNA specific 2 (ADAT2), adenosine deaminase tRNA specific 3 (ADAT3), adenosine deaminase RNA specific B1 (ADARB1), adenosine deaminase RNA specific B2 (ADARB2), adenosine monophosphate deaminase 1 (AMPD1), adenosine monophosphate deaminase 2 (AMPD2), adenosine monophosphate deaminase 3 (AMPD3), adenosine deaminase (ADA), adenosine deaminase 2 (ADA2), adenosine deaminase like (ADAL), adenosine deaminase domain containing 1 (ADAD1), adenosine deaminase domain containing 2 (ADAD2), adenosine deaminase RNA specific (ADAR) and adenosine deaminase RNA specific B1 (ADARB1).
In some embodiments, the nucleobase deaminase is a cytidine deaminase. In some embodiments, the cytidine deaminase is selected from the group consisting of APOBEC3B (A3B), APOBEC3C (A3C), APOBEC3D (A3D), APOBEC3F (A3F), APOBEC3G (A3G), APOBEC3H (A3H), APOBEC1 (A1), APOBEC3 (A3), APOBEC2 (A2), APOBEC4 (A4) and AICDA (AID). In some embodiments, the cytidine deaminase is a human or mouse cytidine deaminase. In some embodiments, the catalytic domain is mouse A3 cytidine deaminase domain 1 (CDA1) or human A3B cytidine deaminase domain 2 (CDA2).
In some embodiments, the nucleobase deaminase inhibitor is an inhibitory domain of a nucleobase deaminase. In some embodiments, the nucleobase deaminase inhibitor is an inhibitory domain of a is a cytidine deaminase. In some embodiments, the nucleobase deaminase inhibitor is an inhibitory domain of an adenosine deaminase. In some embodiments, the nucleobase deaminase inhibitor comprises an amino acid sequence selected from SEQ ID NO: 1-2 and Tables 1 and 2 (SEQ ID NO: 48-135), or an amino acid sequence having at least 85% sequence identity to any of the amino acid sequence selected from SEQ ID NO: 1-2 and Tables 1 and 2. In some embodiments, the nucleobase deaminase inhibitor comprises the amino acid sequence of SEQ ID NO:1, amino acids residues AA76-AA149 of SEQ ID NO:1 or the amino acid sequence of SEQ ID NO:2.
In some embodiments, the first fragment further comprises a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein. In some embodiments, the Cas protein is selected from the group consisting of SpCas9, FnCas9, St1Cas9, St3Cas9, NmCas9, SaCas9, AsCpf1, LbCpf1, FnCpf1, VQR SpCas9, EQR SpCas9, VRER SpCas9, xSpCas9, SpCas9-NG, RHA FnCas9, KKH SaCas9, NmeCas9, StCas9, CjCas9, AsCpf1, FnCpf1, SsCpf1, PcCpf1, BpCpf1, CmtCpf1, LiCpf1, PmCpf1, Pb3310Cpf1, Pb4417Cpf1, BsCpf1, EeCpf1, BhCas12b, AkCas12b, EbCas12b, LsCas12b, RfCas13d, LwaCas13a, PspCas13b, PguCas13b, and RanCas13b.
In some embodiments, the protease cleavage site is a protease cleavage site a protease selected from the group consisting of TuMV protease, PPV protease, PVY protease, ZIKV protease and WNV protease.
In some embodiments, the protease cleavage site is a self-cleavage site. In some embodiments, the protease cleavage site is a TEV protease cleavage site. In some embodiments, the fusion protein further comprises a third fragment comprising a TEV protease or a fragment thereof. In some embodiments, the third fragment comprises a TEV protease fragment which alone is not able to cleave the TEV protease cleavage site.
Also provided, in another embodiment, is a fusion protein comprising: a first fragment comprising a cytidine deaminase or a catalytic domain thereof, a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a first TEV protease fragment, a second fragment comprising a cytidine deaminase inhibitor, and a TEV protease cleavage site between the first fragment and the second fragment, wherein the first TEV protease fragment alone is not able to cleave the TEV protease cleavage site.
In some embodiments, the fusion protein further comprises a uracil glycosylase inhibitor (UGI). In some embodiments, the cytidine deaminase inhibitor, the TEV protease cleavage site, the cytidine deaminase or a catalytic domain thereof, the Cas protein, and the first TEV protease fragment are arranged from the N-terminus to the C-terminus. In some embodiments, the first TEV protease fragment is the N-terminal domain (SEQ ID NO:3) or the C-terminal domain (SEQ ID NO:4) of the TEV protease. In some embodiments, the TEV protease cleavage site has the amino acid sequence of SEQ ID NO:5.
Further provided, in one embodiment, is a method for conducting genomic editing in a cell at a target site, comprising introducing to the cell: (a) a fusion protein of the present disclosure, (b) a guide RNA that targets the target site or a crRNA that targets the target site and a tracrRNA, and further comprises a tag sequence, and (c) a second TEV protease fragment coupled to an RNA recognition peptide that is able to bind the tag sequence.
In some embodiments, one or more of the molecules is introduced to the cell by a polynucleotide encoding the molecule. In some embodiments, the first TEV protease fragment and the second TEV protease fragment, when in interaction, are able to cleave the TEV protease cleavage site. In some embodiments, the second TEV protease fragment is fused to the RNA recognition peptide.
In some embodiments, the tag sequence comprises a MS2 sequence (SEQ ID NO:16). In some embodiments, the RNA recognition peptide comprises a MS2 coat protein (MCP, SEQ ID NO:22). In some embodiments, the tag sequence comprises a PP7 sequence (SEQ ID NO:18) and the RNA recognition peptide comprises a PP7 coat protein (PCP, SEQ ID NO: 23), or the tag sequence comprises a boxB sequence (SEQ ID NO:20) and the RNA recognition peptide comprises a boxB coat protein (N22p, SEQ ID NO:24).
Also provided, in one embodiment, is a kit or package for conducting gene editing, comprising: (a) a fusion protein of the present disclosure, and (b) a second TEV protease fragment coupled to an RNA recognition peptide that is able to bind an RNA sequence.
Yet another embodiment provides a fusion protein comprising: a first fragment comprising first cytidine deaminase or a catalytic domain thereof, and a second fragment comprising an inhibitory domain of a second cytidine deaminase, wherein the first cytidine deaminase is same as or different from the second cytidine deaminase.
In another embodiment, a fusion protein is provided comprising a first fragment comprising: a nucleobase deaminase or a catalytic domain thereof, a nucleobase deaminase inhibitor, a first RNA recognition peptide, and a TEV protease cleavage site between the nucleobase deaminase or a catalytic domain thereof and the nucleobase deaminase inhibitor.
In some embodiments, the fusion protein further comprises a second fragment comprising: a TEV protease fragment which alone is not able to cleave the TEV protease cleavage site, and a second RNA recognition peptide. In some embodiments, the fusion protein further comprises a self-cleavage site between the first fragment and the second fragment.
In some embodiments, the fusion protein further comprises a third fragment comprising a second TEV protease fragment, wherein the first TEV protease fragment is able to cleave the TEV protease site in the presence of the second TEV protease fragment. In some embodiments, the fusion protein further comprises a second self-cleavage site between the second fragment and the third fragment, ad upon cleavage of the second self-cleavage site, the fusion protein releases the second TEV protease fragment which is not fused to any RNA recognition peptide.
Also provided, in one embodiment, is a dual guide RNA system, comprising: a target single guide RNA comprising a first spacer having sequence complementarity to a target nucleic acid sequence proximate to a first PAM site, a helper single guide RNA comprising a second spacer having sequence complementarity to a second nucleic acid sequence proximate to a second PAM site, a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a nucleobase deaminase, wherein the second PAM site is from 34 to 91 bases from the first PAM site. In some embodiments, the second spacer is 8-15 bases in length. In some embodiments, the second spacer is 9-12 bases in length.
In one embodiment, provided is guide RNA comprising a scaffold which comprises, from the 5′ to 3′ direction, a first stem loop portion, a second stem loop portion, a third stem loop portion, and a fourth stem loop portion, wherein the third stem loop comprises five base pairings within. In another embodiment, the present disclosure provides a guide RNA comprising a scaffold derived from SEQ ID NO:31 by introducing a base pairing between the bases at positions 45 and 55. In some embodiments, the scaffold comprises a sequence selected from the group consisting of SEQ ID NO:32-43. In some embodiments, the guide RNA is at least 100, or 120 nucleotides in length.
Another embodiment provides a method for conducting genetic editing in a cell at a target site, comprising introducing to the cell: a first viral particle enclosing a first construct encoding a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a second viral particle enclosing a second construct encoding a reverse-transcriptase fused to an RNA recognition peptide.
In some embodiments, the second construct further encodes a guide RNA comprising an RNA recognition site that the RNA recognition peptide binds to. In some embodiments, the Cas protein is SpCas9-NG (SEQ ID NO:46) or xSpCas9 (SEQ ID NO:47).
