US2022119846A1PendingUtilityA1

Methods and compositions for rna-directed target dna modification and for rna-directed modulation of transcription

Assignee: CHARPENTIER EMMANUELLEPriority: May 25, 2012Filed: Oct 29, 2021Published: Apr 21, 2022
Est. expiryMay 25, 2032(~5.8 yrs left)· nominal 20-yr term from priority
H10P 14/6512H10P 14/20H10H 20/0137C12N 9/22C12N 2310/11C07K 2319/85C07K 2319/71C12N 15/902C12N 15/907C12N 15/102C12N 15/70C12N 2310/32C12N 15/746C12N 15/113C12N 15/111C12N 15/90C12N 15/63C12N 2310/20A61K 38/465C12N 2310/3519C12N 2310/531A01K 67/027A61P 43/00C12N 2310/31A61P 31/00A61P 35/00A61P 31/04C12N 2310/13A61K 48/00A61P 31/12C12Y 301/04A01H 6/4684C12N 2800/80C12N 2310/14C12N 2310/33C12Q 1/686Y02A50/30C12N 5/10C12N 9/226
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Claims

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

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A bacterial cell comprising a chimeric Cas9 protein comprising a Cas9 polypeptide fused to a transcriptional activator polypeptide or a transcription repressor, wherein the Cas9 polypeptide comprises one or more mutations in a RuvC domain and/or an HNH domain. 
     
     
         2 . A composition comprising:
 a buffer, and   a single-molecule DNA-targeting RNA having the structure:   
       
         
           
           
               
               
           
         
       
       wherein the linker is nnnn such that the single-molecule DNA-targeting RNA has the nucleotide sequence nnnnnnnnnnnnnnnnnnnnGUUUUAGAGCUAnnnnUAGCAAGUUAAAAUAAGGCUAGUCCG (SEQ ID NO: 680). 
     
     
         3 . The composition of  claim 2 , wherein the linker is GAAA such that the single-molecule DNA-targeting RNA has the structure: 
       
         
           
           
               
               
           
         
         wherein “20-nt targeting seq” is nnnnnnnnnnnnnnnnnnnn. 
       
     
     
         4 . A method of cleaving a target DNA, the method comprising:
 contacting a target DNA with:   (a) the composition of claim  56 , wherein nnnnnnnnnnnnnnnnnnnn is a DNA-targeting segment that hybridizes with a target sequence of the target DNA; and   (b) a Cas9 protein comprising the  S. pyogenes  Cas9 amino acid sequence set forth as SEQ ID NO.: 2,   wherein said contacting does not take place inside of a cell, and   wherein the target DNA is cleaved.

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