核糖核酸
清脆的
生物
计算生物学
核糖核酸酶
遗传学
基因
作者
Peter H. Yoon,Zeyuan Zhang,Kenneth J. Loi,Benjamin A. Adler,Arushi Lahiri,Kamakshi Vohra,Honglue Shi,Daniel Bellieny‐Rabelo,Marena Trinidad,Ron Boger,Muntathar Al-Shimary,Jennifer A. Doudna
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2024-07-18
卷期号:385 (6708): 538-543
标识
DOI:10.1126/science.adq0553
摘要
The RNA-guided ribonuclease CRISPR-Cas13 enables adaptive immunity in bacteria and programmable RNA manipulation in heterologous systems. Cas13s share limited sequence similarity, hindering discovery of related or ancestral systems. To address this, we developed an automated structural-search pipeline to identify an ancestral clade of Cas13 (Cas13an) and further trace Cas13 origins to defense-associated ribonucleases. Despite being one-third the size of other Cas13s, Cas13an mediates robust programmable RNA depletion and defense against diverse bacteriophages. However, unlike its larger counterparts, Cas13an uses a single active site for both CRISPR RNA processing and RNA-guided cleavage, revealing that the ancestral nuclease domain has two modes of activity. Discovery of Cas13an deepens our understanding of CRISPR-Cas evolution and expands opportunities for precision RNA editing, showcasing the promise of structure-guided genome mining.
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