Evidence map›Paper›PMID 25895170›Full record

ReviewThe FEBS journal2015

Complex elaboration: making sense of meiotic cohesin dynamics.

Susannah Rankin

Abstract readReview
In one paragraph

Review in The FEBS journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.8field-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

43 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. An integrated roadmap of European sea bass (Frontiers in cell and developmental biology · 2026
    Article
  4. Article
  5. Article
  6. Cohesin ring gates are specialized for meiotic cell division.Journal of molecular cell biology · 2025
    Article
  7. CohesinLife (Basel, Switzerland) · 2024
    Article
  8. Article
  9. Review
  10. Establishment of aBiology · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. PDS5A and PDS5B in Cohesin Function and Human Disease.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Meiotic Chromosome Dynamics in Zebrafish.Frontiers in cell and developmental biology · 2021
    Review
  19. Review
  20. Review
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

1 author at 1 institution in 1 country.

Susannah RankinProgram in Cell Cycle and Cancer Biology, Oklahoma Medical Research Foundation, OK, USA.
Oklahoma Medical Research Foundation · US

Funding

Regulation of Chromosome Cohesion during Cell Cycle ProgressionR01GM101250 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI RANKIN, SUSANNAH · 2013 to 2022
$3.2M
NIGMS NIH HHS R01 GM101250NIGMS NIH HHS R01GM101250
6 · The paper itself

Abstract

In mitotically dividing cells, the cohesin complex tethers sister chromatids, the products of DNA replication, together from the time they are generated during S phase until anaphase. Cohesion between sister chromatids ensures accurate chromosome segregation, and promotes normal gene regulation and certain kinds of DNA repair. In somatic cells, the core cohesin complex is composed of four subunits: Smc1, Smc3, Rad21 and an SA subunit. During meiotic cell divisions meiosis-specific isoforms of several of the cohesin subunits are also expressed and incorporated into distinct meiotic cohesin complexes. The relative contributions of these meiosis-specific forms of cohesin to chromosome dynamics during meiotic progression have not been fully worked out. However, the localization of these proteins during chromosome pairing and synapsis, and their unique loss-of-function phenotypes, suggest non-overlapping roles in controlling meiotic chromosome behavior. Many of the proteins that regulate cohesin function during mitosis also appear to regulate cohesin during meiosis. Here we review how cohesin contributes to meiotic chromosome dynamics, and explore similarities and differences between cohesin regulation during the mitotic cell cycle and meiotic progression. A deeper understanding of the regulation and function of cohesin in meiosis will provide important new insights into how the cohesin complex is able to promote distinct kinds of chromosome interactions under diverse conditions.

Indexed as

MeiosisCarrier ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA-Binding ProteinsDNA DamageFemaleHumansMaleNuclear ProteinsPhosphoproteinsPhosphorylationProto-Oncogene ProteinsSex CharacteristicsStructural Maintenance of Chromosome Protein 1Carrier ProteinsCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsDNA-Binding ProteinsNuclear ProteinsPDS5A protein, humanPhosphoproteinsProto-Oncogene ProteinsRAD21 protein, humanREC8 protein, humanSTAG3 protein, humanStructural Maintenance of Chromosome Protein 1WAPL protein, humancell cyclecohesin complexcohesin regulationmeiosis

Identifiers

PMID25895170
PMCPMC4490075
OpenAlexW1980549702

What OpenQuestion holds

Textmetadata
LicenceTDM
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.