Bertoni G, Fujita N, Ishihama A, de Lorenzo V
Department of Microbial Biotechnology, Centro Nacional de Biotecnología CSIC, Campus de Cantoblanco, 28049 Madrid, Spain.
EMBO J. 1998 Sep 1;17(17):5120-8. doi: 10.1093/emboj/17.17.5120.
The sequence elements determining the binding of the sigma54-containing RNA polymerase (sigma54-RNAP) to the Pu promoter of Pseudomonas putida have been examined. Contrary to previous results in related systems, we show that the integration host factor (IHF) binding stimulates the recruitment of the enzyme to the -12/-24 sequence motifs. Such a recruitment, which is fully independent of the activator of the system, XylR, requires the interaction of the C-terminal domain of the alpha subunit of RNAP with specific DNA sequences upstream of the IHF site which are reminiscent of the UP elements in sigma70 promoters. Our data show that this interaction is mainly brought about by the distinct geometry of the promoter region caused by IHF binding and the ensuing DNA bending. These results support the view that binding of sigma54-RNAP to a promoter is a step that can be subjected to regulation by factors (e.g. IHF) other than the sole intrinsic affinity of sigma54-RNAP for the -12/-24 site.
已经对决定含σ54的RNA聚合酶(σ54-RNAP)与恶臭假单胞菌的Pu启动子结合的序列元件进行了研究。与相关系统中的先前结果相反,我们发现整合宿主因子(IHF)的结合会刺激该酶募集到-12 / -24序列基序。这种募集完全独立于系统激活因子XylR,它需要RNAP的α亚基的C末端结构域与IHF位点上游特定的DNA序列相互作用,这些序列让人联想到σ70启动子中的UP元件。我们的数据表明,这种相互作用主要是由IHF结合导致的启动子区域独特几何形状以及随之而来的DNA弯曲引起的。这些结果支持了这样一种观点,即σ54-RNAP与启动子的结合是一个可以受到除σ54-RNAP对-12 / -24位点的唯一内在亲和力之外的其他因子(例如IHF)调控的步骤。