Song C S, Her S, Slomczynska M, Choi S J, Jung M H, Roy A K, Chatterjee B
Department of Cellular and Structural Biology, University of Texas Health Science Center at San Antonio.
Biochem J. 1993 Sep 15;294 ( Pt 3)(Pt 3):779-84. doi: 10.1042/bj2940779.
The far upstream region of the rat androgen receptor (AR) gene has been cloned, and the nucleotide sequence up to -2656 bp established. Nested deletion mutants of rat AR 5' flanking sequences were ligated to the luciferase reporter gene, and their promoter activities were examined in transfected COS1 cells. Results show a critical cis-acting domain located between positions -960 and -940. Deletion of this cis element resulted in a greater than 90% decrease in the promoter activity. A nuclear protein that specifically binds to this 21-nucleotide sequence was identified by gel mobility shift analysis. The -960/-940 cis element has no identify to the binding sequence of any known transcription factor. Furthermore, the cognate binding protein is present in both rat and human (HeLa) cell nuclear extracts. We conclude that a novel trans-activator interacting at the -960/-940 region plays a critical role in the regulation of AR gene expression.
大鼠雄激素受体(AR)基因的远上游区域已被克隆,并确定了至-2656 bp的核苷酸序列。将大鼠AR 5'侧翼序列的嵌套缺失突变体与荧光素酶报告基因连接,并在转染的COS1细胞中检测其启动子活性。结果显示在-960和-940位之间存在一个关键的顺式作用结构域。删除该顺式元件导致启动子活性下降超过90%。通过凝胶迁移率变动分析鉴定出一种与该21核苷酸序列特异性结合的核蛋白。-960/-940顺式元件与任何已知转录因子的结合序列均无同源性。此外,大鼠和人(HeLa)细胞核提取物中均存在同源结合蛋白。我们得出结论,一种在-960/-940区域相互作用的新型反式激活因子在AR基因表达的调控中起关键作用。