METHODS FOR USING A 5'-EXONUCLEASE TO INCREASE HOMOLOGOUS RECOMBINATION IN EUKARYOTIC CELLS

Abstract

Provided herein are materials and methods for gene editing in eukaryotic cells (e.g., plant cells) by homologous recombination, including materials and methods for boosting the frequency of homologous recombination through the application of a 5′-exonuclease for end-processing of DNA double-strand breaks.

Description

TECHNICAL FIELD

This document relates to materials and methods for using a 5′-3′ exonuclease (also referred to herein as a 5′-exonuclease) to increase the frequency of homologous recombination in eukaryotic cells. In some cases, for example, the materials and methods described herein can be used for gene editing in plants by boosting the frequency of homologous recombination through the application of a 5′-exonuclease for end-processing of DNA double-strand breaks.

BACKGROUND

Useful traits can be conferred to living cells by the modification of endogenous DNA, or by integration of heterologous DNA into nuclear or organellar genomes. Some methods for introducing foreign DNA or editing endogenous sequences rely on the cellular homologous recombination (HR) pathway to introduce the desired trait at a specific site in the genome. However, HR derived modifications in eukaryotic cells typically occur at a frequency below the practical limit for detection and isolation of modified cells. The low frequency of HR can be partially overcome by the introduction of a double-strand break (DSB) at the site of interest. In plants, for example, targeted DSBs induced by a site-specific nuclease (SSN) can increase the frequency of HR by two to three orders of magnitude (Puchta et al., Proc Natl Acad Sci USA 93:5055-5060, 1996). In some cases, efficient gene targeting in plants can include the use of a robust nuclease such as clustered, regularly-interspaced short palindromic repeat/CRISPR-associated 9 (CRISPR/Cas9) with a DNA replicon for repair template delivery. Although molecular tools such as CRISPR/Cas9 and DNA replicons have boosted the rate at which HR can be induced, gene targeting remains a low efficiency event.

SUMMARY

This document is based, at least in part, on the discovery that expression of a 5′-exonuclease (e.g., a bacteriophage exonuclease) with traditional gene targeting reagents (e.g., a rare-cutting SSN such as a CRISPR/Cas or transcription activator-like effector (TALE) nuclease) in the presence of a supplied or endogenous repair template can enhance HR between the repair template and a chromosomal target cleaved by the nuclease. As described herein, introduction into eukaryotic cells of a 5′-exonuclease together with a SSN or a site-specific nickase (SSNi) can result in a higher frequency of HR with a provided repair template than the frequency obtained with only the SSN or SSNi and the repair template. For example, the data described herein show at least a 3-fold improvement in HR frequency with a 5′-exonuclease in Nicotiana benthamiana and wheat cells. Thus, the materials and methods provided herein can reduce the labor involved in generating gene targeting events in eukaryotic cells.

Without being bound by a particular mechanism, a nuclear-localized 5′-exonuclease can process DSBs to expose 3′ single-stranded DNA (ssDNA) ends, driving the equilibrium of DSB repair within a cell toward the HR pathway. An exonuclease can be delivered to cells along with other gene targeting reagents, such as one or more SSNs and repair templates. The exonuclease can be used to increase the frequency of, without limitation, gene editing, gene replacement, targeted insertions, and multiple genomic modifications in a single cell. With increased HR efficiency, a wide range of traits can be produced in eukaryotic cells. In plants, for example, such traits may include increased yield, beneficial agronomic characteristics, pathogen or pest resistance, tolerance to biotic and abiotic stressors, herbicide resistance, enhanced nutritional profiles, production of medically or industrially useful compounds, altered genomic structure, and/or different fertility and reproductive characteristics. In mammals, the methods provided herein can, for example, facilitate the editing of mutations that cause disease, or can create traits of value in livestock.

In one aspect, this document features a method for generating a modified eukaryotic cell or organism. The method can include delivering to the cell or the organism a site-specific nuclease (SSN) or site-specific nickase (SSNi), a repair template (RT), and a 5′-exonuclease, wherein the SSN or SSNi, RT, and 5′-exonuclease are delivered in amounts sufficient such that the SSN or SSNi cleaves the endogenous DNA of the cell or the organism at a specific site, and a nucleotide sequence carried within the RT is stably integrated into the endogenous DNA at the site of cleavage via homologous recombination. The SSN or SSNi can be a homing endonuclease, a zinc-finger nuclease (ZFN), a transcription activator-like effector (TALE) nuclease, or a clustered, regularly interspaced, short palindromic repeat (CRISPR)/CRISPR-associated (Cas) nuclease. The cell can be a human cell, or can be from an animal selected from the group consisting of cattle, swine, sheep, goats, bison, horses, donkeys, mules, rabbits, chickens, ducks, geese, turkeys, and pigeons. The cell can be from a monocotyledonous plant (e.g., a monocotyledonous plant selected from the group consisting of maize, rice, wheat, barley, sugarcane, oat, rye, millet, sorghum, switchgrass, turfgrass, and bamboo). The cell can be from a dicotyledenous plant (e.g., a dicotyledonous plant selected from the group consisting of bean, soybean, cotton, pea, cowpea, peanut, almond, walnut, apple, plum, peach, pear, citrus, sugar beet, squash, melon, cassava, tomato, pepper, canola, banana, flax, and sunflower). The cell can be a green algae. The cell can be isolated and regenerated into a whole organism following the homologous recombination. The modified cell can be maintained in culture as a pure or a mixed population.

The genomic DNA of the cell or organism can be modified, or the mitochondrial DNA of the cell or organism can be modified. In some embodiments, the cell can be a plant cell, and plastid DNA of the plant cell can be modified. The SSN or SSNi can be provided to the cell as a DNA that is expressed by the cell, as an RNA that is translated by the cell, or as a protein. The RT can be provided to the cell as a single- or double-stranded DNA. The 5′-exonuclease can be provided to the cell as a DNA that is expressed by the cell, as an RNA that is translated by the cell, or as a protein.

The SSN or SSNi, RT, and 5′-exonuclease can be transiently expressed in the plant cell, wherein only a portion of the RT is integrated during the gene targeting event. The SSN or SSNi, RT, and 5′-exonuclease can be stably integrated into the cell. The 5′-exonuclease can be from T5 bacteriophage, or from T3, T4, or another bacteriophage. The 5′-exonuclease can be derived from a prokaryotic cell, or can be of eukaryotic origin. The 5′-exonuclease can be Exo1. The sequences encoding the SSN and the 5′-exonuclease can be independently and operably linked to one or more constitutive promoters, inducible promoters, tissue-specific promoters, developmentally-regulated promoters, or any combination thereof. The SSN or SSNi, the RT, and the 5′-exonuclease, or any combination thereof, can be carried on a viral replicon derived from a DNA or RNA virus, can be carried within the cell on a full DNA or RNA virus, or can be carried within the cell on a non-replicating nucleic acid fragment.

The method can include delivering to the cell or the organism a SSNi, where the SSNi is Cas9 with a D10A substitution, or where the SSNi is Cas9 with a H840A substitution, where the SSNi is Cas9 with an amino acid substitution, insertion, or deletion other than a D10A or H840A substitution. The SSN or SSNi can cause a site-specific break in the double-stranded DNA.

The method can further include regenerating the cell into a whole organism that contains the modification incorporated by the RT, where no other foreign DNA is present in the organism. The method can further include regenerating the cell into a whole organism that contains the SSN or SSNi, RT, and 5′-exonuclease, or any combination thereof, stably integrated within its DNA.

In another aspect, this document features a method that includes delivering to a cell (i) a SSN or SSNi targeted to a selected sequence within the endogenous DNA of the cell, (ii) a RT, and (iii) a 5′-exonuclease, and regenerating the cell into a whole organism that contains the SSN or SSNi, RT, and 5′-exonuclease, or any combination thereof. The SSN or SSNi, RT, and 5′-exonuclease can be stably integrated within the endogenous DNA of the whole organism. In some embodiments, the whole organism may not contain a modification at the selected sequence, and the method can further include developing from the whole organism a line that is maintained under conditions appropriate for expression of the SSN or SSNi and 5′-exonuclease, and screening the line for a desired modification at the selected sequence. In some embodiments, the whole organism can contain a modification at the selected sequence, and the method can further include selfing or crossing the organism to obtain offspring having the modification at the selected sequence but not containing the SSN or SSNi and the 5′-exonuclease.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. Although methods and materials similar or equivalent to those described herein can be used to practice the invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below. Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.

DESCRIPTION OF DRAWINGS

FIG. 1A is a schematic of expression cassettes optimized for dicots (top) and monocots (bottom). The cassettes contain a Cas9 coding sequence (as an example of a SSN or SSNi) that is released by the P2A ribosomal skipping peptide from the T5 bacteriophage 5′-exonuclease (as an example of a 5′-exonuclease) that is encoded by a downstream sequence. FIG. 1B is a diagram depicting how the expressed 5′-exonuclease resects DSB ends to promote repair by the HR pathway. “2×35S” indicates a double copy of the Cauliflower Mosaic Virus 35S constitutive promoter; “Ubil” indicates the ubiquitin 1 constitutive promoter from corn; “P2A” indicates the ribosomal skipping sequence that results in translational release of the 5′-exonuclease protein from the Cas9 protein; “AtU6” indicates the RNA polymerase III U6 promoter from Arabidopsis thaliana; “TaU6” indicates the RNA polymerase III U6 promoter from wheat; “sgRNA” indicates the single guide RNA sequence that guides the Cas9 nuclease to the target sequence. All cassette elements shown can be borne on the geminivirus-derived replicon contained within the vector. Nucleotide sequences for the example plasmids are set forth in SEQ ID NO:2 (a T-DNA vector for dicotyledonous plants), SEQ ID NO:3 (a particle bombardment vector for monocotyledonous plants), SEQ ID NO:4 (a particle bombardment vector for monocotyledonous plants without a DNA replicon), SEQ ID NO:14 (a particle bombardment vector for monocotyledonous plants with Cas9 as a D10A nickase), and SEQ ID NO:15 (a particle bombardment vector for monocotyledonous plants with Cas9 as a H840A nickase). This vector configuration is in contrast to the negative control vectors that lack the T5 5′-exonuclease, as set forth in SEQ ID NO:11 (a T-DNA vector for dicotyledonous plants), SEQ ID NO:12 (a particle bombardment vector for monocotyledonous plants), and SEQ ID NO:13 (a particle bombardment vector for monocotyledonous plants without a DNA replicon).

