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An upstream region of the H2AZ gene promoter modulates promoter activity in different cell types

机译:H2AZ基因启动子的上游区域调节不同细胞类型中的启动子活性

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Human H2AZ gene promoter fragments that included sequences upstream from the core promoter resulted in decreased activity of reporter constructs transfectcd into several huinnn cell lines, but increased activity in the undiffcrcntiatcd human embryonal carcinoma cell line Tera-2. Differentiation of Tera-2 cells in media containing retinoic acid restored the ability of the upstream region to downregulate H2AZ gene promoter activity. Levels of endogenous H2AZ niRNA were also found to be 2.5-lbld higher in undilTerenti-ated Tera-2 cells than in clilTerentiated Tera-2 cells. A 128 bp region located 234 to 361 bp upstream from the transcription start site of the H2AZ gene was found to be responsible for the modulation of reporter activity. The upstream region also functioned similarly when removed from the H2AZ gene promoter and inserted upstream of the SV40 promoter in reporter constructs. Gel mobility shift studies of fragments of this region revealed two sequence elements, CTCCTCC ami CACGTO, that bound nuclear factors in vitro.
机译:人H2AZ基因启动子片段包括核心启动子上游的序列,导致转染入数种huinnn细胞系的报告基因构建体活性降低,但在未分化的人胚胎癌细胞系Tera-2中活性增强。 Tera-2细胞在含有视黄酸的培养基中的分化恢复了上游区域下调H2AZ基因启动子活性的能力。还发现,未稀释的Tera-2细胞中的内源性H2AZ niRNA水平比未稀释的Tera-2细胞高2.5-lbld。发现位于H2AZ基因转录起始位点上游234到361 bp的128 bp区域负责报告基因活性的调节。当从H2AZ基因启动子中移出并插入报告基因构建体中SV40启动子的上游时,上游区域的功能也相似。该区域片段的凝胶迁移率迁移研究揭示了两个序列元素,CTCCTCC和CACGTO,它们在体外与核因子结合。

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