Systems, methods and compositions for sequence manipulation with optimized functional CRISPR-Cas systems

Patent metadata

Field	Value
Publication number	US-12258595-B2
Application number	US-202218089023-A
Country	US
Kind code	B2
Filing date	Dec 27, 2022
Priority date	Dec 12, 2013
Publication date	Mar 25, 2025
Grant date	Mar 25, 2025

Abstract

The invention provides for systems, methods, and compositions for altering expression of target gene sequences and related gene products. Provided are structural information on the Cas protein of the CRISPR-Cas system, use of this information in generating modified components of the CRISPR complex, vectors and vector systems which encode one or more components or modified components of a CRISPR complex, as well as methods for the design and use of such vectors and components. Also provided are methods of directing CRISPR complex formation in eukaryotic cells and methods for utilizing the CRISPR-Cas system. In particular the present invention comprehends optimized functional CRISPR-Cas enzyme systems.

First claim

What is claimed is:

1. A method for modifying a eukaryotic cell, comprising introducing a CRISPR-Cas system into the eukaryotic cell, wherein the CRISPR-Cas system comprises:
an engineered Cas9 protein comprising at least one mutation such that the Cas9 protein substantially lacks DNA cleavage activity, or a polynucleotide encoding the Cas9 protein;
a chimeric RNA comprising a guide sequence capable of hybridizing to a target sequence in a genomic locus of interest in the eukaryotic cell, and a modified loop comprising an insertion of an aptamer sequence into a tetraloop and/or a stem-loop 2 of the chimeric RNA, or a polynucleotide encoding the chimeric RNA; and
an adaptor protein fused to at least one heterologous functional domain, or a polynucleotide encoding the adaptor protein;
wherein the Cas9 protein forms a CRISPR complex with the chimeric RNA, wherein the adaptor protein binds to the aptamer sequence, and wherein the guide sequence direct sequence-specific binding of the CRISPR complex to the target sequence.

2. The method of claim 1 , wherein the chimeric RNA comprises at least two modified loops, wherein each modified loop is modified by insertion of an aptamer sequence.

3. The method of claim 2 , wherein the at least two modified loops are modified by insertion of the same aptamer sequence.

4. The method of claim 2 , wherein the at least two modified loops are modified by insertion of different aptamer sequences capable of binding to different adaptor proteins.

5. The method of claim 2 , wherein both tetraloop and stem-loop 2 of the chimeric RNA are modified.

6. The method of claim 1 , wherein the Cas9 protein is fused to at least one nuclear localization signal (NLS).

7. The method of claim 1 , wherein the Cas9 protein is fused to at least two NLSs.

8. The method of claim 1 , wherein the Cas9 comprises at least one mutation in a RuvC domain and at least one mutation in a HNH domain.

9. The method of claim 8 , wherein the mutation in the RuvC domain corresponds to D10A of Streptococcus pyogenes Cas9.

10. The method of claim 8 , wherein the mutation in the HNH domain corresponds to H840A, N854A, or N863A of Streptococcus pyogenes Cas9.

11. The method of claim 1 , wherein the adaptor protein comprises a bacteriophage coat protein of MS2, PP7, Qβ, F2, GA, fr, JP501, M12, R17, BZ13, JP34, JP500, KU1, M11, MX1, TW18, VK, SP, FI, ID2, NL95, TW19, AP205, ϕCb5, ϕCb8r, ϕCb12r, ϕCb23r, 7s, PRR1, or a combination thereof.

12. The method of claim 1 , wherein the adaptor protein comprises a bacteriophage coat protein of MS2 or PP7.

13. The method of claim 1 , wherein the aptamer sequence is a MS2 aptamer sequence or a PP7 aptamer sequence.

14. The method of claim 1 , wherein the heterologous functional domain has at least one of: methylase activity, demethylase activity, transcription activation activity, transcription repression activity, transcription release factor activity, histone modification activity, or a combination thereof.

15. The method of claim 1 , wherein the heterologous functional domain comprises a transcriptional activation domain, a transcriptional repressor domain, or an epigenetic effector domain.

16. The method of claim 1 , wherein the heterologous functional domain comprises VP64, p65, MyoD1, HSF1, RTA, SET7/9, or a combination thereof.

17. The method of claim 1 , wherein the heterologous functional domain comprises KRAB, NuE, NcoR, SID, SID4X, or a combination thereof.

18. The method of claim 1 , wherein the Cas9 protein is fused to at least one heterologous functional domain.

19. The method of claim 18 , wherein the heterologous functional domain has at least one of: methylase activity, demethylase activity, transcription activation activity, transcription repression activity, transcription release factor activity, histone modification activity, or a combination thereof.

20. The method of claim 1 , wherein the CRISPR-Cas system comprises the chimeric RNA and the Cas9 protein.

21. The method of claim 1 , wherein the CRISPR-Cas system comprises the chimeric RNA and an mRNA encoding the Cas9 protein.

22. The method of claim 1 , wherein the CRISPR-Cas system comprises one or more vectors encoding the chimeric RNA and the Cas9 protein.

23. The method of claim 1 , wherein the target sequence is a coding sequence, a promoter sequence, an enhancer sequence, or a silencer sequence.

24. The method of claim 1 , wherein the eukaryotic cell is a mammalian cell or a human cell.

25. The method of claim 1 , further comprising introducing to the eukaryotic cell a further CRISPR-Cas system comprising
an engineered Cas9 protein comprising at least one mutation such that the Cas9 protein substantially lacks DNA cleavage activity, wherein the Cas9 protein is fused to at least one heterologous functional domain, or a polynucleotide encoding the Cas9 protein; and
a chimeric RNA comprising a guide sequence capable of hybridizing to a target sequence in a genomic locus of interest in the eukaryotic cell, or a polynucleotide encoding the chimeric RNA.

26. The method of claim 25 , wherein the heterologous functional domain has at least one of: methylase activity, demethylase activity, transcription activation activity, transcription repression activity, transcription release factor activity, histone modification activity, or a combination thereof.

27. The method of claim 25 , wherein the heterologous functional domain comprises a transcriptional activation domain, a transcriptional repressor domain, or an epigenetic effector domain.

28. The method of claim 25 , wherein the heterologous functional domain comprises VP64, p65, MyoD1, HSF1, RTA, SET7/9, or a combination thereof.

29. The method of claim 25 , wherein the heterologous functional domain comprises KRAB, NuE, NcoR, SID, SID4X, or a combination thereof.

30. The method of claim 25 , wherein the heterologous functional domain comprises a DNA methyltransferase domain.

Assignees

• Broad Inst Inc
• Massachusetts Inst Technology
• Univ Tokyo
• Harvard College
• Massachusetts Instit Jte Of Tech

Inventors

• Konermann Silvana
• Trevino Alexandro
• Brigham Mark
• Ran Fei
• Hsu Patrick
• Lin Chie-Yu
• Nureki Osamu
• Nishimasu Hiroshi
• Ishitani Ryuichiro
• Zhang Feng

Classifications

• C12Y301/00

  Hydrolases acting on ester bonds (3.1) · CPC title

• C12Q1/6876

  Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes · CPC title

• C12N15/902

  using homologous recombination · CPC title

• A61K38/465

  acting on ester bonds (3.1), e.g. lipases, ribonucleases · CPC title

• C12N15/907

  in mammalian cells · CPC title