Evidence map›Paper›PMID 21055984›Full record

ArticleMolecular cell2010

Identification of the MMS22L-TONSL complex that promotes homologous recombination.

Eris Duro, Cecilia Lundin, Katrine Ask, Luis Sanchez-Pulido, Thomas J MacArtney, Rachel Toth, Chris P Ponting, Anja Groth, Thomas Helleday, John Rouse

Open access · bronzeAbstract read
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In one paragraph

Article in Molecular cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

83 citing papers in PubMed, 118 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Eris DuroMRC Protein Phosphorylation Unit, College of Life Sciences, University of Dundee, Dundee DD1 5EH, Scotland, UK.
Cecilia Lundin
Katrine Ask
Luis Sanchez-Pulido
Thomas J MacArtney
Rachel Toth
Chris P Ponting
Anja Groth
Thomas Helleday
John Rouse
University of Oxford · GBMRC Protein Phosphorylation and Ubiquitylation Unit · GBUniversity of Copenhagen · DKUniversity of Dundee · GBGenomics (United Kingdom) · GB

Funding

Medical Research Council G0700730Medical Research Council MC_U127070192Medical Research Council MC_U137761446
6 · The paper itself

Abstract

Budding yeast Mms22 is required for homologous recombination (HR)-mediated repair of stalled or broken DNA replication forks. Here we identify a human Mms22-like protein (MMS22L) and an MMS22L-interacting protein, NFκBIL2/TONSL. Depletion of MMS22L or TONSL from human cells causes a high level of double-strand breaks (DSBs) during DNA replication. Both proteins accumulate at stressed replication forks, and depletion of MMS22L or TONSL from cells causes hypersensitivity to agents that cause S phase-associated DSBs, such as topoisomerase (TOP) inhibitors. In this light, MMS22L and TONSL are required for the HR-mediated repair of replication fork-associated DSBs. In cells depleted of either protein, DSBs induced by the TOP1 inhibitor camptothecin are resected normally, but the loading of the RAD51 recombinase is defective. Therefore, MMS22L and TONSL are required for the maintenance of genome stability when unscheduled DSBs occur in the vicinity of DNA replication forks.

Indexed as

Recombination, GeneticAmino Acid SequenceCell Cycle ProteinsCell LineCell SurvivalComputational BiologyDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA-Directed DNA PolymeraseDrug ResistanceHumansModels, BiologicalMolecular ChaperonesMolecular Sequence DataMultienzyme ComplexesMultiprotein ComplexesASF1A protein, humanASF1B protein, humanCell Cycle ProteinsDNA-Binding ProteinsDNA-Directed DNA PolymeraseMMS22L protein, humanMolecular ChaperonesMultienzyme ComplexesMultiprotein ComplexesNF-kappa BNuclear ProteinsRad51 RecombinaseReplisomesTONSL protein, human

Identifiers

PMID21055984
OpenAlexW2008529786

What OpenQuestion holds

Textmetadata
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.