IP Library Granted Patent US 10,563,227
Granted Patent B2
US 10,563,227 · App. 16/382,097 · Granted Feb 18, 2020

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 (Braunschweig, 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 10,563,227
App. No.
16/382,097
Filed
Apr 11, 2019
Granted
Feb 18, 2020
Kind
B2
Art Unit
1636
USPC
435/6
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 (43)

1. A composition comprising

(a) a Cas9 protein or a nucleic acid encoding the Cas9 protein, wherein the Cas9 protein comprises a mutation in a RuvC and/or an HNH domain; and

(b) a DNA-targeting RNA comprising:

(i) a targeter-RNA that is capable of hybridizing with a target sequence of a target DNA, and

(ii) an activator-RNA that is capable of hybridizing with the targeter-RNA to form a double-stranded duplex,

wherein (i) and (ii) are covalently linked,

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

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

3. The composition of claim 2 , further comprising a donor polynucleotide.

4. The composition of claim 1 , comprising the nucleic acid encoding the Cas9 protein.

5. The composition of claim 4 , wherein the nucleic acid encoding the Cas9 protein is an RNA.

6. The composition of claim 5 , further comprising a donor polynucleotide.

7. The composition of claim 4 , wherein the nucleic acid encoding the Cas9 protein is a DNA.

8. The composition of claim 7 , further comprising a donor polynucleotide.

9. The composition of claim 4 , wherein the nucleic acid encoding the Cas9 protein is a plasmid, a cosmid, a minicircle, a phage, or a viral vector.

10. The composition of claim 1 , wherein the activator-RNA comprises the 67 nt tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUG CUUUUUUU (SEQ ID NO: 432).

11. The composition of claim 1 , wherein the activator-RNA comprises the 26 nucleotide tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCG (SEQ ID NO: 397).

12. The composition of claim 1 , wherein the DNA-targeting RNA comprises one or more of: a non-natural internucleoside linkage, a nucleic acid mimetic, a modified sugar moiety, and a modified nucleobase.

13. The composition of claim 12 , wherein the DNA-targeting RNA comprises said non-natural internucleoside linkage and/or said modified sugar moiety.

14. The composition of claim 12 , wherein the DNA-targeting RNA comprises said non-natural internucleoside linkage.

15. The composition of claim 1 , wherein the DNA-targeting RNA comprises one or more of: a phosphorothioate, an inverted polarity linkage, an abasic nucleoside linkage, a locked nucleic acid (LNA), a 2′-O-methoxyethyl modified sugar moiety, a 2′-O-methyl modified sugar moiety, a 2′-O-(2-methoxyethyl) modified sugar moiety, a 2′-fluoro modified sugar moiety, a 2′-dimethylaminooxyethoxy modified sugar moiety, a 2′-dimethylaminoethoxyethoxy modified sugar moiety, a peptide nucleic acid (PNA), a morpholino nucleic acid, and a cyclohexenyl nucleic acid (CeNA).

16. The composition of claim 15 , wherein the DNA-targeting RNA comprises said 2′-O-methyl modified sugar moiety and/or said 2′-fluoro modified sugar moiety.

17. The composition of claim 1 , wherein the DNA-targeting RNA comprises a phosphorothioate internucleoside linkage.

18. A kit comprising

(a) a Cas9 protein or a nucleic acid encoding the Cas9 protein, wherein the Cas9 protein comprises a mutation in a RuvC and/or an HNH domain; and

(b) a DNA-targeting RNA comprising:

(i) a targeter-RNA that is capable of hybridizing with a target sequence of a target DNA, and

(ii) an activator-RNA that is capable of hybridizing with the targeter-RNA to form a double-stranded duplex,

wherein (i) and (ii) are covalently linked,

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

wherein (a) and (b) are separated.

19. The kit of claim 18 , comprising the Cas9 protein.

20. The kit of claim 18 , comprising the nucleic acid encoding the Cas9 protein.

21. The kit of claim 20 , wherein the nucleic acid encoding the Cas9 protein is a DNA.

22. The kit of claim 16 , wherein the DNA-targeting RNA comprises one or more of: a phosphorothioate, an inverted polarity linkage, an abasic nucleoside linkage, a locked nucleic acid (LNA), a 2′-O-methoxyethyl modified sugar moiety, a 2′-O-methyl modified sugar moiety, a 2′-O-(2-methoxyethyl) modified sugar moiety, a 2′-fluoro modified sugar moiety, a 2′-dimethylaminooxyethoxy modified sugar moiety, a 2′-dimethylaminoethoxyethoxy modified sugar moiety, a peptide nucleic acid (PNA), a morpholino nucleic acid, and a cyclohexenyl nucleic acid (CeNA).

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

24. The kit of claim 20 , wherein the nucleic acid encoding the Cas9 protein is a plasmid, a cosmid, a minicircle, a phage, or a viral vector.

25. The kit of claim 20 , wherein the nucleic acid encoding the Cas9 protein is an RNA.

26. The kit of claim 18 , further comprising a donor polynucleotide.

27. The kit of claim 18 , wherein the activator-RNA comprises the 67 nt tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCGUUAUCAACUUGAAAAAGUGGCACCGAGUCGGUG CUUUUUUU (SEQ ID NO: 432).

28. The kit of claim 18 , wherein the activator RNA comprises the 26 nucleotide tracrRNA sequence UAGCAAGUUAAAAUAAGGCUAGUCCG (SEQ ID NO: 397).

29. The kit of claim 18 , wherein the DNA-targeting RNA comprises one or more of: a non-natural internucleoside linkage, a nucleic acid mimetic, a modified sugar moiety, and a modified nucleobase.

30. The kit of claim 29 , wherein the DNA-targeting RNA comprises said non-natural internucleoside linkage and/or said modified sugar moiety.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2019
From: DOUDNA, JENNIFER A.; JINEK, MARTIN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 049038/0831 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2019
From: CHYLINSKI, KRZYSZTOF
To: UNIVERSITY OF VIENNA
Reel/Frame 049038/0842 →
Continuity (6)
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 20190264236A1 · Aug 29, 2019
Cited By (2)
US 12,201,699 US 12,338,436