Evidence map›Paper›PMID 28059715›Full record

ArticleScience (New York, N.Y.)2017

Control of meiotic pairing and recombination by chromosomally tethered 26S proteasome.

Jasvinder S Ahuja, Rima Sandhu, Rana Mainpal, Crystal Lawson, Hanna Henley, Patricia A Hunt, Judith L Yanowitz, G Valentin Börner

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
–field-weighted citation impact
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

62 citing papers in PubMed.

  1. Article
  2. Active maintenance of meiosis-specific chromosome structures inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Ufd2p promotes efficient crossover formation by destabilizing Top2p during meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Review
  5. Article
  6. Active maintenance of meiosis-specific chromosome structures inbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Make it or break it: Protein homeostasis in the synaptonemal complex.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cells · 2023
    Article
  15. Envisioning a role for nuclear actin in prophase I spermatocytes.Frontiers in cell and developmental biology · 2023
    Review
  16. Article
  17. Article
  18. The ubiquitin-proteasome system regulates meiotic chromosome organization.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Proteasome complexes experience profound structural and functional rearrangements throughout mammalian spermatogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Jasvinder S AhujaCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University (CSU), Cleveland, OH, USA.
Rima SandhuCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University (CSU), Cleveland, OH, USA.
Rana MainpalMagee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Crystal LawsonSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, WA, USA.
Hanna HenleyCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University (CSU), Cleveland, OH, USA.
Patricia A HuntSchool of Molecular Biosciences, Center for Reproductive Biology, Washington State University, Pullman, WA, USA.
Judith L YanowitzMagee-Womens Research Institute, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
G Valentin BörnerCenter for Gene Regulation in Health and Disease and Department of Biological, Geological and Environmental Sciences, Cleveland State University (CSU), Cleveland, OH, USA. g.boerner@csuohio.edu.

Funding

Undergraduate Summer Research Supplement for 5R01GM104007-07: Characterization of a Meiotic Crossover Surveillance SystemR01GM104007 · NIGMS · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI YANOWITZ, JUDITH L · 2013 to 2021
$2.6M
Male Germline Development and Estrogenic ExposuresR01HD083177 · NICHD · WASHINGTON STATE UNIVERSITY · PI HUNT, PATRICIA · 2015 to 2019
$1.7M
Nikon A1RSI Confocal MicroscopeS10OD010381 · OD · CLEVELAND STATE UNIVERSITY · PI BARIK, SAILEN · 2012 to 2012
$591k
Control of pairing and recombination during meiosisR15GM099056 · NIGMS · CLEVELAND STATE UNIVERSITY · PI BOERNER, VALENTIN · 2011 to 2011
$284k
COELOMOCYTES IN C.ELEGANS--CELL FATE DETERMINATIONF32HD008715 · NICHD · CARNEGIE INSTITUTION OF WASHINGTON, D.C. · PI YANOWITZ, JUDITH L · 2000 to 2002
$112k
NICHD NIH HHS F32 HD008715NICHD NIH HHS R01 HD083177NIGMS NIH HHS R01 GM104007NIGMS NIH HHS R15 GM099056NIH HHS S10 OD010381
6 · The paper itself

Abstract

During meiosis, paired homologous chromosomes (homologs) become linked via the synaptonemal complex (SC) and crossovers. Crossovers mediate homolog segregation and arise from self-inflicted double-strand breaks (DSBs). Here, we identified a role for the proteasome, the multisubunit protease that degrades proteins in the nucleus and cytoplasm, in homolog juxtaposition and crossing over. Without proteasome function, homologs failed to pair and instead remained associated with nonhomologous chromosomes. Although dispensable for noncrossover formation, a functional proteasome was required for a coordinated transition that entails SC assembly between longitudinally organized chromosome axes and stable strand exchange of crossover-designated DSBs. Notably, proteolytic core and regulatory proteasome particles were recruited to chromosomes by Zip3, the ortholog of mammalian E3 ligase RNF212, and SC protein Zip1 . We conclude that proteasome functions along meiotic chromosomes are evolutionarily conserved.

Indexed as

Crossing Over, GeneticCell NucleusChromosome PairingChromosomes, FungalCysteine Proteinase InhibitorsCytoplasmDNA Breaks, Double-StrandedEvolution, MolecularLeupeptinsMeiosisNuclear ProteinsProteasome Endopeptidase ComplexProteolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSynaptonemal ComplexATP dependent 26S proteasebenzyloxycarbonylleucyl-leucyl-leucine aldehydeCysteine Proteinase InhibitorsLeupeptinsNuclear ProteinsProteasome Endopeptidase ComplexSaccharomyces cerevisiae ProteinsUbiquitin-Protein LigasesZip1 protein, S cerevisiaeZip3 protein, S cerevisiae

Identifiers

PMID28059715
PMCPMC6054871

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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.