TAL effector-mediated DNA modification
Materials and Methods related to gene targeting (e.g., gene targeting with transcription activator-like effector nucleases; “TALENS”) are provided.
1. A method for modifying the genetic material of a cell, comprising:
(a) providing a cell containing a target DNA sequence; and
(b) introducing a transcription activator-like (TAL) effector endonuclease into the cell, the TAL effector endonuclease comprising:
(i) a FokI endonuclease domain that can cleave double stranded DNA, and
(ii) a TAL effector domain comprising a plurality of TAL effector repeat sequences that, in combination, bind to a specific nucleotide sequence in the target DNA sequence,
such that the TAL effector endonuclease cleaves the target DNA sequence within or adjacent to the specific nucleotide sequence in the cell or progeny thereof.
2. The method of claim 1 , further comprising introducing into the cell a nucleic acid comprising a sequence homologous to at least a portion of the target DNA sequence, such that homologous recombination occurs between the target DNA sequence and the nucleic acid.
3. The method of claim 1 , wherein the cell is a eukaryotic cell.
4. The method of claim 1 , wherein the cell is a plant cell.
5. The method of claim 4 , wherein the plant cell is a protoplast.
6. The method of claim 1 , wherein the target DNA is chromosomal DNA.
7. The method of claim 1 , wherein the introducing comprises transfecting the cell with a nucleic acid encoding the TAL effector endonuclease.
8. The method of claim 1 , wherein the introducing comprises mechanically injecting the TAL effector endonuclease into the cell as a protein.
9. The method of claim 1 , wherein the introducing comprises delivering the TAL effector endonuclease into the cell as a protein by means of the bacterial type III secretion system.
10. The method of claim 1 , wherein the introducing comprises introducing the TAL effector endonuclease into the cell as a protein by electroporation.
11. The method of claim 1 , wherein the TAL effector domain that binds to a specific nucleotide sequence within the target DNA sequence comprises 15 or more DNA binding repeats.
12. The method of claim 11 , wherein each DNA binding repeat comprises a repeat variable-diresidue (RVD) that determines recognition of a base pair in the target DNA sequence, wherein each DNA binding repeat is responsible for recognizing one base pair in the target DNA sequence, and wherein the RVD comprises one or more of:
HD for recognizing C;
NG for recognizing T;
NI for recognizing A;
NN for recognizing G;
NS for recognizing A;
HG for recognizing T;
IG for recognizing T;
NK for recognizing G;
HA for recognizing C;
ND for recognizing C;
HI for recognizing C;
HN for recognizing G; and
NA for recognizing G.
13. A method for generating a genetically modified organism, comprising:
(a) providing a cell capable of generating an organism and containing a target DNA sequence in its genome;
(b) introducing a TAL effector endonuclease into the cell, the TAL effector endonuclease comprising:
(i) a FokI endonuclease domain that can cleave double stranded DNA, and
(ii) a TAL effector domain comprising a plurality of TAL effector repeat sequences that, in combination, bind to a specific nucleotide sequence in the target DNA sequence,
such that the TAL effector endonuclease cleaves the target DNA sequence within or adjacent to the specific nucleotide sequence in the cell, or progeny thereof, and introduces a genetic modification to the genome of the cell or progeny thereof; and
(c) generating a genetically modified organism from the cell or progeny resulting from step (b), wherein the organism comprises the genetic modification in its genome.
14. The method of claim 13 , wherein cell is a plant cell and the organism is a plant.
15. The method of claim 14 , wherein the method further comprises obtaining seeds from the plant.