Evidence map›Paper›PMID 35613264›Full record

ArticleScience advances2022

Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad.

Chloé Mayère, Violaine Regard, Aitana Perea-Gomez, Corey Bunce, Yasmine Neirijnck, Cyril Djari, Natividad Bellido-Carreras, Pauline Sararols, Richard Reeves, Simon Greenaway and 14 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
17.6field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  3. Spatiotemporally primed coelomic epithelium and supporting-like cells establish the dual origin of granulosa cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Characterization of Forkhead Box Transcription Factor (Animals : an open access journal from MDPI · 2026
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  14. Ovarian-Specific FOXL2 Protein Expression in Testes from Patients with Complete Androgen Insensitivity Syndrome and Undescended Testes.Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation · 2026
    Article
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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

24 authors at 6 institutions in 5 countries.

Chloé MayèreDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0002-9254-4886
Violaine RegardDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0002-9827-0417
Aitana Perea-GomezUniversité Côte d'Azur, Inserm, CNRS, Institut de Biologie Valrose (iBV), 06108 Nice, France.ORCID 0000-0002-7788-038X
Corey BunceDepartment of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0002-1348-8135
Yasmine NeirijnckDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0001-7236-8451
Cyril DjariDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0001-7666-9024
Natividad Bellido-CarrerasUniversité Côte d'Azur, Inserm, CNRS, Institut de Biologie Valrose (iBV), 06108 Nice, France.ORCID 0000-0003-1207-0711
Pauline SararolsDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.
Richard ReevesMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, UK.
Simon GreenawayMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, UK.
Michelle SimonMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, UK.
Pam SiggersMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, UK.
Diana CondreaInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département de Génétique Fonctionnelle et Cancer, Centre National de la Recherche Scientifique (CNRS UMR7104), Institut National de la Santé et de la Recherche Médicale (INSERM U1258), Université de Strasbourg (UNISTRA), 1 rue Laurent Fries, BP1014267404 ILLKIRCH CEDEX, France.
Françoise KühneDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0003-2118-5756
Ivana GantarWyss Center for Bio and Neuroengineering, Geneva, Switzerland.ORCID 0000-0001-6351-8665
Furong TangUniversité Côte d'Azur, Inserm, CNRS, Institut de Biologie Valrose (iBV), 06108 Nice, France.ORCID 0000-0001-7546-7500
Isabelle StévantDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0002-0193-2526
Laura BattiWyss Center for Bio and Neuroengineering, Geneva, Switzerland.ORCID 0000-0003-3717-8470
Norbert B GhyselinckInstitut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Département de Génétique Fonctionnelle et Cancer, Centre National de la Recherche Scientifique (CNRS UMR7104), Institut National de la Santé et de la Recherche Médicale (INSERM U1258), Université de Strasbourg (UNISTRA), 1 rue Laurent Fries, BP1014267404 ILLKIRCH CEDEX, France.ORCID 0000-0003-4042-6818
Dagmar WilhelmDepartment of Anatomy and Physiology, University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0002-7757-4075
Andy GreenfieldMammalian Genetics Unit, Medical Research Council Harwell Institute, Oxfordshire OX11 0RD, UK.ORCID 0000-0002-1477-1776
Blanche CapelDepartment of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.ORCID 0000-0002-6587-0969
Marie-Christine ChaboissierUniversité Côte d'Azur, Inserm, CNRS, Institut de Biologie Valrose (iBV), 06108 Nice, France.
Serge NefDepartment of Genetic Medicine and Development, University of Geneva, 1211 Geneva, Switzerland.ORCID 0000-0001-5462-0676
University of Geneva · CHCentre National de la Recherche Scientifique · FRMary Lyon Centre at MRC Harwell · GBDuke University · USWyss Center for Bio and Neuroengineering · CHThe University of Melbourne · AU

Funding

OPPOSING PATHWAYS IN MAMMALIAN SEX DETERMINATIONR01HD039963 · NICHD · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2001 to 2025
$4.7M
Opposing Pathways in Mammalian Sex DeterminationR37HD039963 · NICHD · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2011 to 2020
$3.5M
Defining Mechanisms of Ovarian RescueR01HD090050 · NICHD · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2017 to 2021
$1.6M
Medical Research Council MC_U142684167NICHD NIH HHS R01 HD039963NICHD NIH HHS R01 HD090050NICHD NIH HHS R37 HD039963
6 · The paper itself

Abstract

Gonadal sex determination represents a unique model for studying cell fate decisions. However, a complete understanding of the different cell lineages forming the developing testis and ovary remains elusive. Here, we investigated the origin, specification, and subsequent sex-specific differentiation of a previously uncharacterized population of supporting-like cells (SLCs) in the developing mouse gonads. The SLC lineage is closely related to the coelomic epithelium and specified as early as E10.5, making it the first somatic lineage to be specified in the bipotential gonad. SLC progenitors are localized within the genital ridge at the interface with the mesonephros and initially coexpress

Identifiers

PMID35613264
PMCPMC10942771
OpenAlexW4281493142

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Registered trials

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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.