FIG. 2 is a schematic showing expression cassettes optimized for dicots (top) and monocots (bottom). The expression cassettes contain a Cas9 coding sequence (as an example of a SSN) fused to a downstream coding sequence for the T5 bacteriophage 5′-exonuclease (as an example of a 5′-exonuclease). “2×35S” indicates a double copy of the Cauliflower Mosaic Virus 35S constitutive promoter; “Ubil” indicates the ubiquitin 1 constitutive promoter from corn; “mP2A” indicates a mutant version of the ribosomal skipping sequence that does not allow translational release of the 5′-exonuclase protein from the Cas9 protein, thus the two protein domains are fused; “AtU6” indicates the RNA polymerase III U6 promoter from Arabidopsis thaliana; “TaU6” indicates the RNA polymerase III U6 promoter from wheat; “sgRNA” indicates the single guide RNA sequence that guides the Cas9 nuclease to the target sequence. All cassette elements shown can be borne on the geminivirus-derived replicon contained within the vector. The nucleotide sequences of the example plasmids are set forth in SEQ ID NO:5 (a T-DNA vector for dicotyledonous plants) and SEQ ID NO:6 (a particle bombardment vector for monocotyledonous plants).

FIG. 3 is a schematic showing expression cassettes optimized for dicots (top) and monocots (bottom). The cassettes contain a Cas9 coding sequence (as an example of a SSN) expressed independently from the T5 bacteriophage 5′-exonuclease (as an example of a 5′-exonuclease) that is encoded by a downstream sequence. “2×35S” indicates a double copy of the Cauliflower Mosaic Virus 35S constitutive promoter; “Ubil” indicates the ubiquitin 1 constitutive promoter from corn; “CmYLCV” indicates a strong constitutive promoter from the tomato yellow leaf curl virus; “Actin” indicates the constitutive actin 1 promoter from rice; “AtU6” indicates the RNA polymerase III U6 promoter from Arabidopsis thaliana; “TaU6” indicates the RNA polymerase III U6 promoter from wheat; “sgRNA” indicates the single guide RNA sequence that guides the Cas9 nuclease to the target sequence. All cassette elements shown can be borne on the geminivirus-derived replicon contained within the vector. The nucleotide sequences of the example plasmids are set forth in SEQ ID NO:7 (a T-DNA vector for dicotyledonous plants) and SEQ ID NO:8 (a particle bombardment vector for monocotyledonous plants).

FIG. 4 is a schematic showing expression cassettes optimized for dicots (top) and monocots (bottom). The expression cassettes contain a T5 bacteriophage 5′-exonuclease (as an example of a 5′-exonuclease) coding sequence fused to a downstream Cas9 coding sequence (as an example of a SSN). “2×35S” indicates a double copy of the Cauliflower Mosaic Virus 35S constitutive promoter; “Ubil” indicates the ubiquitin 1 constitutive promoter from corn; “mP2A” indicates a mutant version of the ribosomal skipping sequence that does not allow translational release of the 5′-exonuclase protein from the Cas9 protein, thus the two protein domains are fused; “AtU6” indicates the RNA polymerase III U6 promoter from Arabidopsis thaliana; “TaU6” indicates the RNA polymerase III U6 promoter from wheat; “sgRNA” indicates the single guide RNA sequence that guides the Cas9 nuclease to the target sequence. All cassette elements shown can be borne on the geminivirus-derived replicon contained within the vector. Nucleotide sequences of example plasmids are set forth in SEQ ID NO:9 (a T-DNA vector for dicotyledonous plants) and SEQ ID NO:10 (a particle bombardment vector for monocotyledonous plants).

FIG. 5 is a pair of schematics illustrating additional examples of configurations in which the SSN (using CRISPR/Cas9 as an example) and 5′-exonuclease (using the T5 bacteriophage 5′-exonuclease as an example) can be expressed as a fusion protein with a Cas9 or other nuclease. The 5′-exonuclease can be expressed as an N- or C-terminal fusion with a peptide linker of any size and amino acid sequence, resulting in expression of a single protein containing the Cas9 nuclease domain and the 5′-exonuclease domain. The fusion of the SSN with the 5′-exonuclease may boost 5′-end resection by bringing the 5′-exonuclease into close proximity to the SSN-induced DSB.

FIG. 6 is a graph plotting the frequency of HR-mediated gene targeting after introduction of a 5′-exonuclease, a SSN, and a repair template into Nicotiana tabaccum cells by Agroinfiltration of leaves, vs. the frequency when only a SSN and a repair template were introduced. The T-DNA vector used for Agroinfiltration of the 5′-exonuclease is described in FIG. 1A. Gene targeting was measured in Agroinfiltrated tobacco leaves of plants that were about 6 weeks old by restoring function of a truncated GUS reporter gene previously integrated in the plant genome (Wright et al., Plant J 44:693-705, 2005). Five days after infiltration, leaf tissue was stained in a solution containing X-Gluc, and gene targeting was determined based on the stained area and intensity of each treatment. Introduction of the 5′-exonuclease combined with the nuclease and donor template significantly increased the frequency of gene targeting, by 2.8-fold, compared with the nuclease and donor template alone. In all cases, the different components of the system were expressed and replicated in the Bean Yellow Dwarf Virus (BeYDV) replicon system as previously described (Baltes et al., Plant Cell 26:151-163, 2014). The AtCas9 -T5 includes a SSN and RT; the AtCas9 +T5 includes a SSN, RT and the T5 5′-exonuclease.

FIG. 7 is a graph plotting the frequency of HR-mediated gene targeting after introduction of a 5′-exonuclease with a SSN and a repair template into wheat protoplasts, as compared to the frequency when only a SSN and repair template were introduced. The vector used for protoplast transfection of the 5′-exonuclease is shown in FIG. 1A. Gene targeting efficiency was determined in wheat protoplasts transfected with the different DNA constructs as the frequency of targeted integration of a promoter-less T2A:gfp sequence (hereafter referred to as T2A:gfp) into the endogenous Ubiquitin gene by HR. The correct integration of the T2A:gfp mediated by homologous recombination led to GFP expression driven by the native Ubiquitin promoter. Gene targeting was calculated two days after transfection by dividing the number of cells expressing GFP by the total number of cells, and normalized to the transfection efficiency of each experiment. Introduction of the 5′-exonuclease combined with the nuclease and donor template significantly increased the frequency of gene targeting, by 3.6-fold, compared to the nuclease and donor template alone. In all cases, the different components of the system were expressed and replicated in the Wheat Dwarf Virus (WDV) replicon system described by Gil-Humanes et al. (in press).

FIG. 8 is a graph plotting the effect (fold increase) on HR-mediated gene targeting (GT) after co-delivery of a 5′-exonuclease in conjunction with a SSNi. The D10A and H840A amino acid substitutions render the two nuclease domains in Cas9 inactive, making such mutants into nickases than can cleave only one or the other strand of the

DNA (although it is to be noted that in some cases, a Cas9 nickase can have an amino acid substitution, insertion, or deletion other than a D10A or H840A substitution). In all cases the T5 5′-exonuclease was expressed with the active Cas9 nuclease and the D10A nickase or the H840A nickase. Comparable levels of gene targeting were observed for all combinations. The vector used for protoplast transfection of the 5′-exonuclease was the monocot vector shown in FIG. 1A. Wheat protoplast transfection was performed as described for FIG. 7.

FIGS. 9A and 9B show a comparison of HR-mediated gene targeting with the 5′-exonuclease expressed from a functional P2A peptide or as a C-terminal fusion to Cas9 with a mutant P2A peptide. FIG. 9A is a schematic of the proteins resulting from each treatment. FIG. 9B is a graph plotting the frequency of HR-mediated gene targeting with a 5′-exonuclease fused to the Cas9 protein via a mutant P2A peptide vs. a fusion that is translationally released by the functional P2A peptide. Fusion of the 5′-exonuclease to the C-terminus of Cas9 resulted in 1.28-fold increase of the frequency of gene targeting compared to the 5′-exonuclease released from the fusion by a functional P2A peptide. The vectors used for protoplast transfection of the 5′-exonuclease are the monocot vectors described in FIGS. 1A and 2. Wheat protoplast transfection was performed as described for FIG. 7.

FIGS. 10A and 10B show a comparison of HR-mediated gene targeting with the 5′-exonuclease expressed in various configurations. FIG. 10A is a schematic of the proteins resulting from expression of each configuration. FIG. 10B is a graph plotting the fold increase in GT. The TaCas9-P2A-T5 treatment included a SSN, RT and the T5 5′-exonuclease released during translation from the C-terminus of the Cas9 protein; the TaCas9::T5 treatment includes a SSN, RT and the T5 5′-exonuclease fused to the C-terminus of the Cas9 protein with a mutant P2A peptide that does not allow translational release of the exonuclease domain from the Cas9 domain; and the T5:TaCas9 treatment included a SSN, RT and the T5 5′-exonuclease fused to the N-terminus of the Cas9 protein with a mutant P2A peptide that does not allow translational release of the exonuclease domain from the Cas9 domain. Fusion of the 5′-exonuclease to the C-terminus of Cas9 (TaCas9::T5) resulted in 1.28-fold increase of the frequency of gene targeting compared to the 5′-exonuclease released from the fusion by a functional P2A peptide. Fusion of the 5′-exonuclease to the N-terminus of Cas9 (T5::TaCas9) resulted in 1.43-fold increase of the frequency of gene targeting compared to the 5′-exonuclease released from the fusion by a functional P2A peptide. The vectors used for protoplast transfection of the 5′-exonuclease were the monocot vectors described in FIGS. 1, 2, and 4. Wheat protoplast transfection was performed as described for FIG. 7.

FIG. 11 is a graph showing that expression of 5′-exonuclease is an effective method for boosting HR-mediated gene targeting even without geminivirus-derived replicons for reagent delivery. The pCR-TaCas9 treatment included a SSN and RT; the pCR-TaCas9-P2A-T5 treatment included a SSN, RT and the T5 5′-exonuclease released during translation from the C-terminus of the Cas9 protein; the pCR-TaCas9::T5 treatment includes a SSN, RT and the T5 5′-exonuclease fused to the C-terminus of the Cas9 protein with a mutant P2A peptide that does not allow translational release of the exonuclease domain from the Cas9 domain. In this experiment there was no geminivirus replicon. Expression of the T5 5′-exonuclease released during translation from the C-terminus of the Cas9 protein (pCR-TaCas9+T5) resulted in a 2-fold increase compared to the pCR-TaCas9 treatment with only SSN and RT and no 5′-exonuclease. Expression of the T5 5′-exonuclease fused to the C-terminus of the Cas9 protein with a mutant P2A peptide resulted in a 4.4-fold increase compared to the pCR-TaCas9 treatment with only SSN and RT and no 5′-exonuclease. The vectors used for protoplast transfection of the 5′-exonuclease were the monocot vectors without DNA replicons but with expression cassettes described in FIGS. 1A and 2. Wheat protoplast transfection was performed as described for FIG. 7.

