Law E C, Savery N J, Busby S J
School of Biochemistry, University of Birmingham, Edgbaston, Birmingham B15 2TT, U.K.
Biochem J. 1999 Feb 1;337 ( Pt 3)(Pt 3):415-23.
The Escherichia coli cAMP receptor protein (CRP) is a factor that activates transcription at over 100 target promoters. At Class I CRP-dependent promoters, CRP binds immediately upstream of RNA polymerase and activates transcription by making direct contacts with the C-terminal domain of the RNA polymerase alpha subunit (alphaCTD). Since alphaCTD is also known to interact with DNA sequence elements (known as UP elements), we have constructed a series of semi-synthetic Class I CRP-dependent promoters, carrying both a consensus DNA-binding site for CRP and a UP element at different positions. We previously showed that, at these promoters, the CRP-alphaCTD interaction and the CRP-UP element interaction contribute independently and additively to transcription initiation. In this study, we show that the two halves of the UP element can function independently, and that, in the presence of the UP element, the best location for the DNA site for CRP is position -69.5. This suggests that, at Class I CRP-dependent promoters where the DNA site for CRP is located at position -61.5, the two alphaCTDs of RNA polymerase are not optimally positioned. Two experiments to test this hypothesis are presented.
大肠杆菌环磷酸腺苷受体蛋白(CRP)是一种能激活100多个靶启动子转录的因子。在I类CRP依赖性启动子中,CRP结合在RNA聚合酶的紧邻上游,并通过与RNA聚合酶α亚基的C末端结构域(αCTD)直接接触来激活转录。由于已知αCTD也与DNA序列元件(称为UP元件)相互作用,我们构建了一系列半合成的I类CRP依赖性启动子,在不同位置同时携带CRP的共有DNA结合位点和一个UP元件。我们之前表明,在这些启动子中,CRP-αCTD相互作用和CRP-UP元件相互作用对转录起始有独立且累加的贡献。在本研究中,我们表明UP元件的两个部分可以独立发挥作用,并且在存在UP元件的情况下,CRP的DNA位点的最佳位置是-69.5。这表明,在CRP的DNA位点位于-61.5的I类CRP依赖性启动子中,RNA聚合酶的两个αCTD没有处于最佳位置。本文提出了两个实验来检验这一假设。