Evidence map›Paper›PMID 34301885›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Arrest of WNT/β-catenin signaling enables the transition from pluripotent to differentiated germ cells in mouse ovaries.

Morgane Le Rolle, Filippo Massa, Pam Siggers, Laurent Turchi, Agnès Loubat, Bon-Kyoung Koo, Hans Clevers, Andy Greenfield, Andreas Schedl, Marie-Christine Chaboissier and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. eLife · 2023
    Article
  13. Cell cycle regulation for meiosis in mammalian germ cells.The Journal of reproduction and development · 2023
    Review
  14. Current progress onFrontiers in cell and developmental biology · 2023
    Review
  15. Article
  16. Review
  17. Early Gonadal Development and Sex Determination in Mammal.International journal of molecular sciences · 2022
    Review
  18. 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

11 authors at 4 institutions in 4 countries.

Morgane Le RolleCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.ORCID 0000-0002-9720-8320
Filippo MassaCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.ORCID 0000-0003-1362-1239
Pam SiggersMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, United Kingdom.
Laurent TurchiCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.ORCID 0000-0003-2020-5831
Agnès LoubatCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.
Bon-Kyoung KooHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, 3584 CT Utrecht, The Netherlands.
Hans CleversHubrecht Institute, Royal Netherlands Academy of Arts and Sciences, 3584 CT Utrecht, The Netherlands.ORCID 0000-0002-3077-5582
Andy GreenfieldMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, United Kingdom.ORCID 0000-0002-1477-1776
Andreas SchedlCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.ORCID 0000-0001-9380-7396
Marie-Christine ChaboissierCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France.ORCID 0000-0003-0934-8217
Anne-Amandine ChassotCNRS, Inserm, Institut de Biologie Valrose, Université Côte d'Azur, Parc Valrose, 06108 Nice Cedex 2, France; Amandine.CHASSOT@univ-cotedazur.fr.ORCID 0000-0003-1242-9456
Centre National de la Recherche Scientifique · FRMary Lyon Centre at MRC Harwell · GBInstitute of Molecular Biotechnology · ATRoyal Netherlands Academy of Arts and Sciences · NL

Funding

Medical Research Council MC_U142684167
6 · The paper itself

Abstract

Germ cells form the basis for sexual reproduction by producing gametes. In ovaries, primordial germ cells exit the cell cycle and the pluripotency-associated state, differentiate into oogonia, and initiate meiosis. Despite the importance of germ cell differentiation for sexual reproduction, signaling pathways regulating their fate remain largely unknown. Here, we show in mouse embryonic ovaries that germ cell-intrinsic β-catenin activity maintains pluripotency and that its repression is essential to allow differentiation and meiosis entry in a timely manner. Accordingly, in β-catenin loss-of-function and gain-of-function mouse models, the germ cells precociously enter meiosis or remain in the pluripotent state, respectively. We further show that interaction of β-catenin and the pluripotent-associated factor POU5F1 in the nucleus is associated with germ cell pluripotency. The exit of this complex from the nucleus correlates with germ cell differentiation, a process promoted by the up-regulation of

Indexed as

Cell DifferentiationAnimalsbeta CateninFemaleGerm CellsMiceMice, Inbred C57BLOctamer Transcription Factor-3Pluripotent Stem CellsWnt Proteinsbeta CateninCTNNB1 protein, mouseOctamer Transcription Factor-3Pou5f1 protein, mouseWnt Proteinsdifferentiationgerm cellsovaryPOU5F1/OCT4WNT/β-catenin

Identifiers

PMID34301885
PMCPMC8325354
OpenAlexW3184069708

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.