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首页> 外文期刊>Nucleic acids research >Common sets of nuclear factors binding to the conserved promoter sequence motif of two coordinately regulated ER protein genes,GRP78 and GRP94
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Common sets of nuclear factors binding to the conserved promoter sequence motif of two coordinately regulated ER protein genes,GRP78 and GRP94

机译:与两个协调调节的ER蛋白基因GRP78和GRP94的保守启动子序列基序结合的常见核因子集

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The GRP78 and GRP94 are two constitutively expressed ER resident proteins that are coordinately induced in response to stress conditions. The control of their induction is at the transcriptional level. We have previously demonstrated that the GRP78 and the GRP94 promoters share a common regulatory domain which is highly conserved. We report here that within this 36 bp promoter region is a CG/CAAT and a GC-rich sequence motif which are important for basal level and induced expression of the gene. Gel mobility shift assays with HeLa nuclear extracts and the conserved element from GRP78 and GRP94 show two shared, specific protein-DNA complexes. By ultraviolet crosslinking, the sizes of the proteins labeled in the slowermigrating complex are 210?, 110?, a doublet at 90/92? and 70 kD, and in the faster-migrating complex, protein species of about 55 kD. The formation of the second complex can be inhibited by competition with the coding strand of the conserved GRP element in a sequence specific manner. In addition, the Ku autoantigen which is abundant in HeLa cell extracts also binds. The sizes of the nuclear factors binding to the GRP78 and GRP94 conserved promoter elements are strikingly similar, providing further evidence that the two genes are coordinately regulated by common frans-acting factors.
机译:GRP78和GRP94是两个组成性表达的ER驻留蛋白,可响应压力条件而协同诱导。其诱导的控制在转录水平上。先前我们已经证明GRP78和GRP94启动子共享一个高度保守的共同调控域。我们在这里报告,在这个36 bp的启动子区域内是一个CG / CAAT和一个富含GC的序列基序,它们对于基础水平和该基因的诱导表达很重要。用HeLa核提取物和GRP78和GRP94的保守元素进行的凝胶迁移率移动分析显示了两种共有的特异性蛋白质-DNA复合物。通过紫外线交联,在缓慢迁移的复合物中标记的蛋白质的大小为210?,110 ?,在90/92?处为双峰。 70 kD的蛋白质,以及迁移速度更快的复合物中约55 kD的蛋白质。第二种复合物的形成可以通过以序列特异性方式与保守的GRP元件的编码链竞争而被抑制。另外,HeLa细胞提取物中丰富的Ku自身抗原也结合。与GRP78和GRP94保守的启动子元件结合的核因子大小惊人地相似,进一步证明了这两个基因受共同的反作用因子协同调节。

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