Regulatory sequence-based discovery of anti-defense genes in archaeal viruses.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
02 May 2024
Historique:
received: 06 09 2023
accepted: 19 04 2024
medline: 3 5 2024
pubmed: 3 5 2024
entrez: 2 5 2024
Statut: epublish

Résumé

In silico identification of viral anti-CRISPR proteins (Acrs) has relied largely on the guilt-by-association method using known Acrs or anti-CRISPR associated proteins (Acas) as the bait. However, the low number and limited spread of the characterized archaeal Acrs and Aca hinders our ability to identify Acrs using guilt-by-association. Here, based on the observation that the few characterized archaeal Acrs and Aca are transcribed immediately post viral infection, we hypothesize that these genes, and many other unidentified anti-defense genes (ADG), are under the control of conserved regulatory sequences including a strong promoter, which can be used to predict anti-defense genes in archaeal viruses. Using this consensus sequence based method, we identify 354 potential ADGs in 57 archaeal viruses and 6 metagenome-assembled genomes. Experimental validation identified a CRISPR subtype I-A inhibitor and the first virally encoded inhibitor of an archaeal toxin-antitoxin based immune system. We also identify regulatory proteins potentially akin to Acas that can facilitate further identification of ADGs combined with the guilt-by-association approach. These results demonstrate the potential of regulatory sequence analysis for extensive identification of ADGs in viruses of archaea and bacteria.

Identifiants

pubmed: 38698035
doi: 10.1038/s41467-024-48074-x
pii: 10.1038/s41467-024-48074-x
doi:

Substances chimiques

Viral Proteins 0
Archaeal Proteins 0
CRISPR-Associated Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

3699

Subventions

Organisme : Novo Nordisk Fonden (Novo Nordisk Foundation)
ID : NNF21OC0067491
Organisme : Novo Nordisk Fonden (Novo Nordisk Foundation)
ID : NNF17OC0031154
Organisme : Det Frie Forskningsråd (Danish Council for Independent Research)
ID : DFF-0135-00402

Informations de copyright

© 2024. The Author(s).

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Auteurs

Yuvaraj Bhoobalan-Chitty (Y)

Department of Biology, University of Copenhagen, Copenhagen N, Denmark. yuvarajb@bio.ku.dk.

Shuanshuan Xu (S)

Department of Biology, University of Copenhagen, Copenhagen N, Denmark.

Laura Martinez-Alvarez (L)

Department of Biology, University of Copenhagen, Copenhagen N, Denmark.

Svetlana Karamycheva (S)

National Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD, USA.

Kira S Makarova (KS)

National Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD, USA.

Eugene V Koonin (EV)

National Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD, USA.

Xu Peng (X)

Department of Biology, University of Copenhagen, Copenhagen N, Denmark. peng@bio.ku.dk.

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