Compositions and methods for promoting homology directed repair
This application provides improved methods of genome editing. Cas9 molecules can be used to create a break in a genomic region of interest. To increase the likelihood that the break is repaired by HDR (homology-directed repair), the cell can be contacted with molecules that bring a template nucleic acid in close proximity to the break, under conditions that allow the cell to repair the break using the template nucleic acid.
1. A Cas9 system comprising
a Cas9 fusion molecule comprising a Cas9 molecule linked to a template binding domain, and a nucleic acid template system comprising a template binding domain partner and a template nucleic acid,
wherein the template binding domain comprises an affinity for the template binding domain partner and does not bind an endogenous nucleic acid of a cell, wherein the template binding domain partner is exogenous to the cell,
wherein the template binding domain is selected from the group consisting of a TetR repressor protein, or a fragment thereof; a LacI repressor protein, or a fragment thereof; a Gal4 repressor protein, or a fragment thereof; and C1 repressor protein, or a fragment thereof; and
wherein the template binding domain partner is a DNA sequence recognized by a DNA binding protein selected from the group consisting of a Tet-O sequence, a Lac operon O1 sequence, a UAS sequence, and an Operator L and R sequence.
2. The Cas9 system of claim 1 , wherein the template binding domain of the Cas9 fusion molecule is bound to the template binding domain partner.
3. The Cas9 system of claim 2 , wherein the template binding domain of the Cas9 fusion molecule is covalently or non-covalently bound to the template binding domain partner.
4. The Cas9 system of claim 1 , wherein the template binding domain partner is linked to the template nucleic acid.
5. The Cas9 system of claim 1 , wherein the DNA binding protein comprises a TetR repressor, or a fragment of the TetR repressor, and the DNA comprises at least one Tet-O sequence.
6. The Cas9 system of claim 1 , wherein the nucleic acid template system comprises a double stranded nucleic acid sequence or a single stranded nucleic acid sequence.
7. The Cas9 system of claim 1 , wherein the template nucleic acid comprises about 50-500 nucleotides of homology with a target nucleic acid.
8. The Cas9 system of claim 1 , further comprising a gRNA.
9. A cell, or a population of cells, comprising the Cas9 system of claim 1 .
10. An in vitro or ex vivo method of altering a nucleic acid at a target position in a cell, or a population of cells, the method comprising contacting the cell or the population of cells with the Cas9 system of claim 8 , wherein the Cas9 molecule comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 6-89,
wherein the gRNA molecule and Cas9 fusion molecule interact with the nucleic acid, resulting in a cleavage event, wherein the cleavage event is repaired by at least one DNA repair pathway, and
wherein the sequence of the nucleic acid after the cleavage event is different than the sequence of the nucleic acid prior to the cleavage event,
thereby altering the nucleic acid at the target position in the cell, or in the population of cells.
11. The method of claim 10 , further comprising contacting the cell, or the population of cells, with a second gRNA molecule,
wherein the second gRNA molecule and the Cas9 fusion molecule interact with the nucleic acid, resulting in a second cleavage event.
12. The method of claim 10 , wherein the cell, or population of cells, is from a subject suffering from a disease or disorder selected from the group consisting of a blood disease, an immune disease, a neurological disease, a cancer, an infectious disease, a genetic disease, a disorder caused by aberrant mtDNA, a metabolic disease, a disorder caused by aberrant cell cycle, a disorder caused by aberrant angiogenesis, a disorder cause by aberrant DNA damage repair, or a pain disorder.
13. The method of claim 10 , wherein the cell, or population of cells, is from a subject having at least one mutation at the target position.
14. A cell, or a population of cells, altered by the method of claim 10 .
15. A pharmaceutical composition comprising the cell, or the population of cells, of claim 14 .
16. A pharmaceutical composition comprising the Cas9 system of claim 8 .
17. An in vitro or ex vivo method of treating a subject suffering from a disease or disorder, the method comprising contacting a cell, or a population of cells, from the subject with the Cas9 system of claim 8 , wherein the Cas9 molecule comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 6-89,
wherein the gRNA molecule and the Cas9 fusion molecule interact with a nucleic acid at a target position, resulting in a cleavage event,
wherein the cleavage event is repaired by at least one DNA repair pathway, and
wherein the sequence of the nucleic acid after the cleavage event is different than the sequence of the nucleic acid prior to the cleavage event,
thereby treating the subject suffering from the disease or disorder.