Evidence map›Paper›PMID 28873404›Full record

ArticlePLoS genetics2017

Fibroblast growth factor signaling is required for early somatic gonad development in zebrafish.

Dena M Leerberg, Kaori Sano, Bruce W Draper

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.5field-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

34 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Clonal dynamics deviate from neutral drift in zebrafish spermatogenesis.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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  12. Article
  13. The use ofSystems biology in reproductive medicine · 2023
    Article
  14. Comparative Transcriptome Analysis Reveals the Effect ofAnimals : an open access journal from MDPI · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Becoming female: Ovarian differentiation from an evolutionary perspective.Frontiers in cell and developmental biology · 2022
    Review
  19. Sexual determination in zebrafish.Cellular and molecular life sciences : CMLS · 2021
    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

3 authors at 2 institutions in 2 countries.

Dena M LeerbergDepartment of Molecular and Cellular Biology, University of California, Davis, California, United States of America.
Kaori SanoDepartment of Molecular and Cellular Biology, University of California, Davis, California, United States of America.
Bruce W DraperDepartment of Molecular and Cellular Biology, University of California, Davis, California, United States of America.ORCID http://orcid.org/0000-0002-4397-7749
University of California, Davis · USSophia University · JP

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Regulation of Vertebrate Gonad Formation by Fibroblast Growth Factor SignalingR01HD081551 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DRAPER, BRUCE W · 2015 to 2019
$1.6M
NICHD NIH HHS R01 HD081551NIGMS NIH HHS T32 GM007377
6 · The paper itself

Abstract

The vertebrate ovary and testis develop from a sexually indifferent gonad. During early development of the organism, primordial germ cells (the gamete lineage) and somatic gonad cells coalesce and begin to undergo growth and morphogenesis to form this bipotential gonad. Although this aspect of development is requisite for a fertile adult, little is known about the genetic regulation of early gonadogenesis in any vertebrate. Here, we provide evidence that fibroblast growth factor (Fgf) signaling is required for the early growth phase of a vertebrate bipotential gonad. Based on mutational analysis in zebrafish, we show that the Fgf ligand 24 (Fgf24) is required for proliferation, differentiation, and morphogenesis of the early somatic gonad, and as a result, most fgf24 mutants are sterile as adults. Additionally, we describe the ultrastructural elements of the early zebrafish gonad and show that distinct somatic cell populations can be identified soon after the gonad forms. Specifically, we show that fgf24 is expressed in an epithelial population of early somatic gonad cells that surrounds an inner population of mesenchymal somatic gonad cells that are in direct contact with the germ cells, and that fgf24 is required for stratification of the somatic tissue. Furthermore, based on gene expression analysis, we find that differentiation of the inner mesenchymal somatic gonad cells into functional cell types in the larval and early juvenile-stage gonad is dependent on Fgf24 signaling. Finally, we argue that the role of Fgf24 in zebrafish is functionally analogous to the role of tetrapod FGF9 in early gonad development.

Indexed as

AnimalsEmbryonic DevelopmentFemaleFibroblast Growth FactorsGene Expression Regulation, DevelopmentalGonadsMaleMorphogenesisOvarySex DifferentiationSignal TransductionTestisZebrafishZebrafish Proteinsfibroblast growth factor 24, zebrafishFibroblast Growth FactorsZebrafish Proteins

Identifiers

PMID28873404
PMCPMC5600409
OpenAlexW2752062112

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.