Surette M G, Lavoie B D, Chaconas G
Department of Biochemistry, University of Western Ontario, London, Canada.
EMBO J. 1989 Nov;8(11):3483-9. doi: 10.1002/j.1460-2075.1989.tb08513.x.
The first committed step in the in vitro strand transfer reaction of a mini-Mu donor molecule is the formation of a Type 1 complex in which the Mu ends are held together in a non-covalent protein-DNA complex. Efficient formation of this complex at high levels of donor supercoiling (sigma approximately -0.06) requires the Mu A and Escherichia coli HU proteins. At in vivo levels of supercoiling, efficient reaction also requires E. coli integration host factor (IHF). We demonstrate that this supercoiling relief activity of IHF is mediated through an IHF binding site in the Mu early promoter region. This site is part of a larger enhancer-like element which includes operator 1 (01) and part of operator 2 (02) with the IHF site in between. The enhancer-like element stimulates the initial rate of the in vitro reaction 100-fold and acts in a distance-independent fashion. Inversion of the orientation of the element results in a total loss of enhancer activity in the absence of IHF. However, a 10-fold stimulation in the initial rate of reaction is induced by the addition of IHF. Furthermore, correct helical phasing between 01 and 02 is required for maximal activity. The results indicate that a specific geometrical configuration of the enhancer-like element, which includes a sharp bend between 01 and 02, is required for optimal induction of synapsis.
微小 Mu 供体分子体外链转移反应的第一个关键步骤是形成 1 型复合物,其中 Mu 末端通过非共价蛋白质 - DNA 复合物结合在一起。在高水平的供体超螺旋(σ 约为 -0.06)下高效形成这种复合物需要 Mu A 和大肠杆菌 HU 蛋白。在体内超螺旋水平下,高效反应还需要大肠杆菌整合宿主因子(IHF)。我们证明 IHF 的这种超螺旋缓解活性是通过 Mu 早期启动子区域中的 IHF 结合位点介导的。该位点是一个更大的增强子样元件的一部分,该元件包括操纵子 1(O1)和操纵子 2(O2)的一部分,IHF 位点位于两者之间。该增强子样元件将体外反应的初始速率提高了 100 倍,并且以与距离无关的方式起作用。在没有 IHF 的情况下,该元件方向的反转导致增强子活性完全丧失。然而,添加 IHF 会诱导反应初始速率提高 10 倍。此外,O1 和 O2 之间正确的螺旋相位对于最大活性是必需的。结果表明,为了最佳诱导突触形成,需要增强子样元件的特定几何构型,其中包括 O1 和 O2 之间的急剧弯曲。