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http://purl.uniprot.org/citations/18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18442887http://www.w3.org/2000/01/rdf-schema#comment"Little is known about the upstream regulator of Runx2, a master regulator of osteoblast differentiation in bone tissues. To elucidate the molecular mechanism of Runx2 gene expression, we analyzed Runx2 promoter activity in osseous (MC3T3-E1, KS483, Kusa) and non-osseous (NIH3T3, C3H10T1/2, mouse embryonic fibroblasts) cells and also identified Runx2 upstream regulator using a Runx2 promoter-derived luciferase reporter system. After cloning 15 serial deletion constructs from -6832 bp/+390 bp to -37 bp/+390 bp of the Runx2-P1 promoter, we performed a transient transfection assay in osseous and non-osseous cells. A reduction in Runx2 promoter activity was observed in two regions; one was between -3 kb and -1 kb, and the other was between -155 bp and -75 bp. The step-down pattern in promoter activity between -3 kb and -1 kb was observed only in osseous cells. Interestingly, the step-down pattern between -155 bp and -75 bp was revealed in both cell types. Consistently, beta-galactosidase staining in axial skeleton of -3 kb-Runx2-P1-LacZ transgenic mice was positive, but that of all skeletal tissues of -1 kb-Runx2-P1-LacZ transgenic mice was negative. To identify upstream regulators of the Runx2-P1 promoter, we screened 100 transcription factors using Runx2-P1-luciferase reporter constructs in NIH3T3 fibroblasts and HeLa cells. Among them, HIF2A was identified as the strongest activator of Runx2-P1 promoter activity. A HIF2A-responsive site on the Runx2 promoter was identified between -106 bp and -104 bp by mutation analysis. An electrophoretic mobility shift assay and chromatin immunoprecipitation assay confirmed the binding of HIF2A to the Runx2-P1 promoter in vitro and in vivo, respectively. Knock-down using siRNA against HIF2A confirmed that HIF2A is an important regulator of Runx2 gene expression. Collectively, these results suggest that the region between -3 kb and -1 kb is required for the minimal skeletal tissue-specific expression of Runx2, and that the region between -155 bp and -75 bp is important for its basal transcription, which may be in part mediated by HIF2A in bone tissues."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.org/dc/terms/identifier"doi:10.1016/j.gene.2008.03.003"xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Kawaguchi H."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Ikeda T."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Choi J.Y."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Saito T."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Tamiya H."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Jeong J.H."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Jung Y.K."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Ohba S."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Chung U.I."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/author"Yano F."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/name"Gene"xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/pages"53-60"xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/title"Analysis of the Runx2 promoter in osseous and non-osseous cells and identification of HIF2A as a potent transcription activator."xsd:string
http://purl.uniprot.org/citations/18442887http://purl.uniprot.org/core/volume"416"xsd:string
http://purl.uniprot.org/citations/18442887http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18442887
http://purl.uniprot.org/citations/18442887http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18442887
http://purl.uniprot.org/uniprot/#_A0A0D9SEN7-mappedCitation-18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18442887
http://purl.uniprot.org/uniprot/#_E0CY45-mappedCitation-18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18442887
http://purl.uniprot.org/uniprot/#_E0CZ12-mappedCitation-18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18442887
http://purl.uniprot.org/uniprot/#_E0CZC6-mappedCitation-18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18442887
http://purl.uniprot.org/uniprot/#_F7CN98-mappedCitation-18442887http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18442887