Hayes Victoria M, Zhang Jun-Tao, Katz Mark A, Li Yuelong, Kocsis Benjamin, Brinkley David M, Jia Ning, Meeske Alexander J
Department of Microbiology, University of Washington, Seattle, WA, USA.
Department of Biochemistry, SUSTech Homeostatic Medicine Institute, School of Medicine, Southern University of Science and Technology, Shenzhen, Guangdong, China.
Science. 2025 Apr 25;388(6745):387-391. doi: 10.1126/science.adr3656. Epub 2025 Apr 24.
To circumvent CRISPR-Cas immunity, phages express anti-CRISPR factors that inhibit the expression or activities of Cas proteins. Whereas most anti-CRISPRs described to date are proteins, recently described small RNAs called RNA anti-CRISPRs (rAcrs) have sequence homology to CRISPR RNAs (crRNAs) and displace them from cognate Cas nucleases. In this work, we report the discovery of rAcrVIA1-a plasmid-encoded small RNA that inhibits the RNA-targeting CRISPR-Cas13 system in its natural host, . We solved the cryo-electron microscopy structure of the Cas13-rAcr complex, which revealed that rAcrVIA1 adopts a fold nearly identical to crRNA despite sharing negligible sequence similarity. Collectively, our findings expand the diversity of rAcrs and reveal an example of immune antagonism through RNA structural mimicry.
为了规避CRISPR-Cas免疫,噬菌体表达抑制Cas蛋白表达或活性的抗CRISPR因子。虽然迄今为止描述的大多数抗CRISPR都是蛋白质,但最近描述的称为RNA抗CRISPR(rAcrs)的小RNA与CRISPR RNA(crRNAs)具有序列同源性,并将它们从同源Cas核酸酶中置换出来。在这项工作中,我们报告了rAcrVIA1的发现——一种质粒编码的小RNA,它在其天然宿主中抑制靶向RNA的CRISPR-Cas13系统。我们解析了Cas13-rAcr复合物的冷冻电子显微镜结构,结果表明rAcrVIA1尽管序列相似性可忽略不计,但仍采用了与crRNA几乎相同的折叠方式。总的来说,我们的发现扩展了rAcrs的多样性,并揭示了通过RNA结构模拟进行免疫拮抗的一个例子。