Watanabe H, Imai T, Sharp P A, Handa H
Department of Bacteriology, University of Tokyo, Faculty of Medicine, Japan.
Mol Cell Biol. 1988 Mar;8(3):1290-300. doi: 10.1128/mcb.8.3.1290-1300.1988.
Two kinds of trans-acting factors that regulate transcription from the promoter of the adenovirus early-region 4 (E4) have been identified by reconstituting nuclear extracts of HeLa cells. They were designated E4TF1 and E4TF3 for E4 transcription factors. These factors were responsible for efficient and accurate transcription in vitro from the E4 promoter, as were another transcription factor, designated E4TF2, and a crude fraction containing endogenous RNA polymerase II. E4TF1 stimulated transcription from the E4 promoter but not from the major late promoter or the E4 mutant promoter lacking the E4TF1-binding site. Footprint analysis of E4TF1 revealed that it binds to a specific region, residing between 132 and 152 base pairs upstream from the initiation site of the E4 mRNA. E4TF3 also regulated transcription from the E4 promoter. E4TF3 protected four ca. 20-base-pair regions in a DNase I footprinting assay. They were located around 40, 160, 230, and 260 base pairs upstream from the initiation site of E4 mRNA. Specific inhibition of E4 transcription was observed by addition of DNA fragments covering one of the E4TF1- and E4TF3-binding sites to in vitro transcription assays. These results suggest that both E4TF1 and E4TF3 regulate E4 transcription by binding to the specific upstream elements in the E4 promoter. These factors may be involved in the E1A transactivation of E4 transcription.
通过重组HeLa细胞核提取物,已鉴定出两种调节腺病毒早期区域4(E4)启动子转录的反式作用因子。它们被命名为E4转录因子E4TF1和E4TF3。这些因子与另一种名为E4TF2的转录因子以及含有内源性RNA聚合酶II的粗提物一样,负责在体外从E4启动子进行高效且准确的转录。E4TF1刺激从E4启动子的转录,但不刺激主要晚期启动子或缺乏E4TF1结合位点的E4突变启动子的转录。对E4TF1的足迹分析表明,它结合到E4 mRNA起始位点上游132至152个碱基对之间的特定区域。E4TF3也调节从E4启动子的转录。在DNA酶I足迹分析中,E4TF3保护了四个约20个碱基对的区域。它们位于E4 mRNA起始位点上游约40、160、230和260个碱基对处。通过向体外转录试验中添加覆盖E4TF1和E4TF3结合位点之一的DNA片段,观察到对E4转录的特异性抑制。这些结果表明,E4TF1和E4TF3都通过结合E4启动子中的特定上游元件来调节E4转录。这些因子可能参与E1A对E4转录的反式激活作用。