Invention Grant
- Patent Title: Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription
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Application No.: US17079070Application Date: 2020-10-23
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Publication No.: US11242543B2Publication Date: 2022-02-08
- Inventor: Jennifer A. Doudna , Martin Jinek , Krzysztof Chylinski , Emmanuelle Charpentier
- Applicant: The Regents of the University of California , University of Vienna , Emmanuelle Charpentier
- Applicant Address: US CA Oakland; AT Vienna; DE Braunschweig
- Assignee: The Regents of the University of California,University of Vienna,Emmanuelle Charpentier
- Current Assignee: The Regents of the University of California,University of Vienna,Emmanuelle Charpentier
- Current Assignee Address: US CA Oakland; AT Vienna; DE Braunschweig
- Agency: Bozicevic, Field & Francis LLP
- Main IPC: C12N15/11
- IPC: C12N15/11 ; C12N15/63 ; C12N9/22 ; C12N15/113 ; C12N15/10 ; A61K38/46 ; C12N15/90 ; C12Q1/686 ; C12N15/70 ; C12N15/74 ; A01H6/46 ; A01K67/027 ; A61K48/00

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.
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