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大肠杆菌melAB启动子处的转录激活:MelR与RNA聚合酶α亚基C末端结构域的相互作用。

Transcription activation at the Escherichia coli melAB promoter: interactions of MelR with the C-terminal domain of the RNA polymerase alpha subunit.

作者信息

Grainger David C, Belyaeva Tamara A, Lee David J, Hyde Eva I, Busby Stephen J W

机构信息

School of Biosciences, The University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

Mol Microbiol. 2004 Mar;51(5):1311-20. doi: 10.1111/j.1365-2958.2003.03930.x.

Abstract

We have investigated the role of the RNA polymerase alpha subunit during MelR-dependent activation of transcription at the Escherichia coli melAB promoter. To do this, we used a simplified melAB promoter derivative that is dependent on MelR binding at two 18 bp sites, located from position -34 to -51 and from position -54 to -71, upstream of the transcription start site. Results from experiments with hydroxyl radical footprinting, and with RNA polymerase, carrying alpha subunits that were tagged with a chemical nuclease, show that the C-terminal domains of the RNA polymerase alpha subunits are located near position -52 and near position -72 during transcription activation. We demonstrate that the C-terminal domain of the RNA polymerase alpha subunit is needed for open complex formation, and we describe two experiments showing that the RNA polymerase alpha subunit can interact with MelR. Finally, we used alanine scanning to identify determinants in the C-terminal domain of the RNA polymerase alpha subunit that are important for MelR-dependent activation of the melAB promoter.

摘要

我们研究了RNA聚合酶α亚基在大肠杆菌melAB启动子MelR依赖性转录激活过程中的作用。为此,我们使用了一种简化的melAB启动子衍生物,它依赖于MelR结合在转录起始位点上游两个18 bp的位点,分别位于-34至-51位和-54至-71位。用羟基自由基足迹法以及携带用化学核酸酶标记的α亚基的RNA聚合酶进行的实验结果表明,在转录激活过程中,RNA聚合酶α亚基的C末端结构域位于-52位附近和-72位附近。我们证明RNA聚合酶α亚基的C末端结构域对于开放复合物的形成是必需的,并且我们描述了两个实验,表明RNA聚合酶α亚基可以与MelR相互作用。最后,我们使用丙氨酸扫描来确定RNA聚合酶α亚基C末端结构域中对于melAB启动子MelR依赖性激活很重要的决定因素。

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