Crooke E, Thresher R, Hwang D S, Griffith J, Kornberg A
Department of Biochemistry, Stanford University School of Medicine, CA 94305.
J Mol Biol. 1993 Sep 5;233(1):16-24. doi: 10.1006/jmbi.1993.1481.
DnaA protein and the Escherichia coli chromosomal origin (oriC) form an initial complex at an early stage in the initiation of DNA replication. We have used electron microscopy to determine which structure among the several formed in the reconstitution of this multicomponent system is the replicatively active complex. One distinctive structure could be correlated with activity and localized to oriC, whilst several others could not. Formation of an open complex in the next stage of initiation was accompanied by the presence of a structure similar in size and shape to that of the functional initial complex. Whereas the initial complex was observed with either ATP or the ADP-forms of DnaA protein, only the ATP-form was effective in producing the open complex. Mutagenesis of several DNA sequence elements in oriC, known to be important for replication, was employed to determine the effects of these alterations on formation of the initial complex. As judged by electron microscopy and by functional assays, the region containing the four 9-mer dnaA boxes proved to be essential for the formation of the initial complex, while the three contiguous AT-rich 13-mers, known sites for opening of oriC, were not.
DnaA蛋白与大肠杆菌染色体复制起点(oriC)在DNA复制起始的早期阶段形成初始复合物。我们利用电子显微镜来确定在这个多组分系统的重组过程中形成的几种结构中,哪一种是具有复制活性的复合物。一种独特的结构与活性相关并定位于oriC,而其他几种则不然。起始下一阶段开放复合物的形成伴随着一种大小和形状与功能性初始复合物相似的结构的出现。虽然初始复合物在DnaA蛋白的ATP形式或ADP形式下均能观察到,但只有ATP形式能有效产生开放复合物。我们对oriC中几个已知对复制很重要的DNA序列元件进行诱变,以确定这些改变对初始复合物形成的影响。通过电子显微镜和功能分析判断,包含四个9聚体dnaA框的区域对于初始复合物的形成至关重要,而三个相邻的富含AT的13聚体(已知的oriC开放位点)则不然。