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Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria

The modulation of developmental biochemical pathways by mechanical cues is an emerging feature of animal development, but its evolutionary origins have not been explored. Here we show that a common mechanosensitive pathway involving β-catenin specifies early mesodermal identity at gastrulation in ze...

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Autores principales: Brunet, Thibaut, Bouclet, Adrien, Ahmadi, Padra, Mitrossilis, Démosthène, Driquez, Benjamin, Brunet, Anne-Christine, Henry, Laurent, Serman, Fanny, Béalle, Gaëlle, Ménager, Christine, Dumas-Bouchiat, Frédéric, Givord, Dominique, Yanicostas, Constantin, Le-Roy, Damien, Dempsey, Nora M., Plessis, Anne, Farge, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868206/
https://www.ncbi.nlm.nih.gov/pubmed/24281726
http://dx.doi.org/10.1038/ncomms3821
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author Brunet, Thibaut
Bouclet, Adrien
Ahmadi, Padra
Mitrossilis, Démosthène
Driquez, Benjamin
Brunet, Anne-Christine
Henry, Laurent
Serman, Fanny
Béalle, Gaëlle
Ménager, Christine
Dumas-Bouchiat, Frédéric
Givord, Dominique
Yanicostas, Constantin
Le-Roy, Damien
Dempsey, Nora M.
Plessis, Anne
Farge, Emmanuel
author_facet Brunet, Thibaut
Bouclet, Adrien
Ahmadi, Padra
Mitrossilis, Démosthène
Driquez, Benjamin
Brunet, Anne-Christine
Henry, Laurent
Serman, Fanny
Béalle, Gaëlle
Ménager, Christine
Dumas-Bouchiat, Frédéric
Givord, Dominique
Yanicostas, Constantin
Le-Roy, Damien
Dempsey, Nora M.
Plessis, Anne
Farge, Emmanuel
author_sort Brunet, Thibaut
collection PubMed
description The modulation of developmental biochemical pathways by mechanical cues is an emerging feature of animal development, but its evolutionary origins have not been explored. Here we show that a common mechanosensitive pathway involving β-catenin specifies early mesodermal identity at gastrulation in zebrafish and Drosophila. Mechanical strains developed by zebrafish epiboly and Drosophila mesoderm invagination trigger the phosphorylation of β-catenin–tyrosine-667. This leads to the release of β-catenin into the cytoplasm and nucleus, where it triggers and maintains, respectively, the expression of zebrafish brachyury orthologue notail and of Drosophila Twist, both crucial transcription factors for early mesoderm identity. The role of the β-catenin mechanosensitive pathway in mesoderm identity has been conserved over the large evolutionary distance separating zebrafish and Drosophila. This suggests mesoderm mechanical induction dating back to at least the last bilaterian common ancestor more than 570 million years ago, the period during which mesoderm is thought to have emerged.
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spelling pubmed-38682062013-12-20 Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria Brunet, Thibaut Bouclet, Adrien Ahmadi, Padra Mitrossilis, Démosthène Driquez, Benjamin Brunet, Anne-Christine Henry, Laurent Serman, Fanny Béalle, Gaëlle Ménager, Christine Dumas-Bouchiat, Frédéric Givord, Dominique Yanicostas, Constantin Le-Roy, Damien Dempsey, Nora M. Plessis, Anne Farge, Emmanuel Nat Commun Article The modulation of developmental biochemical pathways by mechanical cues is an emerging feature of animal development, but its evolutionary origins have not been explored. Here we show that a common mechanosensitive pathway involving β-catenin specifies early mesodermal identity at gastrulation in zebrafish and Drosophila. Mechanical strains developed by zebrafish epiboly and Drosophila mesoderm invagination trigger the phosphorylation of β-catenin–tyrosine-667. This leads to the release of β-catenin into the cytoplasm and nucleus, where it triggers and maintains, respectively, the expression of zebrafish brachyury orthologue notail and of Drosophila Twist, both crucial transcription factors for early mesoderm identity. The role of the β-catenin mechanosensitive pathway in mesoderm identity has been conserved over the large evolutionary distance separating zebrafish and Drosophila. This suggests mesoderm mechanical induction dating back to at least the last bilaterian common ancestor more than 570 million years ago, the period during which mesoderm is thought to have emerged. Nature Pub. Group 2013-11-27 /pmc/articles/PMC3868206/ /pubmed/24281726 http://dx.doi.org/10.1038/ncomms3821 Text en Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-by/3.0/ This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. To view a copy of this licence visit http://creativecommons.org/licenses/by/3.0/.
spellingShingle Article
Brunet, Thibaut
Bouclet, Adrien
Ahmadi, Padra
Mitrossilis, Démosthène
Driquez, Benjamin
Brunet, Anne-Christine
Henry, Laurent
Serman, Fanny
Béalle, Gaëlle
Ménager, Christine
Dumas-Bouchiat, Frédéric
Givord, Dominique
Yanicostas, Constantin
Le-Roy, Damien
Dempsey, Nora M.
Plessis, Anne
Farge, Emmanuel
Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title_full Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title_fullStr Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title_full_unstemmed Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title_short Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria
title_sort evolutionary conservation of early mesoderm specification by mechanotransduction in bilateria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868206/
https://www.ncbi.nlm.nih.gov/pubmed/24281726
http://dx.doi.org/10.1038/ncomms3821
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