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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2013
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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. |
format | Online Article Text |
id | pubmed-3868206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
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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