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Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly

Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live im...

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Detalles Bibliográficos
Autores principales: Weng, Mo, Wieschaus, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738385/
https://www.ncbi.nlm.nih.gov/pubmed/26754645
http://dx.doi.org/10.1083/jcb.201508056
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author Weng, Mo
Wieschaus, Eric
author_facet Weng, Mo
Wieschaus, Eric
author_sort Weng, Mo
collection PubMed
description Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live imaging and quantitative image analysis, we track the behavior of E-cadherin–rich junction clusters, demonstrating that in the early stages of gastrulation most subapical clusters in mesoderm not only persist, but move apically and enhance in density and total intensity. All three phenomena depend on myosin II and are temporally correlated with the pulses of actomyosin accumulation that drive initial cell shape changes during gastrulation. When contractile myosin is absent, the normal Snail expression in mesoderm, or ectopic Snail expression in ectoderm, is sufficient to drive early disassembly of junctions. In both cases, junctional disassembly can be blocked by simultaneous induction of myosin contractility. Our findings provide in vivo evidence for mechanosensitivity of cell–cell junctions and imply that myosin-mediated tension can prevent Snail-driven EMT.
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spelling pubmed-47383852016-07-18 Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly Weng, Mo Wieschaus, Eric J Cell Biol Research Articles Although Snail is essential for disassembly of adherens junctions during epithelial–mesenchymal transitions (EMTs), loss of adherens junctions in Drosophila melanogaster gastrula is delayed until mesoderm is internalized, despite the early expression of Snail in that primordium. By combining live imaging and quantitative image analysis, we track the behavior of E-cadherin–rich junction clusters, demonstrating that in the early stages of gastrulation most subapical clusters in mesoderm not only persist, but move apically and enhance in density and total intensity. All three phenomena depend on myosin II and are temporally correlated with the pulses of actomyosin accumulation that drive initial cell shape changes during gastrulation. When contractile myosin is absent, the normal Snail expression in mesoderm, or ectopic Snail expression in ectoderm, is sufficient to drive early disassembly of junctions. In both cases, junctional disassembly can be blocked by simultaneous induction of myosin contractility. Our findings provide in vivo evidence for mechanosensitivity of cell–cell junctions and imply that myosin-mediated tension can prevent Snail-driven EMT. The Rockefeller University Press 2016-01-18 /pmc/articles/PMC4738385/ /pubmed/26754645 http://dx.doi.org/10.1083/jcb.201508056 Text en © 2016 Wieschaus and Weng This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Weng, Mo
Wieschaus, Eric
Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title_full Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title_fullStr Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title_full_unstemmed Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title_short Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
title_sort myosin-dependent remodeling of adherens junctions protects junctions from snail-dependent disassembly
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4738385/
https://www.ncbi.nlm.nih.gov/pubmed/26754645
http://dx.doi.org/10.1083/jcb.201508056
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