FIG. 12 is a graph showing that expressing a 5′-exonuclease from a promoter independent from the promoter driving SSN expression is an effective method for boosting HR-mediated gene targeting. The average frequency of gene targeting events was higher for the independently expressed 5′-exonuclease than for the P2A-mediated release of the 5′-exonuclease or the 5′-exonuclease delivered by a C-terminal fusion to Cas9. The T-DNA vector used for Agroinfiltration of the P2A-released 5′-exonuclease is shown in FIG. 1A; the T-DNA vector used for Agroinfiltration of the Cas9 with a C-terminal 5′-exonuclease fusion is shown in FIG. 2; the T-DNA vector used for Agroinfiltration of the independently expressed 5′-exonuclease is shown in FIG. 3. The experiment was conducted as described for FIG. 6.

SEQUENCE LISTING

The nucleic and amino acid sequences listed in the accompanying sequence listing are shown using standard letter abbreviations for nucleotide bases, and three letter code for amino acids, as defined in 37 C.F.R. §1.822. Only one strand of each nucleic acid sequence is shown, but the complementary strand is understood as included by any reference to the displayed strand. The Sequence Listing is submitted as an ASCII text file [SequenceListing.txt, Dec. 13, 2016, 347 kilobytes], which is incorporated by reference herein. In the accompanying sequence listing:

SEQ ID NO:1 is the amino acid sequence of the T5 5′-exonuclease.

SEQ ID NO:2 is the DNA sequence of a T-DNA vector for dicotyledonous plants [pJG376: BeYDV (sgR2+Cas9-P2A-T5+GUSnptII), with T5E translationally released from Cas9 via a P2A ribosomal skipping peptide].

SEQ ID NO:3 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG482: WDV1 (sgUbi6+TaCas9-P2A-T5+T2A-GFP), with T5E translationally released from Cas9 via a P2A ribosomal skipping peptide].

SEQ ID NO:4 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG623: non replicating ctrl (sgUbi6+TaCas9-P2A-T5+T2A-GFP), with T5E translationally released from Cas9 via a P2A ribosomal skipping peptide].

SEQ ID NO:5 is the DNA sequence of a T-DNA vector for dicotyledonous plants [pJG560: BeYDV (sgR2+Cas9:mutP2A:T5-1), with T5E fused to the C-terminus of Cas9 via a mutant (nonreleasing) P2a ribosomal skipping peptide].

SEQ ID NO:6 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG556: WDV1 (sgUbi6+TaCas9:mutP2A:T5+T2A-GFP), with T5E fused to the C-terminus of Cas9 via a mutant (nonreleasing) P2a ribosomal skipping peptide].

SEQ ID NO:7 is the DNA sequence of a T-DNA vector for dicotyledonous plants [pJG562: BeYDV (sgR2+35S:Cas9-CmYLCV:T5-2), with T5E independently expressed from a separate promoter].

SEQ ID NO:8 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG581 (WDV1-Ubi:TaCas9-Act1:T5-sgUbi6-GFP), with T5E independently expressed from a separate (actin) promoter].

SEQ ID NO:9 is the DNA sequence of a T-DNA vector for dicotyledonous plants [BeYDV-T5:mutP2A:Cas9, with T5E fused to the N-terminus of Cas9 via a mutant (nonreleasing) P2a ribosomal skipping peptide].

SEQ ID NO:10 is the DNA sequence of a T-DNA vector for monocotyledonous plants [pJG594: WDV1 (sgUbi6+T5:mutP2A:TaCas9+T2A-GFP), with T5E fused to the N-terminus of Cas9 via a mutant (nonreleasing) P2A ribosomal skipping peptide].

SEQ ID NO:11 is the DNA sequence of a T-DNA vector for dicotyledonous plants [pJG380: BeYDV (sgR2+Cas9+GUSnptII), without T5E (negative control)].

SEQ ID NO:12 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG284: WDV1 (sgUbi6+TaCas9+T2A-GFP), without T5E (negative control)].

SEQ ID NO:13 is the DNA sequence of a particle bombardment vector for monocotyledonous plants without replicon [pJG558: non replicating ctrl (sgUbi6+TaCas9+T2A-GFP), without T5E (negative control)].

SEQ ID NO: 14 is the DNA sequence of a particle bombardment vector for monocotyledonous plants with D10A nickase [pJG596: WDV1 (sgUbi6/sgUbi8+D10ATaCas9-P2A-T5+T2A-GFP)].

SEQ ID NO:15 is the DNA sequence of a particle bombardment vector for monocotyledonous plants with H840A nickase [pJG554: WDV1 (sgUbi6/sgUbi8+H840ATaCas9-P2A-T5+T2A-GFP)].

SEQ ID NO:16 is the DNA sequence of a particle bombardment vector for monocotyledonous plants [pJG624: non replicating ctrl (sgUbi6+TaCas9::T5+T2A-GFP), with T5E fused to the C-terminal end of the SSN in a non-replicating vector].

DETAILED DESCRIPTION

DNA DSBs can be resolved by one of two competing pathways in the cell. The non-homologous end joining pathway (NHEJ) typically predominates in eukaryotic cells, and results in repair by ligation of double-stranded DNA (dsDNA) ends, without the use of a homologous template from which to copy information. This pathway can be useful for generating gene knockouts or insertions, but it is not ideal for producing gene conversion events. The less commonly used HR pathway can be exploited to produce gene conversions that introduce one or more changes into chromosomal DNA via a repair template that contains sequence homologous to the chromosomal target (Puchta and Fauser, Int Dev Biol 57:629-637, 2013). A challenge with gene targeting by HR, however, is the low frequency at which cells undergo HR with the repair template, even with the induction of a DSB.

Gene editing methods can employ a SSN to create a DNA DSB at the target site in a eukaryotic cell. SSNs include, for example, homing endonucleases (HEs; also referred to as meganucleases), zinc-finger nucleases (ZFN), TALE nucleases, or CRISPR/Cas-derived nucleases or other reagents that generate DSBs in a user-defined, sequence-specific manner. Along with the SSN that produces the DSB, a repair template (RT) is delivered to the cell. The RT contains the DNA sequence intended for insertion or editing of the chromosomal DNA, flanked on both sides by sequence homologous to the genomic DNA at the site of the break. In some cases, the cell may be treated with one or more small molecules (e.g., SCR7) or siRNA-based (e.g., hairpins against DNA ligase IV) inhibitors of the non-homologous end joining (NHEJ) pathway for modest boosts in the efficiency of HR (Chu et al., Nature Biotechnol, 33:543-548, 2015). Delivery of the RT on a viral DNA replicon also can boost the efficiency of HR repair (Baltes et al., Plant Cell, 26: 151-163, 2014). Despite these advances, however, the frequency of repair by HR from a supplied RT remains low in eukaryotic cells, typically requiring significant labor or robust selection strategies to identify the desired gene editing event.

As described herein, introducing a 5′-exonuclease together with a SSN into eukaryotic cells can result in a higher frequency of HR with a provided repair template, as compared with the frequency obtained with the SSN alone. A nuclear-localized 5′-exonuclease can process DSBs to expose 3′ ssDNA ends, an essential step for DSB repair by HR (Zhu et al., Cell, 134: 981-994, 2008). Increased end-resection may drive the equilibrium of DSB repair within a cell toward the HR pathway. Such an exonuclease can be conveniently delivered to cells along with the other gene targeting reagents (e.g., the SSN and RT). In some embodiments, the 5′-exonuclease can be delivered via the same method, and as part of the same vector, as the SSN and RT reagents, requiring a minimal increase in the size of the vector elements and no additional effort in sample handling or transformation.

As described herein, simultaneous, coordinated expression of a 5′-exonuclease with traditional gene targeting reagents (e.g., rare-cutting SSNs such as CRISPR/Cas9 or TALE nucleases) in the presence of a supplied or endogenous repair template can enhance HR between the repair template and the chromosomal target that is cleaved by action of the nuclease, presumably by driving the cell toward the HR pathway and thus increasing the frequency at which HR mediated gene editing events can be recovered. A 5′-exonuclease can be used to process the ends of SSN induced DSBs, and to increase the frequency of, without limitation, gene targeting, gene replacement, targeted insertions, and multiple genomic modifications in a single cell. For example, when added to plant cells with a CRISPR/Cas9 nuclease and a DNA replicon repair template, a 5′-exonuclease can provide at least a 3-fold improvement in the efficiency of gene targeting over what was possible without the 5′-exonuclease.

With the increased efficiency of HR, a wide range of traits can be produced. In plants, these can include, without limitation, increased yield, beneficial agronomic characteristics, pathogen or pest resistance, tolerance to biotic and abiotic stresses, herbicide resistance, enhanced nutritional profiles, production of medically or industrially useful compounds, altered genomic structure, and/or different fertility and reproductive characteristics.

The methods provided herein can exploit the natural mechanism of homology searching by exposed 3′-ends of broken double-stranded DNA, which mediates HR. Without being bound by a particular mechanism, the 5′-exonuclease can resect the 5′-ends at the double-stranded break generated by the SSN, potentially increasing the abundance and possibly the size of the exposed 3′-ends.

The systems and methods described herein include at least three components: 1) a SSN for creating the targeted DSB in the cellular DNA, 2) a 5′-exonuclease targeted to the cellular compartment in which the DSB occurs to resect the 5′-ends and drive DSB repair toward the HR pathway, and 3) a RT with homology arms to mediate incorporation of the desired edits into the repaired DNA.

A representative 5′-exonuclease (the bacteriophage T5 exonuclease) sequence is set forth as an example, but this document contemplates the application of any enzyme with 5′-end resection activity of dsDNA ends to improve the efficiency of gene editing by HR. This document also contemplates the use of a “functional variant” of any naturally occurring or synthetic 5′-exonuclease enzyme. Such a mutant is catalytically active, and can have activity that is the same, higher or lower than the parent protein or protein domain.

In some embodiments, the 5′-exonuclease can be from a bacteriophage (e.g., the T2, T3, T4, T5, T7, or lambda bacteriophage), from a prokaryote (e.g., rexB, or the N-terminal exonuclease domain of DNA Polymerase I), or from a eukaryote (e.g., the Xrn1 or Exo1 5′-exonuclease). For example, the T5 bacteriophage 5′-exonuclease is a small protein having the amino acid sequence set forth in SEQ ID NO:1. In some embodiments, the 5′-exonuclease can be expressed as a fusion with the SSN, facilitating its delivery to plant cells by the same methods that can be used to introduce the other gene targeting reagents. The use of such a fusion also can be compatible with transient editing strategies (e.g., the DNA replicon) that can be used to make a genomic sequence modification without integration of unwanted foreign DNA such as, without limitation, the SSN expression cassette. An additional advantage of translational fusions of the 5′-exonuclease to the SSN can be the delivery of the 5′-exonuclease to the site of the DSB at the time the break is made due to its linkage to the SSN. This may increase the frequency at which the 5′-exonuclease is available at the proper place and time to cause resection of the dsDNA ends.

