Evidence map›Paper›PMID 25637499›Full record

ArticleEMBO reports2015

Escape of Sgs1 from Rad9 inhibition reduces the requirement for Sae2 and functional MRX in DNA end resection.

Diego Bonetti, Matteo Villa, Elisa Gobbini, Corinne Cassani, Giulia Tedeschi, Maria Pia Longhese

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 68 citations in OpenAlex.

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  17. CtIP promotes the motor activity of DNA2 to accelerate long-range DNA end resection.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

6 authors at 1 institution in 1 country.

Diego BonettiDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy.
Matteo VillaDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy.
Elisa GobbiniDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy.
Corinne CassaniDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy.
Giulia TedeschiDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy.
Maria Pia LongheseDipartimento di Biotecnologie e Bioscienze, Università di Milano-Bicocca, Milan, Italy mariapia.longhese@unimib.it.
University of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homologous recombination requires nucleolytic degradation (resection) of DNA double-strand break (DSB) ends. In Saccharomyces cerevisiae, the MRX complex and Sae2 are involved in the onset of DSB resection, whereas extensive resection requires Exo1 and the concerted action of Dna2 and Sgs1. Here, we show that the checkpoint protein Rad9 limits the action of Sgs1/Dna2 in DSB resection by inhibiting Sgs1 binding/persistence at the DSB ends. When inhibition by Rad9 is abolished by the Sgs1-ss mutant variant or by deletion of RAD9, the requirement for Sae2 and functional MRX in DSB resection is reduced. These results provide new insights into how early and long-range resection is coordinated.

Indexed as

Cell Cycle ProteinsDNA-Binding ProteinsEndodeoxyribonucleasesEndonucleasesExodeoxyribonucleasesModels, BiologicalMultiprotein ComplexesRecombinational DNA RepairRecQ HelicasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCell Cycle ProteinsDNA-Binding ProteinsEndodeoxyribonucleasesEndonucleasesExodeoxyribonucleasesMRE11 protein, S cerevisiaeMultiprotein ComplexesRAD50 protein, S cerevisiaerad9 proteinRecQ HelicasesSaccharomyces cerevisiae ProteinsSAE2 protein, S cerevisiaeSGS1 protein, S cerevisiaeXRS2 protein, S cerevisiaedouble‐strand breakRad9resectionSaccharomyces cerevisiaeSgs1

Identifiers

PMID25637499
PMCPMC4364874
OpenAlexW2141959693

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.