Chatterjee Sujoy, Basu Arnab, Basu Abhijit, Das Gupta Sujoy K
Bose Institute, Dept. of Microbiology, P1/12 C.I.T. Scheme VIIM, Kolkata 700054, India.
J Bacteriol. 2007 Dec;189(23):8584-92. doi: 10.1128/JB.01155-07. Epub 2007 Sep 28.
Plasmid pAL5000 represents a family of relatively newly discovered cryptic plasmids in gram-positive Actinomycetes bacteria. The replication regions of these plasmids comprise a bicistronic operon, repA-repB, encoding two replication proteins. Located upstream is a cis-acting element that functions as the origin of replication. It comprises an approximately 200-bp segment spanning two binding sites for the replication protein RepB, a low-affinity (L) site and a high-affinity (H) site separated by an approximately 40-bp spacer sequence. The trajectory of the DNA in the RepB-origin complex has been investigated, and it has been found that the origin undergoes significant bending movements upon RepB binding. RepB binding not only led to local bending effects but also caused a long-range polar curvature which affected the DNA sequences 3' to the H site. These movements appear to be essential for the in-phase alignment of the L and H sites that leads to the formation of a looped structure. A novel property of RepB unearthed in this study is its ability to form multimers. This property may be an important factor that determines the overall trajectory of the DNA in the RepB-origin complex. The results presented in this study suggest that the origins of replication of pAL5000 and related plasmids are highly flexible and that multimeric, RepB-like initiator proteins bind the origin and induce local deformations and long-range curvatures which are probably necessary for the proper functioning of the origin.
质粒pAL5000代表了革兰氏阳性放线菌中相对较新发现的一类隐蔽质粒。这些质粒的复制区域包含一个双顺反子操纵子repA-repB,编码两种复制蛋白。位于上游的是一个作为复制起点的顺式作用元件。它由一个约200bp的片段组成,该片段跨越复制蛋白RepB的两个结合位点,一个低亲和力(L)位点和一个高亲和力(H)位点,中间由一个约40bp的间隔序列隔开。已经研究了RepB-复制起点复合物中DNA的轨迹,发现复制起点在RepB结合时会发生显著的弯曲运动。RepB结合不仅导致局部弯曲效应,还会引起长程极性曲率,影响H位点3'端的DNA序列。这些运动似乎对于L位点和H位点的同相位排列至关重要,而这种排列会导致形成环状结构。本研究中发现的RepB的一个新特性是其形成多聚体的能力。这个特性可能是决定RepB-复制起点复合物中DNA整体轨迹的一个重要因素。本研究给出的结果表明,pAL5000及相关质粒的复制起点具有高度灵活性,多聚体形式的、类似RepB的起始蛋白结合复制起点并诱导局部变形和长程曲率,这可能是复制起点正常发挥功能所必需的。