Polynucleotides encoding the fusion proteins of the present disclosure, constructs containing the polynucleotides, cells containing the polynucleotides or the constructs, and compositions comprising any of the above are also provided, without limitation.
It is to be noted that the term “a” or “an” entity refers to one or more of that entity; for example, “an antibody,” is understood to represent one or more antibodies. As such, the terms “a” (or “an”), “one or more,” and “at least one” can be used interchangeably herein.
As used herein, the term “polypeptide” is intended to encompass a singular “polypeptide” as well as plural “polypeptides,” and refers to a molecule composed of monomers (amino acids) linearly linked by amide bonds (also known as peptide bonds). The term “polypeptide” refers to any chain or chains of two or more amino acids, and does not refer to a specific length of the product. Thus, peptides, dipeptides, tripeptides, oligopeptides, “protein”, “amino acid chain” or any other term used to refer to a chain or chains of two or more amino acids, are included within the definition of “polypeptide,” and the term “polypeptide” may be used instead of, or interchangeably with any of these terms. The term “polypeptide” is also intended to refer to the products of post-expression modifications of the polypeptide, including without limitation glycosylation, acetylation, phosphorylation, amidation, derivatization by known protecting/blocking groups, proteolytic cleavage, or modification by non-naturally occurring amino acids. A polypeptide may be derived from a natural biological source or produced by recombinant technology, but is not necessarily translated from a designated nucleic acid sequence. It may be generated in any manner, including by chemical synthesis.
“Homology” or “identity” or “similarity” refers to sequence similarity between two peptides or between two nucleic acid molecules. Homology can be determined by comparing a position in each sequence which may be aligned for purposes of comparison. When a position in the compared sequence is occupied by the same base or amino acid, then the molecules are homologous at that position. A degree of homology between sequences is a function of the number of matching or homologous positions shared by the sequences. An “unrelated” or “non-homologous” sequence shares less than 40% identity, though preferably less than 25% identity, with one of the sequences of the present disclosure.
A polynucleotide or polynucleotide region (or a polypeptide or polypeptide region) has a certain percentage (for example, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 98% or 99%) of “sequence identity” to another sequence means that, when aligned, that percentage of bases (or amino acids) are the same in comparing the two sequences. This alignment and the percent homology or sequence identity can be determined using software programs known in the art, for example those described in Ausubel et al. eds. (2007) Current Protocols in Molecular Biology. Preferably, default parameters are used for alignment. One alignment program is BLAST, using default parameters.
The term “an equivalent nucleic acid or polynucleotide” refers to a nucleic acid having a nucleotide sequence having a certain degree of homology, or sequence identity, with the nucleotide sequence of the nucleic acid or complement thereof. A homolog of a double stranded nucleic acid is intended to include nucleic acids having a nucleotide sequence which has a certain degree of homology with or with the complement thereof. In one aspect, homologs of nucleic acids are capable of hybridizing to the nucleic acid or complement thereof. Likewise, “an equivalent polypeptide” refers to a polypeptide having a certain degree of homology, or sequence identity, with the amino acid sequence of a reference polypeptide. In some aspects, the sequence identity is at least about 70%, 75%, 80%, 85%, 90%, 95%, 98%, or 99%. In some aspects, the equivalent polypeptide or polynucleotide has one, two, three, four or five addition, deletion, substitution and their combinations thereof as compared to the reference polypeptide or polynucleotide. In some aspects, the equivalent sequence retains the activity (e.g., epitope-binding) or structure (e.g., salt-bridge) of the reference sequence.
The term “encode” as it is applied to polynucleotides refers to a polynucleotide which is said to “encode” a polypeptide if, in its native state or when manipulated by methods well known to those skilled in the art, it can be transcribed and/or translated to produce the mRNA for the polypeptide and/or a fragment thereof. The antisense strand is the complement of such a nucleic acid, and the encoding sequence can be deduced therefrom.
Use of Nucleobase Deaminase Inhibitor to Reduce Random Insertions and Deletions
As shown in the experimental examples and
It was discovered surprisingly, however, that the use of the mouse APOBEC3 (mA3) in mA3-BE3 (
Also surprisingly, the mA3-CDA2 domain not only can inhibit the base editing activity of mA3-CDA1, it can also inhibit other nucleobase deaminases. For instance, when mA3-CDA2 was fused to the N-terminus of each of three active BEs, mA3CDA1-BE3, BE3 and hA3A-BE3, the fusion proteins mA3rev-BE3, mA3-CDA2-BE3 and mA3-CDA2-hA3A-BE3 (
Moreover, cleavage of mA3-CDA2 from the fusion proteins restored the base editing efficiency (
Like mA3, the human APOBEC3B (hA3B) also has two cytidine deaminase (CDA) domains, CDA1 and CDA2 (
Using the sequences of mA3-CDA2 and hA3B-CDA1, the instant inventors were able to identify additional nucleobase deaminase inhibitors/domains in the protein database. Table 1 shows 44 proteins/domains that have significant sequence homology to mA3-CDA2 core sequence (
Fusion Proteins
Based on these surprising and expected findings, a fusion protein is designed that can be used to generate a base editor with improved base editing specificity and efficiency. In one embodiment, the present disclosure provides a fusion protein that includes a first fragment comprising a nucleobase deaminase or a catalytic domain thereof, a second fragment comprising a nucleobase deaminase inhibitor, and a protease cleavage site between the first fragment and the second fragment.
A base editor that incorporates such a fusion protein has reduced or even no editing capability and accordingly will generate reduced or no off-target mutations. Upon cleavage of the protease cleavage site and release of the nucleobase deaminase inhibitor from the fusion protein at a target site, the base editor that is at the target site will then be able to edit the target site efficiently.
The term “nucleobase deaminase” as used herein, refers to a group of enzymes that catalyze the hydrolytic deamination of nucleobases such as cytidine, deoxycytidine, adenosine and deoxyadenosine. Non-limiting examples of nucleobase deaminases include cytidine deaminases and adenosine deaminases.
“Cytidine deaminase” refers to enzymes that catalyze the irreversible hydrolytic deamination of cytidine and deoxycytidine to uridine and deoxyuridine, respectively. Cytidine deaminases maintain the cellular pyrimidine pool. A family of cytidine deaminases is APOBEC (“apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like”). Members of this family are C-to-U editing enzymes. Some APOBEC family members have two domains, one domain of APOBEC like proteins is the catalytic domain, while the other domain is a pseudocatalytic domain. More specifically, the catalytic domain is a zinc dependent cytidine deaminase domain and is important for cytidine deamination. RNA editing by APOBEC-1 requires homodimerisation and this complex interacts with RNA binding proteins to form the editosome.
Non-limiting examples of APOBEC proteins include APOBEC1, APOBEC2, APOBEC3A, APOBEC3B, APOBEC3C, APOBEC3D, APOBEC3F, APOBEC3G, APOBEC3H, APOBEC4, and activation-induced (cytidine) deaminase (AID).
Various mutants of the APOBEC proteins are also known that have bring about different editing characteristics for base editors. For instance, for human APOBEC3A, certain mutants (e.g., W98Y, Y130F, Y132D, W104A, D131Y and P134Y) even outperform the wildtype human APOBEC3A in terms of editing efficiency or editing window. Accordingly, the term APOBEC and each of its family member also encompasses variants and mutants that have certain level (e.g., 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99%) of sequence identity to the corresponding wildtype APOBEC protein or the catalytic domain and retain the cytidine deaminating activity. The variants and mutants can be derived with amino acid additions, deletions and/or substitutions. Such substitutions, in some embodiments, are conservative substitutions.
“Adenosine deaminase”, also known as adenosine aminohydrolase, or ADA, is an enzyme (EC 3.5.4.4) involved in purine metabolism. It is needed for the breakdown of adenosine from food and for the turnover of nucleic acids in tissues.
Non-limiting examples of adenosine deaminases include tRNA-specific adenosine deaminase (TadA), adenosine deaminase tRNA specific 1 (ADAT1), adenosine deaminase tRNA specific 2 (ADAT2), adenosine deaminase tRNA specific 3 (ADAT3), adenosine deaminase RNA specific B1 (ADARB1), adenosine deaminase RNA specific B2 (ADARB2), adenosine monophosphate deaminase 1 (AMPD1), adenosine monophosphate deaminase 2 (AMPD2), adenosine monophosphate deaminase 3 (AMPD3), adenosine deaminase (ADA), adenosine deaminase 2 (ADA2), adenosine deaminase like (ADAL), adenosine deaminase domain containing 1 (ADAD1), adenosine deaminase domain containing 2 (ADAD2), adenosine deaminase RNA specific (ADAR) and adenosine deaminase RNA specific B1 (ADARB1).
