Taylor W E, Najmabadi H, Strathearn M, Jou N T, Liebling M, Rajavashisth T, Chanani N, Phung L, Bhasin S
Division of Endocrinology, Metabolism, and Molecular Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, California 90059, USA.
Endocrinology. 1996 Dec;137(12):5407-14. doi: 10.1210/endo.137.12.8940364.
Stem cell factor (SCF) gene expression is regulated by FSH in testicular Sertoli cells. Many functions of FSH are mediated through the second messenger cAMP. We show that cAMP activates transcription of the human SCF promoter in a Sertoli cell line. The human SCF promoter was cloned in cosmid vector pWE15, and its DNA sequence was determined for the promoter region extending 2.3 kilobase pairs upstream from the translation start site at +184 bp. The in vivo messenger RNA (mRNA) start site, by primer-extension studies, was located in exon 1 at +109 bp in human testis mRNA, and at +99 bp in mouse SF7 Sertoli cell line or GC1 germ cell line mRNA. To test which regions of the SCF promoter are necessary for regulation by cAMP, a series of 5'-end deletions of this region were cloned onto the luciferase reporter gene in plasmid pXP1. The SCF promoter region was fused to luciferase downstream (at +120) from its +109 mRNA start site, extending upstream a variable distance to BstXI (-162), BamHI (-313), Bgl2 (-853), or XbaI (-2185). The shortest of these fragments extending only to -162 bp, contains possible SP1 and AP-2 elements. When mouse Sertoli SF7 or human JEG.3 cell lines were transfected with these plasmids, all of the mutants were regulated by 8Br-cAMP or forskolin, as expected for the SCF gene, whereas FSH and TPA had no effect. In the shortest promoter deletion -162, luciferase expression from SF7 cells in serum-free media was at a moderate basal level, but it was induced in six h about 2-fold by 8Br-cAMP, and over 7-fold by forskolin (an adenylate cyclase activator) to high levels, similar to the SV40 positive control promoter. In SCF-luc plasmids extending to -853 or -2185, luciferase expression was still inducible by 8Br-cAMP and forskolin to high levels, but basal promoter activity was repressed to levels over 15-fold lower, in both the absence or presence of testosterone in the media for SF7 cells. The distal portion of the human SCF promoter (between -313 and -853, and also -853 and -2185) inhibits the basal level of transcription, while the proximal region (5' of -162) can mediate activation by cAMP.
干细胞因子(SCF)基因表达在睾丸支持细胞中受促卵泡激素(FSH)调控。FSH的许多功能是通过第二信使环磷酸腺苷(cAMP)介导的。我们发现,cAMP可激活支持细胞系中人SCF启动子的转录。将人SCF启动子克隆到黏粒载体pWE15中,并测定了其从翻译起始位点(+184 bp)上游2.3千碱基对延伸的启动子区域的DNA序列。通过引物延伸研究,体内信使核糖核酸(mRNA)起始位点在人睾丸mRNA的外显子1中位于+109 bp处,在小鼠SF7支持细胞系或GC1生殖细胞系mRNA中位于+99 bp处。为了检测SCF启动子的哪些区域对于cAMP调控是必需的,将该区域的一系列5'端缺失片段克隆到质粒pXP1中的荧光素酶报告基因上。SCF启动子区域在其+109 mRNA起始位点下游(+120处)与荧光素酶融合,向上游延伸不同距离至BstXI(-162)、BamHI(-313)、Bgl2(-853)或XbaI(-2185)。这些片段中最短的仅延伸至-162 bp,包含可能的SP1和AP-2元件。当用这些质粒转染小鼠支持细胞SF7或人JEG.3细胞系时,所有突变体均受8-溴环磷酸腺苷(8Br-cAMP)或福斯可林调控,这与SCF基因的预期情况一致,而FSH和佛波酯(TPA)则无作用。在最短的启动子缺失片段-162中,无血清培养基中SF7细胞的荧光素酶表达处于中等基础水平,但8Br-cAMP在6小时内可诱导其表达约2倍,福斯可林(一种腺苷酸环化酶激活剂)可诱导其表达超过7倍,使其达到高水平,类似于SV40阳性对照启动子。在延伸至-853或-2185的SCF-荧光素酶质粒中,荧光素酶表达仍可被8Br-cAMP和福斯可林诱导至高水平,但基础启动子活性在SF7细胞培养基中无论有无睾酮存在的情况下均被抑制至低15倍以上的水平。人SCF启动子的远端部分(-313至-853之间,以及-853至-2185之间)抑制转录的基础水平,而近端区域(-162的5'端)可介导cAMP的激活作用。