Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2010-8-27
pubmed:abstractText
The Hippo (Hpo) pathway is a central determinant of tissue size in both Drosophila and higher organisms. The core of the pathway is a kinase cascade composed of an upstream kinase Hpo (MST1/2 in mammals) and a downstream kinase Warts (Wts, Lats1/2 in mammals), as well as several scaffold proteins, Sav, dRASSF, and Mats. Activation of the core kinase cassette results in phosphorylation and inactivation of the progrowth transcriptional coactivator Yki, leading to increased apoptosis and reduced tissue growth. The mechanisms that prevent inappropriate Hpo activation remain unclear, and in particular, the identity of the phosphatase that antagonizes Hpo is unknown. Using combined proteomic and RNAi screening approaches, we identify the dSTRIPAK PP2A complex as a major regulator of Hpo signaling. dSTRIPAK depletion leads to increased Hpo activatory phosphorylation and repression of Yki target genes in vivo, suggesting this phosphatase complex prevents Hpo activation during development.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Phosphatase 2, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/RASSF protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Yorkie protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/hpo protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/microtubule star protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/salvador protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/warts protein, Drosophila
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1097-4164
pubmed:author
pubmed:copyrightInfo
Copyright (c) 2010 Elsevier Inc. All rights reserved.
pubmed:issnType
Electronic
pubmed:day
27
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
521-34
pubmed:meshHeading
pubmed-meshheading:20797625-Animals, pubmed-meshheading:20797625-Apoptosis, pubmed-meshheading:20797625-Carrier Proteins, pubmed-meshheading:20797625-Cell Cycle Proteins, pubmed-meshheading:20797625-Cell Line, pubmed-meshheading:20797625-Cell Proliferation, pubmed-meshheading:20797625-Drosophila Proteins, pubmed-meshheading:20797625-Drosophila melanogaster, pubmed-meshheading:20797625-Genomics, pubmed-meshheading:20797625-Genotype, pubmed-meshheading:20797625-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:20797625-Multienzyme Complexes, pubmed-meshheading:20797625-Nuclear Proteins, pubmed-meshheading:20797625-Phenotype, pubmed-meshheading:20797625-Phosphorylation, pubmed-meshheading:20797625-Protein Kinases, pubmed-meshheading:20797625-Protein Phosphatase 2, pubmed-meshheading:20797625-Protein-Serine-Threonine Kinases, pubmed-meshheading:20797625-Proteomics, pubmed-meshheading:20797625-RNA Interference, pubmed-meshheading:20797625-Reproducibility of Results, pubmed-meshheading:20797625-Signal Transduction, pubmed-meshheading:20797625-Tandem Mass Spectrometry, pubmed-meshheading:20797625-Trans-Activators, pubmed-meshheading:20797625-Transfection
pubmed:year
2010
pubmed:articleTitle
Combined functional genomic and proteomic approaches identify a PP2A complex as a negative regulator of Hippo signaling.
pubmed:affiliation
Apoptosis and Proliferation Control Laboratory, Cancer Research UK, London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't