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Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila

In Drosophila imaginal epithelia, cells mutant for the endocytic neoplastic tumor suppressor gene vps25 stimulate nearby untransformed cells to express Drosophila Inhibitor-of-Apoptosis-Protein-1 (DIAP-1), conferring resistance to apoptosis non-cell autonomously. Here, we show that the non-cell auto...

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Autores principales: Graves, Hillary K., Woodfield, Sarah E., Yang, Chih-Chao, Halder, Georg, Bergmann, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367968/
https://www.ncbi.nlm.nih.gov/pubmed/22679484
http://dx.doi.org/10.1371/journal.pone.0037615
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author Graves, Hillary K.
Woodfield, Sarah E.
Yang, Chih-Chao
Halder, Georg
Bergmann, Andreas
author_facet Graves, Hillary K.
Woodfield, Sarah E.
Yang, Chih-Chao
Halder, Georg
Bergmann, Andreas
author_sort Graves, Hillary K.
collection PubMed
description In Drosophila imaginal epithelia, cells mutant for the endocytic neoplastic tumor suppressor gene vps25 stimulate nearby untransformed cells to express Drosophila Inhibitor-of-Apoptosis-Protein-1 (DIAP-1), conferring resistance to apoptosis non-cell autonomously. Here, we show that the non-cell autonomous induction of DIAP-1 is mediated by Yorkie, the conserved downstream effector of Hippo signaling. The non-cell autonomous induction of Yorkie is due to Notch signaling from vps25 mutant cells. Moreover, activated Notch in normal cells is sufficient to induce non-cell autonomous Yorkie activity in wing imaginal discs. Our data identify a novel mechanism by which Notch promotes cell survival non-cell autonomously and by which neoplastic tumor cells generate a supportive microenvironment for tumor growth.
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spelling pubmed-33679682012-06-07 Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila Graves, Hillary K. Woodfield, Sarah E. Yang, Chih-Chao Halder, Georg Bergmann, Andreas PLoS One Research Article In Drosophila imaginal epithelia, cells mutant for the endocytic neoplastic tumor suppressor gene vps25 stimulate nearby untransformed cells to express Drosophila Inhibitor-of-Apoptosis-Protein-1 (DIAP-1), conferring resistance to apoptosis non-cell autonomously. Here, we show that the non-cell autonomous induction of DIAP-1 is mediated by Yorkie, the conserved downstream effector of Hippo signaling. The non-cell autonomous induction of Yorkie is due to Notch signaling from vps25 mutant cells. Moreover, activated Notch in normal cells is sufficient to induce non-cell autonomous Yorkie activity in wing imaginal discs. Our data identify a novel mechanism by which Notch promotes cell survival non-cell autonomously and by which neoplastic tumor cells generate a supportive microenvironment for tumor growth. Public Library of Science 2012-06-05 /pmc/articles/PMC3367968/ /pubmed/22679484 http://dx.doi.org/10.1371/journal.pone.0037615 Text en Graves 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
Graves, Hillary K.
Woodfield, Sarah E.
Yang, Chih-Chao
Halder, Georg
Bergmann, Andreas
Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title_full Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title_fullStr Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title_full_unstemmed Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title_short Notch Signaling Activates Yorkie Non-Cell Autonomously in Drosophila
title_sort notch signaling activates yorkie non-cell autonomously in drosophila
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367968/
https://www.ncbi.nlm.nih.gov/pubmed/22679484
http://dx.doi.org/10.1371/journal.pone.0037615
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