Characterization of the promoter region of the mouse gene encoding the steroidogenic acute regulatory protein

被引:217
作者
Caron, KM
Ikeda, Y
Soo, SC
Stocco, DM
Parker, KL
Clark, BJ
机构
[1] DUKE UNIV, MED CTR, DEPT MED, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, DEPT PHARMACOL, DURHAM, NC 27710 USA
[3] TEXAS TECH UNIV, HLTH SCI CTR, DEPT CELL BIOL & BIOCHEM, LUBBOCK, TX 79430 USA
[4] UNIV LOUISVILLE, SCH MED, DEPT BIOCHEM, LOUISVILLE, KY 40292 USA
关键词
D O I
10.1210/me.11.2.138
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Steroidogenic acute regulatory protein (StAR) delivers cholesterol to the inner mitochondrial membrane, where the cholesterol side-chain cleavage enzyme carries out the first committed step in steroid hormone biosynthesis. StAR expression is restricted to steroidogenic cells and is rapidly induced by treatment with trophic hormones or cAMP. We analyzed the 5'-flanking region of the mouse StAR gene to elucidate the mechanisms that regulate its cell-specific and hormone-induced expression. In transient transfection assays, a luciferase reporter gene driven by the StAR 5'-flanking region was preferentially expressed by steroidogenic Y1 adrenocortical and MA-10 Leydig cells in a cAMP-responsive manner. 5'-Deletion and site-directed mutagenesis studies identified a region between -254 and -113 that is essential for full levels of promoter activity. This region contains a binding site for the orphan nuclear receptor steroidogenic factor-1 (SF-1) that, although not required for hormone induction, is critical for basal promoter activity, thus implicating SF-1 in StAR expression. Analyses of knockout mice deficient in SF-1 further supported an important role for SF-1 in StAR gene expression. These studies provide novel insights into the mechanisms that regulate StAR gene expression and extend our understanding of SF-1's global roles within steroidogenic cells.
引用
收藏
页码:138 / 147
页数:10
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