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Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells
Apico-basal polarity is the defining characteristic of epithelial cells. In Drosophila, apical membrane identity is established and regulated through interactions between the highly conserved Par complex (Bazooka/Par3, atypical protein kinase C and Par6), and the Crumbs complex (Crumbs, Stardust and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400595/ https://www.ncbi.nlm.nih.gov/pubmed/25770183 http://dx.doi.org/10.1242/bio.201410934 |
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author | Shahab, Jaffer Tiwari, Manu D. Honemann-Capito, Mona Krahn, Michael P. Wodarz, Andreas |
author_facet | Shahab, Jaffer Tiwari, Manu D. Honemann-Capito, Mona Krahn, Michael P. Wodarz, Andreas |
author_sort | Shahab, Jaffer |
collection | PubMed |
description | Apico-basal polarity is the defining characteristic of epithelial cells. In Drosophila, apical membrane identity is established and regulated through interactions between the highly conserved Par complex (Bazooka/Par3, atypical protein kinase C and Par6), and the Crumbs complex (Crumbs, Stardust and PATJ). It has been proposed that Bazooka operates at the top of a genetic hierarchy in the establishment and maintenance of apico-basal polarity. However, there is still ambiguity over the correct sequence of events and cross-talk with other pathways during this process. In this study, we reassess this issue by comparing the phenotypes of the commonly used baz(4) and baz(815-8) alleles with those of the so far uncharacterized baz(XR11) and baz(EH747) null alleles in different Drosophila epithelia. While all these baz alleles display identical phenotypes during embryonic epithelial development, we observe strong discrepancies in the severity and penetrance of polarity defects in the follicular epithelium: polarity is mostly normal in baz(EH747) and baz(XR11) while baz(4) and baz(815)(-8) show loss of polarity, severe multilayering and loss of epithelial integrity throughout the clones. Further analysis reveals that the chromosomes carrying the baz(4) and baz(815-8) alleles may contain additional mutations that enhance the true baz loss-of-function phenotype in the follicular epithelium. This study clearly shows that Baz is dispensable for the regulation of polarity in the follicular epithelium, and that the requirement for key regulators of cell polarity is highly dependent on developmental context and cell type. |
format | Online Article Text |
id | pubmed-4400595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-44005952015-04-24 Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells Shahab, Jaffer Tiwari, Manu D. Honemann-Capito, Mona Krahn, Michael P. Wodarz, Andreas Biol Open Research Article Apico-basal polarity is the defining characteristic of epithelial cells. In Drosophila, apical membrane identity is established and regulated through interactions between the highly conserved Par complex (Bazooka/Par3, atypical protein kinase C and Par6), and the Crumbs complex (Crumbs, Stardust and PATJ). It has been proposed that Bazooka operates at the top of a genetic hierarchy in the establishment and maintenance of apico-basal polarity. However, there is still ambiguity over the correct sequence of events and cross-talk with other pathways during this process. In this study, we reassess this issue by comparing the phenotypes of the commonly used baz(4) and baz(815-8) alleles with those of the so far uncharacterized baz(XR11) and baz(EH747) null alleles in different Drosophila epithelia. While all these baz alleles display identical phenotypes during embryonic epithelial development, we observe strong discrepancies in the severity and penetrance of polarity defects in the follicular epithelium: polarity is mostly normal in baz(EH747) and baz(XR11) while baz(4) and baz(815)(-8) show loss of polarity, severe multilayering and loss of epithelial integrity throughout the clones. Further analysis reveals that the chromosomes carrying the baz(4) and baz(815-8) alleles may contain additional mutations that enhance the true baz loss-of-function phenotype in the follicular epithelium. This study clearly shows that Baz is dispensable for the regulation of polarity in the follicular epithelium, and that the requirement for key regulators of cell polarity is highly dependent on developmental context and cell type. The Company of Biologists 2015-03-13 /pmc/articles/PMC4400595/ /pubmed/25770183 http://dx.doi.org/10.1242/bio.201410934 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Shahab, Jaffer Tiwari, Manu D. Honemann-Capito, Mona Krahn, Michael P. Wodarz, Andreas Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title | Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title_full | Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title_fullStr | Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title_full_unstemmed | Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title_short | Bazooka/PAR3 is dispensable for polarity in Drosophila follicular epithelial cells |
title_sort | bazooka/par3 is dispensable for polarity in drosophila follicular epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4400595/ https://www.ncbi.nlm.nih.gov/pubmed/25770183 http://dx.doi.org/10.1242/bio.201410934 |
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