Evidence map›Paper›PMID 27642754›Full record

ArticlePLoS genetics2016

Bmp15 Is an Oocyte-Produced Signal Required for Maintenance of the Adult Female Sexual Phenotype in Zebrafish.

Daniel B Dranow, Kevin Hu, April M Bird, S Terese Lawry, Melissa T Adams, Angelica Sanchez, James F Amatruda, Bruce W Draper

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
17.1field-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

95 citing papers in PubMed, 215 citations in OpenAlex.

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  9. The DNA mismatch repair protein Msh4 is essential for meiosis of male but not for female in zebrafish.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
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  17. Characterizing the Ovarian Cytogenetic Dynamics of Sichuan Bream (International journal of molecular sciences · 2025
    Article
  18. Article
  19. Article
  20. Article

35 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

Daniel B DranowDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.ORCID 0000-0002-5685-3833
Kevin HuDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.
April M BirdDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.ORCID 0000-0003-3552-072X
S Terese LawryDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.
Melissa T AdamsDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.ORCID 0000-0002-3676-0285
Angelica SanchezDepartments of Pediatrics and Molecular Biology, The University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, United States of America.
James F AmatrudaDepartments of Pediatrics and Molecular Biology, The University of Texas Southwestern Medical Center at Dallas, Dallas, Texas, United States of America.
Bruce W DraperDepartment of Molecular and Cellular Biology, University of California Davis, Davis, California, United States of America.ORCID 0000-0002-4397-7749
University of California, Davis · USThe University of Texas Southwestern Medical Center · US

Funding

Generation and Rapid Mapping of Low-Penetrance Disease Alleles in ZebrafishR01CA135731 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI AMATRUDA, JAMES F · 2008 to 2012
$1.6M
NCI NIH HHS R01 CA135731
6 · The paper itself

Abstract

Although the zebrafish is a major model organism, how they determine sex is not well understood. In domesticated zebrafish, sex determination appears to be polygenic, being influenced by multiple genetic factors that may vary from strain to strain, and additionally can be influenced by environmental factors. However, the requirement of germ cells for female sex determination is well documented: animals that lack germ cells, or oocytes in particular, develop exclusively as males. Recently, it has been determined that oocytes are also required throughout the adult life of the animal to maintain the differentiated female state. How oocytes control sex differentiation and maintenance of the sexual phenotype is unknown. We therefore generated targeted mutations in genes for two oocyte produced signaling molecules, Bmp15 and Gdf9 and here report a novel role for Bmp15 in maintaining adult female sex differentiation in zebrafish. Females deficient in Bmp15 begin development normally but switch sex during the mid- to late- juvenile stage, and become fertile males. Additionally, by generating mutations in the aromatase cyp19a1a, we show that estrogen production is necessary for female development and that the function of Bmp15 in female sex maintenance is likely linked to the regulation of estrogen biosynthesis via promoting the development of estrogen-producing granulosa cells in the oocyte follicle.

Indexed as

Signal TransductionAnimalsAromataseBone Morphogenetic Protein 15EstrogensFemaleGrowth Differentiation Factor 9MaleMutationOocytesPhenotypeSex Determination ProcessesZebrafishZebrafish ProteinsAromataseBone Morphogenetic Protein 15Cyp19a1a protein, zebrafishEstrogensGrowth Differentiation Factor 9Zebrafish Proteins

Identifiers

PMID27642754
PMCPMC5028036
OpenAlexW2521989110

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.