Some of the nucleobase deaminases have a single, catalytic domain, while others also have other domains, such as an inhibitory domain as currently discovered by the instant inventors. In some embodiments, therefore, the first fragment only includes the catalytic domain, such as mA3-CDA1 and hA3B-CDA2. In some embodiments, the first fragment includes at least a catalytic core of the catalytic domain. For instance, as demonstrated in the experimental examples, when mA3-CDA1 was truncated at residues 196/197 the CDA1 domain still retained substantial editing efficiencies (
The present disclosure tested two nucleobase deaminase inhibitors, mA3-CDA2 and hA3B-CDA1, which are the inhibitory domains of the corresponding nucleobase deaminase. Additional nucleobase deaminase inhibitors and inhibitory domains were also identified in the protein databases (see Tables 1 and 2). Their biological equivalents (e.g., having at least about 80%, 85%, 90%, 95%, 97%, 98%, 99%, 99.5% sequence identity, or having one, two, or three amino acid addition/deletion/substitution, and having nucleobase deaminase inhibitor activity) can also be prepared with known methods in the art, such as conservative amino acid substitutions. A “nucleobase deaminase inhibitor,” accordingly, refers to a protein or a protein domain that inhibits the deaminase activity of a nucleobase deaminase. In some embodiments, the second fragment includes at least an inhibitory core of the inhibitory protein/domain. For instance, as demonstrated in the experimental examples, when mA3-CDA2 retained residues 334-429, the CDA2 still had the inhibitory effect of base editing (
In some embodiments, the fusion protein further includes a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, optionally in the first fragment, next to the nucleobase deaminase or the catalytic domain thereof.
The term “Cas protein” or “clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein” refers to RNA-guided DNA endonuclease enzymes associated with the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) adaptive immunity system in Streptococcus pyogenes, as well as other bacteria. Cas proteins include Cas9 proteins, Cas12a (Cpf1) proteins, Cas12b (formerly known as C2c1) proteins, Cas13 proteins and various engineered counterparts. Example Cas proteins include SpCas9, FnCas9, St1Cas9, St3Cas9, NmCas9, SaCas9, AsCpf1, LbCpf1, FnCpf1, VQR SpCas9, EQR SpCas9, VRER SpCas9, SpCas9-NG, xSpCas9, RHA FnCas9, KKH SaCas9, NmeCas9, StCas9, CjCas9, AsCpf1, FnCpf1, SsCpf1, PcCpf1, BpCpf1, CmtCpf1, LiCpf1, PmCpf1, Pb3310Cpf1, Pb4417Cpf1, BsCpf1, EeCpf1, BhCas12b, AkCas12b, EbCas12b, LsCas12b, RfCas13d, LwaCas13a, PspCas13b, PguCas13b, RanCas13b and those provided in Table A below.
The protease cleavage site between the first fragment and the second fragment can be any known protease cleavage site (peptide) for any proteases. Non-limiting examples of proteases include TEV protease, TuMV protease, PPV protease, PVY protease, ZIKV protease and WNV protease. The protein sequences of example proteases and their corresponding cleavage sites are provided in Table B.
ACCCAUGUCUGCAGGGCCAAGUGGCACCGAGUCGGUGC
In some embodiments, the protease cleavage site is a self-cleaving peptide, such as the 2A peptides. “2A peptides” are 18-22 amino-acid-long viral oligopeptides that mediate “cleavage” of polypeptides during translation in eukaryotic cells. The designation “2A” refers to a specific region of the viral genome and different viral 2As have generally been named after the virus they were derived from. The first discovered 2A was F2A (foot-and-mouth disease virus), after which E2A (equine rhinitis A virus), P2A (porcine teschovirus-1 2A), and T2A (thosea asigna virus 2A) were also identified. A few non-limiting examples of 2A peptides are provided in SEQ ID NO:26-28.
In some embodiments, the protease cleavage site is a cleavage site (e.g., SEQ ID NO:5) for the TEV protease. In some embodiments, the fusion protein further includes a third fragment that includes the TEV protease or a fragment thereof. In some embodiments, the TEV protease fragment in the fusion protein in not active, that, is, not able to cleave the TEV cleavage site on its own. However, in the presence of the remaining portion of the TEV protease, this fragment will be able to execute the cleavage. As further described below, such an arrangement provides additional control and flexible of the base editing capabilities. The TEV fragment may be the TEV N-terminal domain (e.g., SEQ ID NO:3) or the TEV C-terminal domain (e.g., SEQ ID NO:4).
Various arrangement of the fragments can be made. Non-limiting examples include, from N-terminal side to C-terminal side:
In some embodiments, provided are fusion proteins comprising a first fragment comprising first nucleobase deaminase (e.g., cytidine deaminase) or a catalytic domain thereof, and a second fragment comprising an inhibitory domain of a second nucleobase deaminase, wherein the first nucleobase deaminase is different from the second nucleobase deaminase. In some embodiments, each of the first and second nucleobase deaminases is independently selected from the group of human and mouse APOBEC3B (A3B), APOBEC3C (A3C), APOBEC3D (A3D), APOBEC3F (A3F), APOBEC3G (A3G), APOBEC3H (A3H), APOBEC1 (A1), APOBEC3 (A3), APOBEC2 (A2), APOBEC4 (A4) and AICDA (AID).
The fusion proteins may include other fragments, such as uracil DNA glycosylase inhibitor (UGI) and nuclear localization sequences (NLS).
The “Uracil Glycosylase Inhibitor” (UGI), which can be prepared from Bacillus subtilis bacteriophage PBS1, is a small protein (9.5 kDa) which inhibits E. coli uracil-DNA glycosylase (UDG) as well as UDG from other species. Inhibition of UDG occurs by reversible protein binding with a 1:1 UDG:UGI stoichiometry. UGI is capable of dissociating UDG-DNA complexes. A non-limiting example of UGI is found in Bacillus phage AR9 (YP_009283008.1). In some embodiments, the UGI comprises the amino acid sequence of SEQ ID NO:25 or has at least at least 70%, 75%, 80%, 85%, 90% or 95% sequence identity to SEQ ID NO:25 and retains the uracil glycosylase inhibition activity.
The fusion protein, in some embodiments, may include one or more nuclear localization sequences (NLS).
A “nuclear localization signal or sequence” (NLS) is an amino acid sequence that tags a protein for import into the cell nucleus by nuclear transport. Typically, this signal consists of one or more short sequences of positively charged lysines or arginines exposed on the protein surface. Different nuclear localized proteins may share the same NLS. An NLS has the opposite function of a nuclear export signal (NES), which targets proteins out of the nucleus. A non-limiting example of NLS is the internal SV40 nuclear localization sequence (iNLS).
In some embodiments, a peptide linker is optionally provided between each of the fragments in the fusion protein. In some embodiments, the peptide linker has from 1 to 100 amino acid residues (or 3-20, 4-15, without limitation). In some embodiments, at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80% or 90% of the amino acid residues of peptide linker are amino acid residues selected from the group consisting of alanine, glycine, cysteine, and serine.
For any fusion protein of the present disclosure, biological equivalents thereof are also provided. In some embodiments, the biological equivalents have at least about 70%, 75%, 80%, 85%, 90%, 95%, 98%, or 99% sequence identity with the reference fusion protein. Preferably, the biological equivalents retained the desired activity of the reference fusion protein. In some embodiments, the biological equivalents are derived by including one, two, three, four, five or more amino acid additions, deletions, substitutions, of the combinations thereof. In some embodiments, the substitution is a conservative amino acid substitution.
A “conservative amino acid substitution” is one in which the amino acid residue is replaced with an amino acid residue having a similar side chain. Families of amino acid residues having similar side chains have been defined in the art, including basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). Thus, a nonessential amino acid residue in an immunoglobulin polypeptide is preferably replaced with another amino acid residue from the same side chain family. In another embodiment, a string of amino acids can be replaced with a structurally similar string that differs in order and/or composition of side chain family members.
Non-limiting examples of conservative amino acid substitutions are provided in the table below, where a similarity score of 0 or higher indicates conservative substitution between the two amino acids.
On-Target Activation of Fusion Proteins
The present disclosure also provides compositions and methods in which a fusion protein of the present disclosure, which includes both a nucleobase deaminase or the catalytic domain thereof and an inhibitor, is activated where its activity is desired. The technology is illustrated in
In an illustrative configuration, the fusion protein (A) includes (a) a first fragment comprising a nucleobase deaminase (e.g., cytidine deaminase) or a catalytic domain thereof, optionally with a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a first TEV protease fragment, (b) a second fragment comprising a nucleobase deaminase inhibitor, and (c) a TEV protease cleavage site between the first fragment and the second fragment. In some embodiments, wherein the first TEV protease fragment alone is not able to cleave the TEV protease cleavage site.
When the fusion protein is used, in vitro or in vivo, to conduct gene editing in a cell, two additional molecules can be introduced. In one example, one molecule (B) is a single guide RNA (sgRNA) that further incorporates a tag sequence that can be recognized by an RNA recognition peptide. The sgRNA, alternatively, can be replaced by a crRNA that targets the target site and a CRISPR RNA (crRNA) alone, or in combination with a trans-activating CRISPR RNA (tracrRNA). Examples of tag sequences and corresponding RNA recognition peptides include MS2/MS2 coat protein (MCP), PP7/PP7 coat protein (PCP), and boxB/boxB coat protein (N22p), the sequences of which are provided in Table B. The molecule (B) may be provided as a DNA sequence encoding the RNA molecule.
