抗毒素
清脆的
毒素
核糖核酸
生物
反式激活crRNA
效应器
基因
计算生物学
基因组编辑
CRISPR干扰
引导RNA
遗传学
细胞生物学
作者
Ming Li,Luyao Gong,Feiyue Cheng,Haiying Yu,Dahe Zhao,Rui Wang,Tian Wang,Shengjie Zhang,Jian Zhou,Sergey Shmakov,Eugene V. Koonin,Hua Xiang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-04-29
卷期号:372 (6541)
被引量:69
标识
DOI:10.1126/science.abe5601
摘要
Small RNAs guard CRISPR-Cas The microbial adaptive immunity system CRISPR-Cas benefits microbes by warding off genetic invaders, but it also inflicts a fitness cost because of occasional autoimmune reactions, rendering CRISPR loci evolutionarily unstable. Li et al. identified previously unnoticed toxin-antitoxin RNA pairs embedded within diverse CRISPR-Cas loci. The antitoxin RNA mimics a CRISPR RNA and repurposes the CRISPR immunity effector to transcriptionally repress a toxin RNA that would otherwise arrest cell growth by sequestering a rare transfer RNA. These small RNAs thus form a symbiosis with CRISPR, rendering CRISPR addictive to the host despite its fitness cost. These findings reveal how CRISPR-Cas can operate as a selfish genetic element. Science , this issue p. eabe5601
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