引导RNA
计算生物学
基因组
亚基因组mRNA
基因组工程
CRISPR干扰
细胞生物学
作者
April Pawluk,Nadia Amrani,Yan Zhang,Bianca Garcı́a,Yurima Hidalgo-Reyes,Jooyoung Lee,Alireza Edraki,Megha Shah,Erik J. Sontheimer,Karen L. Maxwell,Alan R. Davidson
出处
期刊:Cell
[Elsevier]
日期:2016-12-01
卷期号:167 (7): 1829-1838.e9
被引量:331
标识
DOI:10.1016/j.cell.2016.11.017
摘要
CRISPR-Cas9 technology would be enhanced by the ability to inhibit Cas9 function spatially, temporally, or conditionally. Previously, we discovered small proteins encoded by bacteriophages that inhibit the CRISPR-Cas systems of their host bacteria. These "anti-CRISPRs" were specific to type I CRISPR-Cas systems that do not employ the Cas9 protein. We posited that nature would also yield Cas9 inhibitors in response to the evolutionary arms race between bacteriophages and their hosts. Here, we report the discovery of three distinct families of anti-CRISPRs that specifically inhibit the CRISPR-Cas9 system of Neisseria meningitidis. We show that these proteins bind directly to N. meningitidis Cas9 (NmeCas9) and can be used as potent inhibitors of genome editing by this system in human cells. These anti-CRISPR proteins now enable "off-switches" for CRISPR-Cas9 activity and provide a genetically encodable means to inhibit CRISPR-Cas9 genome editing in eukaryotes. VIDEO ABSTRACT.
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