The other additional molecule (C), in some embodiments, includes a second TEV protease fragment coupled to the RNA recognition peptide (e.g., MCP, PCP, N22p). The first TEV fragment and the second TEV fragment, in some embodiments, when present together, are able to cleave a TEV protease site.
Such co-presence can be triggered by the molecule (C) binding to the molecule (B) by virtue of the tag sequence-RNA recognition protein interaction. Meanwhile, the fusion protein (A) and the molecule (B) will be both present at the target genome locus for gene editing. Therefore, the molecule (B) brings both of the TEV protease fragments from the fusion protein (A) and molecule (C) together, which will activate the TEV protease, leading to removal of the nucleobase deaminase inhibitor from the fusion protein and activation of the base editor. It can be readily appreciated that such activation only occurs at the target genome site, not at off-target single-stranded DNA regions. As such, base editing does not occur at the single-stranded DNA regions that sgRNA does not bind to (as demonstrated in
“Guide RNAs” are non coding short RNA sequences which bind to the complementary target DNA sequences. A guide RNA first binds to the Cas enzyme and the gRNA sequence guides the complex via pairing to a specific location on the DNA, where Cas performs its endonuclease activity by cutting the target DNA strand. A “single guide RNA,” frequently simply referred to as “guide RNA”, refers to synthetic or expressed single guide RNA (sgRNA) that consists of both the crRNA and tracrRNA as a single construct. The tracrRNA portion is responsible for Cas endonuclease activity and the crRNA portion binds to the target specific DNA region. Therefore, the trans activating RNA (tracrRNA, or scaffold region) and crRNA are two key components and are joined by tetraloop which results in formation of sgRNA.
The scaffold of the guide RNA has a stem-loop structure in itself and attaches to the endonuclease enzyme. A typical scaffold has a structure as illustrated in
With reference to these example scaffold sequences, the fragment of positions 1-12 (e.g., GUUUUAGAGCUA, SEQ ID NO:197; GUUUGAGAGCUA, SEQ ID NO:198) represents the repeat region, which forms about 8-12 base pairings with the anti-repeat, which includes positions 17-30 (e.g., UAGCAAGUUAAAAU, SEQ ID NO:199). The GAAA loop (SEQ ID NO:200) between them is the tetraloop. As shown in SEQ ID NO:17, this entire loop can be replaced with a MS2 sequence. Stem loop 1 roughly includes positions 31-39 and includes a small loop (e.g., UA, AU, AA, or UU, without limitation). Stem loop 1 generally has 3-4 base parings in the stem. Stem loop 2, including positions 48-61 (e.g., AACUUGAAAAAGUG, SEQ ID NO:201), generally includes 4 base parings in the stem, and a GAAA (SEQ ID NO:200) loop which can be totally replaced. The remaining, positions 62-76 (e.g., GCACCGAGUCGGUGC, SEQ ID NO:202; GCACCGAUUCGGUGC; SEQ ID NO:203) constitute stem loop 3, which generally includes 4 base pairings in the stem. The small loop (U and G here in the example) can be any nucleotide.
Accordingly, the sequence of the scaffold can be expressed as: GUUUNAGAGCUAX1UAGCAAGUUNAAAUAAGGCNNGUCCGUUAUCAACUUX2A AGUGGCACCGANUCGGUGC (SEQ ID NO:31), where N represents any base, and X1 and X2 denotes any nucleotide sequence of a length of 2-50 bases. The terms “guide RNA” and “single guide RNA” encompasses those that include additional sequences, such as MS2, PP7 and boxB, inserted into one or more loops in the RNA.
Various embodiments and examples of nucleobase deaminases, catalytic domains, nucleobase deaminase inhibitors, and Cas proteins are provided in the disclosures. For instance, a nucleobase deaminase can be a cytidine deaminases and adenosine deaminases. Non-limiting examples of cytidine deaminases include APOBEC1, APOBEC2, APOBEC3A, APOBEC3B, APOBEC3C, APOBEC3D, APOBEC3F, APOBEC3G, APOBEC3H, APOBEC4, and activation-induced (cytidine) deaminase.
Non-limiting examples of adenosine deaminases include tRNA-specific adenosine deaminase (TadA), adenosine deaminase tRNA specific 1 (ADAT1), adenosine deaminase tRNA specific 2 (ADAT2), adenosine deaminase tRNA specific 3 (ADAT3), adenosine deaminase RNA specific B1 (ADARB1), adenosine deaminase RNA specific B2 (ADARB2), adenosine monophosphate deaminase 1 (AMPD1), adenosine monophosphate deaminase 2 (AMPD2), adenosine monophosphate deaminase 3 (AMPD3), adenosine deaminase (ADA), adenosine deaminase 2 (ADA2), adenosine deaminase like (ADAL), adenosine deaminase domain containing 1 (ADAD1), adenosine deaminase domain containing 2 (ADAD2), adenosine deaminase RNA specific (ADAR) and adenosine deaminase RNA specific B1 (ADARB1).
Example Cas proteins include SpCas9, FnCas9, St1Cas9, St3Cas9, NmCas9, SaCas9, AsCpf1, LbCpf1, FnCpf1, VQR SpCas9, EQR SpCas9, VRER SpCas9, RHA FnCas9, and KKH SaCas9 and those provided in Table A.
The fusion proteins may include other fragments, such as uracil DNA glycosylase inhibitor (UGI) and nuclear localization sequences (NLS), each of which is discussed herein.
The base editors and base editing methods described in this disclosure can be applied to perform high-specificity and high-efficiency base editing in the genome of various eukaryotes.
The present disclosure provides compositions and methods. Such compositions comprise an effective amount of a fusion protein, and an acceptable carrier. In some embodiments, the composition further includes a guide RNA that has a desired complementarity to a target DNA. Such a composition can be used for base editing in a sample.
The fusion proteins and the compositions can be used for base editing. In one embodiment, a method for editing a target polynucleotide is provided, comprising contacting to the target polynucleotide a fusion protein of the present disclosure and a guide RNA having at least partial sequence complementarity to the target polynucleotide, wherein the editing comprises deamination of a cytosine (C) in the target polynucleotide.
In one embodiment, provided is a method of editing a cytosine on a nucleic acid sequence in a sample. In some embodiments, the method entails contacting the sample a fusion protein of the present disclosure, or a polynucleotide encoding the fusion protein. In some embodiments, further added is a suitable guide RNA. Design of the guide RNA is readily available to the skilled artisan.
The contacting between the fusion protein (and the guide RNA) and the target polynucleotide can be in vitro, in particular in a cell culture. When the contacting is ex vivo, or in vivo, the fusion proteins can exhibit clinical/therapeutic significance. The in vivo contacting may be administration to a live subject, such as a human, an animal, a yeast, a plant, a bacterium, a virus, without limitation.
Configurations of Induced and Split Base Editors
Various configurations of constructs have been tested to implement the induced and split base editor (isplitBE) design (
In configuration Pair 9 (
The first molecule can include just a Cas protein, which has a suitable size for packaging in a common vehicle, AAV. The second molecule includes, among others, a nucleobase deaminase (e.g., APOBEC), a nucleobase deaminase inhibitor (e.g., mA3-CDA2), and an RNA recognition peptide (e.g., MCP). A protease cleavage site (e.g., TEV site) is inserted between the nucleobase deaminase and the nucleobase deaminase inhibitor, which enables removal of the nucleobase deaminase inhibitor at proper timing/location. Optionally, the second molecule further includes a UGI.
The third molecule is a fusion between an inactive portion of the protease (e.g., TEVc) fused to different RNA recognition peptide (e.g., N22p). The fourth molecule is a standalone TEVn which, in combination with the first portion, can carry out the protease activity to remove the nucleobase deaminase inhibitor from the second molecule.
The fifth molecule is a helper sgRNA containing an RNA recognition site (e.g., MS2) recognizable by the RNA recognition peptide in the 2nd molecule. The sixth molecule is a regular sgRNA that contains an RNA recognition site (e.g., boxB) recognizable by the RNA recognition peptide in the 3rd molecule.
At the correct target site in the genome (or RNA), both the hsgRNA and the sgRNA will bind, and each recruits a Cas protein to the binding site. The hsgRNA will also recruit the 2nd molecule by virtue of the MS2-MCP binding, and the sgRNA will recruit the 3rd molecule by virtue of the boxB-N22p binding. Therefore, the TEVc of the 3rd molecule is in contact with the TEV site. Since the standalone TEVn is present in the entire cell, it can also be present here, which ensures that the TEVc is active and cleaves the nucleobase deaminase inhibitor from the nucleobase deaminase in molecule 2, thereby activating the nucleobase deaminase.
It is further discovered that an optimal distance between the hsgRNA binding site and the regular sgRNA binding site is from 34-91 bp (from PAM to PAM), with the hsgRNA on the upstream.