In some embodiments, therefore, the methods provided herein include the expression of a 291 amino acid T5 5′-exonuclease polypeptide, which can be expressed from the same promoter as that which drives expression of the SSN. The methods can be compatible with DNA replicons and transient introduction of gene targeting reagents. In addition, the methods can harness the natural biology of the cell, without requiring exposure to chemicals, small molecules, or interfering RNA that could have wider negative impacts on cellular processes unrelated to gene targeting. Further, there is no expected negative effect on the viability or regenerative capacity of cells exposed to the 5′-exonuclease, beyond the effect of exposure to the SSN and repair template alone.

This document provides isolated nucleic acids encoding the SSN molecules and 5′-exonucleases that are useful in the methods disclosed herein. In some embodiments, a nucleic acid can include sequences that encode one or more SSN or SSNi molecules (e.g., a TALE nuclease, a CRISPR/Cas endonuclease, a ZNF, or a meganuclease), as well as sequences that encode one or more 5′-exonucleases (e.g., a T5 5′-exonuclease). Further, a nucleic acid molecule as provided herein can include a repair template sequence.

The terms “nucleic acid” and “polynucleotide” are used interchangeably, and refer to both RNA and DNA, including cDNA, genomic DNA, synthetic (e.g., chemically synthesized) DNA, and DNA (or RNA) containing nucleic acid analogs. Polynucleotides can have any three-dimensional structure. A nucleic acid can be double-stranded or single-stranded (i.e., a sense strand or an antisense single strand). Non-limiting examples of polynucleotides include genes, gene fragments, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers, as well as nucleic acid analogs.

As used herein, “isolated,” when in reference to a nucleic acid, refers to a nucleic acid that is separated from other nucleic acids that are present in a genome, e.g., a plant genome, including nucleic acids that normally flank one or both sides of the nucleic acid in the genome. The term “isolated” as used herein with respect to nucleic acids also includes any non-naturally-occurring sequence, since such non-naturally-occurring sequences are not found in nature and do not have immediately contiguous sequences in a naturally-occurring genome.

An isolated nucleic acid can be, for example, a DNA molecule, provided one of the nucleic acid sequences normally found immediately flanking that DNA molecule in a naturally-occurring genome is removed or absent. Thus, an isolated nucleic acid includes, without limitation, a DNA molecule that exists as a separate molecule (e.g., a chemically synthesized nucleic acid, or a cDNA or genomic DNA fragment produced by PCR or restriction endonuclease treatment) independent of other sequences, as well as DNA that is incorporated into a vector, an autonomously replicating plasmid, a virus (e.g., a pararetrovirus, a retrovirus, lentivirus, adenovirus, or herpes virus), or the genomic DNA of a prokaryote or eukaryote. In addition, an isolated nucleic acid can include a recombinant nucleic acid such as a DNA molecule that is part of a hybrid or fusion nucleic acid. A nucleic acid existing among hundreds to millions of other nucleic acids within, for example, cDNA libraries or genomic libraries, or gel slices containing a genomic DNA restriction digest, is not to be considered an isolated nucleic acid.

A nucleic acid can be made by, for example, chemical synthesis or polymerase chain reaction (PCR) amplification from a template sequence or sequences. PCR refers to a procedure or technique in which target nucleic acids are amplified. PCR can be used to amplify specific sequences from DNA as well as RNA, including sequences from total genomic DNA or total cellular RNA. Various PCR methods are described, for example, in PCR Primer: A Laboratory Manual, Dieffenbach and Dveksler, eds., Cold Spring Harbor Laboratory Press, 1995. Generally, sequence information from the ends of the region of interest or beyond is employed to design oligonucleotide primers that are identical or similar in sequence to opposite strands of the template to be amplified. Various PCR strategies also are available by which site-specific nucleotide sequence modifications can be introduced into a template nucleic acid.

This document also provides purified 5′-exonuclease molecules, as well as purified SSN/SSNi polypeptides. The term “polypeptide” as used herein refers to a compound of two or more subunit amino acids regardless of post-translational modification (e.g., phosphorylation or glycosylation). The subunits may be linked by peptide bonds or other bonds such as, for example, ester or ether bonds. The term “amino acid” refers to either natural and/or unnatural or synthetic amino acids, including D/L optical isomers.

By “isolated” or “purified” with respect to a polypeptide it is meant that the polypeptide is separated to some extent from the cellular components with which it is normally found in nature (e.g., other polypeptides, lipids, carbohydrates, and nucleic acids). A purified polypeptide can yield a single major band on a non-reducing polyacrylamide gel. A purified polypeptide can be at least about 75% pure (e.g., at least 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100% pure). Purified polypeptides can be obtained by, for example, extraction from a natural source, by chemical synthesis, or by recombinant production in a host cell or transgenic plant, and can be purified using, for example, affinity chromatography, immunoprecipitation, size exclusion chromatography, and ion exchange chromatography. The extent of purification can be measured using any appropriate method, including, without limitation, column chromatography, polyacrylamide gel electrophoresis, or high-performance liquid chromatography.

As noted above, this document also contemplates the use of “functional variants” of 5′-exonuclease enzymes, which are catalytically active and can have activity that is the same, higher or lower than the parent protein or protein domain. Functional variants of 5′-exonuclease enzymes can have amino acid sequences that are at least 90% (e.g., at least 95%, at least 98%, or at least 99%) identical to a reference 5′-exonuclease sequence (e.g., the sequence set forth in SEQ ID NO:1). The percent sequence identity between a particular nucleic acid or amino acid sequence and a sequence referenced by a particular sequence identification number is determined as follows. First, a nucleic acid or amino acid sequence is compared to the sequence set forth in a particular sequence identification number using the BLAST 2 Sequences (B12seq) program from the stand-alone version of BLASTZ containing BLASTN version 2.0.14 and BLASTP version 2.0.14. This stand-alone version of BLASTZ can be obtained online at fr.com/blast or at ncbi.nlm.nih.gov. Instructions explaining how to use the B12seq program can be found in the readme file accompanying BLASTZ. B12seq performs a comparison between two sequences using either the BLASTN or BLASTP algorithm. BLASTN is used to compare nucleic acid sequences, while BLASTP is used to compare amino acid sequences. To compare two nucleic acid sequences, the options are set as follows: -i is set to a file containing the first nucleic acid sequence to be compared (e.g., C:\seql.txt); -j is set to a file containing the second nucleic acid sequence to be compared (e.g., C:\seq2.txt); -p is set to blastn; -o is set to any desired file name (e.g., C:\output.txt); -q is set to -1; -r is set to 2; and all other options are left at their default setting. For example, the following command can be used to generate an output file containing a comparison between two sequences: C:\B12seq c:\seql.txt -j c:\seq2.txt -p blastn -o c:\output.txt -q -1 -r 2. To compare two amino acid sequences, the options of B12seq are set as follows: -i is set to a file containing the first amino acid sequence to be compared (e.g., C:\seql.txt); -j is set to a file containing the second amino acid sequence to be compared (e.g., C:\seq2.txt); -p is set to blastp; -o is set to any desired file name (e.g., C:\output.txt); and all other options are left at their default setting. For example, the following command can be used to generate an output file containing a comparison between two amino acid sequences: C:\B12seq c:\seq1.txt -j c:\seq2.txt -p blastp -o c:\output.txt. If the two compared sequences share homology, then the designated output file will present those regions of homology as aligned sequences. If the two compared sequences do not share homology, then the designated output file will not present aligned sequences.

Once aligned, the number of matches is determined by counting the number of positions where an identical nucleotide or amino acid residue is presented in both sequences. The percent sequence identity is determined by dividing the number of matches either by the length of the sequence set forth in the identified sequence (e.g., SEQ ID NO:1), or by an articulated length (e.g., 100 consecutive nucleotides or amino acid residues from a sequence set forth in an identified sequence), followed by multiplying the resulting value by 100. For example, a nucleic acid sequence that has 275 matches when aligned with the sequence set forth in SEQ ID NO:1 is 94.5 percent identical to the sequence set forth in SEQ ID NO:1 (i.e., 275±291×100=94.5). It is noted that the percent sequence identity value is rounded to the nearest tenth. For example, 75.11, 75.12, 75.13, and 75.14 are rounded down to 75.1, while 75.15, 75.16, 75.17, 75.18, and 75.19 are rounded up to 75.2. It also is noted that the length value will always be an integer.

In some embodiments, nucleotide sequences encoding the SSN/SSNi and 5′-exonuclease molecules described herein can be incorporated into a vector. Thus, recombinant nucleic acid constructs (e.g., vectors) also are provided herein. The terms “vector” and “vectors” refer to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. In particular, a “vector” is a replicon, such as a plasmid, phage, or cosmid, into which another DNA segment may be inserted so as to bring about the replication of the inserted segment. A vector can be, without limitation, a viral vector, a plasmid, a RNA vector or a linear or circular DNA or RNA molecule which can consist of chromosomal, non-chromosomal, semi-synthetic, or synthetic nucleic acids. Vectors can be capable of autonomous replication (episomal vector) and/or expression of nucleic acids to which they are linked (expression vectors). Large numbers of suitable vectors are known to those of skill in the art and commercially available.

Generally, a vector is capable of replication when associated with the proper control elements. Suitable vector backbones include, for example, those routinely used in the art such as plasmids, viruses, artificial chromosomes, BACs, YACs, or PACs. The term “vector” includes cloning and expression vectors, as well as viral vectors and integrating vectors. An “expression vector” is a vector that includes one or more expression control sequences, and an “expression control sequence” is a DNA sequence that controls and regulates the transcription and/or translation of another DNA sequence. Suitable expression vectors include, without limitation, plasmids and viral vectors derived from, for example, bacteriophage, baculoviruses, tobacco mosaic virus, herpes viruses, cytomegalovirus, retroviruses, vaccinia viruses, adenoviruses, and adeno-associated viruses. Numerous vectors and expression systems are commercially available from such corporations as Novagen (Madison, Wis.), Clontech (Palo Alto, Calif.), Stratagene (La Jolla, Calif.), and Invitrogen/Life Technologies (Carlsbad, Calif.).

The terms “regulatory region,” “control element,” and “expression control sequence” refer to nucleotide sequences that influence transcription or translation initiation and rate, and stability and/or mobility of the transcript or polypeptide product. Regulatory regions include, without limitation, promoter sequences, enhancer sequences, response elements, protein recognition sites, inducible elements, promoter control elements, protein binding sequences, 5′ and 3′ untranslated regions (UTRs), transcriptional start sites, termination sequences, polyadenylation sequences, introns, and other regulatory regions that can reside within coding sequences, such as secretory signals, Nuclear Localization Sequences (NLS) and protease cleavage sites.

As used herein, “operably linked” means incorporated into a genetic construct so that expression control sequences effectively control expression of a coding sequence of interest. A coding sequence is “operably linked” and “under the control” of expression control sequences in a cell when RNA polymerase is able to transcribe the coding sequence into RNA, which if an mRNA, then can be translated into the protein encoded by the coding sequence. Thus, a regulatory region can modulate, e.g., regulate, facilitate or drive, transcription in the plant cell, plant, or plant tissue in which it is desired to express a modified target nucleic acid.

