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http://purl.uniprot.org/citations/26077467http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26077467http://www.w3.org/2000/01/rdf-schema#comment"The inhibition of p53 activity by histone deacetylase 3 (HDAC3) has been reported, but the precise molecular mechanism is unknown. Here we show that programmed cell death 5 (PDCD5) selectively mediates HDAC3 dissociation from p53, which induces HDAC3 cleavage and ubiquitin-dependent proteasomal degradation. Casein kinase 2 alpha phosphorylates PDCD5 at Ser-119 to enhance its stability and importin 13-mediated nuclear translocation of PDCD5. Genetic deletion of PDCD5 abrogates etoposide (ET)-induced p53 stabilization and HDAC3 cleavage, indicating an essential role of PDCD5 in p53 activation. Restoration of PDCD5(WT) in PDCD5(-/-) MEFs restores ET-induced HDAC3 cleavage. Reduction of both PDCD5 and p53, but not reduction of either protein alone, significantly enhances in vivo tumorigenicity of AGS gastric cancer cells and correlates with poor prognosis in gastric cancer patients. Our results define a mechanism for p53 activation via PDCD5-dependent HDAC3 decay under genotoxic stress conditions."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.org/dc/terms/identifier"doi:10.1038/ncomms8390"xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Lee S.H."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Park S.Y."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Choi H.K."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Choi Y."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Lee P.C."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Seo J."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Choi K.C."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Jeong J.H."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Jeong J.W."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Park E.S."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Jeong M.H."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/author"Yoon H.G."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/name"Nat Commun"xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/pages"7390"xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/title"Programmed cell death 5 mediates HDAC3 decay to promote genotoxic stress response."xsd:string
http://purl.uniprot.org/citations/26077467http://purl.uniprot.org/core/volume"6"xsd:string
http://purl.uniprot.org/citations/26077467http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26077467
http://purl.uniprot.org/citations/26077467http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26077467
http://purl.uniprot.org/uniprot/#_D3Z7Q5-mappedCitation-26077467http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26077467
http://purl.uniprot.org/uniprot/#_P56812-mappedCitation-26077467http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26077467
http://purl.uniprot.org/uniprot/#_A0A158SIS7-mappedCitation-26077467http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26077467