Moreover, even though the proper binding of both hsgRNA and regular sgRNA is required for the intended editing in the target site for regular sgRNA, the editing in the target site for hsgRNA is not desirable. It is discovered herein that when the spacer length of the hsgRNA (spacer is the target complementary region) is from 8-15 bases, such a hsgRNA is still sufficient to provide dual recognition to ensure binding specificity, but greatly reduce the editing in the hsgRNA target site.
In accordance with one embodiment of the disclosure, therefore, provided is a fusion protein comprising a first fragment comprising: a nucleobase deaminase or a catalytic domain thereof, a nucleobase deaminase inhibitor, a first RNA recognition peptide, and a TEV protease cleavage site between the nucleobase deaminase or a catalytic domain thereof and the nucleobase deaminase inhibitor.
In some embodiments, the fusion protein further comprises a second fragment comprising: a TEV protease fragment which alone is not able to cleave the TEV protease cleavage site, and a second RNA recognition peptide. In some embodiments, the fusion protein further comprises a self-cleavage site between the first fragment and the second fragment.
In some embodiments, the fusion protein further comprises a third fragment comprising a second TEV protease fragment, wherein the first TEV protease fragment is able to cleave the TEV protease site in the presence of the second TEV protease fragment. In some embodiments, the fusion protein further comprises a second self-cleavage site between the second fragment and the third fragment, ad upon cleavage of the second self-cleavage site, the fusion protein releases the second TEV protease fragment which is not fused to any RNA recognition peptide.
Also provided, in one embodiment, is a dual guide RNA system, comprising: a target single guide RNA comprising a first spacer having sequence complementarity to a target nucleic acid sequence proximate to a first PAM site, a helper single guide RNA comprising a second spacer having sequence complementarity to a second nucleic acid sequence proximate to a second PAM site, a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a nucleobase deaminase.
In some embodiments, the second PAM site is located within 150 bases, or alternatively within 140, 130, 120, 110, 100, 95, 94, 93, 92, 91, 90, 89, 88, 87, 86, 85, 84, 83, 82, 81, 80, 75 or 70 bases from the second PAM site. In some embodiments, the second PAM site is located at least 10 bases, or alternatively at least 15, 20, 25, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 50, 55, or 60 bases from the first PAM. In some embodiments, the second PAM site is upstream from the first PAM site. In some embodiments, the second PAM site is downstream from the first PAM site. In some embodiments, the distance is from 20-100, 25-95, 30-95, 34-95, 34-91, 34-90, 35-90, 40-90, 40-84, 45-85, or 50-80 bases, without limitation.
In some embodiments, the second (helper) spacer is 8-15 bases in length. In some embodiments, the second spacer is 8-14, 8-13, 8-12, 8-11, 8-10, 9-15, 9-14, 9-13, 9-12, 9-11, 9-10, 10-15, 10-14, 10-13, 10-12, 10-11, 11-15, 11-14, 11-13, 11-12, 12-15, 12-14, 12-13, or 13-15 bases in length. The first spacer, by contrast, is at least 16, 17, 18, or 19 bases in length.
Various “split” base editing systems are also described here, which allow the Cas protein and the nucleobase deaminase to be packaged into separate delivery vehicles (e.g., AAV).
In some embodiments, pairs of regular sgRNA and hsgRNA are provided that can mediate efficient editing to generate early stop codons in PCSK9 genes, which can have clinic benefits. Based on the discoveries here, suitable target sites for sgRNA and hsgRNA have been selected for converting a non-stop codon to a stop codon. Take C-to-T/U editing as an example, a non-stop codon can be CAG, CAA or CGA.
Examples of such target sites are illustrated in Table 4. It is readily understood that the sequences in Table 4 are used to show the location of the target. The actual sgRNA and hsgRNA, however, does not need to bind to the entire sequence. In fact, for hsgRNA for instance, a binding of 8-15 nucleotides could well be enough as explained above. Accordingly, the spacer sequence on the hsgRNA can be complementary to a sub-sequence of any shown in Table 4, or even overlap with any of them. The same is true for sgRNA as well, with a preferred spacer length of 18-24 nucleotides, without limitation.
In one embodiment, provided is a pair of helper guide RNA/guide RNA for editing a human PCSK9 nucleic acid sequence, wherein the guide RNA specifically targets a first site on the PCSK9 nucleic acid to enable base editing to convert a non-stop codon to a stop codon, and wherein the helper guide RNA specifically targets a second site on the PCSK9 nucleic acid that is 20 to 100 bases from the first site. In some embodiments, the second site is about 20-100, 25-95, 30-95, 34-95, 34-91, 34-90, 35-90, 40-90, 40-84, 45-85, or 50-80 bases away from the first site.
In some embodiments, the hsgRNA has a spacer that is 8-15 bases in length. In some embodiments, the spacer is 8-14, 8-13, 8-12, 8-11, 8-10, 9-15, 9-14, 9-13, 9-12, 9-11, 9-10, 10-15, 10-14, 10-13, 10-12, 10-11, 11-15, 11-14, 11-13, 11-12, 12-15, 12-14, 12-13, or 13-15 bases in length. In some embodiments, the sgRNA has a spacer that is at least 16, 17, 18, or 19 bases in length.
Spacer sequences for the sgRNA/hsgRNA can be readily designed. For instance, for each target site shown in Table 4, a spacer may be the complementary sequence of the desired length (i.e., complementary to a sub-sequence of any of SEQ ID NO:166-180 or 181-195). Specific examples of pairs of binding sites include, without limitation, SEQ ID NO:166 and 181; SEQ ID NO:167 and 182; SEQ ID NO:168 and 183; SEQ ID NO:169 and 184; SEQ ID NO:170 and 185; SEQ ID NO:171 and 186; SEQ ID NO:172 and 187; SEQ ID NO:173 and 188; SEQ ID NO:174 and 189; SEQ ID NO:175 and 190; SEQ ID NO:176 and 191; SEQ ID NO:177 and 192; SEQ ID NO:178 and 193; SEQ ID NO:179 and 194; and SEQ ID NO:180 and 195.
Example sgRNA/hsgRNA sequences have also been designed and tested. See Table 3. Moreover, polynucleotide sequences encoding the helper guide RNA and guide RNA are also provided.
With such pairs of sgRNA/hsgRNA sequences, methods of inactivating a PSCK9 gene in a cell can be carried out. In some embodiments, the method entails contacting the cell with a pair of helper guide RNA and guide RNA of the present disclosure, a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a nucleobase deaminase. Each of these elements have been further described in the instant disclosure.
Enhanced Prime Editing
Improved prime editing systems are also provided, in some embodiments. In particular, certain prime editing guide RNA (pegRNA) molecules provided herein have improved stability. These pegRNA contain a scaffold that, compared to the conventional guide RNA, has one additional base pairing (see,
As discussed above, a typical guide RNA scaffold has a structure which includes, from the 5′ to the 3′ end, (a) a repeat region, (b) a tetraloop, (c) an anti-repeat that is at least partially complementary to the repeat region, (d) stem loop 1, (e) a linker, (0 stem loop 2, and (g) stem loop 3. In other words, the scaffold includes 4 stem loops. The third stem loop (counted from 5′ to 3′), also referred to as “Stem loop 2”, includes 4 base pairings in the conventional design. In the new design, this stem loop has 5 base pairing.
In one embodiment, provided is a guide RNA comprising a scaffold which comprises, from the 5′ to 3′ direction, a first stem loop portion, a second stem loop portion, a third stem loop portion, and a fourth stem loop portion, wherein the third stem loop comprises five base pairings within.
The sequence of the scaffold can be expressed as: GUUUNAGAGCUAX1UAGCAAGUUNAAAUAAGGCNNGUCCGUUAUCAACUUX2A AGUGGCACCGANUCGGUGC (SEQ ID NO:31), where N represents any base, and X1 and X2 denotes any nucleotide sequence of a length of 2-50 bases (or 2-40, 3-40, 4-40, 4-30, 2-30, 4-20 bases). Accordingly, in some embodiments, the base pairings comprise one between positions 45 and 55, according to the positions in SEQ ID NO:31. In some embodiments, the scaffold has at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO:31 and includes give base pairings in the third stem loop.
In one embodiment, therefore, provided is a guide RNA comprising a scaffold derived from SEQ ID NO:31 by introducing a base pairing between the bases at position 45 and position 55, and optionally allowing one, two, three, four, or five base additions, deletions, substitutions, or the combination thereof, as long as it maintains the stem loops structure or the scaffold/guide RNA functionality. In some embodiments, the scaffold comprises a sequence selected from the group consisting of SEQ ID NO:32-43. In some embodiments, the guide RNA is at least 100 nucleotides, or 105, 110, 115, 120, 125, 130, 140 or 150 nucleotides in length. In some embodiments, the guide RNA further includes a spacer (e.g., 8-25 nucleotides), a reverse-transcriptase template, and/or a primer-binding site.
