Déthiollaz S, Eichenberger P, Geiselmann J
Département de Biologie Moléculaire, Université de Genève, Switzerland.
EMBO J. 1996 Oct 1;15(19):5449-58.
Transcription from many Escherichia coli promoters can be activated by the cAMP-CRP complex bound at different locations upstream of the promoter. At some locations the mechanism of activation involves direct protein-protein contacts between CRP and the RNA polymerase. We positioned the CRP binding site at various distances from the transcription start site of the malT promoter and measured the in vivo activities of these promoter variants. From the activation profiles we deduce that the protein-protein interactions involved in transcriptional activation are rather rigid. A heterologous protein (IHF) that bends the DNA to a similar degree as does CRP activates transcription when bound at sites equivalent to activating positions for CRP. DNA geometry makes a major contribution to the process of transcriptional activation and DNA upstream of the activator binding site participates in this process. Removal of this DNA decreases the capacity of the malT promoter to be activated by CRP in vitro. We conclude that both DNA topology and direct protein-protein contacts contribute to transcriptional activation and that the relative importance of these two modes of activation depends on the nature of the activator and on the location of the activator binding site.
许多大肠杆菌启动子的转录可被结合在启动子上游不同位置的cAMP-CRP复合物激活。在某些位置,激活机制涉及CRP与RNA聚合酶之间直接的蛋白质-蛋白质相互作用。我们将CRP结合位点定位在距malT启动子转录起始位点不同距离处,并测量了这些启动子变体的体内活性。从激活曲线我们推断,转录激活中涉及的蛋白质-蛋白质相互作用相当严格。一种能将DNA弯曲到与CRP相似程度的异源蛋白质(IHF),当结合在与CRP激活位置相当的位点时,可激活转录。DNA几何结构对转录激活过程起主要作用,激活剂结合位点上游的DNA参与这一过程。去除这段DNA会降低malT启动子在体外被CRP激活的能力。我们得出结论,DNA拓扑结构和直接的蛋白质-蛋白质相互作用都有助于转录激活,并且这两种激活模式的相对重要性取决于激活剂的性质和激活剂结合位点的位置。