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Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila
Drosophila's dorsal closure provides an excellent model system with which to analyze biomechanical processes during morphogenesis. During native closure, the amnioserosa, flanked by two lateral epidermal sheets, forms an eye-shaped opening with canthi at each corner. The dynamics of amnioserosa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230616/ https://www.ncbi.nlm.nih.gov/pubmed/25253724 http://dx.doi.org/10.1091/mbc.E14-07-1190 |
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author | Wells, Adrienne R. Zou, Roger S. Tulu, U. Serdar Sokolow, Adam C. Crawford, Janice M. Edwards, Glenn S. Kiehart, Daniel P. |
author_facet | Wells, Adrienne R. Zou, Roger S. Tulu, U. Serdar Sokolow, Adam C. Crawford, Janice M. Edwards, Glenn S. Kiehart, Daniel P. |
author_sort | Wells, Adrienne R. |
collection | PubMed |
description | Drosophila's dorsal closure provides an excellent model system with which to analyze biomechanical processes during morphogenesis. During native closure, the amnioserosa, flanked by two lateral epidermal sheets, forms an eye-shaped opening with canthi at each corner. The dynamics of amnioserosa cells and actomyosin purse strings in the leading edges of epidermal cells promote closure, whereas the bulk of the lateral epidermis opposes closure. Canthi maintain purse string curvature (necessary for their dorsalward forces), and zipping at the canthi shortens leading edges, ensuring a continuous epithelium at closure completion. We investigated the requirement for intact canthi during closure with laser dissection approaches. Dissection of one or both canthi resulted in tissue recoil and flattening of each purse string. After recoil and a temporary pause, closure resumed at approximately native rates until slowing near the completion of closure. Thus the amnioserosa alone can drive closure after dissection of one or both canthi, requiring neither substantial purse string curvature nor zipping during the bulk of closure. How the embryo coordinates multiple, large forces (each of which is orders of magnitude greater than the net force) during native closure and is also resilient to multiple perturbations are key extant questions. |
format | Online Article Text |
id | pubmed-4230616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42306162015-01-20 Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila Wells, Adrienne R. Zou, Roger S. Tulu, U. Serdar Sokolow, Adam C. Crawford, Janice M. Edwards, Glenn S. Kiehart, Daniel P. Mol Biol Cell Articles Drosophila's dorsal closure provides an excellent model system with which to analyze biomechanical processes during morphogenesis. During native closure, the amnioserosa, flanked by two lateral epidermal sheets, forms an eye-shaped opening with canthi at each corner. The dynamics of amnioserosa cells and actomyosin purse strings in the leading edges of epidermal cells promote closure, whereas the bulk of the lateral epidermis opposes closure. Canthi maintain purse string curvature (necessary for their dorsalward forces), and zipping at the canthi shortens leading edges, ensuring a continuous epithelium at closure completion. We investigated the requirement for intact canthi during closure with laser dissection approaches. Dissection of one or both canthi resulted in tissue recoil and flattening of each purse string. After recoil and a temporary pause, closure resumed at approximately native rates until slowing near the completion of closure. Thus the amnioserosa alone can drive closure after dissection of one or both canthi, requiring neither substantial purse string curvature nor zipping during the bulk of closure. How the embryo coordinates multiple, large forces (each of which is orders of magnitude greater than the net force) during native closure and is also resilient to multiple perturbations are key extant questions. The American Society for Cell Biology 2014-11-05 /pmc/articles/PMC4230616/ /pubmed/25253724 http://dx.doi.org/10.1091/mbc.E14-07-1190 Text en © 2014 Wells, Zou, et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. |
spellingShingle | Articles Wells, Adrienne R. Zou, Roger S. Tulu, U. Serdar Sokolow, Adam C. Crawford, Janice M. Edwards, Glenn S. Kiehart, Daniel P. Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title | Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title_full | Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title_fullStr | Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title_full_unstemmed | Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title_short | Complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in Drosophila |
title_sort | complete canthi removal reveals that forces from the amnioserosa alone are sufficient to drive dorsal closure in drosophila |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230616/ https://www.ncbi.nlm.nih.gov/pubmed/25253724 http://dx.doi.org/10.1091/mbc.E14-07-1190 |
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