Improved prime editor proteins are also provided, in some embodiments. In one embodiment, the prime editor includes a Cas protein and a reverse-transcriptase linked through a linker tested to optimized for the performance of the prime editor. In one embodiment, the prime editor comprises the amino acid sequence of SEQ ID NO:44. In one embodiment, the prime editor comprises the amino acid sequence of SEQ ID NO:45. Both these prime editors have been tested and shown to exhibit superior editing efficiency and specificity.
Various “split” prime editing systems are also described here, which allow the Cas protein and the reverse transcriptase to be packaged into separate delivery vehicles (e.g., AAV).
With the split prime editing systems, methods for conducting genetic editing in a cell at a target site are also provided. In some embodiments, the method entails introducing to the cell a first viral particle enclosing a first construct encoding a clustered regularly interspaced short palindromic repeats (CRISPR)-associated (Cas) protein, and a second viral particle enclosing a second construct encoding a reverse-transcriptase fused to an RNA recognition peptide. In some embodiments, the second construct further encodes a guide RNA comprising an RNA recognition site that the RNA recognition peptide binds to.
In some embodiments, the second construct further encodes a guide RNA comprising an RNA recognition site that the RNA recognition peptide binds to. In some embodiments, the Cas protein is selected from the group consisting of SpCas9, FnCas9, St1Cas9, St3Cas9, NmCas9, SaCas9, AsCpf1, LbCpf1, FnCpf1, VQR SpCas9, EQR SpCas9, VRER SpCas9, SpCas9-NG, xSpCas9, RHA FnCas9, KKH SaCas9, NmeCas9, StCas9, CjCas9, AsCpf1, FnCpf1, SsCpf1, PcCpf1, BpCpf1, CmtCpf1, LiCpf1, PmCpf1, Pb3310Cpf1, Pb4417Cpf1, BsCpf1, EeCpf1, BhCas12b, AkCas12b, EbCas12b, LsCas12b, RfCas13d, LwaCas13a, PspCas13b, PguCas13b, and RanCas13b. In some embodiments, the Cas protein is SpCas9-NG or xSpCas9.
Non-limiting examples of reverse-transcriptases include human immunodeficiency virus (HIV) reverse-transcriptase, moloney murine leukemia virus (MMLV) reverse-transcriptase and avian myeloblastosis virus (AMV) reverse-transcriptase
Single-guide RNAs (sgRNAs) and base editors (BEs) mentioned in the examples are for SpCas9, unless specifically pointed out, e.g., the sgRNA for SaCas9 (Sa-sgRNAs). To test whether the current base editing system can induce C-to-T mutations in ssDNA regions, we used SaD10A nickase and Sa-sgRNA to make a DNA single-stranded break (SSB), which can trigger end recession to generate a ssDNA region. (
To inhibit the activity of cytidine deaminase at non-relevant sites, e.g., ssDNA regions, we proposed to fuse base editors with a base editing inhibitor. Mouse APOBEC3 (mA3) comprises two cytidine deaminase (CDA) domains (CDA1 and CDA2,
Next, we considered whether the cleavage of mA3CDA2 can restore the base editing efficiency. 2A self-cleavage peptides were inserted between mA3CDA2 and the rest part of BE in mA3rev-BE3, mA3CDA2-BE3 and mA3CDA2-hA3A-BE3 to generate mA3rev-2A-BE3, mA3CDA2-2A-BE3 and mA3CDA2-2A-hA3A-BE3 (
Human APOBEC3B (hA3B) also comprises two cytidine deaminase (CDA) domains (CDA1 and CDA2,
Next, we planned to use mA3 to develop novel BEs. The two BEs, mA3rev-BE3 and mA3rev-2A-BE3, were made by splitting mA3 between amino acid (AA)207 and AA208 and then we determined where to split mA3CDA2 can keep the highest editing efficiency (
Furthermore, we tried to determine the minimal region of mA3 that has a base editing inhibitory effect. We deleted various N-terminal parts of mA3CDA2 in mA3rev-BE-237 to develop mA3rev-BE-237-Del-255, mA3rev-BE-237-Del-285 and mA3rev-BE-237-Del-333, which contains the AA256-AA429, AA286-AA429 and AA334-AA429 parts of mA3 as the base editing inhibitor respectively (
In order to develop base editors that do not cause C-to-T mutation in non-relevant ssDNA regions, we replaced the 2A self-cleavage site with a cleavage site of TEV protease in mA3rev-2A-BE3 and then fused the N-terminal part of TEV protease (TEVn) [Gray et al., 2010, Cell, doi: 10.1016/j.cell.2010.07.014] to the C-terminus of mA3rev-2A-BE3 with another TEV cleavage site. The newly developed BE is named BEsafe. In addition, we put one MS2 loop into the sgRNA to generate MS2-sgRNA [Ma et al., 2016, Nature Biotechnology, doi: 10.1038/nbt.3526] and then fused the C-terminal part of TEV protease (TEVc) with MS2 coat protein (MCP), which can bind to MS2 loop (
We then compared the performance of BEsafe and hA3A-BE3 at on-target sites and non-relevant ssDNA regions (
The base editors and base editing method described in this invention could be applied to perform high-specificity and high-efficiency base editing in the genome of various eukaryotes.
For the first time, a base editing system was established to avoid causing C-to-T mutations in non-relevant ssDNA regions and to induce efficient base editing at on-target sites. The BEsafe base editing system and the accompanying methods disclosed in this invention could be utilized to perform highly specific base editing that cannot be implemented by the currently existing BEs as the cytidine deaminases in current BEs can cause unintended mutations in non-relevant ssDNA regions. Importantly, the high specificity and efficiency of this BEsafe base editing system will promote the potential clinical translation, especially in the gene therapies that involve restoring disease-related mutations.
cytidine deaminase
Mus spicilegus A3
Cricetulus
longicaudatus A3
Mus terricolor A3
Mus caroli A3
Mus pahari A3
Mus shortridgei A3
Mus setulosus A3
Grammomys
surdaster A3
Rattus norvegicus A3
Mastomys coucha A3
Cricetulus griseus
Peromyscus leucopus
Mesocricetus auratus
Microtus ochrogaster
Meriones
unguiculatus A3
Dipodomys ordii A3
Jaculus jaculus A3
Chinchilla lanigera
Heterocephalus
glaber A3 (AA277-
Octodon degus A3
Urocitellus parryii
Aotus nancymaae
Cebus capucinus
Saimiri boliviensis
Homo sapiens A3H
Homo sapiens
Pan paniscus A3H
Symphalangus
syndactylus A3H
Macaca mulatta A3H
Theropithecus gelada
Mandrillus
leucophaeus A3H
Bos grunniens A3
Bubalus bubalis A3
virginianus texanus
Sus scrofa A3
Ceratotherium simum
simum A3B (AA232-
Equus caballus A3H
Enhydra lutris
kenyoni A3B
Leptonychotes
weddellii A3H
Ursus arctos
horribilis A3F
Panthera leo
bleyenberghi A3H
Panthera tigris
sumatrae A3H
Tupaia belangeri A3
Pan paniscus A3B
Pan troglodytes A3B
Pan troglodytes A3F
Human sapiens A3F
Macaca leonine
Macaca nemestrina
Rhinopithecus
roxellana A3F
Mandrillus
leucophaeus A3F
Macaca mulatta A3F
Theropithecus gelada
Cercocebus atys A3B
Macaca fascicularis
Macaca mulatta A3B
Macaca leonina A3B
Mandrillus
leucophaeus A3B
Macaca nemestrina
Rhinopithecus bieti
Rhinopithecus
roxellana A3B
Chlorocebus sabaeus
Nomascus
leucogenys A3B
Cercocebus atys A3F
Papio anubis A3F
Chlorocebus aethiops
Chlorocebus sabaeus
Chlorocebus sabaeus
Erythrocebus patas
Macaca fascicularis
Macaca fascicularis
Macaca nemestrina
Macaca leonina A3D
Macaca mulatta A3D
Pan paniscus A3D
Pan troglodytes A3D
Homo sapiens A3D
Nomascus
leucogenys A3D
Saimiri boliviensis
Saimiri boliviensis
Piliocolobus
tephrosceles A3F
palliatus A3F
Pongo abelii A3F
This example developed an efficient method to demonstrate that the APOBEC moiety of base editors (BEs) directly induced mutations at off-target single-stranded DNA (OTss) sites in an sgRNA-independent manner. By testing a series of APOBEC proteins with two cytidine deaminase (CDA) domains, we identified that the catalytically-inactive CDA domains of certain dual-domain APOBECs function as cytidine deaminase inhibitors (CDIs). By taking advantage of this finding and the concept of split-TEV protease, an induced base editor (iBE) by sgRNA-guided cleavage of CDI was developed, which links a nSpCas9-BE and a CDI with a TEV cleavage site. At sgRNA-independent OTss sites, iBE1 remained dormant owing to the covalently linked CDI. Whereas, at on-target sites, iBE1 was activated by sgRNA-guided TEV cleavage of CDI, resulting in efficient base editing. By using ‘enhanced specificity’ SpCas9 nickase, iBE2 was further developed to reduce unintended OTsg mutations. Due to its minimum off-target effects and uncompromised on-target editing efficiency, the editing specificity of iBEs was significantly higher than that of the previously-reported BEs. Thus, the iBE system described in this example provides a new layer of regulation for the specificity of current base editing system and secures its application against off-target mutations.