A promoter is an expression control sequence composed of a region of a DNA molecule, typically within 100 nucleotides upstream of the point at which transcription starts (generally near the initiation site for RNA polymerase II). Promoters are involved in recognition and binding of RNA polymerase and other proteins to initiate and modulate transcription. To bring a coding sequence under the control of a promoter, it typically is necessary to position the translation initiation site of the translational reading frame of the polypeptide between one and about fifty nucleotides downstream of the promoter. A promoter can, however, be positioned as much as about 5,000 nucleotides upstream of the translation start site, or about 2,000 nucleotides upstream of the transcription start site. A promoter typically comprises at least a core (basal) promoter. A promoter also may include at least one control element such as an upstream element. Such elements include upstream activation regions (UARs) and, optionally, other DNA sequences that affect transcription of a polynucleotide such as a synthetic upstream element.

The choice of promoters to be included depends upon several factors, including, but not limited to, efficiency, selectability, inducibility, desired expression level, and cell or tissue specificity. For example, tissue-, organ- and cell-specific promoters that confer transcription only or predominantly in a particular tissue, organ, and cell type, respectively, can be used. In some embodiments, promoters specific to plant tissues such as the stem, parenchyma, ground meristem, vascular bundle, cambium, phloem, cortex, shoot apical meristem, lateral shoot meristem, root apical meristem, lateral root meristem, leaf primordium, leaf mesophyll, or leaf epidermis can be suitable regulatory regions. In some embodiments, promoters that are essentially specific to seeds (“seed-preferential promoters”) can be useful. Seed-specific promoters can promote transcription of an operably linked nucleic acid in endosperm and cotyledon tissue during seed development. Alternatively, constitutive promoters can promote transcription of an operably linked nucleic acid in most or all tissues of a plant, throughout plant development. Other classes of promoters include, but are not limited to, inducible promoters, such as promoters that confer transcription in response to external stimuli such as chemical agents, developmental stimuli, or environmental stimuli.

Non-limiting examples of promoters that can be included in the nucleic acid constructs provided herein include the cauliflower mosaic virus (CaMV) 35S transcription initiation region, the 1′ or 2′ promoters derived from T-DNA of Agrobacterium tumefaciens, promoters from a maize leaf-specific gene described by Busk ((1997) Plant J 11:1285-1295), knl-related genes from maize and other species, promoters from rice actin 1 and Arabidopsis UBI10, and transcription initiation regions from various plant genes such as the maize ubiquitin-1 promoter. Inducible promoters can be induced by pathogens or stress (e.g., cold, heat, UV light, or high ionic concentrations; reviewed in Potenza et al., In vitro Cell Dev Biol 40:1-22, 2004). Inducible promoters also may be induced by chemicals (reviewed in Moore et al., Plant J., 45:651-683, 2006; Padidam, Curr Opin Plant Biol, 6:169-177, 2003; Wang et al., Transgenic Res., 12:529-540, 2003; and Zuo and Chua, Curr Opin Biotechnol, 11:146-151, 2000).

It will be understood that more than one regulatory region may be present in a recombinant polynucleotide, e.g., introns, enhancers, upstream activation regions, and inducible elements.

For example, a 5′ untranslated region (UTR) that is transcribed but is not translated, can lie between the start site of the transcript and the translation initiation codon, and may include the +1 nucleotide. A 3′ UTR can be positioned between the translation termination codon and the end of the transcript. UTRs can have particular functions such as increasing mRNA message stability or translation attenuation. Examples of 3′ UTRs include, but are not limited to polyadenylation signals and transcription termination sequences. A polyadenylation region at the 3′-end of a coding region can also be operably linked to a coding sequence. The polyadenylation region can be derived from the natural gene, from various other plant genes, or from an Agrobacterium T-DNA.

Recombinant nucleic acid constructs can include a polynucleotide sequence inserted into a vector suitable for transformation of cells (e.g., plant cells or animal cells).

Recombinant vectors can be made using, for example, standard recombinant DNA techniques (see, e.g., Sambrook et al. (1989) Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.).

The vectors provided herein also can include, for example, origins of replication, and/or scaffold attachment regions (SARs). In addition, an expression vector can include a tag sequence designed to facilitate manipulation or detection (e.g., purification or localization) of the expressed polypeptide. Tag sequences, such as green fluorescent protein (GFP), glutathione S-transferase (GST), polyhistidine, c-myc, hemagglutinin, or FLAG™ tag (Kodak, New Haven, Conn.) sequences typically are expressed as a fusion with the encoded polypeptide. Such tags can be inserted anywhere within the polypeptide, including at either the carboxyl or amino terminus.

By “delivery vector” or “delivery vectors” is intended any delivery vector which can be used in the presently described methods to put into cell contact or deliver inside cells or subcellular compartments agents/chemicals and molecules (proteins or nucleic acids). It includes, but is not limited to liposomal delivery vectors, viral delivery vectors, drug delivery vectors, chemical carriers, polymeric carriers, lipoplexes, polyplexes, dendrimers, microbubbles (ultrasound contrast agents), nanoparticles, emulsions or other appropriate transfer vectors. These delivery vectors allow delivery of molecules, chemicals, macromolecules (genes, proteins), or other vectors such as plasmids, peptides developed by Diatos. In these cases, delivery vectors are molecule carriers. By “delivery vector” or “delivery vectors” is also intended delivery methods to perform transfection.

In some embodiments, this document provides viral vectors (e.g., geminivirus or adeno-associated virus vectors) and T-DNAs that carry a sequence encoding a 5′-exonuclease, as well as Agrobacterium strains that include such T-DNAs. Other useful viral vectors can include retrovirus, adenovirus, parvovirus (e. g. adeno-associated viruses), coronavirus, negative strand RNA viruses such as orthomyxovirus (e. g., influenza virus), rhabdovirus (e. g., rabies and vesicular stomatitis virus), paramyxovirus (e. g. measles and Sendai), positive strand RNA viruses such as picornavirus and alphavirus, and double-stranded DNA viruses including adenovirus, herpesvirus (e. g., Herpes Simplex virus types 1 and 2, Epstein-Barr virus, cytomegalovirus), and poxvirus (e. g., vaccinia, fowlpox and canarypox) vectors. Further examples of viral vectors include those from Norwalk virus, togavirus, flavivirus, reoviruses, papovavirus, hepadnavirus, and hepatitis virus, for example. Examples of retroviruses include avian leukosis-sarcoma, mammalian C-type, B-type viruses, D type viruses, HTLV-BLV group, lentivirus, and spumavirus (Coffin, “Retroviridae: The viruses and their replication,” In Fundamental Virology, Third Edition, Fields et al., Eds., Lippincott-Raven Publishers, Philadelphia, 1996).

Methods for modifying endogenous DNA (e.g., genomic DNA, mitochondrial DNA, or plastid DNA) also are provided herein. The methods can include introducing one or more 5′-exonuclease and SSN/SSNi nucleic acids or polypeptides into a eukaryotic cell, where the SSN/SSNi is targeted to a particular DNA sequence within the cell. ART containing sequences homologous to the targeted DNA sequence also can be introduced into the cell. The SSN/SSNi and the 5′-exonuclease can be provided to the cell as one or more DNA molecules that are expressed by the cell, as one or more RNA molecules that are translated by the cell, or as one or more proteins. The RT can be provided to the cell as a single-stranded DNA or as a double-stranded DNA.

In some embodiments, the methods can include introducing into a cell a vector that contains a sequence encoding a 5′-exonuclease and, optionally, a sequence encoding a SSN or SSNi, in which the open reading frames of the 5′-exonuclease coding sequence and the optional SSN or SSNi coding sequence are operably linked to a promoter suitable for the species and cell type in which the coding sequence is to be expressed. In some cases, the vector also can contain a RT. The promoter(s) operably linked to the coding sequence(s) can be, without limitation, constitutive, inducible or tissue-specific. The eukaryotic cells modified according to the methods provided herein can be from any species that undergoes HR as a repair pathway for DSBs. These can include, without limitation, any species of monocotyledonous or dicotyledenous plants, or mammalian (e.g., human) cells. In some embodiments, the methods described herein can include the modification of single or multiple cells within a population, followed by isolation of those cells for amplification or maintenance of the cell line or for regeneration of whole organs, tissues, or organisms from a modified cell. In some embodiments, a population of cells can be maintained as a mixture of modified and unmodified cells.

Also provided herein are methods in which one or more SSN and 5′-exonuclease-encoding constructs are used to transform eukaryotic cells, such that a genetically modified cell or organism (e.g., a plant or an animal) is generated. Thus, genetically modified organisms and cells containing the nucleic acids and/or polypeptides described herein also are provided. A transformed cell, as provided herein, has a recombinant nucleic acid construct integrated into its genome (i.e., is stably transformed). A construct can integrate in a homologous manner, such that a nucleotide sequence endogenous to the transformed cell is replaced by the construct, where the construct contains a sequence that corresponds to the endogenous sequence, but that contains one or more modifications with respect to the endogenous sequence. It is noted that while a plant or animal containing such a modified endogenous sequence may be termed a “genetically modified organism” (GMO) herein, the modified endogenous sequence is not considered a transgene.

Alternatively, a cell can be transiently transformed, such that the 5′-exonuclease and SSN/SSNi coding sequences are not integrated into its genome. For example, a plasmid vector containing a 5′-exonuclease and a SSN/SSNi coding sequence can be introduced into a cell, such that the coding sequences are expressed but the vector is not stably integrated in the genome. Transiently transformed cells typically lose some or all of the introduced nucleic acid construct with each cell division, such that the introduced nucleic acid cannot be detected in daughter cells after sufficient number of cell divisions. Nevertheless, expression of the 5′-exonuclease and SSN/SSNi coding sequences is sufficient to achieve homologous recombination between a RT and an endogenous target sequence. Both transiently transformed and stably transformed cells can be useful in the methods described herein.

With particular respect to genetically modified plant cells, cells used in the methods described herein can constitute part or all of a whole plant. Such plants can be grown in a manner suitable for the species under consideration, either in a growth chamber, a greenhouse, or in a field. Genetically modified plants can be bred as desired for a particular purpose, e.g., to introduce a recombinant nucleic acid into other lines, to transfer a recombinant nucleic acid to other species or for further selection of other desirable traits. Alternatively, genetically modified plants can be propagated vegetatively for those species amenable to such techniques. Progeny includes descendants of a particular plant or plant line. Progeny of an instant plant include seeds formed on F₁, F₂, F₃, F₄, F₅, F₆ and subsequent generation plants, or seeds formed on BC₁, BC₂, BC₃, and subsequent generation plants, or seeds formed on F₁BC₁, FB₂, F₁BC₃, and subsequent generation plants. Seeds produced by a genetically modified plant can be grown and then selfed (or outcrossed and selfed) to obtain seeds homozygous for a desired modification.

