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http://purl.uniprot.org/citations/8510931http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8510931http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/8510931http://www.w3.org/2000/01/rdf-schema#comment"The erg gene is a member of the ets gene family. ETS proteins have been shown to bind specifically the (GGA-A/T) motif and to transactivate via this consensus sequence. The human erg products exhibit approximately 70% homology with ETS proteins in their DNA-binding domain. We have isolated three erg cDNAs from a human fetal liver library. Two of them are different from the previously described erg-1 and erg-2 cDNAs (Rao et al., Science, 1987, 237, 635-639), in the middle of their coding sequence and in their 5' part where a novel initiation codon is introduced. These isoforms are generated by alternative RNA splicing from a single gene that leads to the inclusion or exclusion of different exon sequences. The three cDNAs expressed by an in vitro transcription-translation system direct the synthesis of proteins of approximately 38, 49 and 55 kDa. These in vitro erg products were tested for their DNA-binding activity by gel mobility-shift assays with different probes containing the ETS-specific binding site. The results indicated that all these erg isoforms are able to bind the ETS binding site in a specific manner. Our data using transient transfection assays indicate that erg protein isoforms function as transcriptional activators."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Plaza S."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Plaza S."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Stehelin D."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Stehelin D."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Duterque-Coquillaud M."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Duterque-Coquillaud M."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Niel C."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/author"Niel C."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/date"1993"xsd:gYear
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/name"Oncogene"xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/pages"1865-1873"xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/pages"1865-1873"xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/title"New human erg isoforms generated by alternative splicing are transcriptional activators."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/title"New human erg isoforms generated by alternative splicing are transcriptional activators."xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/volume"8"xsd:string
http://purl.uniprot.org/citations/8510931http://purl.uniprot.org/core/volume"8"xsd:string
http://purl.uniprot.org/citations/8510931http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8510931
http://purl.uniprot.org/citations/8510931http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/8510931
http://purl.uniprot.org/citations/8510931http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8510931
http://purl.uniprot.org/citations/8510931http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/8510931