Siam Rania, Brassinga Ann Karen C, Marczynski Gregory T
Department of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada H3A 2B4.
J Bacteriol. 2003 Sep;185(18):5563-72. doi: 10.1128/JB.185.18.5563-5572.2003.
The response regulator CtrA controls chromosome replication by binding to five sites, a, b, c, d, and e, inside the Caulobacter crescentus replication origin (Cori). In this study, we demonstrate that integration host factor (IHF) binds Cori over the central CtrA binding site c. Surprisingly, IHF and CtrA share DNA recognition sequences. Rather than promoting cooperative binding, IHF binding hinders CtrA binding to site c and nearby site d. Unlike other CtrA binding sites, DNA mutations in the CtrA c/IHF site uniquely impair autonomous Cori plasmid replication. These mutations also alter transcription from distant promoters more than 100 bp away. When the CtrA c/IHF site was deleted from the chromosome, these cells grew slowly and became selectively intolerant to a CtrA phosphor-mimic allele (D51E). Since CtrA protein concentration decreases during the cell cycle as IHF protein concentration increases, we propose a model in which IHF displaces CtrA in order to bend Cori and promote efficient chromosome replication.
应答调节因子CtrA通过与新月柄杆菌复制起点(Cori)内的a、b、c、d和e五个位点结合来控制染色体复制。在本研究中,我们证明整合宿主因子(IHF)在中央CtrA结合位点c上与Cori结合。令人惊讶的是,IHF和CtrA共享DNA识别序列。IHF的结合不是促进协同结合,而是阻碍CtrA与位点c及附近位点d的结合。与其他CtrA结合位点不同,CtrA c/IHF位点的DNA突变独特地损害了Cori自主质粒复制。这些突变还会改变距离超过100 bp的远处启动子的转录。当从染色体上删除CtrA c/IHF位点时,这些细胞生长缓慢,并对CtrA磷酸模拟等位基因(D51E)产生选择性不耐受。由于在细胞周期中CtrA蛋白浓度随着IHF蛋白浓度的增加而降低,我们提出了一个模型,其中IHF取代CtrA以弯曲Cori并促进高效的染色体复制。