Structural insights into the inactivation of the type I-F CRISPR-Cas system by anti-CRISPR proteins

被引:4
|
作者
Yang, Lingguang [1 ,2 ]
Zhang, Yi [1 ]
Yin, Peipei [1 ,2 ]
Feng, Yue [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Life Sci & Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing Key Lab Bioproc,State Key Lab Chem Resour, Beijing 100029, Peoples R China
[2] Yichun Univ, Dept Chem & Bioengn, Jiangxi Prov Key Lab Nat Act Pharmaceut Constitue, Yichun, Peoples R China
基金
中国国家自然科学基金;
关键词
CRISPR-Cas systems; anti-CRISPR; type I-F system; structure; adaptive immune system; R-LOOP FORMATION; SURVEILLANCE COMPLEX; EVOLUTIONARY CLASSIFICATION; ANTIVIRAL DEFENSE; VIRAL SUPPRESSORS; STRUCTURE REVEALS; INHIBITION; RNA; MECHANISMS; RECRUITMENT;
D O I
10.1080/15476286.2021.1985347
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
Phage infection is one of the major threats to prokaryotic survival, and prokaryotes in turn have evolved multiple protection approaches to fight against this challenge. Various delicate mechanisms have been discovered from this eternal arms race, among which the CRISPR-Cas systems are the prokaryotic adaptive immune systems and phages evolve diverse anti-CRISPR (Acr) proteins to evade this immunity. Until now, about 90 families of Acr proteins have been identified, out of which 24 families were verified to fight against subtype I-F CRISPR-Cas systems. Here, we review the structural and biochemical mechanisms of the characterized type I-F Acr proteins, classify their inhibition mechanisms into two major groups and provide insights for future studies of other Acr proteins. Understanding Acr proteins in this context will lead to a variety of practical applications in genome editing and also provide exciting insights into the molecular arms race between prokaryotes and phages.
引用
收藏
页码:562 / 573
页数:12
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