Evidence map›Paper›PMID 29507349›Full record

ArticleNature microbiology2018

Anti-CRISPR proteins encoded by archaeal lytic viruses inhibit subtype I-D immunity.

Fei He, Yuvaraj Bhoobalan-Chitty, Lan B Van, Anders L Kjeldsen, Matteo Dedola, Kira S Makarova, Eugene V Koonin, Ditlev E Brodersen, Xu Peng

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
8.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

80 citing papers in PubMed, 139 citations in OpenAlex.

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  11. Newly Established Genetic System for Functional Analysis of MetSV.International journal of molecular sciences · 2023
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Mechanisms regulating the CRISPR-Cas systems.Frontiers in microbiology · 2023
    Review
  18. Review
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Fei HeDanish Archaea Centre, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Yuvaraj Bhoobalan-ChittyDanish Archaea Centre, Department of Biology, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-8104-7657
Lan B VanCentre for Bacterial Stress Response and Persistence, Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Anders L KjeldsenDanish Archaea Centre, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Matteo DedolaDanish Archaea Centre, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Kira S MakarovaNational Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD, USA.
Eugene V KooninNational Center for Biotechnology Information, National Library of Medicine, NIH, Bethesda, MD, USA.ORCID 0000-0003-3943-8299
Ditlev E BrodersenCentre for Bacterial Stress Response and Persistence, Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-5413-4667
Xu PengDanish Archaea Centre, Department of Biology, University of Copenhagen, Copenhagen, Denmark. peng@bio.ku.dk.ORCID 0000-0003-3926-7514
University of Copenhagen · DKAarhus University · DKNational Center for Biotechnology Information · US

Funding

Comparative Analysis Of Completely Sequenced GenomesZIALM000073 · NLM · NATIONAL LIBRARY OF MEDICINE · PI KOONIN, EUGENE V · 2009 to 2025
$43.1M
Finding Protein Sequence Motifs--Methods And ApplicationsZIALM000061 · NLM · NATIONAL LIBRARY OF MEDICINE · PI KOONIN, EUGENE V · 2009 to 2025
$10.6M
Intramural NIH HHS ZIA LM000073
6 · The paper itself

Abstract

Viruses employ a range of strategies to counteract the prokaryotic adaptive immune system, clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas), including mutational escape and physical blocking of enzymatic function using anti-CRISPR proteins (Acrs). Acrs have been found in many bacteriophages but so far not in archaeal viruses, despite the near ubiquity of CRISPR-Cas systems in archaea. Here, we report the functional and structural characterization of two archaeal Acrs from the lytic rudiviruses, SIRV2 and SIRV3. We show that a 4 kb deletion in the SIRV2 genome dramatically reduces infectivity in Sulfolobus islandicus LAL14/1 that carries functional CRISPR-Cas subtypes I-A, I-D and III-B. Subsequent insertion of a single gene from SIRV3, gp02 (AcrID1), which is conserved in the deleted fragment, successfully restored infectivity. We demonstrate that AcrID1 protein inhibits the CRISPR-Cas subtype I-D system by interacting directly with Cas10d protein, which is required for the interference stage. Sequence and structural analysis of AcrID1 show that it belongs to a conserved family of compact, dimeric αβ-sandwich proteins characterized by extreme pH and temperature stability and a tendency to form protein fibres. We identify about 50 homologues of AcrID1 in four archaeal viral families demonstrating the broad distribution of this group of anti-CRISPR proteins.

Indexed as

CRISPR-Associated ProteinsCRISPR-Cas SystemsRepressor ProteinsRudiviridaeSulfolobusCRISPR-Associated ProteinsRepressor Proteins

Identifiers

PMID29507349
PMCPMC11249088
OpenAlexW2789786861

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.