Chemically modified guide RNAs for CRISPR/CAS-mediated gene regulation
Provided herein are methods for inducing CRISPR/Cas-based gene regulation (e.g., genome editing or gene expression) of a target nucleic acid (e.g., target DNA or target RNA) in a cell. The methods include using modified single guide RNAs (sgRNAs) that enhance gene regulation of the target nucleic acid in a primary cell for use in ex vivo therapy or in a cell in a subject for use in in vivo therapy. Additionally, provided herein are methods for preventing or treating a genetic disease in a subject by administering a sufficient amount of a modified sgRNA to correct a mutation in a target gene associated with the genetic disease.
1. A method for inducing gene regulation of a target nucleic acid in a primary cell, the method comprising:
introducing into the primary cell:
(a) a modified single guide RNA (sgRNA) comprising a first nucleotide sequence that is complementary to the target nucleic acid and a second nucleotide sequence that interacts with a CRISPR-associated protein (Cas) polypeptide, wherein:
(i) about 10% to about 30% of nucleotides in the first nucleotide sequence and/or about 1% to about 10% of nucleotides in the second nucleotide sequence are modified nucleotides;
(ii) the modified sgRNA comprises a modified nucleotide within five nucleotides from the 5′ end of the first nucleotide sequence and/or within five nucleotides from the 3′ end of the second nucleotide sequence; and
(iii) the modified nucleotides are selected from the group consisting of a 2′-O-methyl 3′-phosphorothioate (MS) nucleotide, a 2′-O-methyl 3′-thioPACE (MSP) nucleotide, and a combination thereof; and
(b) a Cas polypeptide, an mRNA encoding the Cas polypeptide, or a recombinant expression vector comprising a nucleotide sequence encoding the Cas polypeptide,
wherein the modified sgRNA guides the Cas polypeptide to the target nucleic acid, and wherein the modified sgRNA induces a gene regulation of the target nucleic acid with an enhanced activity relative to a corresponding unmodified sgRNA.
2. The method of claim 1 , wherein the enhanced activity comprises increased stability of the modified sgRNA and/or increased specificity of the modified sgRNA for the target nucleic acid.
3. The method of claim 1 , wherein the target nucleic acid comprises a target DNA or a target RNA.
4. The method of claim 3 , wherein the gene regulation comprises genome editing of the target DNA.
5. The method of claim 4 , wherein the genome editing comprises homologous-directed repair (HDR) or nonhomologous end joining (NHEJ) of the target DNA.
6. The method of claim 4 , further comprising introducing a recombinant donor repair template into the primary cell.
7. The method of claim 6 , wherein the recombinant donor repair template comprises two nucleotide sequences comprising two non-overlapping, homologous portions of the target DNA, wherein one of the two homologous portions is located at the 5′ end and the other homologous portion is located at the 3′ end of the recombinant donor template, wherein each homologous portion is homologous to a corresponding region of the target DNA to undergo genome editing.
8. The method of claim 6 , wherein the recombinant donor repair template comprises a synthetic single-stranded oligodeoxynucleotide (ssODN) template comprising a nucleotide sequence encoding a mutation to correct a single nucleotide polymorphism (SNP) and two nucleotide sequences comprising two non-overlapping, homologous portions that are homologous to corresponding regions of the target DNA, wherein one of the two homologous portions is located at the 5′ end and the other homologous portion is located at the 3′ end of the recombinant donor template.
9. The method of claim 3 , wherein the gene regulation comprises inhibition or activation of gene expression of the target DNA or the target RNA using a Cas polypeptide that is endonuclease-deficient.
10. The method of claim 1 , wherein the primary cell is isolated from a multicellular organism prior to introducing the modified sgRNA and the Cas polypeptide into the primary cell.
11. The method of claim 10 , wherein the multicellular organism is a plant, a multicellular protist, a multicellular fungus, or an animal.
12. The method of claim 1 , wherein the primary cell is a stem cell or an immune cell.
13. The method of claim 12 , wherein the stem cell is a hematopoietic stem and progenitor cell (HSPC), a mesenchymal stem cell, a neural stem cell, or an organ stem cell.
14. The method of claim 12 , wherein the immune cell is a T cell, a natural killer cell, a monocyte, a peripheral blood mononuclear cell (PBMC), or a peripheral blood lymphocyte (PBL).
15. The method of claim 10 , wherein the primary cell or a progeny thereof is returned to the multicellular organism after introducing the modified sgRNA and the Cas polypeptide into the primary cell.
16. The method of claim 1 , comprising introducing (a) and (b) to a population of primary cells each comprising the target nucleic acid.
17. The method of claim 16 , wherein the modified sgRNA induces the gene regulation of the target nucleic acid in at least about 30% of the population of primary cells.
18. The method of claim 16 , wherein the modified sgRNA induces the gene regulation of the target nucleic acid in at least about 40% of the population of primary cells.
19. The method of claim 16 , wherein the modified sgRNA induces the gene regulation of the target nucleic acid in at least about 50% of the population of primary cells.
20. The method of claim 16 , wherein the modified sgRNA induces the gene regulation of the target nucleic acid in at least about 60% of the population of primary cells.
21. The method of claim 1 , wherein the first nucleotide sequence is about 20 nucleotides in length.
22. The method of claim 1 , wherein at least two nucleotides in the first nucleotide sequence are modified nucleotides.
23. The method of claim 1 , wherein one or more modified nucleotides are located within five nucleotides from the 5′-end of the first nucleotide sequence.
24. The method of claim 1 , wherein from about 10% to about 30% of the nucleotides in the first nucleotide sequence are modified nucleotides.
25. The method of claim 1 , wherein the second nucleotide sequence is about 80 nucleotides in length.
26. The method of claim 1 , wherein at least two nucleotides in the second nucleotide sequence are modified nucleotides.
27. The method of claim 1 , wherein one or more modified nucleotides are located within five nucleotides from the 3′-end of the second nucleotide sequence.
28. The method of claim 1 , wherein from about 1% to about 10% of the nucleotides in the second nucleotide sequence are modified nucleotides.
29. The method of claim 1 , wherein the modified sgRNA comprises one, two, or three consecutive or non-consecutive modified nucleotides at or near the 5′-end of the first nucleotide sequence and one, two, or three consecutive or non-consecutive modified nucleotides at or near the 3′-end of the second nucleotide sequence.
30. The method of claim 29 , wherein the modified sgRNA comprises three consecutive modified nucleotides at the 5′-end of the first nucleotide sequence and three consecutive modified nucleotides at the 3′-end of the second nucleotide sequence.
31. The method of claim 1 , wherein the modified sgRNA is chemically synthesized.
32. The method of claim 1 , further comprising introducing into the primary cell a second modified single guide RNA (sgRNA), wherein the second modified sgRNA guides the Cas polypeptide to a second target nucleic acid that is different from the target nucleic acid.
33. The method of claim 1 , comprising introducing into the primary cell the mRNA encoding the Cas polypeptide.
34. The method of claim 1 , wherein the Cas polypeptide is a Cas9 polypeptide, a variant thereof, or a fragment thereof.
35. The method of claim 1 , wherein the step of introducing into the primary cell comprises electroporating the primary cell.
36. The method of claim 1 ,
wherein the modified sgRNA in (a) and the Cas polypeptide in (b) are introduced into the primary cell in a ribonucleoprotein (RNP) complex.
37. The method of claim 1 , wherein the gene regulation induced by the introduction of (a) and (b) is stable in the primary cell for at least 24 hours.