Evidence map›Paper›PMID 40928873›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

The RecBC complex protects single-stranded DNA gaps during lesion bypass.

Gaëlle Philippin, Pauline Dupaigne, Élodie Chrabaszcz, Maialen Iturralde, Mauro Modesti, Eric Le Cam, Vincent Pagès, Luisa Laureti

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Gaëlle PhilippinCancer Research Center of Marseille: Team DNA Damage and Genome Instability|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.ORCID 0000-0003-4554-8152
Pauline DupaigneGenome Integrity and Cancers, UMR 9019 CNRS, Université-Paris-Saclay, Gustave Roussy, Villejuif Cedex F-94805, France.ORCID 0000-0001-7033-4055
Élodie ChrabaszczCancer Research Center of Marseille: Team DNA Damage and Genome Instability|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.
Maialen IturraldeCancer Research Center of Marseille: Team DNA Damage and Genome Instability|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.
Mauro ModestiCancer Research Center of Marseille: Team Homologous Recombination, Non Homologous End Joining and Maintenance of Genomic Integrity|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.ORCID 0000-0002-4964-331X
Eric Le CamGenome Integrity and Cancers, UMR 9019 CNRS, Université-Paris-Saclay, Gustave Roussy, Villejuif Cedex F-94805, France.
Vincent Pagès *Cancer Research Center of Marseille: Team DNA Damage and Genome Instability|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.ORCID 0000-0002-3059-2903
Luisa Laureti *Cancer Research Center of Marseille: Team DNA Damage and Genome Instability|CNRS, Inserm, Institut Paoli-Calmettes, Aix Marseille Université, Marseille 13009, France.ORCID 0000-0002-7863-4922

Funding

Agence Nationale de la Recherche (ANR) ANR (17-CE12-0015)Fondation pour la Recherche Médicale (FRM) Equipe FRM-EQU201903007797
6 · The paper itself

Abstract

Following encounter with an unrepaired DNA lesion, replication is halted and can restart downstream of the lesion leading to the formation of a single-stranded DNA (ssDNA) gap. To complete replication, this ssDNA gap is filled in by one of the two lesion tolerance pathways: the error-prone Translesion Synthesis (TLS) or the error-free Homology Directed Gap Repair (HDGR). In the present work, we evidence a role for the RecBC complex distinct from its canonical function in homologous recombination at DNA double strand breaks. We show that upon lesion encounter RecBC (independently of its catalytic activity and of the RecD subunit) is required to protect the nascent DNA in order to promote efficient lesion bypass. In the absence of RecBC, our data indicate that the nuclease ExoI can access and degrade the nascent DNA, affecting both TLS and HDGR mechanisms. We show that the recruitment of RecBC becomes particularly important at strong blocking lesions, when postreplicative ssDNA gaps persist and are covered by the ssDNA binding proteins. This protective role of RecBC is reminiscent of the role of BRCA2 in protecting the nascent DNA in human cells, highlighting once again the evolutionary conservation of DNA replication mechanisms across all living organisms.

Indexed as

DNA RepairDNA, Single-StrandedExodeoxyribonuclease VDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA DamageDNA ReplicationEscherichia coliEscherichia coli ProteinsHumansDNA-Binding ProteinsDNA, Single-StrandedEscherichia coli ProteinsExodeoxyribonuclease VDNA damage toleranceDNA lesionRecBCsingle-stranded DNA gaptranslesion synthesis

Identifiers

PMID40928873
PMCPMC12452888

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Registered trials

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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.