Evidence map›Paper›PMID 24040125›Full record

ArticlePloS one2013

Retinoic acid metabolic genes, meiosis, and gonadal sex differentiation in zebrafish.

Adriana Rodríguez-Marí, Cristian Cañestro, Ruth A BreMiller, Julian M Catchen, Yi-Lin Yan, John H Postlethwait

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 91 citations in OpenAlex.

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  10. Zoological research · 2024
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  12. Review
  13. Article
  14. Identification and Expression Pattern ofAnimals : an open access journal from MDPI · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 2 institutions in 2 countries.

Adriana Rodríguez-MaríInstitute of Neuroscience, University of Oregon, Eugene, Oregon, United States of America ; Departament de Genètica, Universitat de Barcelona, Barcelona, Spain.
Cristian Cañestro
Ruth A BreMiller
Julian M Catchen
Yi-Lin Yan
John H Postlethwait
University of Oregon · USUniversitat de Barcelona · ES

Funding

Zebrafish FacilityP01HD022486 · NICHD · UNIVERSITY OF OREGON · PI EISEN, JUDITH S · 1987 to 2017
$28.8M
Resources for Teleost Gene Duplicates and Human DiseaseR01OD011116 · OD · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2012 to 2020
$5.4M
RESOURCES FOR TELEOST GENE DUPLICATES AND HUMAN DISEASER01RR020833 · NCRR · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2005 to 2011
$3.6M
Mechanisms of Sex Determination in ZebrafishR01GM085318 · NIGMS · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2010 to 2018
$2.1M
NCRR NIH HHS 2R01RR020833NCRR NIH HHS R01 RR020833NICHD NIH HHS 5P01HD022486NICHD NIH HHS P01 HD022486NIGMS NIH HHS 1R01GM085318NIGMS NIH HHS R01 GM085318NIH HHS R01 OD011116NIH HHS R01OD011116PHS HHS 2009SGR336
6 · The paper itself

Abstract

To help understand the elusive mechanisms of zebrafish sex determination, we studied the genetic machinery regulating production and breakdown of retinoic acid (RA) during the onset of meiosis in gonadogenesis. Results uncovered unexpected mechanistic differences between zebrafish and mammals. Conserved synteny and expression analyses revealed that cyp26a1 in zebrafish and its paralog Cyp26b1 in tetrapods independently became the primary genes encoding enzymes available for gonadal RA-degradation, showing lineage-specific subfunctionalization of vertebrate genome duplication (VGD) paralogs. Experiments showed that zebrafish express aldh1a2, which encodes an RA-synthesizing enzyme, in the gonad rather than in the mesonephros as in mouse. Germ cells in bipotential gonads of all zebrafish analyzed were labeled by the early meiotic marker sycp3, suggesting that in zebrafish, the onset of meiosis is not sexually dimorphic as it is in mouse and is independent of Stra8, which is required in mouse but was lost in teleosts. Analysis of dead-end knockdown zebrafish depleted of germ cells revealed the germ cell-independent onset and maintenance of gonadal aldh1a2 and cyp26a1 expression. After meiosis initiated, somatic cell expression of cyp26a1 became sexually dimorphic: up-regulated in testes but not ovaries. Meiotic germ cells expressing the synaptonemal complex gene sycp3 occupied islands of somatic cells that lacked cyp26a1 expression, as predicted by the hypothesis that Cyp26a1 acts as a meiosis-inhibiting factor. Consistent with this hypothesis, females up-regulated cyp26a1 in oocytes that entered prophase-I meiotic arrest, and down-regulated cyp26a1 in oocytes resuming meiosis. Co-expression of cyp26a1 and the pluripotent germ cell stem cell marker pou5f1(oct4) in meiotically arrested oocytes was consistent with roles in mouse to promote germ cell survival and to prevent apoptosis, mechanisms that are central for tipping the sexual fate of gonads towards the female pathway in zebrafish.

Indexed as

AnimalsBiomarkersCytochrome P-450 Enzyme SystemFemaleGene Expression Regulation, DevelopmentalGerm CellsGonadsMaleMeiosisMicePhylogenyRetinal DehydrogenaseRetinoic Acid 4-HydroxylaseSex DifferentiationSignal TransductionTretinoinBiomarkersCyp26a1 protein, mousecyp26a1 protein, zebrafishCyp26b1 protein, mouseCytochrome P-450 Enzyme SystemRetinal DehydrogenaseRetinoic Acid 4-HydroxylaseTretinoinZebrafish Proteins

Identifiers

PMID24040125
PMCPMC3769385
OpenAlexW2075553349

What OpenQuestion holds

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LicenceCC BY
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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.