Evidence map›Paper›PMID 32781981›Full record

ArticleBMC genomics2020

Sex chromosome and sex locus characterization in goldfish, Carassius auratus (Linnaeus, 1758).

Ming Wen, Romain Feron, Qiaowei Pan, Justine Guguin, Elodie Jouanno, Amaury Herpin, Christophe Klopp, Cedric Cabau, Margot Zahm, Hugues Parrinello and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  15. Insights into chromosomal evolution and sex determination of Pseudobagrus ussuriensis (Bagridae, Siluriformes) based on a chromosome-level genome.DNA research : an international journal for rapid publication of reports on genes and genomes · 2022
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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

16 authors at 10 institutions in 7 countries.

Ming WenState Key Laboratory of Developmental Biology of Freshwater Fish, College of Life Science, Hunan Normal University, Changsha, China.
Romain FeronINRAE, LPGP, 35000, Rennes, France.
Qiaowei PanINRAE, LPGP, 35000, Rennes, France.
Justine GuguinINRAE, LPGP, 35000, Rennes, France.
Elodie JouannoINRAE, LPGP, 35000, Rennes, France.
Amaury HerpinINRAE, LPGP, 35000, Rennes, France.
Christophe KloppPlate-forme bio-informatique Genotoul, Mathématiques et Informatique Appliquées de Toulouse, INRAE, Castanet Tolosan, France.
Cedric CabauSIGENAE, GenPhySE, Université de Toulouse, INRAE, ENVT, Castanet Tolosan, France.
Margot ZahmSIGENAE, GenPhySE, Université de Toulouse, INRAE, ENVT, Castanet Tolosan, France.
Hugues ParrinelloMontpellier GenomiX (MGX), c/o Institut de Génomique Fonctionnelle, 141 rue de la Cardonille, 34094, Montpellier Cedex 05, France.
Laurent JournotMontpellier GenomiX (MGX), c/o Institut de Génomique Fonctionnelle, 141 rue de la Cardonille, 34094, Montpellier Cedex 05, France.
Shawn M BurgessTranslational and Functional Genomics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
Yoshihiro OmoriLaboratory of Functional Genomics, Graduate School of Bioscience, Nagahama Institute of Bioscience and Technology, Nagahama, Shiga, Japan.
John H PostlethwaitInstitute of Neuroscience, University of Oregon, Eugene, Oregon, USA.
Manfred SchartlDevelopmental Biochemistry, Biozentrum, University of Würzburg, Würzburg, Germany.
Yann GuiguenINRAE, LPGP, 35000, Rennes, France. yann.guiguen@inrae.fr.ORCID http://orcid.org/0000-0001-5464-6219
École Nationale Vétérinaire de Toulouse · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRMontpellier GenomiX · FRSIB Swiss Institute of Bioinformatics · CHHunan Normal University · CNInstitut National de la Recherche Agronomique · MANagahama Institute of Bio-Science and Technology · JPNational Human Genome Research Institute · USOregon State University · USTexas State University · US

Funding

Resources for Teleost Gene Duplicates and Human DiseaseR01OD011116 · OD · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2012 to 2020
$5.4M
Mechanisms of Sex Determination in ZebrafishR01GM085318 · NIGMS · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2010 to 2018
$2.1M
Mechanisms of Sex Determination in ZebrafishR35GM139635 · NIGMS · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2021 to 2025
$1.9M
NIGMS NIH HHS R01 GM085318NIGMS NIH HHS R35 GM139635NIH HHS 5R01GM085318NIH HHS R01 OD011116NIH HHS R01OD011116
6 · The paper itself

Abstract

backgroundGoldfish is an important model for various areas of research, including neural development and behavior and a species of significant importance in aquaculture, especially as an ornamental species. It has a male heterogametic (XX/XY) sex determination system that relies on both genetic and environmental factors, with high temperatures being able to produce female-to-male sex reversal. Little, however, is currently known on the molecular basis of genetic sex determination in this important cyprinid model. Here we used sequencing approaches to better characterize sex determination and sex-chromosomes in an experimental strain of goldfish.

resultsOur results confirmed that sex determination in goldfish is a mix of environmental and genetic factors and that its sex determination system is male heterogametic (XX/XY). Using reduced representation (RAD-seq) and whole genome (pool-seq) approaches, we characterized sex-linked polymorphisms and developed male specific genetic markers. These male specific markers were used to distinguish sex-reversed XX neomales from XY males and to demonstrate that XX female-to-male sex reversal could even occur at a relatively low rearing temperature (18 °C), for which sex reversal has been previously shown to be close to zero. We also characterized a relatively large non-recombining region (~ 11.7 Mb) on goldfish linkage group 22 (LG22) that contained a high-density of male-biased genetic polymorphisms. This large LG22 region harbors 373 genes, including a single candidate as a potential master sex gene, i.e., the anti-Mullerian hormone gene (amh). However, no sex-linked polymorphisms were detected in the coding DNA sequence of the goldfish amh gene.

conclusionsThese results show that our goldfish strain has a relatively large sex locus on LG22, which is likely the Y chromosome of this experimental population. The presence of a few XX males even at low temperature also suggests that other environmental factors in addition to temperature could trigger female-to-male sex reversal. Finally, we also developed sex-linked genetic markers, which will be important tools for future research on sex determination in our experimental goldfish population. However, additional work would be needed to explore whether this sex locus is conserved in other populations of goldfish.

Indexed as

GoldfishSex Determination ProcessesAnimalsFemaleGenetic LinkageMaleSex ChromosomesY ChromosomeGoldfishMale genome assemblyPoolseqRADseqSex determinationSex markers

Identifiers

PMID32781981
PMCPMC7430817
OpenAlexW3048833694

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.