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Regulating mechanical tension at compartment boundaries in Drosophila

During animal development, cells with similar function and fate often stay together and sort out from cells with different fates. In Drosophila wing imaginal discs, cells of anterior and posterior fates are separated by a straight compartment boundary. Separation of anterior and posterior cells requ...

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Autores principales: Michel, Marcus, Dahmann, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036931/
https://www.ncbi.nlm.nih.gov/pubmed/27362651
http://dx.doi.org/10.1080/19336934.2016.1207028
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author Michel, Marcus
Dahmann, Christian
author_facet Michel, Marcus
Dahmann, Christian
author_sort Michel, Marcus
collection PubMed
description During animal development, cells with similar function and fate often stay together and sort out from cells with different fates. In Drosophila wing imaginal discs, cells of anterior and posterior fates are separated by a straight compartment boundary. Separation of anterior and posterior cells requires the homeodomain-containing protein Engrailed, which is expressed in posterior cells. Engrailed induces the expression of the short-range signaling molecule Hedgehog in posterior cells and confines Hedgehog signal transduction to anterior cells. Transduction of the Hedgehog signal in anterior cells is required for the separation of anterior and posterior cells. Previous work showed that this separation of cells involves a local increase in mechanical tension at cell junctions along the compartment boundary. However, how mechanical tension was locally increased along the compartment boundary remained unknown. A recent paper now shows that the difference in Hedgehog signal transduction between anterior and posterior cells is necessary and sufficient to increase mechanical tension. The local increase in mechanical tension biases junctional rearrangements during cell intercalations to maintain the straight shape of the compartment boundary. These data highlight how developmental signals can generate patterns of mechanical tension important for tissue organization.
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spelling pubmed-50369312016-10-05 Regulating mechanical tension at compartment boundaries in Drosophila Michel, Marcus Dahmann, Christian Fly (Austin) Extra View During animal development, cells with similar function and fate often stay together and sort out from cells with different fates. In Drosophila wing imaginal discs, cells of anterior and posterior fates are separated by a straight compartment boundary. Separation of anterior and posterior cells requires the homeodomain-containing protein Engrailed, which is expressed in posterior cells. Engrailed induces the expression of the short-range signaling molecule Hedgehog in posterior cells and confines Hedgehog signal transduction to anterior cells. Transduction of the Hedgehog signal in anterior cells is required for the separation of anterior and posterior cells. Previous work showed that this separation of cells involves a local increase in mechanical tension at cell junctions along the compartment boundary. However, how mechanical tension was locally increased along the compartment boundary remained unknown. A recent paper now shows that the difference in Hedgehog signal transduction between anterior and posterior cells is necessary and sufficient to increase mechanical tension. The local increase in mechanical tension biases junctional rearrangements during cell intercalations to maintain the straight shape of the compartment boundary. These data highlight how developmental signals can generate patterns of mechanical tension important for tissue organization. Taylor & Francis 2016-06-30 /pmc/articles/PMC5036931/ /pubmed/27362651 http://dx.doi.org/10.1080/19336934.2016.1207028 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Extra View
Michel, Marcus
Dahmann, Christian
Regulating mechanical tension at compartment boundaries in Drosophila
title Regulating mechanical tension at compartment boundaries in Drosophila
title_full Regulating mechanical tension at compartment boundaries in Drosophila
title_fullStr Regulating mechanical tension at compartment boundaries in Drosophila
title_full_unstemmed Regulating mechanical tension at compartment boundaries in Drosophila
title_short Regulating mechanical tension at compartment boundaries in Drosophila
title_sort regulating mechanical tension at compartment boundaries in drosophila
topic Extra View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036931/
https://www.ncbi.nlm.nih.gov/pubmed/27362651
http://dx.doi.org/10.1080/19336934.2016.1207028
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