Author
Listed:
- Shouyue Zhang
(Tsinghua University)
- Ao Sun
(Tsinghua University)
- Jing-Mei Qian
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Shuo Lin
(Tsinghua University)
- Wenjing Xing
(Tsinghua University)
- Yun Yang
(Tsinghua University)
- Han-Zhou Zhu
(Tsinghua University)
- Xin-Yi Zhou
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Yan-Shuo Guo
(Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Yun Liu
(Tsinghua University)
- Yu Meng
(Tsinghua University)
- Shu-Lin Jin
(Tsinghua University)
- Wenhao Song
(Tsinghua University)
- Cheng-Ping Li
(Tsinghua University)
- Zhaofu Li
(Tsinghua University)
- Shuai Jin
(Tsinghua University
University of Chinese Academy of Sciences
Chinese Academy of Sciences)
- Jian-Hua Wang
(National Institute of Biological Sciences
Tsinghua University)
- Meng-Qiu Dong
(National Institute of Biological Sciences
Tsinghua University)
- Caixia Gao
(University of Chinese Academy of Sciences
Chinese Academy of Sciences)
- Chunlai Chen
(Tsinghua University)
- Yang Bai
(Chinese Academy of Sciences
University of Chinese Academy of Sciences
Peking University)
- Jun-Jie Gogo Liu
(Tsinghua University)
Abstract
The CRISPR system is an adaptive immune system found in prokaryotes that defends host cells against the invasion of foreign DNA1. As part of the ongoing struggle between phages and the bacterial immune system, the CRISPR system has evolved into various types, each with distinct functionalities2. 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 invasions3,4. 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.
Suggested Citation
Shouyue Zhang & Ao Sun & Jing-Mei Qian & Shuo Lin & Wenjing Xing & Yun Yang & Han-Zhou Zhu & Xin-Yi Zhou & Yan-Shuo Guo & Yun Liu & Yu Meng & Shu-Lin Jin & Wenhao Song & Cheng-Ping Li & Zhaofu Li & Sh, 2024.
"Pro-CRISPR PcrIIC1-associated Cas9 system for enhanced bacterial immunity,"
Nature, Nature, vol. 630(8016), pages 484-492, June.
Handle:
RePEc:nat:nature:v:630:y:2024:i:8016:d:10.1038_s41586-024-07486-x
DOI: 10.1038/s41586-024-07486-x
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