Evidence map›Paper›PMID 29272351›Full record

ArticleEndocrinology2018

Nuclear Androgen Receptor Regulates Testes Organization and Oocyte Maturation in Zebrafish.

Camerron M Crowder, Christopher S Lassiter, Daniel A Gorelick

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
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  3. Review
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  6. Genes · 2024
    Article
  7. Article
  8. Review
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  10. Direct male development in chromosomally ZZ zebrafish.Frontiers in cell and developmental biology · 2024
    Article
  11. Review
  12. Article
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  17. Article
  18. Article
  19. Stage Specific Transcriptomic Analysis and Database for Zebrafish Oogenesis.Frontiers in cell and developmental biology · 2022
    Article
  20. Control of testes mass by androgen receptor paralogs in a cichlid.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2022
    Article
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 1 country.

Camerron M CrowderDepartment of Pharmacology & Toxicology, University of Alabama at Birmingham, Birmingham, Alabama.
Christopher S LassiterDepartment of Biology, Roanoke College, Salem, Virginia.
Daniel A GorelickDepartment of Pharmacology & Toxicology, University of Alabama at Birmingham, Birmingham, Alabama.
University of Alabama at Birmingham · USRoanoke College · US

Funding

Mentored Experiences in Research, Instruction and Teaching (MERIT) Program - administrative supplementK12GM088010 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI SCHNEIDER, DAVID ALAN · 2009 to 2024
$9.2M
INVESTIGATING ARYL HYDROCARBON RECEPTOR-COFACTOR INTERACTIONS THAT MEDIATE TOXICITYR01ES026337 · NIEHS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Daniel Gorelick · 2016 to 2026
$3.9M
NIEHS NIH HHS R01 ES026337NIGMS NIH HHS K12 GM088010
6 · The paper itself

Abstract

Androgens act through the nuclear androgen receptor (AR) to regulate gonad differentiation and development. In mice, AR is necessary for spermatogenesis, testis development, and formation of external genitalia in males and oocyte maturation in females. However, the extent to which these phenotypes are conserved in nonmammalian vertebrates is not well understood. Here, we generate zebrafish with a mutation in the ar gene (aruab105/105) and examine the role of AR in sexual determination and gonad development. We found that zebrafish AR regulates male sexual determination, because the majority of aruab105/105 mutant embryos developed ovaries and displayed female secondary sexual characteristics. The small percentage of mutants that developed testes displayed female secondary sexual characteristics, exhibited structurally disorganized testes, and were unable to release or produce normal levels of sperm, demonstrating that AR is necessary for zebrafish testis development and fertility. In females, we found that AR regulates oocyte maturation and fecundity. The aruab105/105 mutant females developed ovaries filled primarily with immature stage I oocytes and few mature stage III oocytes. Two genes whose expression is enriched in wild-type ovaries compared with testes (cyp19a1a, foxl2a) were upregulated in ar mutant testes, and two genes enriched in testes (amh, dmrt1) were upregulated in ar mutant ovaries. These findings demonstrate that AR regulates sexual determination, testis development, and oocyte maturation and suggest that AR regulates sexually dimorphic gene expression. The ar mutant we developed will be useful for modeling human endocrine function in zebrafish.

Indexed as

AnimalsAnimals, Genetically ModifiedCell NucleusEmbryo, NonmammalianFemaleFertilityMaleOogenesisReceptors, AndrogenSex DifferentiationSpermatogenesisTestisZebrafishReceptors, Androgen

Identifiers

PMID29272351
PMCPMC5788001
OpenAlexW2951231225

What OpenQuestion holds

Textmetadata
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.