Evidence map›Paper›PMID 32597755›Full record

ArticleeLife2020

Tetramerisation of the CRISPR ring nuclease Crn3/Csx3 facilitates cyclic oligoadenylate cleavage.

Januka S Athukoralage, Stuart McQuarrie, Sabine Grüschow, Shirley Graham, Tracey M Gloster, Malcolm F White

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Diversity and abundance of ring nucleases in type III CRISPR-Cas loci.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Type III CRISPR-Cas: beyond the Cas10 effector complex.Trends in biochemical sciences · 2024
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Enzymatic properties of CARF-domain proteins inFrontiers in microbiology · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Januka S AthukoralageBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.ORCID 0000-0002-1666-0180
Stuart McQuarrieBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.ORCID 0000-0003-4828-4842
Sabine GrüschowBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.
Shirley GrahamBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.ORCID 0000-0002-2608-3815
Tracey M GlosterBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.ORCID 0000-0003-4692-2222
Malcolm F WhiteBiomedical Sciences Research Complex, School of Biology, University of St Andrews, St Andrews, United Kingdom.ORCID 0000-0003-1543-9342
New York State Department of Health · US

Funding

Biotechnology and Biological Sciences Research Council BB/S000313/1Biotechnology and Biological Sciences Research Council BB/T004789/1Wellcome Trust
6 · The paper itself

Abstract

Type III CRISPR systems detect foreign RNA and activate the cyclase domain of the Cas10 subunit, generating cyclic oligoadenylate (cOA) molecules that act as a second messenger to signal infection, activating nucleases that degrade the nucleic acid of both invader and host. This can lead to dormancy or cell death; to avoid this, cells need a way to remove cOA from the cell once a viral infection has been defeated. Enzymes specialised for this task are known as ring nucleases, but are limited in their distribution. Here, we demonstrate that the widespread CRISPR associated protein Csx3, previously described as an RNA deadenylase, is a ring nuclease that rapidly degrades cyclic tetra-adenylate (cA

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsArchaeoglobus fulgidusCatalysisCatalytic DomainCRISPR-Associated ProteinsEndonucleasesEscherichia coliKineticsMethanosarcinaModels, MolecularOligonucleotidesProtein MultimerizationRibonucleasesRNASecond Messenger SystemsSignal TransductionCRISPR-Associated ProteinsEndonucleasesOligonucleotidesRibonucleasesRNAarchaeoglobus fulgidusbiochemistryCARF domainchemical biologycooperative enzymeCRISPRCsx3cyclic tetra-adenylate

Identifiers

PMID32597755
PMCPMC7371418
OpenAlexW3037297286

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.