Evidence map›Paper›PMID 36912817›Full record

ArticleThe CRISPR journal2023

Functional and Phylogenetic Diversity of Cas10 Proteins.

Tanner Wiegand, Royce Wilkinson, Andrew Santiago-Frangos, Mackenzie Lynes, Roland Hatzenpichler, Blake Wiedenheft

Abstract read
In one paragraph

Article in The CRISPR journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  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. Cat1 forms filament networks to degrade NADScience (New York, N.Y.) · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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.

Tanner WiegandDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.ORCID 0000-0002-0528-268X
Royce WilkinsonDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.
Andrew Santiago-FrangosDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.
Mackenzie LynesDepartment of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, USA.
Roland HatzenpichlerDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.
Blake WiedenheftDepartment of Microbiology and Cell Biology, Montana State University, Bozeman, Montana, USA.ORCID 0000-0001-9297-5304

Funding

Structural and functional understanding of bacterial defense and viral counter defenseR35GM134867 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI Blake A Wiedenheft · 2020 to 2026
$3.8M
Mechanisms of CRISPR-mediated immunity and applications beyond editingK99GM147842 · NIGMS · MONTANA STATE UNIVERSITY - BOZEMAN · PI SANTIAGO-FRANGOS, ANDREW · 2022 to 2023
$171k
NIGMS NIH HHS K99 GM147842NIGMS NIH HHS R35 GM134867
6 · The paper itself

Abstract

Cas10 proteins are large subunits of type III CRISPR RNA (crRNA)-guided surveillance complexes, many of which have nuclease and cyclase activities. Here, we use computational and phylogenetic methods to identify and analyze 2014 Cas10 sequences from genomic and metagenomic databases. Cas10 proteins cluster into five distinct clades that mirror previously established CRISPR-Cas subtypes. Most Cas10 proteins (85.0%) have conserved polymerase active-site motifs, while HD-nuclease domains are less well conserved (36.0%). We identify Cas10 variants that are split over multiple genes or genetically fused to nucleases activated by cyclic nucleotides (i.e., NucC) or components of toxin-antitoxin systems (i.e., AbiEii). To clarify the functional diversification of Cas10 proteins, we cloned, expressed, and purified five representatives from three phylogenetically distinct clades. None of the Cas10s are functional cyclases in isolation, and activity assays performed with polymerase domain active site mutants indicate that previously reported Cas10 DNA-polymerase activity may be a result of contamination. Collectively, this work helps clarify the phylogenetic and functional diversity of Cas10 proteins in type III CRISPR systems.

Indexed as

CRISPR-Associated ProteinsGene EditingBacterial ProteinsCRISPR-Cas SystemsPhylogenyBacterial ProteinsCRISPR-Associated Proteins

Identifiers

PMID36912817
PMCPMC10123807

What OpenQuestion holds

Textmetadata
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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.