Phage Against the Machine: Discovery and Mechanism of Type V Anti-CRISPRs

被引:6
|
作者
Marino, Nicole D. [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
FERTILITY INHIBITION; CPF1; CLASSIFICATION; SPECIFICITIES; ENDONUCLEASE; COMPLEX; SYSTEMS; CAS12A; GENES;
D O I
10.1016/j.jmb.2023.168054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The discovery of diverse bacterial CRISPR-Cas systems has reignited interest in understanding bacterial defense pathways while yielding exciting new tools for genome editing. CRISPR-Cas systems are widely distributed in prokaryotes, found in 40% of bacteria and 90% of archaea, where they function as adaptive immune systems against bacterial viruses (phage) and other mobile genetic elements. In turn, phage have evolved inhibitors, called anti-CRISPR proteins, to prevent targeting. Type V CRISPR-Cas12 sys-tems have emerged as a particularly exciting arena in this co-evolutionary arms race. Type V anti-CRISPRs have highly diverse and novel mechanisms of action, some of which appear to be unusually potent or widespread. In this review, we discuss the discovery and mechanism of these anti-CRISPRs as well as future areas for exploration.(c) 2023 Elsevier Ltd. All rights reserved.
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页数:8
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