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促进 CRISPR PcrIIC1 相关 Cas9 系统增强细菌免疫。

Pro-CRISPR PcrIIC1-associated Cas9 system for enhanced bacterial immunity.

机构信息

Beijing Frontier Research Center for Biological Structure, Beijing Advanced Innovation Center for Structural Biology, State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.

State Key Laboratory of Plant Genomics, CAS-JIC Centre of Excellence for Plant and Microbial Sciences, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.

出版信息

Nature. 2024 Jun;630(8016):484-492. doi: 10.1038/s41586-024-07486-x. Epub 2024 May 29.

Abstract

The CRISPR system is an adaptive immune system found in prokaryotes that defends host cells against the invasion of foreign DNA. As part of the ongoing struggle between phages and the bacterial immune system, the CRISPR system has evolved into various types, each with distinct functionalities. Type II Cas9 is the most extensively studied of these systems and has diverse subtypes. It remains uncertain whether members of this family can evolve additional mechanisms to counter viral invasions. Here we identify 2,062 complete Cas9 loci, predict the structures of their associated proteins and reveal three structural growth trajectories for type II-C Cas9. We found that novel associated genes (NAGs) tended to be present within the loci of larger II-C Cas9s. Further investigation revealed that CbCas9 from Chryseobacterium species contains a novel β-REC2 domain, and forms a heterotetrameric complex with an NAG-encoded CRISPR-Cas-system-promoting (pro-CRISPR) protein of II-C Cas9 (PcrIIC1). The CbCas9-PcrIIC1 complex exhibits enhanced DNA binding and cleavage activity, broader compatibility for protospacer adjacent motif sequences, increased tolerance for mismatches and improved anti-phage immunity, compared with stand-alone CbCas9. Overall, our work sheds light on the diversity and 'growth evolutionary' trajectories of II-C Cas9 proteins at the structural level, and identifies many NAGs-such as PcrIIC1, which serves as a pro-CRISPR factor to enhance CRISPR-mediated immunity.

摘要

CRISPR 系统是一种存在于原核生物中的适应性免疫系统,可抵御外来 DNA 的入侵。作为噬菌体和细菌免疫系统之间持续斗争的一部分,CRISPR 系统已经进化成多种类型,每种类型都具有不同的功能。其中,II 型 Cas9 是研究最广泛的系统,具有多种亚型。目前尚不清楚该家族的成员是否能够进化出其他机制来抵御病毒入侵。在这里,我们鉴定了 2062 个完整的 Cas9 基因座,预测了它们相关蛋白的结构,并揭示了 II 型-Cas9 的三种结构生长轨迹。我们发现,新的相关基因(NAGs)往往存在于较大的 II-Cas9 基因座内。进一步的研究表明,来自黄杆菌属的 CbCas9 含有一个新的β-REC2 结构域,并与 II-Cas9(PcrIIC1)的 NAG 编码的 CRISPR-Cas 系统促进(pro-CRISPR)蛋白形成异四聚体复合物。与独立的 CbCas9 相比,CbCas9-PcrIIC1 复合物表现出增强的 DNA 结合和切割活性、更广泛的原间隔邻近基序序列兼容性、更高的错配容忍度和改善的抗噬菌体免疫能力。总的来说,我们的工作揭示了 II-Cas9 蛋白在结构水平上的多样性和“生长进化”轨迹,并鉴定了许多 NAGs,如 PcrIIC1,它作为一种 pro-CRISPR 因子,可增强 CRISPR 介导的免疫。

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