Evidence map›Paper›PMID 25414342›Full record

ArticleNucleic acids research2014

Rad51/Dmc1 paralogs and mediators oppose DNA helicases to limit hybrid DNA formation and promote crossovers during meiotic recombination.

Alexander Lorenz, Alizée Mehats, Fekret Osman, Matthew C Whitby

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.The Journal of clinical endocrinology and metabolism · 2022
    Article
  6. Article
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  8. Intragenic meiotic recombination in Schizosaccharomyces pombe is sensitive to environmental temperature changes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2020
    Article
  9. DNA Helicase Mph1Developmental cell · 2020
    Article
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  11. Article
  12. Article
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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

4 authors at 1 institution in 1 country.

Alexander LorenzDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK The Institute of Medical Sciences (IMS), University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK a.lorenz@abdn.ac.uk.
Alizée MehatsDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Fekret OsmanDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Matthew C WhitbyDepartment of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK a.lorenz@abdn.ac.uk.
University of Oxford · GB

Funding

Wellcome Trust 090767/Z/09/Z
6 · The paper itself

Abstract

During meiosis programmed DNA double-strand breaks (DSBs) are repaired by homologous recombination using the sister chromatid or the homologous chromosome (homolog) as a template. This repair results in crossover (CO) and non-crossover (NCO) recombinants. Only CO formation between homologs provides the physical linkages guiding correct chromosome segregation, which are essential to produce healthy gametes. The factors that determine the CO/NCO decision are still poorly understood. Using Schizosaccharomyces pombe as a model we show that the Rad51/Dmc1-paralog complexes Rad55-Rad57 and Rdl1-Rlp1-Sws1 together with Swi5-Sfr1 play a major role in antagonizing both the FANCM-family DNA helicase/translocase Fml1 and the RecQ-type DNA helicase Rqh1 to limit hybrid DNA formation and promote Mus81-Eme1-dependent COs. A common attribute of these protein complexes is an ability to stabilize the Rad51/Dmc1 nucleoprotein filament, and we propose that it is this property that imposes constraints on which enzymes gain access to the recombination intermediate, thereby controlling the manner in which it is processed and resolved.

Indexed as

Recombination, GeneticAdenosine TriphosphatasesDNA-Binding ProteinsDNA Breaks, Double-StrandedDNA, FungalDNA HelicasesDNA RepairEndonucleasesGene DeletionMeiosisRec A RecombinasesSchizosaccharomyces pombe ProteinsAdenosine TriphosphatasesDNA-Binding ProteinsDNA, FungalDNA HelicasesEndonucleasesFml1 protein, S pombeMUS81 protein, S pombeRec A RecombinasesRHP55 protein, S pombeRhp57 protein, S pombeRlp1 protein, S pombeRqh1 protein, S pombeSchizosaccharomyces pombe ProteinsSfr1 protein, S pombeSwi5 protein, S pombeSws1 protein, S pombe

Identifiers

PMID25414342
PMCPMC4267644
OpenAlexW1965520614

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.