Evidence map›Paper›PMID 27170622›Full record

ArticleEMBO reports2016

High density of REC8 constrains sister chromatid axes and prevents illegitimate synaptonemal complex formation.

Ana Agostinho, Otto Manneberg, Robin van Schendel, Abrahan Hernández-Hernández, Anna Kouznetsova, Hans Blom, Hjalmar Brismar, Christer Höög

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. CpG site methylation regulates mouse Rec8 gene promoter activity.The Journal of reproduction and development · 2025
    Article
  4. Article
  5. Article
  6. Mapping separase-mediated cleavage in situ.NAR genomics and bioinformatics · 2022
    Article
  7. Ectopic expression of meiotic cohesin generates chromosome instability in cancer cell line.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Chromosome architecture and homologous recombination in meiosis.Frontiers in cell and developmental biology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Chromosome Organization in Early Meiotic Prophase.Frontiers in cell and developmental biology · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Ana AgostinhoDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden ana.agostinho@ki.se.ORCID 0000-0001-6270-7384
Otto MannebergScience for Life Laboratory, Department of Applied Physics, Royal Institute of Technology, Solna, Sweden.
Robin van SchendelDepartment of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Abrahan Hernández-HernándezDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Anna KouznetsovaDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Hans BlomScience for Life Laboratory, Department of Applied Physics, Royal Institute of Technology, Solna, Sweden.
Hjalmar BrismarScience for Life Laboratory, Department of Applied Physics, Royal Institute of Technology, Solna, Sweden.
Christer HöögDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEScience for Life Laboratory · SELeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During meiosis, cohesin complexes mediate sister chromatid cohesion (SCC), synaptonemal complex (SC) assembly and synapsis. Here, using super-resolution microscopy, we imaged sister chromatid axes in mouse meiocytes that have normal or reduced levels of cohesin complexes, assessing the relationship between localization of cohesin complexes, SCC and SC formation. We show that REC8 foci are separated from each other by a distance smaller than 15% of the total chromosome axis length in wild-type meiocytes. Reduced levels of cohesin complexes result in a local separation of sister chromatid axial elements (LSAEs), as well as illegitimate SC formation at these sites. REC8 but not RAD21 or RAD21L cohesin complexes flank sites of LSAEs, whereas RAD21 and RAD21L appear predominantly along the separated sister-chromatid axes. Based on these observations and a quantitative distribution analysis of REC8 along sister chromatid axes, we propose that the high density of randomly distributed REC8 cohesin complexes promotes SCC and prevents illegitimate SC formation.

Indexed as

Synaptonemal ComplexAnimalsCell Cycle ProteinsChromatidsChromosomal Proteins, Non-HistoneChromosome SegregationCohesinsMaleMeiosisMiceMice, KnockoutNuclear ProteinsPhosphoproteinsProtein SubunitsSister Chromatid ExchangeSpermatocytesCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsNuclear ProteinsPhosphoproteinsProtein SubunitsRec8 protein, mousecohesinmeiosissister chromatid cohesionsuper‐resolution microscopysynaptonemal complex

Identifiers

PMID27170622
PMCPMC5278604
OpenAlexW2373930832

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.