Response element binding proteins and intracellular vitamin D binding proteins: novel regulators of vitamin D trafficking, action and metabolism

被引:48
作者
Adams, JS
Chen, H
Chun, R
Gacad, MA
Encinas, C
Ren, SY
Nguyen, L
Wu, SX
Hewison, M
Barsony, J
机构
[1] Univ Calif Los Angeles, Cedars Sinai Med Ctr, Sch Med, Burns & Allen Res Inst, Los Angeles, CA 90024 USA
[2] Univ Birmingham, Dept Med Sci, Birmingham B15 2TT, W Midlands, England
[3] NIDDKD, Lab Cell Biochem & Biol, NIH, Bethesda, MD 20892 USA
关键词
vitamin D; binding proteins; receptors; transcription; resistance; metabolism; traffic; heat shock proteins; heterogeneous nuclear ribonucleoproteins;
D O I
10.1016/j.jsbmb.2004.03.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Using vitamin D-resistant New World primates as model of natural diversity for sterol/steroid action and metabolism, two families of novel intracellular vitamin D regulatory proteins have been discovered and their human homologs elucidated. The first family of proteins, heterogeneous nuclear ribonucleoproteins (hnRNPs), initially considered to function only as pre-mRNA-interacting proteins, have been demonstrated to be potent cis-acting, trans-dominant regulators of vitamin D hormone-driven gene transactivation. The second group of proteins bind 25-hydroxylated vitamin D metabolites. Their overexpression increases vitamin D receptor (VDR)-directed target gene expression. We found that these intracellular vitamin D binding proteins (IDBPs) are homologous to proteins in the heat shock protein-70 family. Our ongoing studies indicate directly or indirectly through a series of protein interactions that the IDBPs interact with hydroxylated vitamin D metabolites and facilitate their intracellular targeting. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:461 / 465
页数:5
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