Evidence map›Paper›PMID 12556476›Full record

ArticleMolecular and cellular biology2003

Loss of HR6B ubiquitin-conjugating activity results in damaged synaptonemal complex structure and increased crossing-over frequency during the male meiotic prophase.

Willy M Baarends, Evelyne Wassenaar, Jos W Hoogerbrugge, Gert van Cappellen, Henk P Roest, Jan Vreeburg, Marja Ooms, Jan H J Hoeijmakers, J Anton Grootegoed

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

38 citing papers in PubMed, 106 citations in OpenAlex.

  1. Article
  2. Review
  3. The role of ubiquitin-conjugating enzyme in the process of spermatogenesis.Reproductive biology and endocrinology : RB&E · 2024
    Review
  4. Review
  5. The ubiquitin-proteasome system regulates meiotic chromosome organization.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. A universal method for sequential immunofluorescent analysis of chromatin and chromatin-associated proteins on chromosome spreads.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2013
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Meiotic functions of RAD18.Journal of cell science · 2011
    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

9 authors at 2 institutions in 2 countries.

Willy M BaarendsDepartment of Reproduction and Development, Erasmus University Rotterdam, 3000 DR Rotterdam, The Netherlands. barrends@endov.fgg.eur.nl
Evelyne Wassenaar
Jos W Hoogerbrugge
Gert van Cappellen
Henk P Roest
Jan Vreeburg
Marja Ooms
Jan H J Hoeijmakers
J Anton Grootegoed
Pediatrics and Genetics · USErasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitin-conjugating enzymes HR6A and HR6B are the two mammalian homologs of Saccharomyces cerevisiae RAD6. In yeast, RAD6 plays an important role in postreplication DNA repair and in sporulation. HR6B knockout mice are viable, but spermatogenesis is markedly affected during postmeiotic steps, leading to male infertility. In the present study, increased apoptosis of HR6B knockout primary spermatocytes was detected during the first wave of spermatogenesis, indicating that HR6B performs a primary role during the meiotic prophase. Detailed analysis of HR6B knockout pachytene nuclei showed major changes in the synaptonemal complexes. These complexes were found to be longer. In addition, we often found depletion of synaptonemal complex proteins from near telomeric regions in the HR6B knockout pachytene nuclei. Finally, we detected an increased number of foci containing the mismatch DNA repair protein MLH1 in these nuclei, reflecting a remarkable and consistent increase (20 to 25%) in crossing-over frequency. The present findings reveal a specific requirement for the ubiquitin-conjugating activity of HR6B in relation to dynamic aspects of the synaptonemal complex and meiotic recombination in spermatocytes.

Indexed as

Crossing Over, GeneticMeiosisUbiquitin-Conjugating EnzymesAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell DeathDNA RepairLigasesMaleMiceMice, Inbred C57BLMice, KnockoutMutationMutL Protein Homolog 1Neoplasm ProteinsAdaptor Proteins, Signal TransducingCarrier ProteinsLigasesMlh1 protein, mouseMutL Protein Homolog 1Neoplasm ProteinsNuclear ProteinsUbe2a protein, mouseUbe2b protein, mouseUbiquitinUbiquitin-Conjugating Enzymes

Identifiers

PMID12556476
PMCPMC141135
OpenAlexW2158787911

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.