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http://purl.uniprot.org/citations/14618271http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/14618271http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/14618271http://www.w3.org/2000/01/rdf-schema#comment"In vertebrates, different isoforms of fibroblast growth factor 2 (FGF2) exist, which differ by their N-terminal extension. They show different localization and expression levels and exert distinct biological effects. Nevertheless, genetic inactivation of all FGF2 isoforms in the mouse results in only mild phenotypes. Here, we analyzed mouse FGF2, and show that, as in the human, mouse FGF2 contains CTG-initiated high molecular-weight (HMW) isoforms, which contain a nuclear localization signal, and which mediate localization of this isoform to the nucleus. Using green fluorescent protein-FGF2 fusions, we furthermore observed, that C-terminal deletions disable nuclear localization of the short low-molecular-weight (LMW) 18-kDa isoform. This loss of specific localization is accompanied by a loss in heparin binding. We therefore suggest that, first, localization of mouse FGF2 is comparable to that in other vertebrates and, second, FGF2 contains at least two sequences important for nuclear localization, a nuclear localization sequence at the N terminus which is only contained in the HMW isoform, and another sequence at the C terminus, which is only required for localization of the LMW 18-kDa isoform."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.org/dc/terms/identifier"doi:10.1007/s00018-003-3258-6"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.org/dc/terms/identifier"doi:10.1007/s00018-003-3258-6"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Vuadens F."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Vuadens F."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Beermann F."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Beermann F."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Foletti A."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/author"Foletti A."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/name"Cell. Mol. Life Sci."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/name"Cell Mol Life Sci"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/pages"2254-2265"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/pages"2254-2265"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/title"Nuclear localization of mouse fibroblast growth factor 2 requires N-terminal and C-terminal sequences."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/title"Nuclear localization of mouse fibroblast growth factor 2 requires N-terminal and C-terminal sequences."xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/volume"60"xsd:string
http://purl.uniprot.org/citations/14618271http://purl.uniprot.org/core/volume"60"xsd:string
http://purl.uniprot.org/citations/14618271http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/14618271
http://purl.uniprot.org/citations/14618271http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/14618271
http://purl.uniprot.org/citations/14618271http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/14618271
http://purl.uniprot.org/citations/14618271http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/14618271