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http://purl.uniprot.org/citations/28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28286232http://www.w3.org/2000/01/rdf-schema#comment"Steroid receptor coactivator-1 (SRC-1), a well-studied coactivator of estrogen receptor (ER), is known to play an important and functional role in the development and maintenance of bone tissue. Previous reports suggest SRC-1 maintains bone mineral density primarily through its interaction with ER. Here we demonstrate that SRC-1 can also affect bone development independent of estrogen signaling as ovariectomized SRC-1 knockout (SRC-1 KO) mouse had decreased bone mineral density. To identify estrogen-independent SRC-1 target genes in osteoblastogenesis, we undertook an integrated analysis utilizing ChIP-Seq and mRNA microarray in transformed osteoblast-like U2OS-ERα cells. We identified critical osteoblast differentiation genes regulated by SRC-1, but not by estrogen including alkaline phosphatase and osteocalcin. Ex vivo primary culture of osteoblasts from SRC-1 wild-type and KO mice confirmed the role of SRC-1 in osteoblastogenesis, associated with altered ALPL levels. Together, these data indicate that SRC-1 can impact osteoblast function in an ER-independent manner."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.org/dc/terms/identifier"doi:10.1016/j.mce.2017.03.005"xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Lu X."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Li W."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Chen K."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Liao L."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Rae J.M."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Oesterreich S."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Hartmaier R.J."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Watters R.J."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Gillihan R.M."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/author"Osmanbeyoglu H.U."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/name"Mol Cell Endocrinol"xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/pages"21-27"xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/title"Steroid receptor coactivator-1 can regulate osteoblastogenesis independently of estrogen."xsd:string
http://purl.uniprot.org/citations/28286232http://purl.uniprot.org/core/volume"448"xsd:string
http://purl.uniprot.org/citations/28286232http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28286232
http://purl.uniprot.org/citations/28286232http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28286232
http://purl.uniprot.org/uniprot/#_A8K1V4-mappedCitation-28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28286232
http://purl.uniprot.org/uniprot/#_A0A1W2P7S6-mappedCitation-28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28286232
http://purl.uniprot.org/uniprot/#_A0A1W2P881-mappedCitation-28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28286232
http://purl.uniprot.org/uniprot/#_A0A1W2P6K7-mappedCitation-28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28286232
http://purl.uniprot.org/uniprot/#_A0A1W2P7C1-mappedCitation-28286232http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28286232