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http://purl.uniprot.org/citations/16630820http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16630820http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16630820http://www.w3.org/2000/01/rdf-schema#comment"The Wnt pathway controls cell fates, tissue homeostasis, and cancer. Its activation entails the association of beta-catenin with nuclear TCF/LEF proteins and results in transcriptional activation of target genes. The mechanism by which nuclear beta-catenin controls transcription is largely unknown. Here we genetically identify a novel Wnt/Wg pathway component that mediates the transcriptional outputs of beta-catenin/Armadillo. We show that Drosophila Hyrax and its human ortholog, Parafibromin, components of the Polymerase-Associated Factor 1 (PAF1) complex, are required for nuclear transduction of the Wnt/Wg signal and bind directly to the C-terminal region of beta-catenin/Armadillo. Moreover, we find that the transactivation potential of Parafibromin/Hyrax depends on the recruitment of Pygopus to beta-catenin/Armadillo. Our results assign to the tumor suppressor Parafibromin an unexpected role in Wnt signaling and provide a molecular mechanism for Wnt target gene control, in which the nuclear Wnt signaling complex directly engages the PAF1 complex, thereby controlling transcriptional initiation and elongation by RNA Polymerase II."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.org/dc/terms/identifier"doi:10.1016/j.cell.2006.01.053"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.org/dc/terms/identifier"doi:10.1016/j.cell.2006.01.053"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Basler K."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Basler K."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Hausmann G."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Hausmann G."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Mosimann C."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/author"Mosimann C."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/name"Cell"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/name"Cell"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/pages"327-341"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/pages"327-341"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/title"Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/title"Parafibromin/Hyrax activates Wnt/Wg target gene transcription by direct association with beta-catenin/Armadillo."xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/volume"125"xsd:string
http://purl.uniprot.org/citations/16630820http://purl.uniprot.org/core/volume"125"xsd:string
http://purl.uniprot.org/citations/16630820http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16630820
http://purl.uniprot.org/citations/16630820http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16630820
http://purl.uniprot.org/citations/16630820http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16630820
http://purl.uniprot.org/citations/16630820http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16630820