IP Library Granted Patent US 11,008,590
Granted Patent B2
US 11,008,590 · App. 17/102,059 · Granted May 18, 2021

Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription

Inventors: Jennifer A. Doudna (Berkeley, CA); Martin Jinek (Berkeley, CA); Krzysztof Chylinski (Vienna, AT); Emmanuelle Charpentier (Berlin, DE)
Assignees: The Regents of The University of California; University of Vienna; Emmanuelle Charpentier
C12N15/907A01H6/4684A01K67/027A61K38/465C12N9/22C12N15/102C12N15/111C12N15/113C12N15/63C12N15/70C12N15/746C12N15/90C12N15/902C12Q1/686A61K48/00C12N2310/11C12N2310/13C12N2310/14C12N2310/20C12N2310/31C12N2310/32C12N2310/33C12N2310/3519C12N2310/531C12N2800/80C12Y301/04
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Quick Facts
Patent No.
US 11,008,590
App. No.
17/102,059
Filed
Nov 23, 2020
Granted
May 18, 2021
Kind
B2
Art Unit
1636
USPC
800/18
Abstract

The present disclosure provides a DNA-targeting RNA that comprises a targeting sequence and, together with a modifying polypeptide, provides for site-specific modification of a target DNA and/or a polypeptide associated with the target DNA. The present disclosure further provides site-specific modifying polypeptides. The present disclosure further provides methods of site-specific modification of a target DNA and/or a polypeptide associated with the target DNA The present disclosure provides methods of modulating transcription of a target nucleic acid in a target cell, generally involving contacting the target nucleic acid with an enzymatically inactive Cas9 polypeptide and a DNA-targeting RNA. Kits and compositions for carrying out the methods are also provided. The present disclosure provides genetically modified cells that produce Cas9; and Cas9 transgenic non-human multicellular organisms.

Claims (50)

1. A composition comprising

(1) a Cas9 protein or a nucleic acid encoding the Cas9 protein, wherein the Cas9 protein is a Streptococcus pyogenes Cas9; and

(2) a DNA-targeting RNA, or one or more nucleic acids encoding the DNA-targeting RNA, wherein the DNA-targeting RNA comprises:

(a) a targeter-RNA comprising:

(i) a first nucleotide sequence that is complementary to a target sequence of a target DNA, and (ii) a second nucleotide sequence that hybridizes with an activator-RNA, wherein the first and second nucleotide sequences are heterologous to one another; and

(b) the activator-RNA, which hybridizes with the second nucleotide sequence of the targeter-RNA to form a double-stranded RNA (dsRNA) duplex, wherein the activator-RNA hybridizes with the targeter-RNA to form a total of 8 to 15 base pairs,

wherein the DNA-targeting RNA is capable of forming a complex with the Cas9 protein and guiding the complex to the target sequence of the target DNA.

2. The composition of claim 1 , wherein the targeter-RNA and the activator-RNA are not covalently linked to one another by intervening nucleotides.

3. The composition of claim 1 , wherein the targeter-RNA and the activator-RNA are two separate RNA molecules.

4. The composition of claim 1 , wherein the first nucleotide sequence is 18 to 25 nucleotides long.

5. The composition of claim 1 , further comprising a nuclease inhibitor.

6. The composition of claim 1 , wherein the Cas9 protein comprises a mutation in a RuvC and/or an HNH domain.

7. The composition of claim 1 , wherein the Cas9 protein comprises a heterologous polypeptide.

8. The composition of claim 7 , wherein the heterologous polypeptide comprises an endosomolytic domain, an influenza HA domain, an IF2 domain, a GST domain, a GRPE domain, a 6×His tag, a hemagglutinin (HA) tag, or green fluorescent protein.

9. The composition of claim 1 , wherein the Cas9 protein is fused to a protein transduction domain (PTD).

10. The composition of claim 1 , wherein the DNA-targeting RNA is capable of firming a complex with the Cas9 protein and guiding the complex to the target sequence to cleave the target DNA.

11. The composition of claim 10 , further comprising a donor polynucleotide.

12. The composition of claim 1 , wherein the DNA-targeting RNA is capable of forming a complex with the Cas9 protein and guiding the complex to the target sequence to cleave the target DNA.

13. The composition of claim 12 , further comprising a donor polynucleotide.

14. The composition of claim 1 , wherein the composition comprises a protein-RNA complex comprising the Cas9 protein and the DNA-targeting RNA.

15. The composition of claim 1 , comprising the DNA-targeting RNA and the nucleic acid encoding the Cas9 protein.

16. The composition of claim 1 , comprising the nucleic acid encoding the Cas9 protein and/or the one or more nucleic acids encoding the DNA-targeting RNA.

17. The composition of claim 16 , wherein the nucleic acid encoding the Cas9 protein is an RNA.

18. The composition of claim 16 , wherein the nucleic acid encoding the Cas9 protein is a DNA.

19. The composition of claim 16 , wherein the nucleic acid encoding the Cas9 protein and/or the one or more nucleic acids encoding the DNA-targeting RNA, is a plasmid, a cosmid, a minicircle, a phage, or a viral vector.

