Sandhoff T W, Hales D B, Hales K H, McLean M P
Department of Obstetrics and Gynecology, University of South Florida College of Medicine, Tampa 33606, USA.
Endocrinology. 1998 Dec;139(12):4820-31. doi: 10.1210/endo.139.12.6345.
Steroidogenic acute regulatory (StAR) protein is synthesized in response to tropic hormones to facilitate cholesterol transport to the inner mitochondrial membrane-bound P450 side-chain cleavage enzyme (P450scc), the first enzymatic step in the steroid hormone biosynthetic pathway. Gonadotropins activate expression of their target genes via the cAMP second messenger system. We have demonstrated that cAMP administration to rat luteal cells stimulates expression of both StAR messenger RNA and protein. Because cholesterol delivery is the first regulated step in steroidogenesis, and because StAR messenger RNA levels are increased in response to tropic hormone and cAMP stimulation, the mechanism by which tropic hormones/cAMP stimulate transcription needs to be elucidated. To this end, approximately 2.7 kb of the rat StAR promoter was isolated and sequenced. Sequence analysis revealed the presence of a TATA-like element as well as multiple regulatory motifs including steroidogenic factor 1 (SF-1) binding sites, an estrogen receptor half-site, and two AP-1 sites within the promoter region. 5'-RACE experiments determined the transcription start site to be located 82 bp upstream of the ATG translation start codon. Electrophoretic mobility shift assays and supershift analysis demonstrated SF-1 binding to three SF-1 binding sites in the rat StAR promoter with high affinity and two SF-1 binding sites with low affinity. Transfection of mouse Y1 adrenal tumor cells and human bladder carcinoma cells (HTB9s) with the rat StAR promoter demonstrated that SF-1 was able to activate transcription of the luciferase reporter gene and that the rat StAR promoter was responsive to cAMP. Nested deletions of the rat StAR promoter (1.9 kb) identified a region between -1413 and -998 that is essential for maximal activation of the rat StAR gene in HTB9 cells; however, deletion of this region does not affect responsiveness to cAMP. 5'-Deletion and site-directed mutagenesis experiments demonstrated that the SF-1 motifs identified within the rat StAR promoter (located at positions -764, -455, and -106) were sufficient to activate transcription as well as confer cAMP responsiveness to the rat StAR gene. Site-directed mutagenesis studies using the smallest promoter fragment demonstrated that the two proximal SF-1 binding sites are crucial for StAR gene transcription, both at a basal level and in response to cAMP stimulation. These studies provide novel insights into the regulation of the rat StAR gene at the transcriptional level by SF-1.
类固醇生成急性调节(StAR)蛋白是在促性腺激素的作用下合成的,以促进胆固醇转运至线粒体内膜结合的细胞色素P450侧链裂解酶(P450scc),这是类固醇激素生物合成途径中的第一步酶促反应。促性腺激素通过环磷酸腺苷(cAMP)第二信使系统激活其靶基因的表达。我们已经证明,向大鼠黄体细胞施用cAMP可刺激StAR信使核糖核酸(mRNA)和蛋白的表达。由于胆固醇转运是类固醇生成中的首个受调控步骤,且StAR mRNA水平会因促性腺激素和cAMP刺激而升高,因此需要阐明促性腺激素/cAMP刺激转录的机制。为此,分离并测序了大鼠StAR启动子约2.7 kb的片段。序列分析揭示了一个类似TATA的元件以及多个调控基序,包括类固醇生成因子1(SF-1)结合位点、一个雌激素受体半位点以及启动子区域内的两个激活蛋白-1(AP-1)位点。5'-RACE实验确定转录起始位点位于ATG翻译起始密码子上游82 bp处。电泳迁移率变动分析和超迁移分析表明,SF-1以高亲和力结合大鼠StAR启动子中的三个SF-1结合位点,并以低亲和力结合两个SF-1结合位点。用大鼠StAR启动子转染小鼠Y1肾上腺肿瘤细胞和人膀胱癌细胞(HTB9s)表明,SF-1能够激活荧光素酶报告基因的转录,且大鼠StAR启动子对cAMP有反应。大鼠StAR启动子(1.9 kb)的嵌套缺失鉴定出一个位于-1413至-998之间的区域,该区域对于HTB9细胞中大鼠StAR基因的最大激活至关重要;然而,删除该区域并不影响对cAMP的反应性。5'-缺失和定点诱变实验表明,在大鼠StAR启动子中鉴定出的SF-1基序(位于-764、-455和-106位)足以激活转录并赋予大鼠StAR基因对cAMP的反应性。使用最小启动子片段的定点诱变研究表明,两个近端SF-1结合位点对于StAR基因转录至关重要,无论是在基础水平还是对cAMP刺激的反应中。这些研究为SF-1在转录水平上对大鼠StAR基因的调控提供了新的见解。