Method to inactivate a mutant allele of an
Methods for inactivating in a cell a mutant allele of the elastase, neutrophil expressed gene (ELANE gene) gene having a mutation associated with severe congenital neutropenia (SCN) or cyclic neutropenia (CyN) wherein the mutant allele is selected from the group consisting of the ELANE mutants set forth in Table 1, the method comprising introducing to the cell a composition comprising: a CRISPR nuclease or a sequence encoding the CRISPR nuclease; and a first RNA molecule comprising a guide sequence portion having 17-30 nucleotides, wherein a complex of the CRISPR nuclease and the first RNA molecule affects a double strand break in the mutant allele of the ELANE gene the method optionally further comprising introduction of a second RNA molecule comprising a guide sequence portion capable of complexing with a CRISPR nuclease, wherein the complex of the second RNA molecule and CRISPR nuclease affects a second double strand break in the ELANE gene.
1. An ex vivo or in vitro method of modifying in a cell a mutant allele of the elastase, neutrophil expressed (ELANE) gene wherein the mutant allele has a mutation associated with severe congenital neutropenia (SCN) or cyclic neutropenia (CyN), the method comprising introducing to the cell a composition comprising:
(a) a CRISPR nuclease, or a DNA polynucleotide encoding said CRISPR nuclease, wherein said CRISPR nuclease comprises:
(i) the amino acid sequence of SEQ ID NO: 31123, 31124, 31125, or 31126; or
(ii) the amino acid sequence encoded by the nucleotide sequence of SEQ ID NO: 31131 or 31132; and
(b) a first RNA molecule, or a DNA polynucleotide encoding the first RNA molecule, wherein said first RNA molecule comprises:
(i) a CRISPR RNA (crRNA) molecule and a transactivating CRISPR RNA (tracrRNA) molecule; or
(ii) a single-guide RNA (sgRNA) molecule,
wherein the first RNA molecule comprises (I) a guide sequence portion comprising 20, 21, or 22 contiguous nucleotides of the sequence set forth in SEQ ID NO: 5519; or (II) a guide sequence portion comprising SEQ ID NO: 5469, 5482, or 5519, wherein the CRISPR nuclease and the first RNA molecule form a complex, and wherein said complex binds to the mutant allele of the ELANE gene and introduces a double strand break in the mutant allele of the ELANE gene.
2. The method of claim 1 , further comprising introduction of a second RNA molecule, or a DNA polynucleotide encoding the second RNA molecule, wherein the second RNA molecule comprises (i) a crRNA molecule and a tracrRNA molecule or (ii) an sgRNA molecule,
wherein the second RNA molecule and the CRISPR nuclease form a complex, and
wherein the complex of the second RNA molecule and CRISPR nuclease introduces a second double strand break in the mutant allele of the ELANE gene.
3. The method of claim 2 , wherein the second double strand break is within a non-coding region of the ELANE gene.
4. The method of claim 1 , comprising obtaining a cell with a mutant allele of the ELANE gene associated with severe congenital neutropenia (SCN) or CyN from a subject with a mutant allele of the ELANE gene associated with SCN or CyN and/or suffering from SCN or CyN.
5. The method of claim 4 , comprising obtaining the cell from the subject by (i) mobilization and apheresis, (ii) apheresis, (iii) mobilization, or (iv) bone marrow aspiration.
6. The method of claim 4 , wherein a cytokine is introduced to the cell prior to introducing the composition to the cell.
7. The method of claim 4 , wherein the cell is expanded by culturing the cell to obtain a larger quantity of the cells, and wherein the cells are cultured with one or more of: stem cell factor (SCF), interleukin 3 (IL-3), and granulocyte-macrophage colony-stimulating factor (GM-CSF);
wherein the cells are cultured with at least one cytokine.
8. The method of claim 7 , wherein the at least one cytokine is a recombinant human cytokine.