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Basal level transcriptional regulation of the human angiotensin II type 1 receptor gene

机译:人类血管紧张素II 1型受体基因的基础水平转录调控

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The peptide hormone angiotensin II regulates a variety of physiological responses which are mediated by its interaction with high affinity G protein-coupled receptors localized on the surface of target cells. To gain insights into the transcriptional regulation of the human angiotensin II type 1 receptor (hAT_1R) gene, we have isolated 1 kb of the 5'-flanking sequence of this gene. Expression constructs containing various 5'-deletions of the hAt_1R promoter region, fused upstream to the luciferase reporter gene, were transiently transfected into H295-R, HEC-1B and A549 cells. It was demonstrated that a 145 bp sequence within the promoter region was required for basal level expression of the hAT_1R gene in all of the three cell lines investigated. Computer analysis indicated the existence of numerous putative transcription factor binding sites in this region. Further detailed deletion data suggested essential transcription factor binding sites between -98 and -79 bp. Electrophoretic mobility shift assays revealed that four protein-DNA complexes were formed within the -98 to -79 bp region of the hAT_1R gene when incubated with H295-R cell nuclear extract. Site-directed mutagenesis experiments showed that a putative Sp1 binding site was critical for the basal level expression of the hAT_1R gene.
机译:肽激素血管紧张素II调节多种生理反应,这些反应是由其与定位在靶细胞表面的高亲和力G蛋白偶联受体相互作用而介导的。为了深入了解人类血管紧张素II 1型受体(hAT_1R)基因的转录调控,我们分离了该基因5'侧翼序列的1 kb。将含有hAt_1R启动子区域各种5'缺失的表达构建体(与荧光素酶报道基因上游融合)瞬时转染到H295-R,HEC-1B和A549细胞中。已经证明,在所研究的所有三种细胞系中,hAT_1R基因的基础水平表达都需要启动子区域内的145 bp序列。计算机分析表明在该区域中存在许多推定的转录因子结合位点。进一步的详细删除数据表明,必需的转录因子结合位点在-98和-79 bp之间。电泳迁移率变动分析表明,与H295-R细胞核提取物孵育时,在hAT_1R基因的-98至-79 bp区域内形成了四个蛋白质-DNA复合物。定点诱变实验表明,假定的Sp1结合位点对于hAT_1R基因的基础水平表达至关重要。

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