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Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo

The establishment and maintenance of apical–basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization....

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Autores principales: Choi, Wangsun, Harris, Nathan J., Sumigray, Kaelyn D., Peifer, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608504/
https://www.ncbi.nlm.nih.gov/pubmed/23363604
http://dx.doi.org/10.1091/mbc.E12-10-0736
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author Choi, Wangsun
Harris, Nathan J.
Sumigray, Kaelyn D.
Peifer, Mark
author_facet Choi, Wangsun
Harris, Nathan J.
Sumigray, Kaelyn D.
Peifer, Mark
author_sort Choi, Wangsun
collection PubMed
description The establishment and maintenance of apical–basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being “downstream” of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway.
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spelling pubmed-36085042013-06-16 Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo Choi, Wangsun Harris, Nathan J. Sumigray, Kaelyn D. Peifer, Mark Mol Biol Cell Articles The establishment and maintenance of apical–basal cell polarity is critical for assembling epithelia and maintaining organ architecture. Drosophila embryos provide a superb model. In the current view, apically positioned Bazooka/Par3 is the initial polarity cue as cells form during cellularization. Bazooka then helps to position both adherens junctions and atypical protein kinase C (aPKC). Although a polarized cytoskeleton is critical for Bazooka positioning, proteins mediating this remained unknown. We found that the small GTPase Rap1 and the actin-junctional linker Canoe/afadin are essential for polarity establishment, as both adherens junctions and Bazooka are mispositioned in their absence. Rap1 and Canoe do not simply organize the cytoskeleton, as actin and microtubules become properly polarized in their absence. Canoe can recruit Bazooka when ectopically expressed, but they do not obligatorily colocalize. Rap1 and Canoe play continuing roles in Bazooka localization during gastrulation, but other polarity cues partially restore apical Bazooka in the absence of Rap1 or Canoe. We next tested the current linear model for polarity establishment. Both Bazooka and aPKC regulate Canoe localization despite being “downstream” of Canoe. Further, Rap1, Bazooka, and aPKC, but not Canoe, regulate columnar cell shape. These data reshape our view, suggesting that polarity establishment is regulated by a protein network rather than a linear pathway. The American Society for Cell Biology 2013-04-01 /pmc/articles/PMC3608504/ /pubmed/23363604 http://dx.doi.org/10.1091/mbc.E12-10-0736 Text en © 2013 Choi 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 of Cell BD; are registered trademarks of The American Society of Cell Biology.
spellingShingle Articles
Choi, Wangsun
Harris, Nathan J.
Sumigray, Kaelyn D.
Peifer, Mark
Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title_full Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title_fullStr Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title_full_unstemmed Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title_short Rap1 and Canoe/afadin are essential for establishment of apical–basal polarity in the Drosophila embryo
title_sort rap1 and canoe/afadin are essential for establishment of apical–basal polarity in the drosophila embryo
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608504/
https://www.ncbi.nlm.nih.gov/pubmed/23363604
http://dx.doi.org/10.1091/mbc.E12-10-0736
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