Xie Y Q, Takimoto K, Pitot H C, Miskimins W K, Lindahl R
Department of Biochemistry and Molecular Biology, University of South Dakota School of Medicine, Vermillion 57069, USA.
Nucleic Acids Res. 1996 Nov 1;24(21):4185-91. doi: 10.1093/nar/24.21.4185.
The Class 3 aldehyde dehydrogenase gene (ALDH-3) is differentially expressed. Expression is either constitutive or xenobiotic inducible via an aromatic hydrocarbon (Ah) receptor-mediated pathway, depending upon the tissue. A series of studies were performed to examine the regulation of rat ALDH-3 basal expression. DNase I footprint analysis identified four DNA regions within the proximal 1 kb of the 5' flanking region of rat ALDH-3 which interact with regulatory proteins. Reporter gene and gel mobility shift assays indicate that Sp1-like proteins interact with two proximal DNase I footprinted sites to confer strong promoter activity. Two distal DNase I footprinted sites are found within a region that inhibits rat ALDH-3 promoter activity. This negative region is bound by NF1-like proteins and/or unique proteins. This 1 kb 5' flanking region of rat ALDH-3 may act constitutively in many cell types. In contrast with other Ah receptor regulated genes, no DNA elements or transcription factors acting within this region appear to be involved in regulating xenobiotic-inducible expression of rat ALDH-3.
3类醛脱氢酶基因(ALDH-3)存在差异表达。其表达情况取决于组织,要么是组成型表达,要么通过芳烃(Ah)受体介导的途径由外源性物质诱导表达。开展了一系列研究以检测大鼠ALDH-3基础表达的调控情况。DNA酶I足迹分析确定了大鼠ALDH-3 5'侧翼区近端1 kb内与调控蛋白相互作用的四个DNA区域。报告基因和凝胶迁移率变动分析表明,类Sp1蛋白与两个近端DNA酶I足迹位点相互作用,赋予强启动子活性。在一个抑制大鼠ALDH-3启动子活性的区域内发现了两个远端DNA酶I足迹位点。该负性区域由类NF1蛋白和/或独特蛋白结合。大鼠ALDH-3的这个1 kb 5'侧翼区可能在许多细胞类型中组成性发挥作用。与其他Ah受体调控基因不同,该区域内似乎不存在参与调控大鼠ALDH-3外源性诱导表达的DNA元件或转录因子。