Genetically modified cells (e.g., plant cells or animal cells) can be grown in suspension culture, or tissue or organ culture, if desired. For the purposes of the methods provided herein, solid and/or liquid tissue culture techniques can be used. When using solid medium, cells can be placed directly onto the medium or can be placed onto a filter film that is then placed in contact with the medium. When using liquid medium, cells can be placed onto a floatation device, e.g., a porous membrane that contacts the liquid medium. Solid medium typically is made from liquid medium by adding agar. For example, a solid medium can be Murashige and Skoog (MS) medium containing agar and a suitable concentration of an auxin, e.g., 2,4-dichlorophenoxyacetic acid (2,4-D), and a suitable concentration of a cytokinin, e.g., kinetin.

The SSN/SSNi and 5′-exonuclease (and, in some cases, the RT) can be delivered to eukaryotic cells by any method suitable for transfection of nucleic acids for the species and cell type being treated. These include, for example, particle bombardment or Agrobacterium mediated transformation of plant cells or tissues, electroporation, and PEG transfection of protoplasts or mammalian cells. In some embodiments, as polypeptides per se using delivery vectors associated or combined with any cellular permeabilization techniques such as sonoporation or electroporation or derivatives of these techniques Delivery vectors and vectors can be associated or combined with any cellular permeabilization techniques such as sonoporation or electroporation or derivatives of these techniques.

A cell can be transformed with one recombinant nucleic acid construct or with a plurality (e.g., 2, 3, 4, or 5) of recombinant nucleic acid constructs. If multiple constructs are utilized, they can be transformed simultaneously or sequentially. Techniques for transforming a wide variety of species are known in the art. The polynucleotides and/or recombinant vectors described herein can be introduced into the genome of a host using any of a number of known methods, including electroporation, microinjection, and biolistic methods. Alternatively, polynucleotides or vectors can be combined with suitable T-DNA flanking regions and introduced into a conventional Agrobacterium tumefaciens host vector. Such Agrobacterium tumefaciens-mediated transformation techniques, including disarming and use of binary vectors, are well known in the art. Other gene transfer and transformation techniques include protoplast transformation through calcium or PEG, electroporation-mediated uptake of naked DNA, liposome-mediated transfection, electroporation, viral vector-mediated transformation, and microprojectile bombardment (see, e.g., U.S. Pat. Nos. 5,538,880, 5,204,253, 5,591,616, and 6,329,571). If a plant cell or tissue culture is used as the recipient tissue for transformation, plants can be regenerated from transformed cultures using techniques known to those skilled in the art.

In some embodiments, a nuclease (5′-exonuclease and/or a SSN/SSNi) can be directly introduced into a cell. For example, a polypeptide can be introduced into a cell by mechanical injection, by delivery via a bacterial type III secretion system, by electroporation, or by Agrobacterium mediated transfer. See, e.g., Vergunst et al. (2000) Science 290:979-982 for a discussion of the Agrobacterium VirB/D4 transport system, and its use to mediate transfer of a nucleoprotein T complex into plant cells.

The nucleic acids, vectors, and polypeptides described herein can be introduced into any of a number of cell types, including plant cells, animal cells, or in some embodiments, algae cells (e.g., green algae cells). In the context of the present document, “eukaryotic cells” refer to a fungal, yeast, plant or animal cell or a cell line derived from the organisms listed herein and established for in vitro culture. For example, suitable fungal cells include cells from the genus Aspergillus, Penicillium, Acremonium, Trichoderma, Chrysoporium, Mortierella, Kluyveromyces or Pichia. More specifically, the fungus can be of the species Aspergillus niger, Aspergillus nidulans, Aspergillus oryzae, Aspergillus terreus, Penicillium chrysogenum, Penicillium citrinum, Acremonium Chrysogenum, Trichoderma reesei, Mortierella alpine, Chrysosporium lucknowense, Kluyveromyces lactis, Pichia pastoris or Pichia ciferrii.

With further respect to plants, the nucleic acids, vectors, and polypeptides described herein can be introduced into any of a number of monocotyledonous and dicotyledonous plants and plant cell systems, including dicots such as safflower, alfalfa, soybean, coffee, amaranth, rapeseed (high erucic acid and canola), peanut, sunflower, bean, soybean, cotton, pea, cowpea, peanut, almond, walnut, apple, plum, peach, pear, citrus, sugar beet, squash, melon, cassava, tomato, pepper, canola, banana, flax, as well as monocots such as oil palm, sugarcane, banana, sudangrass, corn, wheat, rye, barley, oat, rice, millet, sorghum, maize, switchgrass, turfgrass, and bamboo. Also suitable are gymnosperms such as fir and pine.

Thus, the methods described herein can be utilized with dicotyledonous plants belonging, for example, to the orders Magniolales, Illiciales, Laurales, Piperales, Aristochiales, Nymphaeales, Ranunculales, Papeverales, Sarraceniaceae, Trochodendrales, Hamamelidales, Eucomiales, Leitneriales, Myricales, Fagales, Casuarinales, Caryophyllales, Batales, Polygonales, Plumbaginales, Dilleniales, Theales, Malvales, Urticales, Lecythidales, Violales, Salicales, Capparales, Ericales, Diapensales, Ebenales, Primulales, Rosales, Fabales, Podostemales, Haloragales, Myrtales, Cornales, Proteales, Santales, Rafflesiales, Celastrales, Euphorbiales, Rhamnales, Sapindales, Juglandales, Geraniales, Polygalales, Umbellales, Gentianales, Polemoniales, Lamiales, Plantaginales, Scrophulariales, Campanulales, Rubiales, Dipsacales, and Asterales. The methods described herein also can be utilized with monocotyledonous plants such as those belonging to the orders Alismatales, Hydrocharitales, Najadales, Triuridales, Commelinales, Eriocaulales, Restionales, Poales, Juncales, Cyperales, Typhales, Bromeliales, Zingiberales, Arecales, Cyclanthales, Pandanales, Arales, Lilliales, and Orchidales, or with plants belonging to Gymnospermae, e.g., Pinales, Ginkgoales, Cycadales and Gnetales.

The methods can be used over a broad range of plant species, including species from the dicot genera Atropa, Alseodaphne, Anacardium, Arachis, Beilschmiedia, Brassica, Carthamus, Cocculus, Croton, Cucumis, Citrus, Citrullus, Capsicum, Catharanthus, Cocos, Coffea, Cucurbita, Daucus, Duguetia, Eschscholzia, Ficus, Fragaria, Glaucium, Glycine, Gossypium, Helianthus, Hevea, Hyoscyamus, Lactuca, Landolphia, Linum, Litsea, Lycopersicon, Lupinus, Manihot, Majorana, Malus, Medicago, Nicotiana, Olea, Parthenium, Papaver, Persea, Phaseolus, Pistacia, Pisum, Pyrus, Prunus, Raphanus, Ricinus, Senecio, Sinomenium, Stephania, Sinapis, Solanum, Theobroma, Trifolium, Trigonella, Vicia, Vinca, Vitis, and Vigna; the monocot genera Allium, Andropogon, Aragrostis, Asparagus, Avena, Cynodon, Elaeis, Festuca, Festulolium, Heterocallis, Hordeum, Lemna, Lolium, Musa, Oryza, Panicum, Pannesetum, Phleum, Poa, Secale, Sorghum, Triticum, and Zea; or the gymnosperm genera Abies, Cunninghamia, Picea, Pinus, and Pseudotsuga.

The plant can be of the genus Arabidospis, Nicotiana, Solanum, Lactuca, Brassica, Oryza, Asparagus, Pisum, Medicago, Zea, Hordeum, Secale, Triticum, Capsicum, Cucumis, Cucurbita, Citrullis, Citrus, or Sorghum. In some embodiments, the plant can be of the species Arabidospis thaliana, Nicotiana tabaccum, Solanum lycopersicum, Solanum tuberosum, Solanum melongena, Solanum esculentum, Lactuca saliva, Brassica napus, Brassica oleracea, Brassica rapa, Oryza glaberrima, Oryza sativa, Asparagus officinalis, Pisum sativum, Medicago sativa, Zea mays, Hordeum vulgare, Secale cereal, Triticum aestivum, Triticum durum, Capsicum sativus, Cucurbita pepo, Citrullus lanatus, Cucumis melo, Citrus aurantifolia, Citrus maxima, Citrus medica, or Citrus reticulata.

Examples of useful animal cells include those of the genus Homo, Rattus, Mus, Sus, Bos, Danio, Canis, Felis, Equus, Salmo, Oncorhynchus, Gallus, Meleagris, Drosophila, or Caenorhabditis; in some embodiments, the animal cell can be of the species Homo sapiens, Rattus norvegicus, Mus musculus, Sus scrofa, Bos taurus, Danio rerio, Canis lupus, Felis catus, Equus caballus, Oncorhynchus mykiss, Gallus gallus, or Meleagris gallopavo; the animal cell can be a fish cell from Salmo salar, Teleost fish or zebrafish species as non-limiting examples. The animal cell also can be an insect cell from Drosophila melanogaster as a non-limiting example; the animal cell can also be a worm cell from Caenorhabditis elegans as a non-limiting example. In some embodiments, an animal cell can be from a cow, pig, sheep, goat, bison, horse, donkey, mule, rabbit, chicken, duck, goose, turkey, or pigeon.

A transformed cell, callus, tissue, or plant can be identified and isolated by selecting or screening the engineered cells for particular traits or activities, e.g., those encoded by marker genes or antibiotic resistance genes. Such screening and selection methodologies are well known to those having ordinary skill in the art. In addition, physical and biochemical methods can be used to identify transformants. These include Southern analysis or PCR amplification for detection of a polynucleotide; Northern blots, S1 RNase protection, primer-extension, or RT-PCR amplification for detecting RNA transcripts; enzymatic assays for detecting enzyme or ribozyme activity of polypeptides and polynucleotides; and protein gel electrophoresis, Western blots, immunoprecipitation, and enzyme-linked immunoassays to detect polypeptides. Other techniques such as in situ hybridization, enzyme staining, and immunostaining also can be used to detect the presence or expression of polypeptides and/or polynucleotides. Methods for performing all of the referenced techniques are well known. Polynucleotides that are stably incorporated into plant cells can be introduced into other plants using, for example, standard breeding techniques.

The methods provided herein can further include steps such as isolating a modified cell and regenerating it into a whole organism, or maintaining a plurality of modified cells in culture as a pure or a mixed population. In some cases, the whole organism may not contain the desired modification at the targeted site due to inaction of the SSN/SSNi and/or the 5′-exonuclease. Such organisms can be developed into one or more lines that can be maintained under conditions appropriate for expression of the SSN/SSNi and 5′-exonuclease, which then can be screened for the desired modification. In some cases, the whole organism may contain the desired modification at the targeted site, and also may contain the stably integrated SSN or SSNi, RT, and 5′-exonuclease, or any combination thereof. In such cases, the method may further include selfing or crossing the organism to obtain offspring having the desired modification without the stably integrated SSN/SSNi and 5′-exonuclease. When the cell is a plant cell, the methods provided herein can further include steps such as generating a plant containing the transformed cell, generating progeny of the plant, selecting or screening for plants containing the desired modification at the targeted site, generating progeny of the selected plants, and testing the plants (e.g., tissue, seed, precursor cells, or whole plants) or progeny of the plants for recombination at the target nucleotide sequence. In some cases, the methods can include out-crossing the selected plants to remove the SSN/SSNi and/or 5′-exonuclease, and/or screening the selected or out-crossed plants for the absence of the SSN/SSNi and/or 5′-exonuclease.

