Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
The tyrosine phosphatase PTPN14 is a negative regulator of YAP activity
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2833385
Author(s) Michaloglou, C.; Lehmann, W.; Martin, T.; Delaunay, C.; Hueber, A.; Barys, L.; Niu, H.; Billy, E.; Wartmann, M.; Ito, M.; Wilson, C. J.; Digan, M. E.; Bauer, A.; Voshol, H.; Christofori, G.; Sellers, W. R.; Hofmann, F.; Schmelzle, T.
Author(s) at UniBasel Christofori, Gerhard M.
Year 2013
Title The tyrosine phosphatase PTPN14 is a negative regulator of YAP activity
Journal PLoS ONE
Volume 8
Number 4
Keywords Cell Line; Epithelial Cells/cytology/metabolism; Humans; Phosphoproteins/genetics/ metabolism; Protein Binding; Protein Tyrosine Phosphatases, Non-Receptor/genetics/ metabolism; Signal Transduction/physiology
Abstract 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.
Publisher Public Library of Science
ISSN/ISBN 1932-6203
edoc-URL http://edoc.unibas.ch/dok/A6338674
Full Text on edoc No
Digital Object Identifier DOI 10.1371/journal.pone.0061916
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/23613971
ISI-Number WOS:000317893400129
Document type (ISI) Article
 
   

MCSS v5.8 PRO. 0.380 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
03/05/2024