Kawasaki Y, Matsunaga F, Kano Y, Yura T, Wada C
Institute for Virus Research, Kyoto University, Japan.
Mol Gen Genet. 1996 Nov 27;253(1-2):42-9. doi: 10.1007/s004380050294.
Replication of mini-F plasmids requires the initiator protein RepE, which binds specifically to four iterons within the origin (ori2), as well as some host factors that are involved in chromosomal DNA replication. To understand the role of host factors and RepE in the early steps of mini-F DNA replication, we examined the effects of RepE and the Escherichia coli proteins DnaA and HU on the localized melting of ori2 DNA in a purified in vitro system. We found that the binding of RepE to an iteron causes a 50 degrees bend at or around the site of binding. RepE and HU exhibited synergistic effects on the localized melting within the ori2 region, as detected by sensitivity to the single-strand specific P1 endonuclease. This opening of duplex DNA occurred around the 13mer of ori2, whose sequence closely resembles the set of 13mers found in the chromosomal origin oriC. Further addition of DnaA to the reaction mixture increased the efficiency of melting and appeared to extend melting to the adjacent AT-rich region. Moreover, DNA melting with appreciably higher efficiencies was observed with mutant forms of RepE that were previously shown to be hyperactive both in DNA binding in vitro and in initiator activity in vivo. We propose that the binding of RepE to four iterons of ori2 causes bending at the sites of RepE binding and, with the assistance of HU, induces a localized melting in the 13mer region. The addition of DnaA extends melting to the AT-rich region, which could then serve as the entry site for the DnaB-DnaA complex, much as has been documented for oriC dependent replication.
微小F质粒的复制需要起始蛋白RepE,它特异性结合于复制起点(ori2)内的四个重复子,同时还需要一些参与染色体DNA复制的宿主因子。为了了解宿主因子和RepE在微小F DNA复制早期步骤中的作用,我们在一个纯化的体外系统中研究了RepE以及大肠杆菌蛋白DnaA和HU对ori2 DNA局部解链的影响。我们发现RepE与一个重复子的结合会在结合位点或其周围引起50度的弯曲。通过对单链特异性P1核酸内切酶的敏感性检测发现,RepE和HU对ori2区域内的局部解链具有协同作用。双链DNA的这种解链发生在ori2的13聚体周围,其序列与染色体复制起点oriC中发现的13聚体序列非常相似。向反应混合物中进一步添加DnaA可提高解链效率,并似乎将解链扩展到相邻的富含AT的区域。此外,使用先前在体外DNA结合和体内起始活性方面均表现出高活性的RepE突变形式,观察到了效率明显更高的DNA解链。我们提出,RepE与ori2的四个重复子结合会在RepE结合位点处引起弯曲,并在HU的协助下,诱导13聚体区域的局部解链。DnaA的添加将解链扩展到富含AT的区域,然后该区域可作为DnaB-DnaA复合物的进入位点,这与oriC依赖性复制中所记录的情况非常相似。