RNA-mediated CRISPR-Cas13 inhibition through crRNA structural mimicry
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, <i>Listeria seeligeri</i>. 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.
Authors
- V. Hayes
- Benjamin L. Kocsis
- Ning Jia (ORCID: https://orcid.org/0000-0002-0672-454X)
- Alexander J. Meeske (ORCID: https://orcid.org/0000-0003-3878-531X)
- Mark A. Katz (ORCID: https://orcid.org/0000-0002-5532-7276)
- Juntao Zhang (ORCID: https://orcid.org/0000-0002-6871-4494)
- Yuelong Li (ORCID: https://orcid.org/0000-0001-5466-779X)
- David M. Brinkley (ORCID: https://orcid.org/0000-0002-6472-9330)
Institutions
- University of Washington (US)
- Southern University of Science and Technology (CN)
Publication Details
- Journal
- Science
- Published
- 2025-04-24
- DOI
- https://doi.org/10.1126/science.adr3656
- Citations
- 4
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 3.22