Evidence map›Paper›PMID 40093061›Full record

ArticlebioRxiv : the preprint server for biology2025

The basic helix-loop-helix transcription factor TCF4 recruits the Mediator Complex to activate gonadal genes and drive ovarian development.

E V O'Neil, S M Dupont, R Singh, B Capel

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

E V O'NeilDepartment of Cell Biology, Duke University School of Medicine, Durham NC 27710.ORCID 0000-0002-4919-2715
S M DupontDepartment of Cell Biology, Duke University School of Medicine, Durham NC 27710.ORCID 0000-0003-4607-2715
R SinghDepartment of Cell Biology, Duke University School of Medicine, Durham NC 27710.ORCID 0000-0002-4084-7340
B CapelDepartment of Cell Biology, Duke University School of Medicine, Durham NC 27710.ORCID 0000-0002-6587-0969

Funding

Defining Mechanisms of Ovarian RescueR01HD090050 · NICHD · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2017 to 2021
$1.6M
NICHD NIH HHS R01 HD090050
6 · The paper itself

Abstract

The bipotential gonad is the precursor organ to both the ovary and testis and develops as part of the embryonic urogenital system. In mice, gonadogenesis initiates around embryonic day 9.5 (E9.5), when coelomic epithelial (CE) cells overlaying the mesonephric ducts proliferate and acquire competence to differentiate into the somatic cell types of the embryonic gonad, the pre-supporting cell (Sertoli cells in the testis and granulosa cells in the ovary) and the interstitial cell lineages. While some transcription factors that drive gonadal cell fate are known, we found that basic helix-loop-helix (bHLH) binding sites are highly represented upstream of granulosa and interstitial genes. We investigated the bHLH Transcription Factor 4 (TCF4), which is expressed in GATA4+ somatic cells in both sexes prior to sex determination, maintained in ovarian pre-supporting cells and interstitial cells of both sexes, but silenced specifically in male pre-supporting cells. In a

Indexed as

developmentgonadTCF4

Identifiers

PMID40093061
PMCPMC11908221

What OpenQuestion holds

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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.