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p120 Catenin Is Required for the Stress Response in Drosophila

p120ctn is a ubiquitously expressed core component of cadherin junctions and essential for vertebrate development. Surprisingly, Drosophila p120ctn (dp120ctn) is dispensable for adherens junctions and development, which has discouraged Drosophila researchers from further pursuing the biological role...

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Detalles Bibliográficos
Autores principales: Stefanatos, Rhoda K., Bauer, Christin, Vidal, Marcos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861524/
https://www.ncbi.nlm.nih.gov/pubmed/24349561
http://dx.doi.org/10.1371/journal.pone.0083942
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author Stefanatos, Rhoda K.
Bauer, Christin
Vidal, Marcos
author_facet Stefanatos, Rhoda K.
Bauer, Christin
Vidal, Marcos
author_sort Stefanatos, Rhoda K.
collection PubMed
description p120ctn is a ubiquitously expressed core component of cadherin junctions and essential for vertebrate development. Surprisingly, Drosophila p120ctn (dp120ctn) is dispensable for adherens junctions and development, which has discouraged Drosophila researchers from further pursuing the biological role of dp120ctn. Here we demonstrate that dp120ctn loss results in increased heat shock sensitivity and reduced animal lifespan, which are completely rescued by ectopic expression of a dp120ctn-GFP transgene. Transcriptomic analysis revealed multiple relish/NF-κB target genes differentially expressed upon loss of dp120ctn. Importantly, this aberrant gene expression was rescued by overexpression of dp120ctn-GFP or heterozygosity for relish. Our results uncover a novel role for dp120ctn in the regulation of animal stress response and immune signalling. This may represent an ancient role of p120ctn and can influence further studies in Drosophila and mammals.
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spelling pubmed-38615242013-12-17 p120 Catenin Is Required for the Stress Response in Drosophila Stefanatos, Rhoda K. Bauer, Christin Vidal, Marcos PLoS One Research Article p120ctn is a ubiquitously expressed core component of cadherin junctions and essential for vertebrate development. Surprisingly, Drosophila p120ctn (dp120ctn) is dispensable for adherens junctions and development, which has discouraged Drosophila researchers from further pursuing the biological role of dp120ctn. Here we demonstrate that dp120ctn loss results in increased heat shock sensitivity and reduced animal lifespan, which are completely rescued by ectopic expression of a dp120ctn-GFP transgene. Transcriptomic analysis revealed multiple relish/NF-κB target genes differentially expressed upon loss of dp120ctn. Importantly, this aberrant gene expression was rescued by overexpression of dp120ctn-GFP or heterozygosity for relish. Our results uncover a novel role for dp120ctn in the regulation of animal stress response and immune signalling. This may represent an ancient role of p120ctn and can influence further studies in Drosophila and mammals. Public Library of Science 2013-12-12 /pmc/articles/PMC3861524/ /pubmed/24349561 http://dx.doi.org/10.1371/journal.pone.0083942 Text en © 2013 Stefanatos et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Stefanatos, Rhoda K.
Bauer, Christin
Vidal, Marcos
p120 Catenin Is Required for the Stress Response in Drosophila
title p120 Catenin Is Required for the Stress Response in Drosophila
title_full p120 Catenin Is Required for the Stress Response in Drosophila
title_fullStr p120 Catenin Is Required for the Stress Response in Drosophila
title_full_unstemmed p120 Catenin Is Required for the Stress Response in Drosophila
title_short p120 Catenin Is Required for the Stress Response in Drosophila
title_sort p120 catenin is required for the stress response in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861524/
https://www.ncbi.nlm.nih.gov/pubmed/24349561
http://dx.doi.org/10.1371/journal.pone.0083942
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