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http://purl.uniprot.org/citations/8799135http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8799135http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8799135http://www.w3.org/2000/01/rdf-schema#comment"A constitutively active form of fibroblast growth factor 2 (FGFR2) was identified in rat osteosarcoma (ROS) cells by an expression cloning strategy. Unlike other tyrosine kinase receptors activated by N-terminal truncation in tumors, this receptor, FGFR2-ROS, contains an altered C terminus generated from chromosomal rearrangement with a novel gene, designated FGFR activating gene 1 (FRAG1). While the removal of the C terminus slightly activates FGFR2, the presence of the FRAG1 sequence drastically stimulates the transforming activity and autophosphorylation of the receptor. FGFR2-ROS is expressed as a unusually large protein and is highly phosphorylated in NIH 3T3 transfectants. FRAG1 is ubiquitously expressed and encodes a predicted protein of 28 kDa lacking significant structural similarity to known proteins. Epitope-tagged FRAG1 protein showed a perinuclear localization by immunofluorescence staining. The highly activated state of FGFR2-ROS appears to be attributed to constitutive dimer formation and higher phosphorylation level as well as possibly altered subcellular localization. These results indicate a unique mechanism of receptor activation by a C terminus alteration through a chromosomal fusion with FRAG1."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.org/dc/terms/identifier"doi:10.1073/pnas.93.17.8956"xsd:string
http://purl.uniprot.org/citations/8799135http://purl.org/dc/terms/identifier"doi:10.1073/pnas.93.17.8956"xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Miki T."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Miki T."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Sakaguchi K."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Sakaguchi K."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Horii Y."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Horii Y."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Yamanaka R."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Yamanaka R."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Lorenzi M.V."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/author"Lorenzi M.V."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/date"1996"xsd:gYear
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/date"1996"xsd:gYear
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/name"Proc. Natl. Acad. Sci. U.S.A."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/pages"8956-8961"xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/pages"8956-8961"xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/title"FRAG1, a gene that potently activates fibroblast growth factor receptor by C-terminal fusion through chromosomal rearrangement."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/title"FRAG1, a gene that potently activates fibroblast growth factor receptor by C-terminal fusion through chromosomal rearrangement."xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/volume"93"xsd:string
http://purl.uniprot.org/citations/8799135http://purl.uniprot.org/core/volume"93"xsd:string