Jalinot P, Kédinger C
Nucleic Acids Res. 1986 Mar 25;14(6):2651-69. doi: 10.1093/nar/14.6.2651.
The adenovirus type 2 early EIIa (EIIaE) transcriptional control region exhibits an EIa-dependent enhancer activity (Imperiale et al., 1985, Proc. Natl. Acad. Sci. USA 82, 381-385). We have determined the sequence requirements for this enhancer activity by analysing the enhancing capacity of the entire EIIa promoter region, or portions of it, when inserted approximately 400 bp upstream of the rabbit beta-globin gene. Globin-specific transcription efficiency from the resulting recombinants was measured after transfection into HeLa cells, both in the presence and absence of the EIa products. It was found that the minimal EIIa element with bidirectional, EIa-dependent enhancer activity extends between -111 and -27 relative to the EIIaE major startsite (+1). Furthermore an extensive deletion analysis revealed, within this element, three functionally distinct regions: a central region between about -90 and -70, corresponding to an essential EIIaE upstream promoter element, and two flanking control elements (about 20 bp each) which, in the absence of the EIa products, exert a negative effect on the enhancer activity. Deletion of either one of these control elements renders the EIIaE enhancer activity constitutive, suggesting that the EIa products stimulate the EIIaE enhancer by relieving the negative control mediated by these sequences.
腺病毒2型早期EIIa(EIIaE)转录控制区表现出依赖于ElIa的增强子活性(Imperiale等人,1985年,《美国国家科学院院刊》82卷,381 - 385页)。我们通过分析整个EIIa启动子区域或其部分区域插入兔β - 珠蛋白基因上游约400 bp处时的增强能力,确定了这种增强子活性的序列要求。在转染入HeLa细胞后,分别在存在和不存在ElIa产物的情况下,测量了所得重组体中珠蛋白特异性转录效率。发现具有双向、依赖于ElIa的增强子活性的最小EIIa元件相对于EIIaE主要起始位点(+1)在 - 111至 - 27之间延伸。此外,广泛的缺失分析在该元件内揭示了三个功能不同的区域:一个约 - 90至 - 70之间的中央区域,对应于一个必需的EIIaE上游启动子元件,以及两个侧翼控制元件(每个约20 bp),在不存在ElIa产物时,它们对增强子活性产生负面影响。删除这些控制元件中的任何一个都会使EIIaE增强子活性组成型,这表明ElIa产物通过解除由这些序列介导的负调控来刺激EIIaE增强子。