Evidence map›Paper›PMID 24076219›Full record

ArticleMolecular cell2013

Cooperative control of holliday junction resolution and DNA repair by the SLX1 and MUS81-EME1 nucleases.

Dennis Castor, Nidhi Nair, Anne-Cécile Déclais, Christophe Lachaud, Rachel Toth, Thomas J Macartney, David M J Lilley, J Simon C Arthur, John Rouse

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
10.8field-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

106 citing papers in PubMed, 147 citations in OpenAlex.

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  20. Coordinated roles of SLX4 and MutSβ in DNA repair and the maintenance of genome stability.Critical reviews in biochemistry and molecular biology · 2021
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Dennis CastorMRC Protein Phosphorylation and Ubiquitylation Unit, College of Life Sciences, University of Dundee, Dundee DD1 5EH, Scotland, UK.
Nidhi Nair
Anne-Cécile Déclais
Christophe Lachaud
Rachel Toth
Thomas J Macartney
David M J Lilley
J Simon C Arthur
John Rouse
University of Dundee · GBMRC Protein Phosphorylation and Ubiquitylation Unit · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E001777/1Cancer Research UK 11722Medical Research Council MC_U127070192Medical Research Council MC_UU_12016/1
6 · The paper itself

Abstract

Holliday junctions (HJs) are X-shaped DNA structures that arise during homologous recombination, which must be removed to enable chromosome segregation. The SLX1 and MUS81-EME1 nucleases can both process HJs in vitro, and they bind in close proximity on the SLX4 scaffold, hinting at possible cooperation. However, the cellular roles of mammalian SLX1 are not yet known. Here, we use mouse genetics and structure function analysis to investigate SLX1 function. Disrupting the murine Slx1 and Slx4 genes revealed that they are essential for HJ resolution in mitotic cells. Moreover, SLX1 and MUS81-EME1 act together to resolve HJs in a manner that requires tethering to SLX4. We also show that SLX1, like MUS81-EME1, is required for repair of DNA interstrand crosslinks, but this role appears to be independent of HJ cleavage, at least in mouse cells. These findings shed light on HJ resolution in mammals and on maintenance of genome stability.

Indexed as

DNA, CruciformDNA RepairAmino Acid SequenceAnimalsBase SequenceBlotting, WesternCells, CulturedDNADNA-Binding ProteinsEmbryo, MammalianEndodeoxyribonucleasesEndonucleasesFibroblastsHEK293 CellsHumansMiceDNADNA-Binding ProteinsDNA, CruciformEme1 protein, mouseEndodeoxyribonucleasesEndonucleasesMus81 protein, mouseRecombinasesSLX1 protein, mouseSlx4 protein, mouse

Identifiers

PMID24076219
PMCPMC3808987
OpenAlexW1980830652

What OpenQuestion holds

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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.