Cargando…

Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis

Smoltification is a metamorphic event in salmon life history, which initiates downstream migration and pre-adapts juvenile salmon for seawater entry. While a number of reports concern thyroid hormones and smoltification, few and inconclusive studies have addressed the potential role of thyrotropin (...

Descripción completa

Detalles Bibliográficos
Autores principales: Fleming, Mitchell S., Maugars, Gersende, Lafont, Anne-Gaëlle, Rancon, Jocelyn, Fontaine, Romain, Nourizadeh-Lillabadi, Rasoul, Weltzien, Finn-Arne, Yebra-Pimentel, Elena Santidrian, Dirks, Ron, McCormick, Stephen D., Rousseau, Karine, Martin, Patrick, Dufour, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418267/
https://www.ncbi.nlm.nih.gov/pubmed/30872608
http://dx.doi.org/10.1038/s41598-019-40019-5
_version_ 1783403701656879104
author Fleming, Mitchell S.
Maugars, Gersende
Lafont, Anne-Gaëlle
Rancon, Jocelyn
Fontaine, Romain
Nourizadeh-Lillabadi, Rasoul
Weltzien, Finn-Arne
Yebra-Pimentel, Elena Santidrian
Dirks, Ron
McCormick, Stephen D.
Rousseau, Karine
Martin, Patrick
Dufour, Sylvie
author_facet Fleming, Mitchell S.
Maugars, Gersende
Lafont, Anne-Gaëlle
Rancon, Jocelyn
Fontaine, Romain
Nourizadeh-Lillabadi, Rasoul
Weltzien, Finn-Arne
Yebra-Pimentel, Elena Santidrian
Dirks, Ron
McCormick, Stephen D.
Rousseau, Karine
Martin, Patrick
Dufour, Sylvie
author_sort Fleming, Mitchell S.
collection PubMed
description Smoltification is a metamorphic event in salmon life history, which initiates downstream migration and pre-adapts juvenile salmon for seawater entry. While a number of reports concern thyroid hormones and smoltification, few and inconclusive studies have addressed the potential role of thyrotropin (TSH). TSH is composed of a α-subunit common to gonadotropins, and a β-subunit conferring hormone specificity. We report the presence and functional divergence of duplicated TSH β-subunit paralogs (tshβa and tshβb) in Atlantic salmon. Phylogeny and synteny analyses allowed us to infer that they originated from teleost-specific whole genome duplication. Expression profiles of both paralogs in the pituitary were measured by qPCR throughout smoltification in Atlantic salmon from the endangered Loire-Allier population raised in a conservation hatchery. This revealed a striking peak of tshβb expression in April, concomitant with downstream migration initiation, while tshβa expression remained relatively constant. In situ hybridization showed two distinct pituitary cell populations, tshβa cells in the anterior adenohypophysis, and tshβb cells near to the pituitary stalk, a location comparable to the pars tuberalis TSH cells involved in seasonal physiology and behaviour in birds and mammals. Functional divergence of tshβ paralogs in Atlantic salmon supports a specific role of tshβb in smoltification.
format Online
Article
Text
id pubmed-6418267
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64182672019-03-18 Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis Fleming, Mitchell S. Maugars, Gersende Lafont, Anne-Gaëlle Rancon, Jocelyn Fontaine, Romain Nourizadeh-Lillabadi, Rasoul Weltzien, Finn-Arne Yebra-Pimentel, Elena Santidrian Dirks, Ron McCormick, Stephen D. Rousseau, Karine Martin, Patrick Dufour, Sylvie Sci Rep Article Smoltification is a metamorphic event in salmon life history, which initiates downstream migration and pre-adapts juvenile salmon for seawater entry. While a number of reports concern thyroid hormones and smoltification, few and inconclusive studies have addressed the potential role of thyrotropin (TSH). TSH is composed of a α-subunit common to gonadotropins, and a β-subunit conferring hormone specificity. We report the presence and functional divergence of duplicated TSH β-subunit paralogs (tshβa and tshβb) in Atlantic salmon. Phylogeny and synteny analyses allowed us to infer that they originated from teleost-specific whole genome duplication. Expression profiles of both paralogs in the pituitary were measured by qPCR throughout smoltification in Atlantic salmon from the endangered Loire-Allier population raised in a conservation hatchery. This revealed a striking peak of tshβb expression in April, concomitant with downstream migration initiation, while tshβa expression remained relatively constant. In situ hybridization showed two distinct pituitary cell populations, tshβa cells in the anterior adenohypophysis, and tshβb cells near to the pituitary stalk, a location comparable to the pars tuberalis TSH cells involved in seasonal physiology and behaviour in birds and mammals. Functional divergence of tshβ paralogs in Atlantic salmon supports a specific role of tshβb in smoltification. Nature Publishing Group UK 2019-03-14 /pmc/articles/PMC6418267/ /pubmed/30872608 http://dx.doi.org/10.1038/s41598-019-40019-5 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fleming, Mitchell S.
Maugars, Gersende
Lafont, Anne-Gaëlle
Rancon, Jocelyn
Fontaine, Romain
Nourizadeh-Lillabadi, Rasoul
Weltzien, Finn-Arne
Yebra-Pimentel, Elena Santidrian
Dirks, Ron
McCormick, Stephen D.
Rousseau, Karine
Martin, Patrick
Dufour, Sylvie
Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title_full Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title_fullStr Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title_full_unstemmed Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title_short Functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
title_sort functional divergence of thyrotropin beta-subunit paralogs gives new insights into salmon smoltification metamorphosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418267/
https://www.ncbi.nlm.nih.gov/pubmed/30872608
http://dx.doi.org/10.1038/s41598-019-40019-5
work_keys_str_mv AT flemingmitchells functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT maugarsgersende functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT lafontannegaelle functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT ranconjocelyn functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT fontaineromain functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT nourizadehlillabadirasoul functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT weltzienfinnarne functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT yebrapimentelelenasantidrian functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT dirksron functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT mccormickstephend functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT rousseaukarine functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT martinpatrick functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis
AT dufoursylvie functionaldivergenceofthyrotropinbetasubunitparalogsgivesnewinsightsintosalmonsmoltificationmetamorphosis