反式激活crRNA
生物
清脆的
效应器
核酸酶
计算生物学
遗传学
DNA
核糖核酸
Cas9
核酸内切酶
基因
细胞生物学
作者
Sergey Shmakov,Omar O. Abudayyeh,Kira S. Makarova,Yuri I. Wolf,Jonathan S. Gootenberg,Ekaterina Semenova,Leonid Minakhin,Julia Joung,Silvana Konermann,Konstantin Severinov,Feng Zhang,Eugene V. Koonin
出处
期刊:Molecular Cell
[Elsevier]
日期:2015-10-25
卷期号:60 (3): 385-397
被引量:1068
标识
DOI:10.1016/j.molcel.2015.10.008
摘要
Microbial CRISPR-Cas systems are divided into Class 1, with multisubunit effector complexes, and Class 2, with single protein effectors. Currently, only two Class 2 effectors, Cas9 and Cpf1, are known. We describe here three distinct Class 2 CRISPR-Cas systems. The effectors of two of the identified systems, C2c1 and C2c3, contain RuvC-like endonuclease domains distantly related to Cpf1. The third system, C2c2, contains an effector with two predicted HEPN RNase domains. Whereas production of mature CRISPR RNA (crRNA) by C2c1 depends on tracrRNA, C2c2 crRNA maturation is tracrRNA independent. We found that C2c1 systems can mediate DNA interference in a 5′-PAM-dependent fashion analogous to Cpf1. However, unlike Cpf1, which is a single-RNA-guided nuclease, C2c1 depends on both crRNA and tracrRNA for DNA cleavage. Finally, comparative analysis indicates that Class 2 CRISPR-Cas systems evolved on multiple occasions through recombination of Class 1 adaptation modules with effector proteins acquired from distinct mobile elements.
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