Methods
Cell Culture and Transfection
HEK293FT cells from ATCC were maintained in DMEM (10566, Gibco/Thermo Fisher Scientific)+10% FBS (16000-044, Gibco/Thermo Fisher Scientific) and regularly tested to exclude mycoplasma contamination.
For base editing in genomic DNA, HEK293FT cells were seeded in a 24-well plate at a density of 1.1×105 per well and transfected with 250 μl serum-free Opti-MEM that contained 5.35 μl LIPOFECTAMINE LTX (Life, Invitrogen), 2.14 μl LIPOFECTAMINE plus (Life, Invitrogen), 1 μg pCMV-BE3 (or hA3B-BE3, hA3BCDA2-nSpCas9-BE, hA3D-BE3, hA3DCDA2-nSpCas9-BE, hA3F-BE3, hA3FCDA2-nSpCas9-BE, hA3G-BE3, hA3GCDA2-nSpCas9-BE, mA3-BE3, mA3CDA1-nSpCas9-BE, mA3CDA2-mA3CDA1-nSpCas9-BE, hA3FCDA1-mA3CDA1-nSpCas9-BE, hA3BCDA1-mA3CDA1-nSpCas9-BE, mA3CDA2-rA1-nSpCas9-BE, hA3FCDA1-rA1-nSpCas9-BE, hA3BCDA1-rA1-nSpCas9-BE, hA3A-BE3, mA3CDA2-hA3A-nSpCas9-BE, hA3FCDA1-hA3A-nSpCas9-BE, hA3BCDA1-hA3A-nSpCas9-BE, mA3CDA2F1-mA3CDA1-nSpCas9-BE, mA3CDA2F2-mA3CDA1-nSpCas9-BE, mA3CDA2F3-mA3CDA1-nSpCas9-BE, mA3CDA1-T2A-mA3CDA1-nSpCas9-BE, EGFP-mA3CDA1-nSpCas9-BE, EGFP-T2A-mA3CDA1-nSpCas9-BE, mA3CDA1-T2A-rA1-nSpCas9-BE, EGFP-rA1-nSpCas9-BE, EGFP-T2A-rA1-nSpCas9-BE, mA3CDA1-T2A-hA3A-nSpCas9-BE, EGFP-hA3A-nSpCas9-BE, EGFP-T2A-hA3A-nSpCas9-BE, pCMV-dSpCas9, iBE1, iBE2, mA3CDA1-TS-mA3CDA1-nSpCas9HF1-BE-NTEV or mA3CDA1-TS-mA3CDA1-nHypaSpCas9-BE-NTEV) expression vector, 0.64 μg sgRNA expression vector without or with 0.5 μg Sa-sg-SaD10A expression vector. After 24 hr, puromycin (ant-pr-1, InvivoGen) was added to the medium at the final concentration of 4 μg/ml. After another 48 hr, the genomic DNA was extracted from the cells with QuickExtract™ DNA Extraction Solution (QE09050, Epicentre) for subsequent sequencing analysis.
DNA Library Preparation and Sequencing
Target genomic sequences were PCR amplified by high-fidelity DNA polymerase PrimeSTAR HS (Clonetech) with primer sets flanking examined sgRNA target sites. Indexed DNA libraries were prepared by using the TruSeq ChIP Sample Preparation Kit (Illumina) with minor modifications. Briefly, the PCR products amplified from genomic DNA regions were fragmented by Covaris S220. The fragmented DNAs were then PCR amplified by using the TruSeq ChIP Sample Preparation Kit (Illumina). After quantitated with Qubit High-Sensitivity DNA kit (Invitrogen), PCR products with different tags were pooled together for deep sequencing by using the Illumina Hiseq X10 (2×150) or NextSeq 500 (2×150) at CAS-MPG Partner Institute for Computational Biology Omics Core, Shanghai, China. Raw read qualities were evaluated by FastQC. For paired-end sequencing, only R1 reads were used. Adaptor sequences and read sequences on both ends with Phred quality score lower than 30 were trimmed. Trimmed reads were then mapped with the BWA-MEM algorithm (BWA v0.7.17) to target sequences. After piled up with samtools (v1.9), base substitutions were further calculated.
Base Substitution Calculation
Base substitutions were selected at each position of the examined sgRNA target sites that were mapped with at least 1000 independent reads, and obvious base substitutions were only observed at the targeted base editing sites. Base substitution frequencies were calculated by dividing base substitution reads by total reads. For each sgRNA, the ratio of C-to-T base substitution over indel was calculated by dividing the sum of C-to-T base substitution frequencies at all editing sites by the indel frequency of 50-bp region around sgRNA target site (from upstream eight nucleotides to the target site to downstream 19 nucleotides to PAM sites).
Results
Cytosine or adenine base editors (CBEs/BEs or ABEs) that fuse native cytidine deaminases or in vitro evolved adenosine deaminases with CRISPR-Cas9 have been developed to induce targeted C-to-T or adenine to guanine (A-to-G) conversions with high efficiencies. Because BEs use catalytically dead Cas9 (dCas9) protein or Cas9 nickase (nCas9) to direct their binding to genomic DNA, unintended base substitutions were expected to be induced at OTsg sites that are partially complementary to sgRNA. In this scenario, the use of high-fidelity Cas9 in BEs can reduce these OTsg mutations. Meanwhile, since free APOBECs can induce unexpected C-to-T mutations in single-stranded DNA (ssDNA) regions, the APOBEC moiety of BEs may directly trigger unexpected mutations at OTss sites. In other words, the off-target mutations induced by BEs may also occur at OTss sites independent of the guidance of sgRNA; however, OTss mutations were not revealed due to the lack of a quantitative and reproducible way for detection.
This example set up an efficient method to quantitatively evaluate BE-induced OTss mutations by co-expressing S. aureus and S. pyogenes Cas9 orthologs (CESSCO). In CESSCO, the expression of nSaCas9/Sa-sgRNA pairs generated DNA single-strand breaks (SSBs) at specific genomic loci and led to the formation of a genomic ssDNA region in a programmable way. At the same time, co-expressed BE3 in the absence of sgRNA (sgRNA means Sp-sgRNA hereafter) was used to examine whether sgRNA-independent C-to-T base substitutions can be induced by BE3 alone in the ssDNA regions generated around nSaCas9/Sa-sgRNA-introduced SSBs. After deep-sequencing the genomic regions targeted by nSaCas9/Sa-sgRNA, it was clearly shown that C-to-T mutations at OTss sites were induced by the rat APOBEC1 (rA1)-containing BE3 but not by dSpCas9 in the absence of sgRNA, confirming that OTss mutations are caused by the APOBEC moiety of BEs in an sgRNA-independent manner.
This example then sought to reduce OTss mutations by exploiting members of APOBEC family suitable for highly-specific BE construction. Most of commonly used BEs were constructed with single domain APOBECs, such as rA1 in BE3, but not with dual-domain APOBECs. Usually, in APOBECs with two CDA domains, one is catalytically active, while the other one is catalytically inactive, which plays a regulatory role on the cytidine deamination activity and thus may be suited for constructing highly-specific BEs with reduced OTss effects. To attempt this possibility, we constructed and compared the C-to-T editing efficiencies of ten paired BEs, which have either one catalytically active CDA domain or two CDA domains of five dual-domain APOBECs (
As revealed in
To examine whether the inhibitory function is general, we covalently linked the catalytically inactive CDA domains of mA3, hA3F or hA3B individually to the N-terminus of mA3CDA1-nSpCas9-BE (
Next, we sought to test whether the cleavage of mA3CDI (mA3CDA2) from its covalently-linked BEs can restore their base editing capacity. We used self-cleaving peptides (T2A) to link mA3CDI and mA3CDA1-nSpCas9-BE for examination. After self-cleavage of mA3CDI, the editing efficiency of mA3CDI-T2A-mA3CDA1-nSpCas9-BE was regained to the levels similar to EGFP-mA3CDA1-nSpCas9-BE or EGFP-T2A-mA3CDA1-nSpCas9-BE, ˜10-fold higher than that of the non-cleavable-mA3CDI fused BE. The self-cleavage of mA3CDI from BE3 and hA3A-BE3 also enhanced their editing efficiencies, albeit to different extents.
