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The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity
The Hippo (Hpo) pathway is a novel signaling pathway that controls organ size in Drosophila and mammals and is deregulated in a variety of human cancers. It consists of a set of kinases that, through a number of phosphorylation events, inactivate YAP, a transcriptional co-activator that controls cel...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628344/ https://www.ncbi.nlm.nih.gov/pubmed/23613971 http://dx.doi.org/10.1371/journal.pone.0061916 |
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author | Michaloglou, Chrysiis Lehmann, Waltraut Martin, Typhaine Delaunay, Clara Hueber, Andreas Barys, Louise Niu, Honglin Billy, Eric Wartmann, Markus Ito, Moriko Wilson, Christopher J. Digan, Mary Ellen Bauer, Andreas Voshol, Hans Christofori, Gerhard Sellers, William R. Hofmann, Francesco Schmelzle, Tobias |
author_facet | Michaloglou, Chrysiis Lehmann, Waltraut Martin, Typhaine Delaunay, Clara Hueber, Andreas Barys, Louise Niu, Honglin Billy, Eric Wartmann, Markus Ito, Moriko Wilson, Christopher J. Digan, Mary Ellen Bauer, Andreas Voshol, Hans Christofori, Gerhard Sellers, William R. Hofmann, Francesco Schmelzle, Tobias |
author_sort | Michaloglou, Chrysiis |
collection | PubMed |
description | The Hippo (Hpo) pathway is a novel signaling pathway that controls organ size in Drosophila and mammals and is deregulated in a variety of human cancers. It consists of a set of kinases that, through a number of phosphorylation events, inactivate YAP, a transcriptional co-activator that controls cellular proliferation and apoptosis. We have identified PTPN14 as a YAP-binding protein that negatively regulates YAP activity by controlling its localization. Mechanistically, we find that the interaction of ectopic YAP with PTPN14 can be mediated by the respective WW and PPxY motifs. However, the PTPN14 PPxY motif and phosphatase activity appear to be dispensable for the negative regulation of endogenous YAP, likely suggesting more complex mechanisms of interaction and modulation. Finally, we demonstrate that PTPN14 downregulation can phenocopy YAP activation in mammary epithelial cells and synergize with YAP to induce oncogenic transformation. |
format | Online Article Text |
id | pubmed-3628344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36283442013-04-23 The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity Michaloglou, Chrysiis Lehmann, Waltraut Martin, Typhaine Delaunay, Clara Hueber, Andreas Barys, Louise Niu, Honglin Billy, Eric Wartmann, Markus Ito, Moriko Wilson, Christopher J. Digan, Mary Ellen Bauer, Andreas Voshol, Hans Christofori, Gerhard Sellers, William R. Hofmann, Francesco Schmelzle, Tobias PLoS One Research Article The Hippo (Hpo) pathway is a novel signaling pathway that controls organ size in Drosophila and mammals and is deregulated in a variety of human cancers. It consists of a set of kinases that, through a number of phosphorylation events, inactivate YAP, a transcriptional co-activator that controls cellular proliferation and apoptosis. We have identified PTPN14 as a YAP-binding protein that negatively regulates YAP activity by controlling its localization. Mechanistically, we find that the interaction of ectopic YAP with PTPN14 can be mediated by the respective WW and PPxY motifs. However, the PTPN14 PPxY motif and phosphatase activity appear to be dispensable for the negative regulation of endogenous YAP, likely suggesting more complex mechanisms of interaction and modulation. Finally, we demonstrate that PTPN14 downregulation can phenocopy YAP activation in mammary epithelial cells and synergize with YAP to induce oncogenic transformation. Public Library of Science 2013-04-16 /pmc/articles/PMC3628344/ /pubmed/23613971 http://dx.doi.org/10.1371/journal.pone.0061916 Text en © 2013 Michaloglou 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 Michaloglou, Chrysiis Lehmann, Waltraut Martin, Typhaine Delaunay, Clara Hueber, Andreas Barys, Louise Niu, Honglin Billy, Eric Wartmann, Markus Ito, Moriko Wilson, Christopher J. Digan, Mary Ellen Bauer, Andreas Voshol, Hans Christofori, Gerhard Sellers, William R. Hofmann, Francesco Schmelzle, Tobias The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title | The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title_full | The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title_fullStr | The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title_full_unstemmed | The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title_short | The Tyrosine Phosphatase PTPN14 Is a Negative Regulator of YAP Activity |
title_sort | tyrosine phosphatase ptpn14 is a negative regulator of yap activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628344/ https://www.ncbi.nlm.nih.gov/pubmed/23613971 http://dx.doi.org/10.1371/journal.pone.0061916 |
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