| Literature DB >> 28603751 |
Tao Zhang1, Yangbin Gao2, Rongchen Wang1, Yunde Zhao1,2.
Abstract
CRISPR/Cas9-mediated genome editing relies on a guide RNA (gRNA) molecule to generate sequence-specific DNA cleavage, which is a prerequisite for gene editing. Here we establish a method that enables production of gRNAs from any promoters, in any organisms, and in vitro (Gao and Zhao, 2014). This method also makes it feasible to conduct tissue/cell specific gene editing.Entities:
Keywords: CRISPR; Genome editing; RNA polymerase II promoter; RNA transcription; Ribozyme
Year: 2017 PMID: 28603751 PMCID: PMC5463609 DOI: 10.21769/BioProtoc.2148
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325