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Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish

BACKGROUND: Teleost fishes exhibit remarkably diverse and plastic sexual developmental patterns. One of the most astonishing is the rapid socially controlled female-to-male (protogynous) sex change observed in bluehead wrasses (Thalassoma bifasciatum). Such functional sex change is widespread in mar...

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Autores principales: Liu, Hui, Lamm, Melissa S., Rutherford, Kim, Black, Michael A., Godwin, John R., Gemmell, Neil J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660848/
https://www.ncbi.nlm.nih.gov/pubmed/26613014
http://dx.doi.org/10.1186/s13293-015-0044-8
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author Liu, Hui
Lamm, Melissa S.
Rutherford, Kim
Black, Michael A.
Godwin, John R.
Gemmell, Neil J.
author_facet Liu, Hui
Lamm, Melissa S.
Rutherford, Kim
Black, Michael A.
Godwin, John R.
Gemmell, Neil J.
author_sort Liu, Hui
collection PubMed
description BACKGROUND: Teleost fishes exhibit remarkably diverse and plastic sexual developmental patterns. One of the most astonishing is the rapid socially controlled female-to-male (protogynous) sex change observed in bluehead wrasses (Thalassoma bifasciatum). Such functional sex change is widespread in marine fishes, including species of commercial importance, yet its underlying molecular basis remains poorly explored. METHODS: RNA sequencing was performed to characterize the transcriptomic profiles and identify genes exhibiting sex-biased expression in the brain (forebrain and midbrain) and gonads of bluehead wrasses. Functional annotation and enrichment analysis were carried out for the sex-biased genes in the gonad to detect global differences in gene products and genetic pathways between males and females. RESULTS: Here we report the first transcriptomic analysis for a protogynous fish. Expression comparison between males and females reveals a large set of genes with sex-biased expression in the gonad, but relatively few such sex-biased genes in the brain. Functional annotation and enrichment analysis suggested that ovaries are mainly enriched for metabolic processes and testes for signal transduction, particularly receptors of neurotransmitters and steroid hormones. When compared to other species, many genes previously implicated in male sex determination and differentiation pathways showed conservation in their gonadal expression patterns in bluehead wrasses. However, some critical female-pathway genes (e.g., rspo1 and wnt4b) exhibited unanticipated expression patterns. In the brain, gene expression patterns suggest that local neurosteroid production and signaling likely contribute to the sex differences observed. CONCLUSIONS: Expression patterns of key sex-related genes suggest that sex-changing fish predominantly use an evolutionarily conserved genetic toolkit, but that subtle variability in the standard sex-determination regulatory network likely contributes to sexual plasticity in these fish. This study not only provides the first molecular data on a system ideally suited to explore the molecular basis of sexual plasticity and tissue re-engineering, but also sheds some light on the evolution of diverse sex determination and differentiation systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-015-0044-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46608482015-11-27 Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish Liu, Hui Lamm, Melissa S. Rutherford, Kim Black, Michael A. Godwin, John R. Gemmell, Neil J. Biol Sex Differ Research BACKGROUND: Teleost fishes exhibit remarkably diverse and plastic sexual developmental patterns. One of the most astonishing is the rapid socially controlled female-to-male (protogynous) sex change observed in bluehead wrasses (Thalassoma bifasciatum). Such functional sex change is widespread in marine fishes, including species of commercial importance, yet its underlying molecular basis remains poorly explored. METHODS: RNA sequencing was performed to characterize the transcriptomic profiles and identify genes exhibiting sex-biased expression in the brain (forebrain and midbrain) and gonads of bluehead wrasses. Functional annotation and enrichment analysis were carried out for the sex-biased genes in the gonad to detect global differences in gene products and genetic pathways between males and females. RESULTS: Here we report the first transcriptomic analysis for a protogynous fish. Expression comparison between males and females reveals a large set of genes with sex-biased expression in the gonad, but relatively few such sex-biased genes in the brain. Functional annotation and enrichment analysis suggested that ovaries are mainly enriched for metabolic processes and testes for signal transduction, particularly receptors of neurotransmitters and steroid hormones. When compared to other species, many genes previously implicated in male sex determination and differentiation pathways showed conservation in their gonadal expression patterns in bluehead wrasses. However, some critical female-pathway genes (e.g., rspo1 and wnt4b) exhibited unanticipated expression patterns. In the brain, gene expression patterns suggest that local neurosteroid production and signaling likely contribute to the sex differences observed. CONCLUSIONS: Expression patterns of key sex-related genes suggest that sex-changing fish predominantly use an evolutionarily conserved genetic toolkit, but that subtle variability in the standard sex-determination regulatory network likely contributes to sexual plasticity in these fish. This study not only provides the first molecular data on a system ideally suited to explore the molecular basis of sexual plasticity and tissue re-engineering, but also sheds some light on the evolution of diverse sex determination and differentiation systems. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-015-0044-8) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-25 /pmc/articles/PMC4660848/ /pubmed/26613014 http://dx.doi.org/10.1186/s13293-015-0044-8 Text en © Liu et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liu, Hui
Lamm, Melissa S.
Rutherford, Kim
Black, Michael A.
Godwin, John R.
Gemmell, Neil J.
Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title_full Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title_fullStr Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title_full_unstemmed Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title_short Large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
title_sort large-scale transcriptome sequencing reveals novel expression patterns for key sex-related genes in a sex-changing fish
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4660848/
https://www.ncbi.nlm.nih.gov/pubmed/26613014
http://dx.doi.org/10.1186/s13293-015-0044-8
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