These results served as a critical proof-of-concept for developing an iBE system for precise base editing with low OTss mutations. iBE1 was constructed by using TEV protease cleavage site (TS) to link three critical modules, i.e., mA3CDI, mA3CDA1-nSpCas9-BE and the N-terminal half of TEV protease (NTEV) (
After being expressed in cells, iBE1 remained dormant in the sgRNA-independent OTss regions as expected (
As Cas9 has been known to induce unintended editing at OTsg sites that have partial sequence complementarity to the sgRNA, we also aimed to further reduce OTsg mutations by replacing the unmodified nSpCas9 in iBE1 with its engineered versions that have improved targeting specificity (
As an early developed BE, the editing efficiency of BE3 is restricted under certain conditions and additional BEs with improved editing efficiencies were developed later, e.g., AncBE4max or hA3A-BE3. hA3A-BE3 is a highly active BE in various contexts and we thus compared the performance of iBE2 to that of hA3A-BE3, in terms of editing efficiency and specificity (
In this example, we first developed an efficient method (CESSCO) to quantitatively evaluate sgRNA-independent OTss mutations and confirmed that the BEs with a regular APOBEC-nCas9 backbone indeed induced OTss mutations in an sgRNA-independent manner (
By substituting nSpCas9 with the specificity-improved enSpCas9, highly-specific iBE2 was developed to further reduce unintended editing at OTsg sites (
This example tested a number of different configurations of molecules for implementing the induced and split base editor (isplitBE) system.
The working process of isplitBE is illustrated in
At a target site (ON, left lower branch), each of the hsgRNA and sgRNA binds to two adjacent sites on a target DNA, and the MCP- and N22p-containing fusion proteins bind to the MS2 tag and boxB tag of the hsgRNA and sgRNA, respectively. Due to proximity of TEVc (in the presence of free TEVn) and the TEV site, the TEVc/TEVn cleaves the TEV site, removing the mA3CDA2 from the APOBEC. Without the attached mA3CDA2, the APOBEC can highly efficiently carry out the desired editing.
At off-target sites, which may be a non-specific binding site (OTss, lower middle branch) or a site that only binds one of the guide RNAs, the TEVc/TEVn complex is not recruited to the TEV site-containing fusion protein, and thus the APOBEC cannot be activated. By contrast, in the conventional BE system (
Ten different configurations (Pairs 1-10), as illustrated in
In Pair 4, the rA1 and the nCas9 proteins were placed on different constructs. rA1 was further fused to an MCP protein which recognizes a MS2 tag on the helper sgRNA. In Pair 5, a mA3CDA2 was further fused to the rA1, via a TEV recognition site (black solid box). In Pair 6, a TEV protein was further fused, through a self-cleavage site 2A, to the rA1-mA3CDA2 fusion. Self cleavage of 2A would release the TEV from the fusion protein.
Pair 7 is different from Pair 6 by fusing the TEV to a N22p protein, which would recognize the boxB tag on the sgRNA. In Pair 8, the TEV protein was divided into TEVn and TEVc, separated by the 2A self cleavage site. In Pair 9, only the TEVc was fused to a N22p while the TEVn was free of any RNA tag-binding proteins. In Pair 10, the helper sgRNA targeted GFP, rather than a nearby site.
The constructs in
Likewise, all of these configurations were tested with the FANCF-ON, Sa-VEGFA-7-OTss and FANCF-OTsg sites (see schematic diagram in
A further testing was done with the V1B-ON, Sa-SITE42-OTss and V1B-OTsg sites (see schematic diagram in
Out of the 10 tested configurations, Pair 9 exhibited the best performance in terms of editing specificity. Pair 9 employs two sgRNA, a helper sgRNA (hsgRNA) and a regular sgRNA. The dual use of sgRNA further enhances specificity as it requires that both target sites are in proximity from each other.
In a first assay of this example, the optimal distance between the two target sites was assessed. A schematic diagram is presented in
The second assay tested the effect of hsgRNA spacer length on base editing efficiency and precision.
The overall efficiency of the isplitBE system was compared to the conventional BE3. The results are shown in
Normal cells have a background level of C-to-T mutations attributable to their endogenous APOBEC3 activities. To obtain a more accurate measurement of off-target C-to-T mutations, an APOBEC3 knockout 293FT cell line (293FT-A3KO) was used.
This example then compared transcriptome-wide C-to-U mutations induced by isplitBE-mA3, BE3 and hA3A-BE3-Y130F (Y130F). The numbers of transcriptome-wide C-to-T(U) mutations induced by Cas9, BE3, hA3A-BE3-Y130F (Y130F) and isplitBE-mA3 are shown in
Proprotein convertase subtilisin/kexin type 9 (PCSK9) is an enzyme encoded by the PCSK9 gene in humans on chromosome 1. It is the 9th member of the proprotein convertase family of proteins that activate other proteins. PCSK9 is inactive when first synthesized, because a section of peptide chains blocks their activity; proprotein convertases remove that section to activate the enzyme. The PCSK9 gene contains one of 27 loci associated with increased risk of coronary artery disease.
PCSK9 is ubiquitously expressed in many tissues and cell types. PCSK9 binds to the receptor for low-density lipoprotein particles (LDL), which typically transport 3,000 to 6,000 fat molecules (including cholesterol) per particle, within extracellular fluid. The LDL receptor (LDLR), on liver and other cell membranes, binds and initiates ingestion of LDL-particles from extracellular fluid into cells, thus reducing LDL particle concentrations. If PCSK9 is blocked, more LDLRs are recycled and are present on the surface of cells to remove LDL-particles from the extracellular fluid. Therefore, blocking PCSK9 can lower blood LDL-particle concentrations.
This example tested an approach to inactivate PCSK9 by introducing stop codons through base editing using the present technology. The sequences of the sgRNA/hsgRNA used are shown in Table 3, and the target sites on PCSK9 are shown in Table 4.
The numbers of stop codons generated by base editing were measured for the human PCSK9 gene.
This example confirms the applicability of the induced and split base editor (isplitBE) design in other types of base editors. The inhibitor used was mA3CDA2 and the editor was adenine base editor (ABE).
A schematic diagram illustrating the co-transfection of sgRNA and ABE fused with mA3CDA2 (or not as control) is shown in
The conventional base editors are limited to base transitions, not base transversions, insertions or deletions. Recently, a primer editing system was proposed, which employs a primer editor (PE) by conjugating a Cas9 nickase with a reverse transcriptase (RTase). The PE system can write genomes with almost any intended changes, including all types of base substitutions, small indels, and their combinations. The overall efficiency and specificity of the PE systems, however, are still limited.
In a first assay, this example tested a new design for the primer editing guide RNA (pegRNA). Conventionally, each guide RNA includes a scaffold. A commonly used scaffold sequence is GUUUUAGAGCUAGAAAUAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUU GAAAAAGUGGCACCGAGUCGGUGC (SEQ ID NO:29). Another example is GUUUUAGAGCUAGAAAUAGCAAGUUAAAAUAAGGCAUGUCCGUUAUCAACUU GAAAAAGUGGCACCGAUUCGGUGC (SEQ ID NO:30). A more generic consensus sequence is GUUUNAGAGCUAX1UAGCAAGUUNAAAUAAGGCNNGUCCGUUAUCAACUUX2A AGUGGCACCGANUCGGUGC (SEQ ID NO:31), where N represents any base, and X1 and X2 denotes any nucleotide sequence of a length of 2-50 bases.
The scaffold is expected to form a secondary structure (illustrated in
A new scaffold was therefore prepared, which forms a new pairing between positions 48 (e.g., A in SEQ ID NO:30) and 61 (e.g., G in SEQ ID NO:30). In the examples shown in
Constructs for testing the conventional pegRNA and the newly designed, enhanced pegRNA (epegRNA) were prepare as shown in
Likewise, according to the schematic diagram in
A complete prime editor requires a construct (about 11 kb) that is much larger than what an AAV vehicle can accommodate. Accordingly, a Split PE system was designed and tested. The original PE system is illustrated on the left panel of
An example co-transfection system is illustrated in
The present disclosure is not to be limited in scope by the specific embodiments described which are intended as single illustrations of individual aspects of the disclosure, and any compositions or methods which are functionally equivalent are within the scope of this disclosure. It will be apparent to those skilled in the art that various modifications and variations can be made in the methods and compositions of the present disclosure without departing from the spirit or scope of the disclosure. Thus, it is intended that the present disclosure cover the modifications and variations of this disclosure provided they come within the scope of the appended claims and their equivalents.
All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/074577 | Feb 2019 | WO | international |
This application is a continuation of U.S. application Ser. No. 17/427,040, filed Jul. 29, 2021, now U.S. Pat. No. 11,384,353, which is a U.S. National Stage Application under 35 U.S.C. § 371 of International Application No. PCT/CN2020/074218, filed Feb. 3, 2020, which claims the priority to PCT/CN2019/074577, filed on Feb. 2, 2019, the contents of each of which are hereby incorporated by reference in their entirety into the present disclosure.
| Entry |
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| Adikususma et al., “Versatile single-step-assembly CRISPR/Cas9 vectors for dual gRNA expression”, PLOS One, 12(12): e0187236. 2017. |
| Li, M. et al “First-In-Class Small Molecule Inhibitors of the Single-Strand DNA Cytosine Deaminase APOBEC3G” ACS Chem Biol. Mar. 16, 2012; 7(3): 506-517. doi:10.1021/cb200440y (25 pages). |
| Number | Date | Country | |
|---|---|---|---|
| 20230094769 A1 | Mar 2023 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 17427040 | US | |
| Child | 17862354 | US |
