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A new experimental model for the investigation of sequential hermaphroditism

The stunning sexual transformation commonly triggered by age, size or social context in some fishes is one of the best examples of phenotypic plasticity thus far described. To date our understanding of this process is dominated by studies on a handful of subtropical and tropical teleosts, often in w...

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Autores principales: Goikoetxea, A., Muncaster, S., Todd, E. V., Lokman, P. M., Robertson, H. A., De Farias e Moraes, C. E., Damsteegt, E. L., Gemmell, N. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613207/
https://www.ncbi.nlm.nih.gov/pubmed/34819550
http://dx.doi.org/10.1038/s41598-021-02063-y
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author Goikoetxea, A.
Muncaster, S.
Todd, E. V.
Lokman, P. M.
Robertson, H. A.
De Farias e Moraes, C. E.
Damsteegt, E. L.
Gemmell, N. J.
author_facet Goikoetxea, A.
Muncaster, S.
Todd, E. V.
Lokman, P. M.
Robertson, H. A.
De Farias e Moraes, C. E.
Damsteegt, E. L.
Gemmell, N. J.
author_sort Goikoetxea, A.
collection PubMed
description The stunning sexual transformation commonly triggered by age, size or social context in some fishes is one of the best examples of phenotypic plasticity thus far described. To date our understanding of this process is dominated by studies on a handful of subtropical and tropical teleosts, often in wild settings. Here we have established the protogynous New Zealand spotty wrasse, Notolabrus celidotus, as a temperate model for the experimental investigation of sex change. Captive fish were induced to change sex using aromatase inhibition or manipulation of social groups. Complete female-to-male transition occurred over 60 days in both cases and time-series sampling was used to quantify changes in hormone production, gene expression and gonadal cellular anatomy. Early-stage decreases in plasma 17β-estradiol (E2) concentrations or gonadal aromatase (cyp19a1a) expression were not detected in spotty wrasse, despite these being commonly associated with the onset of sex change in subtropical and tropical protogynous (female-to-male) hermaphrodites. In contrast, expression of the masculinising factor amh (anti-Müllerian hormone) increased during early sex change, implying a potential role as a proximate trigger for masculinisation. Collectively, these data provide a foundation for the spotty wrasse as a temperate teleost model to study sex change and cell fate in vertebrates.
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spelling pubmed-86132072021-11-26 A new experimental model for the investigation of sequential hermaphroditism Goikoetxea, A. Muncaster, S. Todd, E. V. Lokman, P. M. Robertson, H. A. De Farias e Moraes, C. E. Damsteegt, E. L. Gemmell, N. J. Sci Rep Article The stunning sexual transformation commonly triggered by age, size or social context in some fishes is one of the best examples of phenotypic plasticity thus far described. To date our understanding of this process is dominated by studies on a handful of subtropical and tropical teleosts, often in wild settings. Here we have established the protogynous New Zealand spotty wrasse, Notolabrus celidotus, as a temperate model for the experimental investigation of sex change. Captive fish were induced to change sex using aromatase inhibition or manipulation of social groups. Complete female-to-male transition occurred over 60 days in both cases and time-series sampling was used to quantify changes in hormone production, gene expression and gonadal cellular anatomy. Early-stage decreases in plasma 17β-estradiol (E2) concentrations or gonadal aromatase (cyp19a1a) expression were not detected in spotty wrasse, despite these being commonly associated with the onset of sex change in subtropical and tropical protogynous (female-to-male) hermaphrodites. In contrast, expression of the masculinising factor amh (anti-Müllerian hormone) increased during early sex change, implying a potential role as a proximate trigger for masculinisation. Collectively, these data provide a foundation for the spotty wrasse as a temperate teleost model to study sex change and cell fate in vertebrates. Nature Publishing Group UK 2021-11-24 /pmc/articles/PMC8613207/ /pubmed/34819550 http://dx.doi.org/10.1038/s41598-021-02063-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Goikoetxea, A.
Muncaster, S.
Todd, E. V.
Lokman, P. M.
Robertson, H. A.
De Farias e Moraes, C. E.
Damsteegt, E. L.
Gemmell, N. J.
A new experimental model for the investigation of sequential hermaphroditism
title A new experimental model for the investigation of sequential hermaphroditism
title_full A new experimental model for the investigation of sequential hermaphroditism
title_fullStr A new experimental model for the investigation of sequential hermaphroditism
title_full_unstemmed A new experimental model for the investigation of sequential hermaphroditism
title_short A new experimental model for the investigation of sequential hermaphroditism
title_sort new experimental model for the investigation of sequential hermaphroditism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8613207/
https://www.ncbi.nlm.nih.gov/pubmed/34819550
http://dx.doi.org/10.1038/s41598-021-02063-y
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