The methods described herein can be used in a variety of situations. In agriculture, for example, methods described herein are useful to facilitate homologous recombination at a target site can be used to remove a previously integrated transgene (e.g., a herbicide resistance transgene) from a plant line, variety, or hybrid. The methods described herein also can be used to modify an endogenous gene such that the enzyme encoded by the gene confers herbicide resistance, e.g., modification of an endogenous 5-enolpyruvyl shikimate-3-phosphate (EPSP) synthase gene such that the modified enzyme confers resistance to glyphosate herbicides. As another example, the methods described herein are useful to facilitate homologous recombination at regulatory regions for one or more endogenous genes in a plant or mammal metabolic pathway (e.g., fatty acid biosynthesis), such that expression of such genes is modified in a desired manner. The methods described herein are useful to facilitate homologous recombination in an animal (e.g., a rat or a mouse) in one or more endogenous genes of interest involved in, as non-limiting examples, metabolic and internal signaling pathways such as those encoding cell-surface markers, genes identified as being linked to a particular disease, and any genes known to be responsible for a particular phenotype of an animal cell.

In some embodiment, this document features a method for generating a modified eukaryotic cell or organism by delivering to the cell or the organism (1) a SSN/SSNi targeted to an endogenous DNA sequence and (2) a 5′-exonuclease, with or without an exogenous RT, where the SSN/SSNi and 5′-exonuclease are delivered in sufficient amounts such that the SSN/SSNi cleaves the endogenous DNA of the cell or the organism at a specific site targeted by the SSN/SSNi, the 5′-exonuclease cleaves the DNA ends a the DBS, and a nucleotide sequence carried within the RT is stably integrated into the endogenous DNA at the site of cleavage via homologous recombination.

After the nucleic acid(s) encoding the SSN, RT, and 5′-exonuclease have been delivered into the cell and HR mediated gene editing has occurred, any of a variety of methods can be used to determine whether the event was successful, or to isolate correctly modified cells. These include, without limitation, the use of a selectable marker (e.g., the nptll gene) or phenotypic reporter (e.g., the eGFP gene) rendered active by the HR event, or the use of molecular methods such as PCR and sequencing or Southern blotting to detect the recombinant sequence.

The invention will be further described in the following examples, which do not limit the scope of the invention described in the claims.

EXAMPLES

Example 1

Plasmids for Delivering Gene Targeting Reagents

To determine whether a 5′-exonuclease can boost the frequency of HR when delivered with an SSN and RT, two series of plasmids were generated to provide these reagents to plant cells. For testing in dicotyledonous plant cells, T-DNA vectors were generated with constitutive expression of Cas9 from the 2×35s promoter and of the sgRNA from the AtU6 promoters. In addition these vectors contained the T5 bacteriophage 5′-exonuclease codon-optimized for expression in plants that was expressed together with the Cas9 as a C-terminal, translationally released protein via the P2A ribosomal skipping sequence (FIG. 1 and SEQ ID NO:2), as a fusion protein C-terminal to the Cas9 (FIG. 2 and SEQ ID NO:5), or as a distinct protein expressed from an independent promoter (FIG. 3 and SEQ ID NO:7). These configurations were compared to a negative control vector that lacked the T5 5′-exonuclease (SEQ ID NO:11). All T-DNA vectors were configured to deliver the SSN, RT and 5′-exonuclease on a DNA replicon derived from the mild strain of the BeYDV.

For testing in monocotyledonous plant cells, plasmid vectors were generated with constitutive expression of Cas9 from the maize ubiquitin 1 (Ubi1) promoter and of the sgRNA from the wheat U6 promoter (TaU6). In addition these vectors contained the T5 bacteriophage 5′-exonuclease codon-optimized for expression in plants that was expressed together with the Cas9 as a C-terminal, translationally released protein via the P2A ribosomal skipping sequence (FIG. 1 and SEQ ID NO:3), as a fusion protein C-terminal to the Cas9 (FIG. 2 and SEQ ID NO:6), as a distinct protein expressed from an independent promoter (FIG. 3 and SEQ ID NO:8), or as a fusion protein N-terminal to the Cas9 (FIG. 4 and SEQ ID NO:10). The T5 5′-exonuclease is also expressed from an independent promoter. These configurations were compared to a negative control vector that lacked the T5 5′-exonuclease (SEQ ID NO:12). To examine whether a 5′-exonuclease is useful for increasing the frequency of HR-mediated gene targeting in plant cells with a SSNi instead of a SSN, vectors were generated containing the T5 bacteriophage 5′-exonuclease codon-optimized for expression in plants that was expressed together with the D10A Cas9 nickase (FIG. 1 and SEQ ID NO:14) or the H840A Cas9 nickase (FIG. 1 and SEQ ID NO:15) as a C-terminal, translationally released protein via the P2A ribosomal skipping sequence These vectors were configured to deliver the SSN, RT and 5′-exonuclease on a DNA replicon derived from the wheat dwarf virus.

To test the utility of a 5′-exonuclease for increasing the frequency of HR-mediated gene targeting in plant cells without the use of DNA replicons, a third series of vectors was generated for testing in wheat protoplasts. These vectors contained the T5 bacteriophage 5′-exonuclease codon-optimized for expression in plants that was expressed together with the Cas9 as a C-terminal, translationally released protein via the P2A ribosomal skipping sequence (FIG. 1 and SEQ ID NO:4), and as a fusion protein C-terminal to the Cas9 (FIG. 2 and SEQ ID NO:16). No replicon was contained in these vectors. These configurations were compared to a negative control vector that lacked the T5 5′-exonuclease (SEQ ID NO:13).

Example 2

A 5′-Exonuclease Boosts the Frequency of Gene Targeting by Homologous Recombination in Dicotyledenous Somatic Plant Cells

To evaluate the stimulatory effect of a 5′-exonuclease on gene targeting by HR in dicots, Agroinfection was used to deliver T-DNA vectors with (FIG. 1 and SEQ ID NO:2) and without (SEQ ID NO:11) the T5 bacteriophage 5′-exonuclease into whole leaves of tobacco plants carrying an integrated transgene with a truncated β-glucuronidase (GUS) gene (Wright et al., Plant J, 44:693-705, 2005). Gene targeting by HR restored GUS expression, providing a highly quantitative output for relative HR frequency under the treatment conditions. Tobacco plants were grown in a growth chamber at 21° C. with 60% humidity under a 16-h-light and 8-h-dark cycle during 4-6 weeks before performing the infiltration experiments. For each infiltrated leaf, one of the halves was syringe infiltrated with an Agrobacterium solution containing a control plasmid (pLSLZ.D.R, described by Baltes et al., Plant Cell, 26:151, 2014) and the other half was infiltrated with one of the T-DNA vectors with (FIG. 1 and SEQ ID NO:2) and without (SEQ ID NO:11) the T5 bacteriophage 5′-exonuclease. About four to six leaves were infiltrated with each treatment in each experiment. Five days after infiltration, leaf tissue was stained in a solution containing X-Gluc. Whole leaves were scanned and the intensity and area of the expressed GUS was estimated by image quantification using the Image J software. For each treatment HR efficiency was determined as the normalized area of each treatment compared with the pLSLZ.D.R control.

As shown in FIG. 6, a 2.8-fold increase in GT was observed when the 5′-exonuclease was provided in addition to the SSN and RT, compared to when the 5′-exonuclease was not included. This indicated a significant boost in the frequency of GT by HR when a 5′-exonuclease is provided to dicotyledonous cells in conjunction with a SSN and RT.

To determine whether the stimulatory effect of a 5′-exonuclease on gene targeting by HR could be boosted by different configurations of 5′-exonuclease expression, Agroinfection was used to deliver T-DNA vectors with a Cas9::5′-exonuclease fusion (FIG. 2 and SEQ ID NO:5) or with 5′-exonuclease independently expressed from Cas9 by the use of distinct constitutive promoters (FIG. 3 and SEQ ID NO:7) into whole leaves of the tobacco plants previously described. The average GT frequencies obtained with these vectors was 1.5- and 1.8-fold higher, respectively, than the average GT frequency obtained with the 5′-exonuclease expressed as a translational release from the P2A peptide (FIG. 12). This indicates the alternate 5′-exonuclease expression configurations are capable of boosting the efficiency of HR-mediated GT and that both configurations may be slightly advantageous to expressing the 5′-exonuclease as a translational release from the P2A peptide.

Example 3

A 5′-Exonuclease Boosts the Frequency of Gene Targeting by Homologous Recombination in Monocotyledonous Plant Protoplasts

To determine the stimulatory effect of a 5′-exonuclease on gene targeting by HR in monocots, vectors with (FIG. 1 and SEQ ID NO:3) and without (SEQ ID NO:12) the T5 bacteriophage 5′-exonuclease were delivered into leaf cell protoplasts of wheat by PEG-mediated transfection. The RT carried a T2A eGFP sequence and homology arms for HR with the ubiquitin gene in each of the three wheat genomes (Gil-Humanes et al., in press). Thus, proper HR events produced eGFP positive cells that were counted and normalized to the transfection efficiency. Wheat plants (Tricitum aestivum cv Bobwhite) were used for these experiments. Seeds were germinated and grown for 10-15 days at 20° C. day and 14° C. night temperatures with a relative air humidity of 60% under a 16 hour photo-period. For isolation of wheat protoplasts (plant cells lacking the cell wall) approximately twenty plantlets were harvested, cut into ˜1 mm strips with a razor blade, and digested with an enzyme solution as described elsewhere (Shan et al., Nature Protocols, 9:2395-2410, 2014). About 200,000 cells were transfected with each treatment mixing 20 μg of DNA and 240 μl of 40% (w/v) PEG solution (40% PEG 4000, 0.2 M mannitol, and 0.1 M CaCl₂). Transfected protoplasts were incubated in 6-well plates at 24° C. during 48 hours in the dark before analysis in a fluorescence microscope. HR efficiency was calculated by dividing the number of protoplasts expressing eGFP by the total number of cells, and normalizing to the transformation efficiency of each experiment. Image J software was used to count the number of eGFP positive cells and total number of cells in 10 random pictures for each treatment and experiment.

