GENOME EDITING OF HUMAN NEURAL STEM CELLS USING NUCLEASES

1 . A method for generating a genetically modified human neural stem cell, the method comprising:

introducing into an isolated human neural stem cell:

(a) a donor template comprising: (i) a transgene cassette comprising a transgene; and (ii) two nucleotide sequences comprising two non-overlapping, homologous portions of a safe harbor locus, wherein the nucleotide sequences are located at the 5′ and 3′ ends of the transgene cassette; and

(b) a DNA nuclease or a nucleotide sequence encoding the DNA nuclease, wherein the DNA nuclease is a CRISPR-associated protein (Cas) polypeptide capable of creating a double-strand break in the safe harbor locus to induce insertion of the transgene into the safe harbor locus, thereby generating a genetically modified human neural stem cell,

wherein the safe harbor locus comprises the IL2Rγ or HBB gene.

2 . (canceled)

3 . The method of claim 1 , wherein the transgene encodes a protein associated with a genetic disorder of the central nervous system.

4 . The method of claim 1 , wherein the transgene encodes a neuroprotective or neuroregenerative protein, a variant thereof, a fragment thereof, or a peptide mimetic thereof.

5 . The method of claim 1 , wherein the nucleotide sequence encoding the DNA nuclease comprises RNA.

6 . The method of claim 1 , further comprising introducing into the human neural stem cell a DNA-targeting RNA, a truncated DNA-targeting RNA, or a nucleotide sequence encoding the DNA-targeting RNA or truncated DNA-targeting RNA.

7 . The method of claim 6 , wherein the DNA nuclease comprises a Cas polypeptide or a nucleotide sequence encoding the Cas polypeptide, and wherein the DNA-targeting RNA comprises a single guide RNA (sgRNA) or a truncated sgRNA comprising a first nucleotide sequence complementary to a portion of the safe harbor locus and a second nucleotide sequence that interacts with the Cas polypeptide.

8 . (canceled)

9 . The method of claim 1 , wherein the donor template further comprises a selectable marker.

10 . The method of claim 9 , wherein the selectable marker comprises a marker that is not expressed on a cell of the central nervous system.

11 . The method of claim 9 , wherein the selectable marker is a cell surface protein.

12 . The method of claim 11 , wherein the cell surface protein is selected from the group consisting of CD1, CD2, CD4, CD8α, CD10, CD19, CD20, a variant thereof, a fragment thereof, a derivative thereof, and a combination thereof.

13 . A genetically modified human neural stem cell produced by the method of claim 1 .

14 . A pharmaceutical composition comprising the genetically modified human neural stem cell of claim 13 and a pharmaceutically acceptable carrier.

15 . A method for preventing or treating a neurodegenerative disease or a neurological injury in a human subject in need thereof, the method comprising:

administering to the human subject an effective amount of the pharmaceutical composition of claim 14 .

16 . The method of claim 15 , wherein the genetically modified human neural stem cell is autologous to the subject.

17 . The method of claim 15 , wherein the genetically modified human neural stem cell is allogeneic to the subject.

18 . A kit comprising:

(a) a donor template comprising: (i) a transgene cassette comprising a transgene; and (ii) two nucleotide sequences comprising two non-overlapping, homologous portions of a safe harbor locus, wherein the nucleotide sequences are located at the 5′ and 3′ ends of the transgene cassette, and wherein the safe harbor locus comprises the IL2Rγ or HBB gene;

(b) a DNA nuclease or a nucleotide sequence encoding the DNA nuclease, wherein the DNA nuclease is a CRISPR-associated protein (Cas) polypeptide; and

(c) an isolated human neural stem cell.

19 . A genetically modified human neural stem cell comprising a transgene cassette comprising a transgene, wherein the transgene cassette is located within a safe harbor locus comprising the IL2Rγ or HBB gene.