Molecular basis for inhibition of type III-B CRISPR-Cas by an archaeal viral anti-CRISPR protein

Cell Host Microbe. 2023 Nov 8;31(11):1837-1849.e5. doi: 10.1016/j.chom.2023.10.003. Epub 2023 Oct 30.

Abstract

Despite a wide presence of type III clustered regularly interspaced short palindromic repeats, CRISPR-associated (CRISPR-Cas) in archaea and bacteria, very few anti-CRISPR (Acr) proteins inhibiting type III immunity have been identified, and even less is known about their inhibition mechanism. Here, we present the discovery of a type III CRISPR-Cas inhibitor, AcrIIIB2, encoded by Sulfolobus virus S. islandicus rod-shaped virus 3 (SIRV3). AcrIIIB2 inhibits type III-B CRISPR-Cas immune response to protospacers encoded in middle/late-expressed viral genes. Investigation of the interactions between S. islandicus type III-B CRISPR-Cas Cmr-α-related proteins and AcrIIIB2 reveals that the Acr does not bind to Csx1 but rather interacts with the Cmr-α effector complex. Furthermore, in vitro assays demonstrate that AcrIIIB2 can block the dissociation of cleaved target RNA from the Cmr-α complex, thereby inhibiting the Cmr-α turnover, thus preventing host cellular dormancy and further viral genome degradation by the type III-B CRISPR-Cas immunity.

Keywords: Acr inhibition mechanism; CRISPR-Cas turnover; anti-CRISPR; type III CRISPR.

MeSH terms

  • Archaea / metabolism
  • Archaeal Viruses* / metabolism
  • CRISPR-Associated Proteins* / genetics
  • CRISPR-Cas Systems
  • Viral Proteins / genetics

Substances

  • Viral Proteins
  • CRISPR-Associated Proteins