Molecular basis for inhibition of type III-B CRISPR-Cas by an archaeal viral anti-CRISPR protein

被引:8
作者
Lin, Jinzhong [1 ]
Alfastsen, Lauge [1 ]
Bhoobalan-Chitty, Yuvaraj [1 ]
Peng, Xu [1 ]
机构
[1] Univ Copenhagen, Dept Biol, Ole Maaloes Vej 5, DK-2200 Copenhagen N, Denmark
关键词
DNA CLEAVAGE; CSM COMPLEX; TARGET RNA; SYSTEM; DEGRADATION; CLASSIFICATION; MECHANISMS; BIOLOGY; BINDING; ROLES;
D O I
10.1016/j.chom.2023.10.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite a wide presence of type III clustered regularly interspaced short palindromic repeats, CRISPR-associated (CRISPR-Cas) in archaea and bacteria, very few anti-CRISPR (Acr) proteins inhibiting type III immunity have been identified, and even less is known about their inhibition mechanism. Here, we present the discovery of a type III CRISPR-Cas inhibitor, AcrIIIB2, encoded by Sulfolobus virus S. islandicus rod-shaped virus 3 (SIRV3). AcrIIIB2 inhibits type III-B CRISPR-Cas immune response to protospacers encoded in middle/lateexpressed viral genes. Investigation of the interactions between S. islandicus type III-B CRISPR-Cas Cmra-related proteins and AcrIIIB2 reveals that the Acr does not bind to Csx1 but rather interacts with the Cmr-a effector complex. Furthermore, in vitro assays demonstrate that AcrIIIB2 can block the dissociation of cleaved target RNA from the Cmr-a complex, thereby inhibiting the Cmr-a turnover, thus preventing host cellular dormancy and further viral genome degradation by the type III-B CRISPR-Cas immunity.
引用
收藏
页码:1837 / +
页数:19
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