As shown in FIG. 7, a 3.6-fold increase in GT was observed when the 5′-exonuclease was provided in addition to the SSN and RT compared to when the 5′-exonuclease was not included. This result indicated a significant boost in the frequency of GT by HR when a 5′-exonuclease is provided to monocotyledonous cells in conjunction with a SSN and RT.

To further determine whether the stimulatory effect of a 5′-exonuclease on gene targeting by HR in monocots could be extended to benefit HR due to the activity of SSNs, the combination of the T5 bacteriophage 5′-exonuclease with either the D10A Cas9 nickase (FIG. 1 and SEQ ID NO:14) or the H840A Cas9 nickase (FIG. 1 and SEQ ID NO:15) was tested in the wheat protoplast system described above. As shown in FIG. 8, a similar stimulatory effect of the 5′-exonuclease on GT by HR repair events was observed with both the D10A and H840A nickases normalized to the 5′-exonuclease delivered with the Cas9 SSN, indicating a similarly significant boost in the frequency of GT by HR when a 5′-exonuclease is used for GT by HR repair in conjunction with a SSN, compared with a SSN alone.

Example 4

A 5′-Exonuclease can be Fused to a SSN for Greater Stimulation of Gene Targeting by Homologous Recombination

To determine whether the stimulatory effect of a 5′-exonuclease on gene targeting by HR could be further boosted by direct fusion of the 5′-exonuclease domain with the SSN, studies were conducted using a vector (FIG. 2 and SEQ ID NO:6) containing a mutated P2A sequence (Szymczak et al., Nature Biotechnol, 5:589-594, 2004; and Donnelly et al., J Gen Virol, 5:1027-1041, 2001) that does not allow translational release of the T5 bacteriophage 5′-exonuclease from the C-terminal end of the Cas9 nuclease during translation. In the wheat protoplast system described above, a 1.3-fold increase in the GT frequency of the fusion system was observed, compared to the translationally-released (active P2A) system (FIG. 9). This indicated a 5′-exonuclease linked to a SSN by a C-terminal fusion is more effective at stimulating HR than expressing the enzymes as unlinked protein domains. This synergistic effect is likely due to the SSN holding the 5′-exonuclease in close proximity to the DSB, increasing the frequency of 5′ end resection by the exonuclease.

To further determine whether a 5′-exonuclease might have a greater stimulatory effect on gene targeting by HR when expressed as an N-terminal fusion to the SSN, a series of the previously described monocot vectors were tested against a vector (FIG. 4 and SEQ ID NO:10) expressing the T5 bacteriophage 5′-exonuclease fused to the N-terminus of the Cas9 SSN by mutated P2A sequence (Szymczak et al., supra; and Donnelly et al., supra) in the wheat protoplast system described above. As shown in FIG. 10, the 5′-exonuclease as an N-terminal fusion to the Cas9 SSN produced the highest efficiency of GT by HR, indicating this configuration as the most favorable for boosting GT by positioning the 5′-exonuclease near the DSB to 5′ end processing. To delineate the ideal fusion configuration of the 5′-exonuclease with the SSN, a series of vectors with various linker peptides joining the C-terminal end of the 5′-exonuclease domain with the N-terminal end of the SSN is generated and tested in the wheat protoplast system. The linker peptides include various lengths, to determine the optimal distance between the 5′-exonuclease and the SSN domains, and various amino acid compositions to determine the optimal linker flexibility for positioning of both protein domains on the DNA target for optimal processivity. This vector series is tested in the wheat protoplast system to determine the configuration for driving the highest frequency of GT events.

To optimize the expression parameters for the 5′-exonuclease domain, a second codon-optimized version of the bacteriophage 5′-exonuclease protein is tested in the best linker fusion configuration. This experiment indicates whether 5′-exonuclease expression is rate limiting for 5′-exonuclease processivity of DSBs.

Example 5

A 5′-Exonuclease can Boost the Frequency of Gene Targeting by Homologous Recombination With a Non-Replicating SSN and RT

To demonstrate the efficacy of a 5′-exonuclease for boosting the efficiency of HR independent of a DNA replicon for amplifying the SSN and RT, a series of vectors without a DNA replicon was tested in the wheat protoplast system. This series contained vectors either without (SEQ ID NO:13) a T5 bacteriophage 5′-exonuclease or with it as a P2A translational release (FIG. 1 and SEQ ID NO:4) or a fusion to the C-terminal end of the SSN (FIG. 2 and SEQ ID NO:16). As shown in FIG. 11, the 5′-exonuclease fused to the C-terminal end of the SSN produced a 2.1-fold increase in GT events compared to the control without a 5′-exonuclease. This indicates a significant boost in the frequency of GT by HR when a 5′-exonuclease is provided in conjunction with a SSN and a RT, regardless of whether a DNA replicon is included for amplification of the gene targeting reagents.

Other Embodiments

It is to be understood that while the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the invention, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims.

Claims

1. A method for generating a modified eukaryotic cell or organism, comprising delivering to the cell or the organism a site-specific nuclease (SSN) or site-specific nickase (SSNi), a repair template (RT), and a 5′-exonuclease, wherein the SSN or SSNi, RT, and 5′-exonuclease are delivered in amounts sufficient such that the SSN or SSNi cleaves the endogenous DNA of the cell or the organism at a specific site, and a nucleotide sequence carried within the RT is stably integrated into the endogenous DNA at the site of cleavage via homologous recombination.

2. The method of claim 1, wherein the SSN or SSNi is a homing endonuclease, a zinc-finger nuclease (ZFN), a transcription activator-like effector (TALE) nuclease, or a clustered, regularly interspaced, short palindromic repeat (CRISPR)/CRISPR-associated (Cas) nuclease.

3. The method of claim 1, wherein the cell is a human cell.

4. The method of claim 1, wherein the cell is from an animal selected from the group consisting of cattle, swine, sheep, goats, bison, horses, donkeys, mules, rabbits, chickens, ducks, geese, turkeys, and pigeons.

5. The method of claim 1, wherein the cell is from a monocotyledonous plant.

6. The method of claim 5, wherein the monocotyledonous plant is selected from the group consisting of maize, rice, wheat, barley, sugarcane, oat, rye, millet, sorghum, switchgrass, turfgrass, and bamboo.

7. The method of claim 1, wherein the cell is from a dicotyledenous plant.

8. The method of claim 7, wherein the dicotyledonous plant is selected from the group consisting of bean, soybean, cotton, pea, cowpea, peanut, almond, walnut, apple, plum, peach, pear, citrus, sugar beet, squash, melon, cassava, tomato, pepper, canola, banana, flax, and sunflower.

9. The method of claim 1, wherein the cell is a green algae.

10. The method of claim 1, wherein the cell is isolated and regenerated into a whole organism following the homologous recombination.

11. The method of claim 1, wherein the modified cell is maintained in culture as a pure or a mixed population.

12. The method of claim 1, wherein the genomic DNA of the cell or organism is modified.

13. The method of claim 1, wherein the mitochondrial DNA of the cell or organism is modified.

14. The method of claim 1, wherein the cell is a plant cell, and wherein plastid DNA of the plant cell is modified.

15. The method of claim 1, wherein the SSN or SSNi is provided to the cell as a DNA that is expressed by the cell.

16. The method of claim 1, wherein the SSN or SSNi is provided to the cell as an RNA that is translated by the cell.

17. The method of claim 1, wherein the SSN or SSNi is provided to the cell as a protein.

18. The method of claim 1, wherein the RT is provided to the cell as a single- or double-stranded DNA.

19. The method of claim 1, wherein the 5′-exonuclease is provided to the cell as a DNA that is expressed by the cell.

20. The method of claim 1, wherein the 5′-exonuclease is provided to the cell as an RNA that is translated by the cell.

21. The method of claim 1, wherein the 5′-exonuclease is provided to the cell as a protein.

22. The method of claim 1, wherein the SSN or SSNi, RT, and 5′-exonuclease are transiently expressed in the plant cell, and wherein only a portion of the RT is integrated during the gene targeting event.

23. The method of claim 1, wherein the SSN or SSNi, RT, and 5′-exonuclease are stably integrated into the cell.

24. The method of claim 1, wherein the 5′-exonuclease is from T5 bacteriophage.

25. The method of claim 1, wherein the 5′-exonuclease is from T3, T4, or another bacteriophage.

26. The method of claim 1, wherein the 5′-exonuclease is derived from a prokaryotic cell.

27. The method of claim 1, wherein the 5′-exonuclease is of eukaryotic origin.

28. The method of claim 1, wherein the 5′-exonuclease is Exo1.

29. The method of claim 1, wherein the sequences encoding the SSN and the 5′-exonuclease are independently and operably linked to one or more constitutive promoters, inducible promoters, tissue-specific promoters, developmentally-regulated promoters, or any combination thereof.

30. The method of claim 1, wherein the SSN or SSNi, the RT, and the 5′-exonuclease, or any combination thereof, are carried on a viral replicon derived from a DNA or RNA virus, or are carried within the cell on a full DNA or RNA virus.

31. The method of claim 1, wherein the SSN or SSNi, the RT, and the 5′-exonuclease, or any combination thereof, are carried within the cell on a non-replicating nucleic acid fragment.

32. The method of claim 1, comprising delivering to the cell or the organism a SSNi, wherein the SSNi is Cas9 with a D10A substitution.

33. The method of claim 1, comprising delivering to the cell or the organism a SSNi, wherein the SSNi is Cas9 with a H840A substitution.

34. The method of claim 1, comprising delivering to the cell or the organism a SSNi, wherein the SSNi is Cas9 with an amino acid substitution, insertion, or deletion other than a D10A or H840A substitution.

35. The method of claim 1, wherein the SSN or SSNi causes a site-specific break in the double-stranded DNA.

36. The method of claim 1, further comprising regenerating the cell into a whole organism that contains the modification incorporated by the RT, wherein no other foreign DNA is present in the organism.

37. The method of claim 1, further comprising regenerating the cell into a whole organism that contains the SSN or SSNi, RT, and 5′-exonuclease, or any combination thereof, stably integrated within its DNA.

38. A method comprising delivering to a cell (i) a SSN or SSNi targeted to a selected sequence within the endogenous DNA of the cell, (ii) a RT, and (iii) a 5′-exonuclease, and regenerating the cell into a whole organism that contains the SSN or SSNi, RT, and 5′-exonuclease, or any combination thereof.

39. The method of claim 38, wherein the SSN or SSNi, RT, and 5′-exonuclease are stably integrated within the endogenous DNA of the whole organism.

40. The method of claim 38, wherein the whole organism does not contain a modification at the selected sequence, and wherein the method further comprises developing from the whole organism a line that is maintained under conditions appropriate for expression of the SSN or SSNi and 5′-exonuclease, and screening the line for a desired modification at the selected sequence.

41. The method of claim 38, wherein the whole organism contains a modification at the selected sequence, and wherein the method further comprises selfing or crossing the organism to obtain offspring having the modification at the selected sequence but not containing the SSN or SSNi and the 5′-exonuclease.