Positive and negative regulatory regions in promoters of human glutathione transferase alpha genes.

M Lorper, W A Schulz, F Morel, U Warskulat, H Sies
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引用次数: 12

Abstract

The human glutathione transferase (GST, EC 2.5.1.18) alpha class locus comprises several genes and pseudogenes. Genomic DNA encoding several human alpha-class-related genes and pseudogenes was cloned and characterized. Three distinct but highly similar 5'-flanking regions of GST alpha genes as well as a series of 5'-deletions were investigated for promoter activity by fusion to the luciferase reporter gene. Transient transfection of these luciferase constructs into human hepatoblastoma, kidney carcinoma, nephroblastoma or bladder carcinoma cells revealed that the promoters are active and contain both positive and negative regulatory regions that behave in a cell-type specific fashion. The 150 bp proximal promoter regions of the three sequences retained the same relative activities as the full length promoters. Two of them were equally active, whereas the third one showed only 20% of the activity of the two stronger promoters. Site-directed mutagenesis indicated that a conspicuous insertion of three nucleotides (TTT) in the weak promoter is not responsible for the different activities.

人谷胱甘肽转移酶基因启动子的正调控区和负调控区。
人谷胱甘肽转移酶(GST, EC 2.5.1.18) α类位点由多个基因和假基因组成。克隆并鉴定了几个人类α类相关基因和假基因的基因组DNA。通过与荧光素酶报告基因融合,研究了GST α基因的三个不同但高度相似的5'侧区域以及一系列5'缺失的启动子活性。将这些荧光素酶构建体瞬间转染到人肝母细胞瘤、肾癌、肾母细胞瘤或膀胱癌细胞中,发现启动子是活跃的,并且包含以细胞类型特异性方式行为的正调控区和负调控区。三个序列的近端150 bp启动子区与全长启动子区保持相同的相对活性。其中两种活性相同,而第三种活性仅为两种较强启动子的20%。位点定向突变表明,弱启动子中明显插入的三个核苷酸(TTT)不是导致不同活性的原因。
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