Evidence map›Paper›PMID 27010650›Full record

ArticlePLoS genetics2016

The SMC-5/6 Complex and the HIM-6 (BLM) Helicase Synergistically Promote Meiotic Recombination Intermediate Processing and Chromosome Maturation during Caenorhabditis elegans Meiosis.

Ye Hong, Remi Sonneville, Ana Agostinho, Bettina Meier, Bin Wang, J Julian Blow, Anton Gartner

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  7. Review
  8. Loss of NSE-4 Perturbs Genome Stability and DNA Repair inInternational journal of molecular sciences · 2022
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  12. Article
  13. BRCA1 and BRCA2 Tumor Suppressor Function in Meiosis.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. A Role forCells · 2020
    Article
  16. Article
  17. Frontiers in plant science · 2019
    Article
  18. Article
  19. Article
  20. Article
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

7 authors at 1 institution in 1 country.

Ye HongCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
Remi SonnevilleCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
Ana AgostinhoCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
Bettina MeierCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
Bin WangCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
J Julian BlowCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
Anton GartnerCentre for Gene Regulation and Expression, University of Dundee, Dundee, United Kingdom.
University of Dundee · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J015199/1Cancer Research UK 14301Cancer Research UK C303/A14301Cancer Research UK C303/A7399Wellcome TrustWellcome Trust 090944/Z/09/Z
6 · The paper itself

Abstract

Meiotic recombination is essential for the repair of programmed double strand breaks (DSBs) to generate crossovers (COs) during meiosis. The efficient processing of meiotic recombination intermediates not only needs various resolvases but also requires proper meiotic chromosome structure. The Smc5/6 complex belongs to the structural maintenance of chromosome (SMC) family and is closely related to cohesin and condensin. Although the Smc5/6 complex has been implicated in the processing of recombination intermediates during meiosis, it is not known how Smc5/6 controls meiotic DSB repair. Here, using Caenorhabditis elegans we show that the SMC-5/6 complex acts synergistically with HIM-6, an ortholog of the human Bloom syndrome helicase (BLM) during meiotic recombination. The concerted action of the SMC-5/6 complex and HIM-6 is important for processing recombination intermediates, CO regulation and bivalent maturation. Careful examination of meiotic chromosomal morphology reveals an accumulation of inter-chromosomal bridges in smc-5; him-6 double mutants, leading to compromised chromosome segregation during meiotic cell divisions. Interestingly, we found that the lethality of smc-5; him-6 can be rescued by loss of the conserved BRCA1 ortholog BRC-1. Furthermore, the combined deletion of smc-5 and him-6 leads to an irregular distribution of condensin and to chromosome decondensation defects reminiscent of condensin depletion. Lethality conferred by condensin depletion can also be rescued by BRC-1 depletion. Our results suggest that SMC-5/6 and HIM-6 can synergistically regulate recombination intermediate metabolism and suppress ectopic recombination by controlling chromosome architecture during meiosis.

Indexed as

Recombination, GeneticAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsChromosomesHumansMeiosisMultiprotein ComplexesBRC-1 protein, C elegansCaenorhabditis elegans ProteinsCell Cycle ProteinsHIM-6 protein, C elegansMultiprotein ComplexesSMC-5 protein, C elegansSMC-6 protein, C elegans

Identifiers

PMID27010650
PMCPMC4807058
OpenAlexW2303717154

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.