Evidence map›Paper›PMID 28516917›Full record

ArticleNature communications2017

Maternal age-dependent APC/C-mediated decrease in securin causes premature sister chromatid separation in meiosis II.

Ibtissem Nabti, Rosanna Grimes, Hema Sarna, Petros Marangos, John Carroll

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
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  9. Review
  10. Article
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  12. Separase and Roads to Disengage Sister Chromatids during Anaphase.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Oocyte aging: looking beyond chromosome segregation errors.Journal of assisted reproduction and genetics · 2022
    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

5 authors at 3 institutions in 4 countries.

Ibtissem NabtiDevelopment and Stem Cells Program, Department of Anatomy and Developmental Biology, Monash Biomedicine Discovery Institute, Monash University, Melbourne, VIC 3800, Australia.
Rosanna GrimesDivision of Biosciences, Department of Cell and Developmental Biology, University College London, London WC1E 6BT, UK.
Hema SarnaDivision of Biosciences, Department of Cell and Developmental Biology, University College London, London WC1E 6BT, UK.
Petros MarangosDivision of Biosciences, Department of Cell and Developmental Biology, University College London, London WC1E 6BT, UK.
John CarrollDevelopment and Stem Cells Program, Department of Anatomy and Developmental Biology, Monash Biomedicine Discovery Institute, Monash University, Melbourne, VIC 3800, Australia.
University College London · GBMonash University · AUUniversity of Ioannina · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sister chromatid attachment during meiosis II (MII) is maintained by securin-mediated inhibition of separase. In maternal ageing, oocytes show increased inter-sister kinetochore distance and premature sister chromatid separation (PSCS), suggesting aberrant separase activity. Here, we find that MII oocytes from aged mice have less securin than oocytes from young mice and that this reduction is mediated by increased destruction by the anaphase promoting complex/cyclosome (APC/C) during meiosis I (MI) exit. Inhibition of the spindle assembly checkpoint (SAC) kinase, Mps1, during MI exit in young oocytes replicates this phenotype. Further, over-expression of securin or Mps1 protects against the age-related increase in inter-sister kinetochore distance and PSCS. These findings show that maternal ageing compromises the oocyte SAC-APC/C axis leading to a decrease in securin that ultimately causes sister chromatid cohesion loss. Manipulating this axis and/or increasing securin may provide novel therapeutic approaches to alleviating the risk of oocyte aneuploidy in maternal ageing.

Indexed as

MeiosisAnaphase-Promoting Complex-CyclosomeAnimalsChromatidsChromosome SegregationFemaleGene Expression RegulationKinetochoresMaternal AgeMiceM Phase Cell Cycle CheckpointsOocytesPhenotypeProtein Serine-Threonine KinasesSecurinSeparaseAnaphase-Promoting Complex-CyclosomeProtein Serine-Threonine KinasesPTTG1 protein, mouseSecurinSeparaseTtk protein, mouse

Identifiers

PMID28516917
PMCPMC5454377
OpenAlexW2616610686

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.