Evidence map›Paper›PMID 33901174›Full record

ArticlePLoS genetics2021

Aurora kinase A is essential for meiosis in mouse oocytes.

Cecilia S Blengini, Patricia Ibrahimian, Michaela Vaskovicova, David Drutovic, Petr Solc, Karen Schindler

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2021. 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
6.4field-weighted citation impact, top 2% 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, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

6 authors at 2 institutions in 2 countries.

Cecilia S BlenginiDepartment of Genetics; Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.ORCID 0000-0003-2978-0955
Patricia IbrahimianDepartment of Genetics; Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.ORCID 0000-0003-4040-9639
Michaela VaskovicovaInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.ORCID 0000-0003-4928-5732
David DrutovicInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.ORCID 0000-0001-7099-3042
Petr SolcInstitute of Animal Physiology and Genetics of the Czech Academy of Sciences, Libechov, Czech Republic.ORCID 0000-0003-4571-3891
Karen SchindlerDepartment of Genetics; Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.ORCID 0000-0001-6113-1184
Czech Academy of Sciences, Institute of Animal Physiology and Genetics · CZRutgers, The State University of New Jersey · US

Funding

Signaling Mechanisms that Control Chromosome Segregation during Female Meiosis (Equipment Administrative Supplement)R35GM136340 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI Karen A Schindler · 2020 to 2026
$3.1M
Control of mammalian meiosis I through protein kinase signalingR01GM112801 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI SCHINDLER, KAREN A · 2015 to 2019
$1.9M
NIGMS NIH HHS R01 GM112801NIGMS NIH HHS R35 GM136340
6 · The paper itself

Abstract

The Aurora protein kinases are well-established regulators of spindle building and chromosome segregation in mitotic and meiotic cells. In mouse oocytes, there is significant Aurora kinase A (AURKA) compensatory abilities when the other Aurora kinase homologs are deleted. Whether the other homologs, AURKB or AURKC can compensate for loss of AURKA is not known. Using a conditional mouse oocyte knockout model, we demonstrate that this compensation is not reciprocal because female oocyte-specific knockout mice are sterile, and their oocytes fail to complete meiosis I. In determining AURKA-specific functions, we demonstrate that its first meiotic requirement is to activate Polo-like kinase 1 at acentriolar microtubule organizing centers (aMTOCs; meiotic spindle poles). This activation induces fragmentation of the aMTOCs, a step essential for building a bipolar spindle. We also show that AURKA is required for regulating localization of TACC3, another protein required for spindle building. We conclude that AURKA has multiple functions essential to completing MI that are distinct from AURKB and AURKC.

Indexed as

AnimalsAurora Kinase AAurora Kinase BAurora Kinase CCell Cycle ProteinsCell Nucleus DivisionChromosome SegregationFemaleFetal ProteinsGene Expression Regulation, DevelopmentalHumansMeiosisMiceMicrotubule-Associated ProteinsMicrotubule-Organizing CenterOocytesAurkb protein, mouseAurkc protein, mouseAurora Kinase AAurora Kinase BAurora Kinase CCell Cycle ProteinsFetal ProteinsMicrotubule-Associated ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTACC3 protein, mouse

Identifiers

PMID33901174
PMCPMC8102010
OpenAlexW3159672342

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.