Evidence map›Paper›PMID 28757209›Full record

ArticleMolecular cell2017

Smarcal1-Mediated Fork Reversal Triggers Mre11-Dependent Degradation of Nascent DNA in the Absence of Brca2 and Stable Rad51 Nucleofilaments.

Arun Mouli Kolinjivadi, Vincenzo Sannino, Anna De Antoni, Karina Zadorozhny, Mairi Kilkenny, Hervé Técher, Giorgio Baldi, Rong Shen, Alberto Ciccia, Luca Pellegrini and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 270 papers.

0numbers the graph read from it
0cells of the map it votes in
270citing papers in PubMed
15.8field-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

270 citing papers in PubMed, 369 citations in OpenAlex.

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

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

12 authors at 5 institutions in 4 countries.

Arun Mouli KolinjivadiDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy.
Vincenzo SanninoDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy.
Anna De AntoniDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy.
Karina ZadorozhnyDepartment of Biology, Masaryk University, Brno 625 00, Czech Republic.
Mairi KilkennyDepartment of Biochemistry, Tennis Court Road, University of Cambridge, Cambridge CB2 1GA, UK.
Hervé TécherDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy.
Giorgio BaldiDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy.
Rong ShenDepartment of Biochemistry, Tennis Court Road, University of Cambridge, Cambridge CB2 1GA, UK.
Alberto CicciaDepartment of Genetics and Development, Columbia University Irving Medical Center, New York, NY 10032, USA.
Luca PellegriniDepartment of Biochemistry, Tennis Court Road, University of Cambridge, Cambridge CB2 1GA, UK. Electronic address: lp212@cam.ac.uk.
Lumir KrejciDepartment of Biology, Masaryk University, Brno 625 00, Czech Republic; National Centre for Biomolecular Research, Masaryk University, Brno 625 00, Czech Republic; International Clinical Research Center, St. Anne's University Hospital, Brno 656 91, Czech Republic. Electronic address: lkrejci@chemi.muni.cz.
Vincenzo CostanzoDNA Metabolism Laboratory, IFOM, FIRC Institute for Molecular Oncology, 20139 Milan, Italy. Electronic address: vincenzo.costanzo@ifom.eu.
FIRC Institute of Molecular Oncology · ITUniversity of Cambridge · GBColumbia University Irving Medical Center · USMasaryk University · CZUniversity Hospital Brno · CZ

Funding

Replication fork remodeling and genomic stabilityR01CA197774 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Alberto Ciccia · 2016 to 2026
$4.2M
NCI NIH HHS R01 CA197774Wellcome Trust
6 · The paper itself

Abstract

Brca2 deficiency causes Mre11-dependent degradation of nascent DNA at stalled forks, leading to cell lethality. To understand the molecular mechanisms underlying this process, we isolated Xenopus laevis Brca2. We demonstrated that Brca2 protein prevents single-stranded DNA gap accumulation at replication fork junctions and behind them by promoting Rad51 binding to replicating DNA. Without Brca2, forks with persistent gaps are converted by Smarcal1 into reversed forks, triggering extensive Mre11-dependent nascent DNA degradation. Stable Rad51 nucleofilaments, but not RPA or Rad51

Indexed as

DNA ReplicationAnimalsBinding SitesBRCA2 ProteinDNADNA-Binding ProteinsDNA HelicasesDNA Polymerase IDNA Polymerase IIIEndodeoxyribonucleasesExodeoxyribonucleasesFemaleGenomic InstabilityHumansMaleMRE11 Homologue ProteinBRCA2 ProteinDNADNA-Binding ProteinsDNA HelicasesDNA Polymerase IDNA Polymerase IIIEndodeoxyribonucleasesExodeoxyribonucleasesMRE11 Homologue ProteinMRE11 protein, humanMRE11 protein, S cerevisiaeRAD51 protein, humanRAD51 protein, XenopusRad51 RecombinaseSaccharomyces cerevisiae ProteinsSMARCAL1 protein, humanXenopus ProteinsBrca2DNA replicationfork protectionMre11Rad51Xenopus laevis

Identifiers

PMID28757209
PMCPMC5594205
OpenAlexW2737658553

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.