Evidence map›Paper›PMID 23874232›Full record

ArticlePLoS genetics2013

The cohesion protein SOLO associates with SMC1 and is required for synapsis, recombination, homolog bias and cohesion and pairing of centromeres in Drosophila Meiosis.

Rihui Yan, Bruce D McKee

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Structure and function of the synaptonemal complex.The Journal of cell biology · 2026
    Review
  2. The deubiquitinase Usp7 inProceedings of the National Academy of Sciences of the United States of America · 2024
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  3. Article
  4. Review
  5. Review
  6. Article
  7. A Brief History ofGenes · 2022
    Review
  8. Article
  9. Molecular basis of reproductive senescence: insights from model organisms.Journal of assisted reproduction and genetics · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Article
  16. Article
  17. The cohesin complex in mammalian meiosis.Genes to cells : devoted to molecular & cellular mechanisms · 2019
    Review
  18. Article
  19. Review
  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

2 authors at 1 institution in 1 country.

Rihui YanDepartment of Biochemistry, Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee, USA.
Bruce D McKee
University of Tennessee at Knoxville · US

Funding

STIMULATION OF CHROMOSOME PAIRING AND EXCHANGE BY RDNAR01GM040489 · NIGMS · UNIVERSITY OF WISCONSIN EAU CLAIRE · PI MCKEE, BRUCE D. · 1988 to 2017
$4.0M
NIGMS NIH HHS R01 GM040489NIGMS NIH HHS R01 GM40489
6 · The paper itself

Abstract

Cohesion between sister chromatids is mediated by cohesin and is essential for proper meiotic segregation of both sister chromatids and homologs. solo encodes a Drosophila meiosis-specific cohesion protein with no apparent sequence homology to cohesins that is required in male meiosis for centromere cohesion, proper orientation of sister centromeres and centromere enrichment of the cohesin subunit SMC1. In this study, we show that solo is involved in multiple aspects of meiosis in female Drosophila. Null mutations in solo caused the following phenotypes: 1) high frequencies of homolog and sister chromatid nondisjunction (NDJ) and sharply reduced frequencies of homolog exchange; 2) reduced transmission of a ring-X chromosome, an indicator of elevated frequencies of sister chromatid exchange (SCE); 3) premature loss of centromere pairing and cohesion during prophase I, as indicated by elevated foci counts of the centromere protein CID; 4) instability of the lateral elements (LE)s and central regions of synaptonemal complexes (SCs), as indicated by fragmented and spotty staining of the chromosome core/LE component SMC1 and the transverse filament protein C(3)G, respectively, at all stages of pachytene. SOLO and SMC1 are both enriched on centromeres throughout prophase I, co-align along the lateral elements of SCs and reciprocally co-immunoprecipitate from ovarian protein extracts. Our studies demonstrate that SOLO is closely associated with meiotic cohesin and required both for enrichment of cohesin on centromeres and stable assembly of cohesin into chromosome cores. These events underlie and are required for stable cohesion of centromeres, synapsis of homologous chromosomes, and a recombination mechanism that suppresses SCE to preferentially generate homolog crossovers (homolog bias). We propose that SOLO is a subunit of a specialized meiotic cohesin complex that mediates both centromeric and axial arm cohesion and promotes homolog bias as a component of chromosome cores.

Indexed as

AnimalsCell Cycle ProteinsCentromereChromosomal Proteins, Non-HistoneChromosomesChromosome SegregationDrosophilaDrosophila ProteinsFemaleMaleMeiosisRecombination, GeneticSister Chromatid ExchangeStructural Maintenance of Chromosome Protein 1Synaptonemal ComplexCell Cycle ProteinsChromosomal Proteins, Non-HistoneDrosophila Proteinssolo protein, DrosophilaStructural Maintenance of Chromosome Protein 1

Identifiers

PMID23874232
PMCPMC3715423
OpenAlexW2078523916

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LicenceCC BY
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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.