Proximal promoter binding protein contributes to developmental, tissue-restricted expression of the rat osteocalcin gene
Authors
Heinrichs, Arianne A.J.Bortell, Rita
Bourke, Michael
Lian, Jane B.
Stein, Gary S.
Stein, Janet L.
UMass Chan Affiliations
Department of Cell BiologyDocument Type
Journal ArticlePublication Date
1995-01-01Keywords
AnimalsBase Sequence
Cell Differentiation
Cell Extracts
DNA
Gene Expression Regulation, Developmental
Humans
Molecular Sequence Data
Organ Specificity
Osteoblasts
Osteocalcin
Promoter Regions, Genetic
Rats
Cell Biology
Metadata
Show full item recordAbstract
Osteocalcin is a 6 kD tissue-specific calcium binding protein associated with the bone extracellular matrix. The osteocalcin gene is developmentally expressed in postoproliferative rat osteoblasts with regulation at least in part at the transcriptional level. Multiple, basal promoter and enhancer elements which control transcriptional activity in response to physiological mediators, including steroid hormones, have been identified in the modularly organized osteocalcin gene promoter. The osteocalcin box (OC box) is a highly conserved basal regulatory element residing between nucleotides -99 and -76 of the proximal promoter. We recently established by in vivo competition analysis that protein interactions at the CCAAT motif, which is the central core of the rat OC box, are required for support of basal transcription [Heinrichs et al. J Cell Biochem 53:240-250, 1993]. In this study, by the combined utilization of electrophoretic mobility shift analysis, UV cross linking, and DNA affinity chromatography, we have identified a protein that binds to the rat OC box. Results are presented that support involvement of the OC box-binding protein in regulating selective expression of the osteocalcin gene during differentiation of the rat osteoblast phenotype and suggest that this protein is tissue restricted.Source
J Cell Biochem. 1995 Jan;57(1):90-100. Link to article on publisher's siteDOI
10.1002/jcb.240570110Permanent Link to this Item
http://hdl.handle.net/20.500.14038/49656PubMed ID
7721961Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1002/jcb.240570110