Authors
Bidwell, Joseph P.Van Wijnen, Andre J.
Fey, Edward G.
Merriman, Harold L.
Penman, Sheldon
Stein, Janet L.
Stein, Gary S.
Lian, Jane B.
Document Type
Journal ArticlePublication Date
1994-04-01Keywords
Animals; Base Sequence; Cell Nucleus; DNA; DNA-Binding Proteins; Molecular Sequence Data; Nuclear Matrix; Nuclear Proteins; Osteosarcoma; Proto-Oncogene Proteins c-jun; Rats; Receptors, Calcitriol; Transcription Factors; Tumor Cells, Cultured; Vitamin DLife Sciences
Medicine and Health Sciences
Metadata
Show full item recordAbstract
The subnuclear distribution of the vitamin D receptor was investigated to begin addressing the contribution of nuclear architecture to vitamin D-responsive control of gene expression in ROS 17/2.8 rat osteosarcoma cells. The nuclear matrix is an anastomosing network of filaments that is functionally associated with DNA replication, transcription, and RNA processing. The representation of vitamin D receptor in the nuclear matrix and nonmatrix nuclear fractions was determined by the combined application of 1) sequence-specific interactions with the vitamin D receptor binding element of the rat bone-specific osteocalcin gene promoter and 2) Western blot analysis. Both methods confirmed the presence of vitamin D receptor in the nonmatrix nuclear fraction and the absence of detectable vitamin D receptors associated with the nuclear matrix. In contrast, these same nuclear matrix proteins preparations exhibited association with the general transcription factor AP-1 and a bone tissue-specific promoter binding factor NMP2. NMP-2 exhibits recognition for a promoter domain contiguous to the vitamin D-responsive element of the osteocalcin gene, although the vitamin D receptor does not appear to be a component of the nuclear matrix proteins. Interrelationships between nuclear matrix proteins and nonmatrix nuclear proteins, in mediating steroid hormone responsiveness of a vitamin D-regulated promoter, are therefore suggested.Source
J Cell Biochem. 1994 Apr;54(4):494-500. Link to article on publisher's siteDOI
10.1002/jcb.240540417Permanent Link to this Item
http://hdl.handle.net/20.500.14038/32429PubMed ID
8014199Related Resources
Link to article in PubMedae974a485f413a2113503eed53cd6c53
10.1002/jcb.240540417