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Bacteriophages suppress CRISPR–Cas immunity using RNA-based anti-CRISPRs.

Authors :
Camara-Wilpert, Sarah
Mayo-Muñoz, David
Russel, Jakob
Fagerlund, Robert D.
Madsen, Jonas S.
Fineran, Peter C.
Sørensen, Søren J.
Pinilla-Redondo, Rafael
Source :
Nature; Nov2023, Vol. 623 Issue 7987, p601-607, 7p
Publication Year :
2023

Abstract

Many bacteria use CRISPR–Cas systems to combat mobile genetic elements, such as bacteriophages and plasmids1. In turn, these invasive elements have evolved anti-CRISPR proteins to block host immunity2,3. Here we unveil a distinct type of CRISPR–Cas Inhibition strategy that is based on small non-coding RNA anti-CRISPRs (Racrs). Racrs mimic the repeats found in CRISPR arrays and are encoded in viral genomes as solitary repeat units4. We show that a prophage-encoded Racr strongly inhibits the type I-F CRISPR–Cas system by interacting specifically with Cas6f and Cas7f, resulting in the formation of an aberrant Cas subcomplex. We identified Racr candidates for almost all CRISPR–Cas types encoded by a diverse range of viruses and plasmids, often in the genetic context of other anti-CRISPR genes5. Functional testing of nine candidates spanning the two CRISPR–Cas classes confirmed their strong immune inhibitory function. Our results demonstrate that molecular mimicry of CRISPR repeats is a widespread anti-CRISPR strategy, which opens the door to potential biotechnological applications6.In response to bacterial CRISPR–Cas immunity, phages and plasmids have evolved small non-coding RNA anti-CRISPRs, known as Racrs, that sequester Cas proteins in abberrant complexes and thereby inhibit immunity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00280836
Volume :
623
Issue :
7987
Database :
Complementary Index
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
173635543
Full Text :
https://doi.org/10.1038/s41586-023-06612-5