Jänne M, Hammond G L
Department of Obstetrics & Gynecology, and Medical Research Council of Canada Group in Fetal and Neonatal Health and Development, University of Western Ontario, Canada.
J Biol Chem. 1998 Dec 18;273(51):34105-14. doi: 10.1074/jbc.273.51.34105.
Hepatocytes are the major source of sex hormone-binding globulin (SHBG), a glycoprotein that transports sex steroids in the blood and regulates their access to target tissues. The human SHBG proximal promoter was analyzed by DNase I footprinting, and the functional significance of 6 footprinted regions (FP1-FP6) within the proximal promoter was studied in human HepG2 hepatoblastoma cells. Two footprinted regions (FP1 and FP3) contain binding sites for the chicken ovalbumin upstream promoter-transcription factor (COUP-TF) and hepatocyte nuclear factor-4 (HNF-4). In experiments where SHBG promoter-luciferase reporter gene constructs were co-transfected into HepG2 cells with COUP-TF and/or HNF-4 expression vectors, HNF-4 markedly increased transcription, whereas COUP-TF suppressed this probably by displacing HNF-4 from their common FP1-binding site. This COUP-TF/HNF-4-binding site within FP1 includes a TTTAA sequence, located at nucleotides -30/-26 upstream of the transcription start site, which fails to interact with human TFIID, TATA-binding protein in vitro. When this sequence was replaced with an idealized HNF-4-binding site, the transcriptional activity of the promoter increased in HepG2 cells. Taken together, these data imply that an interplay between COUP-TF and HNF-4 at a site within FP1 regulates human SHBG expression and that HNF-4 controls transcription from this TATA-less promoter by somehow substituting for TATA-binding protein in the recruitment of a transcription preinitiation complex.
肝细胞是性激素结合球蛋白(SHBG)的主要来源,SHBG是一种糖蛋白,在血液中运输性类固醇并调节它们进入靶组织。通过DNA酶I足迹法分析了人SHBG近端启动子,并在人HepG2肝癌细胞中研究了近端启动子内6个足迹区域(FP1 - FP6)的功能意义。两个足迹区域(FP1和FP3)含有鸡卵清蛋白上游启动子转录因子(COUP - TF)和肝细胞核因子4(HNF - 4)的结合位点。在将SHBG启动子 - 荧光素酶报告基因构建体与COUP - TF和/或HNF - 4表达载体共转染到HepG2细胞的实验中,HNF - 4显著增加转录,而COUP - TF可能通过从它们共同的FP1结合位点取代HNF - 4来抑制转录。FP1内的这个COUP - TF/HNF - 4结合位点包括一个TTTAA序列,位于转录起始位点上游核苷酸 - 30/-26处,在体外它不与人TFIID(TATA结合蛋白)相互作用。当这个序列被理想的HNF - 4结合位点取代时,启动子在HepG2细胞中的转录活性增加。综上所述,这些数据表明在FP1内的一个位点上COUP - TF和HNF - 4之间的相互作用调节人SHBG的表达,并且HNF - 4通过在募集转录起始前复合物中以某种方式替代TATA结合蛋白来控制这个无TATA启动子的转录。