Bidwell J P, van Wijnen A J, Fey E G, Merriman H, Penman S, Stein J L, Stein G S, Lian J B
Department of Cell Biology, University of Massachusetts, Worcester 01655.
J Cell Biochem. 1994 Apr;54(4):494-500. doi: 10.1002/jcb.240540417.
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.
为了初步探讨核结构对ROS 17/2.8大鼠骨肉瘤细胞中维生素D反应性基因表达调控的作用,研究了维生素D受体在细胞核内的分布情况。核基质是一个相互连接的丝状网络,在功能上与DNA复制、转录和RNA加工相关。通过联合应用以下两种方法来确定维生素D受体在核基质和非核基质核组分中的表达情况:1)与大鼠骨特异性骨钙素基因启动子的维生素D受体结合元件进行序列特异性相互作用;2)蛋白质免疫印迹分析。两种方法均证实维生素D受体存在于非核基质核组分中,而与核基质相关的维生素D受体未被检测到。相反,这些相同的核基质蛋白制剂显示与一般转录因子AP-1和骨组织特异性启动子结合因子NMP2有关联。NMP-2对与骨钙素基因维生素D反应元件相邻的启动子结构域具有识别作用,尽管维生素D受体似乎不是核基质蛋白的组成部分。因此,提示了核基质蛋白与非核基质核蛋白之间在介导维生素D调节启动子的类固醇激素反应性方面的相互关系。