Evidence map›Paper›PMID 33905417›Full record

ArticlePloS one2021

Protection of the C. elegans germ cell genome depends on diverse DNA repair pathways during normal proliferation.

Bettina Meier, Nadezda V Volkova, Ye Hong, Simone Bertolini, Víctor González-Huici, Tsvetana Petrova, Simon Boulton, Peter J Campbell, Moritz Gerstung, Anton Gartner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

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  11. MutantCancers · 2022
    Article
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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

10 authors at 4 institutions in 3 countries.

Bettina MeierCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.ORCID 0000-0002-9227-6519
Nadezda V VolkovaEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, United Kingdom.ORCID 0000-0003-3368-3920
Ye HongCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.
Simone BertoliniCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.
Víctor González-HuiciCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.ORCID 0000-0002-6977-1060
Tsvetana PetrovaCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.ORCID 0000-0003-2425-2459
Simon BoultonFrancis Crick Institute, London, United Kingdom.
Peter J CampbellCancer, Ageing and Somatic Mutation Program, Wellcome Sanger Institute, Hinxton, United Kingdom.
Moritz GerstungEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, United Kingdom.
Anton GartnerCentre for Gene Regulation and Expression, University of Dundee, Dundee, Scotland.ORCID 0000-0003-4639-9902
University of Dundee · GBEuropean Bioinformatics Institute · GBThe Francis Crick Institute · GBUniversity of Cambridge · GB

Funding

Cancer Research UK 28990Wellcome TrustWellcome Trust RG70175Worldwide Cancer Research 18-0644
6 · The paper itself

Abstract

Maintaining genome integrity is particularly important in germ cells to ensure faithful transmission of genetic information across generations. Here we systematically describe germ cell mutagenesis in wild-type and 61 DNA repair mutants cultivated over multiple generations. ~44% of the DNA repair mutants analysed showed a >2-fold increased mutagenesis with a broad spectrum of mutational outcomes. Nucleotide excision repair deficiency led to higher base substitution rates, whereas polh-1(Polη) and rev-3(Polζ) translesion synthesis polymerase mutants resulted in 50-400 bp deletions. Signatures associated with defective homologous recombination fall into two classes: 1) brc-1/BRCA1 and rad-51/RAD51 paralog mutants showed increased mutations across all mutation classes, 2) mus-81/MUS81 and slx-1/SLX1 nuclease, and him-6/BLM, helq-1/HELQ or rtel-1/RTEL1 helicase mutants primarily accumulated structural variants. Repetitive and G-quadruplex sequence-containing loci were more frequently mutated in specific DNA repair backgrounds. Tandem duplications embedded in inverted repeats were observed in helq-1 helicase mutants, and a unique pattern of 'translocations' involving homeologous sequences occurred in rip-1 recombination mutants. atm-1/ATM checkpoint mutants harboured structural variants specifically enriched in subtelomeric regions. Interestingly, locally clustered mutagenesis was only observed for combined brc-1 and cep-1/p53 deficiency. Our study provides a global view of how different DNA repair pathways contribute to prevent germ cell mutagenesis.

Indexed as

DNA RepairGene Expression RegulationGenome, HelminthMutationAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell ProliferationChromosome MappingDeoxyribonucleasesDNA DamageDNA-Directed DNA PolymeraseDNA HelicasesDNA, HelminthDNA ReplicationEndonucleasesBRC-1 protein, C elegansCaenorhabditis elegans ProteinsDeoxyribonucleasesDNA-Directed DNA PolymeraseDNA HelicasesDNA, HelminthEndonucleasesHELQ-1 protein, C elegansHIM-6 protein, C elegansIsoenzymesMUS-81 protein, C elegansPOLH-1 protein, C elegansrad-51 protein, C elegansRad51 Recombinasercq-5 protein, C elegansSLX-1 protein, C elegansY-Family DNA Polymerases

Identifiers

PMID33905417
PMCPMC8078821
OpenAlexW3158926467

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.