Keaveney M, Klug J, Gannon F
Department of Microbiology, University College Galway, Ireland.
DNA Seq. 1992;2(6):347-58. doi: 10.3109/10425179209020816.
We present the sequence of 2770 nucleotides of 5' flanking sequence of the human estrogen receptor (hER) gene. The positions of potential binding sites for a number of trans-acting factors including Sp1, OTF-1, INR, TATA and CAAT box factors as well as several half palindromic hormone responsive elements (HREs) have been mapped by comparison with the consensus binding sequences. A long alternating purine/pyrimidine (APP) tract which has the potential for structural diversity as indicated by site-specific cleavage with S1 nuclease is another feature of this region. The organization of this promoter region is compared to that of other cloned members of this family. The potential roles that these sequences may play in the transcriptional regulation of this gene are discussed.
我们展示了人类雌激素受体(hER)基因5'侧翼序列的2770个核苷酸序列。通过与共有结合序列比较,已确定了包括Sp1、OTF-1、INR、TATA和CAAT盒因子等多种反式作用因子以及几个半回文激素反应元件(HRE)潜在结合位点的位置。一个长的交替嘌呤/嘧啶(APP)序列,经S1核酸酶位点特异性切割显示具有结构多样性的潜力,是该区域的另一个特征。将该启动子区域的结构与该家族其他克隆成员的结构进行了比较。讨论了这些序列在该基因转录调控中可能发挥的潜在作用。