20. The composition of claim 1 , wherein the activator-RNA comprises the 67 nt tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGU GCUUUUUUU (SEQ ID NO: 432); or the 26 nucleotide tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCG (SEQ ID NO: 397).

21. The composition of claim 1 , comprising the DNA-targeting RNA, wherein the DNA-targeting RNA comprises one or more non-natural internucleoside linkages, one or more nucleic acid mimetics, one or more modified sugar moieties, and/or one or more modified nucleobases.

22. The composition of claim 1 , comprising the DNA-targeting RNA, wherein the DNA-targeting RNA comprises one or more phosphorothioates, one or more inverted polarity linkages, one or more abasic nucleoside linkages, one or more locked nucleic acids (LNAs), one or more 2′-O-methoxyethyl modified sugar moieties, one or more 2′-O-methyl modified sugar moieties, one or more 2′-O-(2-methoxyethyl) modified sugar moieties, one or more 2′-fluoro modified sugar moieties, one or more 2′-dimethylaminooxyethoxy modified sugar moieties, one or more 2′-dimethylaminoethoxyethoxy modified sugar moieties, one or more peptide nucleic acids (PNAs), one or more morpholino nucleic acids, and/or one or more cyclohexenyl nucleic acids (CeNAs).

23. The composition of claim 22 , wherein the DNA-targeting RNA comprises said one or more 2′-O-methyl modified sugar moieties and/or said one or more 2′-fluoro modified sugar moieties.

24. The composition of claim 1 , comprising the DNA-targeting RNA, wherein the targeter-RNA and/or the activator-RNA are conjugated to a heterologous moiety.

25. A composition comprising

(1) a Cas9 protein or a nucleic acid encoding the Cas9 protein, wherein the Cas9 protein is a Streptococcus pyogenes Cas9; and

(2) a DNA-targeting RNA, or one or more nucleic acids encoding the DNA-targeting RNA, wherein the DNA-targeting RNA comprises:

(a) a targeter-RNA comprising:

(i) a first nucleotide sequence that is complementary to a target sequence of a target DNA, and (ii) a second nucleotide sequence that hybridizes with an activator-RNA, wherein the first and second nucleotide sequences are heterologous to one another; and

(b) the activator-RNA, which hybridizes with the second nucleotide sequence of the targeter-RNA to form a double-stranded RNA (dsRNA) duplex, wherein the activator-RNA hybridizes with the targeter-RNA to form a total of 8 to 15 base pairs,

wherein the activator-RNA comprises the 67 nt tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCGUUUAUCAACUUGAAAAAGUGGCACCGAGUCGGU GCUUUUUUU (SEQ ID NO: 432), and

wherein the DNA-targeting RNA is capable of forming a complex with the Cas9 protein and guiding the complex to the target sequence of the target DNA.

26. A kit comprising:

(1) a Cas9 protein or a nucleic acid encoding the Cas9 protein, wherein the Cas9 protein is a Streptococcus pyogenes Cas9; and

(2) a DNA-targeting RNA, or one or more nucleic acids encoding the DNA-targeting RNA, wherein the DNA-targeting RNA comprises:

(a) a targeter-RNA comprising:

(i) a first nucleotide sequence that is complementary to a target sequence of a target DNA, and (ii) a second nucleotide sequence that hybridizes with an activator-RNA, wherein the first and second nucleotide sequences are heterologous to one another; and

(b) the activator-RNA, which hybridizes with the second nucleotide sequence of the targeter-RNA to form a double-stranded RNA (dsRNA) duplex, wherein the activator-RNA hybridizes with the targeter-RNA to form a total of 8 to 1 base pairs,

wherein the DNA-targeting RNA is capable of forming a complex with the Cas9 protein and guiding the complex to the target sequence of the target DNA; and

wherein (a) and (b) are separated.

27. The kit of claim 26 , wherein the first nucleotide sequence is 18 to 25 nucleotides long.

28. The kit of claim 26 , wherein the activator-RNA comprises the 67 in tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGU GCUUUUUUU (SEQ ID NO: 432); or the 26 nucleotide tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCG (SEQ 11) NO: 397).

29. The kit of claim 26 , wherein the Cas9 protein comprises a mutation in a RuvC and/or an HNH domain.

30. The kit of claim 26 , wherein the Cas9 protein comprises a heterologous polypeptide.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2020
From: DOUDNA, JENNIFER A.; JINEK, MARTIN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 054535/0254 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 3, 2020
From: CHYLINSKI, KRZYSZTOF
To: UNIVERSITY OF VIENNA
Reel/Frame 054535/0306 →
Continuity (7)
Continuation 16385360 · Apr 16, 2019
Continuation 13842859 · Mar 15, 2013
Provisional Application 61765576 · Feb 15, 2013
Provisional Application 61757640 · Jan 28, 2013
Provisional Application 61716256 · Oct 19, 2012
Provisional Application 61652086 · May 25, 2012
Related Publication 20210108231A1 · Apr 15, 2021
Cited By (2)
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