Wade J T, Belyaeva T A, Hyde E I, Busby S J
School of Biosciences, The University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
EMBO J. 2001 Dec 17;20(24):7160-7. doi: 10.1093/emboj/20.24.7160.
The Escherichia coli melAB promoter is co-dependent upon two transcription activators, MelR and the cyclic AMP receptor protein, CRP. In this study we demonstrate positive co-operativity between the binding of MelR and CRP at the melAB promoter, which provides a simple mechanism for its co-dependence. MelR binds to four sites, centred at positions -42.5, -62.5, -100.5 and -120.5 relative to the melAB transcription start point. When MelR is pre-bound, CRP is able to bind to a target located between MelR at positions -62.5 and -100.5. This increases the occupation of the two downstream sites for MelR, which is essential for transcription activation. We have identified residues within activating region 1 (AR1) of CRP that are important in transcription activation of the melAB promoter. At simple CRP-dependent promoters, the surface of CRP containing these residues is involved in contacting the RNA polymerase alpha subunit. Our results show that, at the melAB promoter, the surface of CRP containing AR1 contacts MelR rather than RNA polymerase. Thus, MelR and CRP activate transcription by a novel mechanism in which they bind co-operatively to adjacent sites and form a bacterial enhanceosome.
大肠杆菌melAB启动子的活性依赖于两种转录激活因子,即MelR和环腺苷酸受体蛋白(CRP)。在本研究中,我们证明了MelR和CRP在melAB启动子上的结合存在正协同效应,这为其依赖性提供了一种简单的机制。MelR结合到四个位点,这些位点相对于melAB转录起始点的中心位置分别为-42.5、-62.5、-100.5和-120.5。当MelR预先结合时,CRP能够结合到位于MelR在-62.5和-100.5位点之间的一个靶点上。这增加了MelR对两个下游位点的占据,而这对于转录激活至关重要。我们已经确定了CRP激活区域1(AR1)内对melAB启动子转录激活很重要的残基。在简单的依赖CRP的启动子中,含有这些残基的CRP表面参与与RNA聚合酶α亚基的接触。我们的结果表明,在melAB启动子上,含有AR1的CRP表面与MelR而非RNA聚合酶接触。因此,MelR和CRP通过一种新机制激活转录,即它们协同结合到相邻位点并形成细菌增强体。