IP Library Patent Application 18134317
Patent Application
App. No. 18/134,317

CRISPR-CAS COMPONENT SYSTEMS, METHODS AND COMPOSITIONS FOR SEQUENCE MANIPULATION

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Patent No.
US None
App. No.
18/134,317
Abstract

The invention provides for systems, methods, and compositions for manipulation of sequences and/or activities of target sequences. Provided are vectors and vector systems, some of which encode one or more components of a CRISPR complex, as well as methods for the design and use of such vectors. Also provided are methods of directing CRISPR complex formation in eukaryotic cells and methods for selecting specific cells by introducing precise mutations utilizing the CRISPR/Cas system.

Claims (38)

1 . An ex vivo human cell comprising:

(i) a Cas9 comprising one or more SV40 large T-antigen nuclear localization signals, and

(ii) an RNA molecule,

wherein the Cas9 is complexed with the RNA molecule, and wherein the RNA molecule and the Cas9 do not occur naturally together.

2 . The ex vivo human cell of claim 1 , wherein at least one of the one or more SV40 large T-antigen nuclear localization signals is at the C-terminus of the Cas9.

3 . The ex vivo human cell of claim 1 , wherein at least one of the one or more SV40 large T-antigen nuclear localization signals is the N-terminus of the Cas9.

4 . The ex vivo human cell of claim 1 , wherein the S. pyogenes Cas9 is flanked on each end by one or more SV40 large T-antigen nuclear localization signals.

5 . The ex vivo human cell of claim 1 , wherein the SV40 large T-antigen nuclear localization signals comprise the sequence PKKKRKV (SEQ ID NO: 1).

6 . The ex vivo human cell of claim 1 , wherein the Cas9 is an S. pyogenes Cas9.

7 . The ex vivo human cell of claim 1 , wherein the RNA molecule comprises one or more methylated nucleotides.

8 . The ex vivo human cell of claim 1 , wherein the RNA molecule comprises a sequence complementary to a target DNA sequence in the ex vivo human cell.

9 . The ex vivo human cell of claim 8 , wherein the RNA molecule comprises a sequence that is hybridized to the target DNA sequence in the ex vivo human cell.

10 . The ex vivo human cell of claim 8 , wherein the target sequence comprises a non-coding sequence.

11 . The ex vivo human cell of claim 8 , wherein the non-coding sequence comprises a regulatory element.

12 . The ex vivo human cell of claim 1 , wherein the sequence complementary to a target DNA sequence e is between 15-25 nucleotides in length.

13 . An ex vivo human cell comprising:

(i) an S. pyogenes Cas9 comprising one or more SV40 large T-antigen nuclear localization signals, and

(ii) an RNA molecule,

wherein the Cas9 is complexed with the RNA molecule, and wherein the RNA molecule and the Cas9 do not occur naturally together.

14 . The ex vivo human cell of claim 13 , wherein at least one of the one or more SV40 large T-antigen nuclear localization signals is at the C-terminus of the S. pyogenes Cas9.

15 . The ex vivo human cell of claim 13 , wherein the S. pyogenes Cas9 comprises two SV40 large T-antigen nuclear localization signals.

16 . The ex vivo human cell of claim 13 , wherein the SV40 large T-antigen nuclear localization signals comprise the sequence PKKKRKV (SEQ ID NO: 1).

17 . The ex vivo human cell of claim 13 , wherein the RNA molecule comprises one or more methylated nucleotides.

18 . The ex vivo human cell of claim 13 , wherein the RNA molecule comprises a sequence complementary to a target DNA sequence in the ex vivo human cell.

19 . The ex vivo human cell of claim 18 , wherein the RNA molecule comprises a sequence that is hybridized to the target DNA sequence in the ex vivo human cell.

20 . The ex vivo human cell of claim 18 , wherein the target DNA sequence comprises a non-coding sequence.

21 . The ex vivo human cell of claim 20 , wherein the non-coding sequence comprises a regulatory element.

22 . An ex vivo human cell comprising:

(i) an S. pyogenes Cas9 comprising two nuclear localization signals flanking the Cas9, and

(ii) a non-naturally occurring RNA molecule, wherein the RNA molecule comprises one or more methylated nucleotides,

wherein the S. pyogenes Cas9 is complexed with the RNA molecule.

23 . The ex vivo human cell of claim 22 , wherein at least one of the nuclear localization signals is an SV40 large T-antigen nuclear localization signal.

24 . The ex vivo human cell of claim 23 , wherein the SV40 large T-antigen nuclear localization signal comprises the sequence PKKKRKV (SEQ ID NO: 1).

25 . The ex vivo human cell of claim 22 , wherein the RNA molecule comprises a sequence complementary to a target DNA sequence in the ex vivo human cell.

26 . The ex vivo human cell of claim 25 , wherein the RNA molecule comprises a sequence that is hybridized to the target DNA sequence in the ex vivo human cell.

27 . The ex vivo human cell of claim 25 , wherein the target DNA sequence comprises a non-coding sequence.

28 . The ex vivo human cell of claim 28 , wherein the non-coding sequence comprises a regulatory element.

29 . The ex vivo human cell of claim 22 , wherein the RNA molecule comprises a sequence complementary to a target DNA sequence between 15-25 nucleotides in length and a tracr-mate sequence that comprises the sequence GUUUUAGAGCUA.

Assignments (2)
LICENSE Recorded Apr 3, 2025
From: BROAD INSTITUTE, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 070737/0520 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2023
From: ZHANG, FENG
To: THE BROAD INSTITUTE, INC.; MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 063317/0206 →