Homology directed repair compositions for the treatment of hemoglobinopathies
The present disclosure provides improved compositions for the homology directed repair of the human globin locus for the prevention, treatment, or amelioration of at least one symptom of a hemoglobinopathy.
1. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and
a DNA donor repair template having the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,
whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.
2. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 17.
3. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 18.
4. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 19.
5. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 20.
6. The method of claim 1 , wherein the DNA donor repair template has the sequence as set forth in SEQ ID NO: 21.
7. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell
one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and
a DNA donor repair template having at least 99% sequence identity to the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,
whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.
8. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 17.
9. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 18.
10. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 19.
11. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 20.
12. The method of claim 7 , wherein the DNA donor repair template has the sequence having at least 99% sequence identity to the sequence as set forth in SEQ ID NO: 21.
13. A method for increasing gamma globin expression in a hematopoietic stem or progenitor cell comprising introducing into the cell
one or more engineered nucleases that cleave a target site set forth in SEQ ID NO: 9 and
a DNA donor repair template having at least 98% sequence identity to the sequence as set forth in SEQ ID NOs: 17, 18, 19, 20, or 21,
whereby the DNA donor repair template is inserted into the cell genome by homology directed repair at a double strand break introduced by the one or more engineered nucleases.
14. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 17.
15. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 18.
16. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 19.
17. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 20.
18. The method of claim 13 , wherein the DNA donor repair template has the sequence having at least 98% sequence identity to the sequence as set forth in SEQ ID NO: 21.