CAS9 proteins including ligand-dependent inteins
Some aspects of this disclosure provide compositions, methods, systems, and kits for controlling the activity of RNA-programmable endonucleases, such as Cas9, or for controlling the activity of proteins comprising a Cas9 variant fused to a functional effector domain, such as a nuclease, nickase, recombinase, deaminase, transcriptional activator, transcriptional repressor, or epigenetic modifying domain. For example, the inventive proteins provided comprise a ligand-dependent intein, the presence of which inhibits one or more activities of the protein (e.g., gRNA binding, enzymatic activity, target DNA binding). The binding of a ligand to the intein results in self-excision of the intein, restoring the activity of the protein.
1. A polynucleotide encoding a Cas9 protein comprising an intein.
2. The polynucleotide of claim 1 , wherein an activity of the Cas9 protein is disrupted by the intein, and wherein the disrupted activity is restored upon excision of the intein from the Cas9 protein.
3. The polynucleotide of claim 1 , wherein the Cas9 protein is capable of binding a guide RNA (gRNA) prior to excision of the intein.
4. The polynucleotide of claim 1 , wherein the Cas9 protein has no or minimal gRNA binding activity prior to excision of the intein.
5. The polynucleotide of claim 1 , wherein the intein is a ligand-dependent intein.
6. The polynucleotide of claim 1 , wherein the intein comprises a ligand-binding domain.
7. The polynucleotide of claim 1 , wherein the Cas9 protein comprises a nuclease-inactivated Cas9 (dCas9) domain.
8. The polynucleotide of claim 1 , wherein the Cas9 protein is a Cas9 nickase.
9. The polynucleotide of claim 1 , wherein the Cas9 protein further comprises a nucleic acid-editing domain.
10. The polynucleotide of claim 9 , wherein the nucleic acid-editing domain is a deaminase domain.
11. The polynucleotide of claim 10 , wherein the intein is a ligand-dependent intein.
12. The polynucleotide of claim 10 , wherein the Cas9 protein comprises a nuclease-inactivated Cas9 (dCas9) domain.
13. The polynucleotide of claim 10 , wherein the Cas9 protein is a Cas9 nickase.
14. The polynucleotide of claim 10 , wherein the Cas9 protein and the deaminase domain are separated by a linker.
15. The polynucleotide of claim 14 , wherein linker is a peptide linker.
16. The polynucleotide of claim 1 , wherein (a) the intein is a ligand-dependent intein, (b) the Cas9 protein comprises a dCas9 domain or is a Cas9 nickase, and (c) the Cas9 protein further comprises a deaminase domain.
17. The polynucleotide of claim 1 , wherein the Cas9 protein comprises a Cas9 domain having the amino acid sequence of SEQ ID NO: 2, SEQ ID NO: 4 or SEQ ID NO: 5, or an amino acid sequence that has at least 90% sequence identity with SEQ ID NO: 2, SEQ ID NO: 4 or SEQ NO: 5.
18. A method for site-specific DNA cleavage, comprising:
(a) introducing the polynucleotide of claim 1 into the cell under conditions where the Cas9 protein is expressed;
(b) contacting the Cas9 protein with a ligand, wherein binding of the ligand to the intein induces self-excision of the intein; and
(c) contacting a DNA with the Cas9 protein, wherein the Cas9 protein is associated with a gRNA,
wherein self-excision of the intein from the Cas9 protein in step (b) allows the Cas9 protein to cleave the DNA, thereby producing cleaved DNA.
19. A method of editing DNA in a cell, comprising:
(a) introducing the polynucleotide of claim 16 into the cell under conditions where the Cas9 protein is expressed;
(b) introducing into the cell a gRNA capable of targeting the Cas9 protein to a target nucleotide sequence; and
(c) contacting the cell with a ligand that binds to the ligand-dependent intein and induces self-excision of the intein, thereby restoring the Cas9 protein;
(d) contacting the target nucleotide sequence with the restored Cas9 protein, thereby editing DNA.