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http://purl.uniprot.org/citations/17488777http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17488777http://www.w3.org/2000/01/rdf-schema#comment"Neurotrophin receptor-interacting MAGE homolog (NRAGE) has been recently identified as a cell-death inducer, involved in molecular events driving cells through apoptotic networks during neuronal development. Recently, we have focused on the functional role of Che-1, also known as apoptosis-antagonizing transcription factor (AATF), a protein involved in cell cycle control and gene transcription. Increasing evidence suggests that Che-1 is involved in apoptotic signalling in neural tissues. In cortical neurons Che-1 exhibits an anti-apoptotic activity, protecting cells from neuronal damage induced by amyloid beta-peptide. Here, we report that Che-1 interacts with NRAGE and that an EGFP-NRAGE fusion protein inhibits nuclear localization of Che-1, by sequestering it within the cytoplasmic compartment. Furthermore, NRAGE overexpression downregulates endogenous Che-1 by targeting it for proteasome-dependent degradation. Finally, we propose that Che-1 is a functional antagonist of NRAGE, because its overexpression completely reverts NRAGE-induced cell-death."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.org/dc/terms/identifier"doi:10.1242/jcs.03454"xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Bruno T."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Corbi N."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"De Nicola F."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Fanciulli M."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Floridi A."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Iezzi S."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Mattei E."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Passananti C."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Ciotti M.T."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Di Certo M.G."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/author"Desantis A."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/name"J Cell Sci"xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/pages"1852-1858"xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/title"NRAGE associates with the anti-apoptotic factor Che-1 and regulates its degradation to induce cell death."xsd:string
http://purl.uniprot.org/citations/17488777http://purl.uniprot.org/core/volume"120"xsd:string
http://purl.uniprot.org/citations/17488777http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17488777
http://purl.uniprot.org/citations/17488777http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17488777
http://purl.uniprot.org/uniprot/Q9JKX4#attribution-6FE57E2527E546B16AE050A507D58328http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/17488777
http://purl.uniprot.org/uniprot/Q9QYH6#attribution-948B1B9B1369A6F165D1E51156ADA23Bhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/17488777
http://purl.uniprot.org/uniprot/#_A0A0G2JG51-mappedCitation-17488777http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17488777
http://purl.uniprot.org/uniprot/#_A0A0G2JEK0-mappedCitation-17488777http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17488777