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Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses
Fishes exhibit remarkably diverse, and plastic, patterns of sexual development, most striking of which is sequential hermaphroditism, where individuals readily reverse sex in adulthood. How this stunning example of phenotypic plasticity is controlled at a genetic level remains poorly understood. Sev...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568253/ https://www.ncbi.nlm.nih.gov/pubmed/31218121 http://dx.doi.org/10.7717/peerj.7032 |
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author | Thomas, Jodi T. Todd, Erica V. Muncaster, Simon Lokman, P Mark Damsteegt, Erin L. Liu, Hui Soyano, Kiyoshi Gléonnec, Florence Lamm, Melissa S. Godwin, John R. Gemmell, Neil J. |
author_facet | Thomas, Jodi T. Todd, Erica V. Muncaster, Simon Lokman, P Mark Damsteegt, Erin L. Liu, Hui Soyano, Kiyoshi Gléonnec, Florence Lamm, Melissa S. Godwin, John R. Gemmell, Neil J. |
author_sort | Thomas, Jodi T. |
collection | PubMed |
description | Fishes exhibit remarkably diverse, and plastic, patterns of sexual development, most striking of which is sequential hermaphroditism, where individuals readily reverse sex in adulthood. How this stunning example of phenotypic plasticity is controlled at a genetic level remains poorly understood. Several genes have been implicated in regulating sex change, yet the degree to which a conserved genetic machinery orchestrates this process has not yet been addressed. Using captive and in-the-field social manipulations to initiate sex change, combined with a comparative qPCR approach, we compared expression patterns of four candidate regulatory genes among three species of wrasses (Labridae)—a large and diverse teleost family where female-to-male sex change is pervasive, socially-cued, and likely ancestral. Expression in brain and gonadal tissues were compared among the iconic tropical bluehead wrasse (Thalassoma bifasciatum) and the temperate spotty (Notolabrus celidotus) and kyusen (Parajulus poecilepterus) wrasses. In all three species, gonadal sex change was preceded by downregulation of cyp19a1a (encoding gonadal aromatase that converts androgens to oestrogens) and accompanied by upregulation of amh (encoding anti-müllerian hormone that primarily regulates male germ cell development), and these genes may act concurrently to orchestrate ovary-testis transformation. In the brain, our data argue against a role for brain aromatase (cyp19a1b) in initiating behavioural sex change, as its expression trailed behavioural changes. However, we find that isotocin (it, that regulates teleost socio-sexual behaviours) expression correlated with dominant male-specific behaviours in the bluehead wrasse, suggesting it upregulation mediates the rapid behavioural sex change characteristic of blueheads and other tropical wrasses. However, it expression was not sex-biased in temperate spotty and kyusen wrasses, where sex change is more protracted and social groups may be less tightly-structured. Together, these findings suggest that while key components of the molecular machinery controlling gonadal sex change are phylogenetically conserved among wrasses, neural pathways governing behavioural sex change may be more variable. |
format | Online Article Text |
id | pubmed-6568253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65682532019-06-19 Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses Thomas, Jodi T. Todd, Erica V. Muncaster, Simon Lokman, P Mark Damsteegt, Erin L. Liu, Hui Soyano, Kiyoshi Gléonnec, Florence Lamm, Melissa S. Godwin, John R. Gemmell, Neil J. PeerJ Aquaculture, Fisheries and Fish Science Fishes exhibit remarkably diverse, and plastic, patterns of sexual development, most striking of which is sequential hermaphroditism, where individuals readily reverse sex in adulthood. How this stunning example of phenotypic plasticity is controlled at a genetic level remains poorly understood. Several genes have been implicated in regulating sex change, yet the degree to which a conserved genetic machinery orchestrates this process has not yet been addressed. Using captive and in-the-field social manipulations to initiate sex change, combined with a comparative qPCR approach, we compared expression patterns of four candidate regulatory genes among three species of wrasses (Labridae)—a large and diverse teleost family where female-to-male sex change is pervasive, socially-cued, and likely ancestral. Expression in brain and gonadal tissues were compared among the iconic tropical bluehead wrasse (Thalassoma bifasciatum) and the temperate spotty (Notolabrus celidotus) and kyusen (Parajulus poecilepterus) wrasses. In all three species, gonadal sex change was preceded by downregulation of cyp19a1a (encoding gonadal aromatase that converts androgens to oestrogens) and accompanied by upregulation of amh (encoding anti-müllerian hormone that primarily regulates male germ cell development), and these genes may act concurrently to orchestrate ovary-testis transformation. In the brain, our data argue against a role for brain aromatase (cyp19a1b) in initiating behavioural sex change, as its expression trailed behavioural changes. However, we find that isotocin (it, that regulates teleost socio-sexual behaviours) expression correlated with dominant male-specific behaviours in the bluehead wrasse, suggesting it upregulation mediates the rapid behavioural sex change characteristic of blueheads and other tropical wrasses. However, it expression was not sex-biased in temperate spotty and kyusen wrasses, where sex change is more protracted and social groups may be less tightly-structured. Together, these findings suggest that while key components of the molecular machinery controlling gonadal sex change are phylogenetically conserved among wrasses, neural pathways governing behavioural sex change may be more variable. PeerJ Inc. 2019-06-11 /pmc/articles/PMC6568253/ /pubmed/31218121 http://dx.doi.org/10.7717/peerj.7032 Text en ©2019 Thomas et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Aquaculture, Fisheries and Fish Science Thomas, Jodi T. Todd, Erica V. Muncaster, Simon Lokman, P Mark Damsteegt, Erin L. Liu, Hui Soyano, Kiyoshi Gléonnec, Florence Lamm, Melissa S. Godwin, John R. Gemmell, Neil J. Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title | Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title_full | Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title_fullStr | Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title_full_unstemmed | Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title_short | Conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
title_sort | conservation and diversity in expression of candidate genes regulating socially-induced female-male sex change in wrasses |
topic | Aquaculture, Fisheries and Fish Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6568253/ https://www.ncbi.nlm.nih.gov/pubmed/31218121 http://dx.doi.org/10.7717/peerj.7032 |
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