Woelker B, Messer W
Max-Planck-Institut für Molekulare Genetik, Berlin-Dahlem, Germany.
Nucleic Acids Res. 1993 Nov 11;21(22):5025-33. doi: 10.1093/nar/21.22.5025.
Two distinct regions in the replication origin, oriC, of Escherichia coli are separately distorted upon initiation complex formation by the initiator protein DnaA. The AT-rich region in the left part of oriC and the start site region in the right part of oriC. Chemical modification of single-stranded DNA was observed at both regions whereas endonuclease recognition of DNA mini-bulges specifically occurred in the start site region. We show that the helical phasing of binding sites for DnaA protein in oriC is important for origin function. An insertion or deletion of one helical turn between the two rightmost binding sites does not alter the efficiency of replication initiation, whereas all modifications of distance by less or more than one helical turn result in inactivation of oriC. DnaA binding and helical distortions in the AT-rich region as well as in the start site region are not affected in the distance mutants irrespective of their functionality in vivo. We propose a specific compact nucleoprotein structure for the initiation complex.
在大肠杆菌复制起点oriC中,有两个不同区域在起始蛋白DnaA形成起始复合物时分别发生扭曲。oriC左侧富含AT的区域和oriC右侧的起始位点区域。在这两个区域均观察到单链DNA的化学修饰,而DNA小凸起的核酸内切酶识别则特异性地发生在起始位点区域。我们表明,oriC中DnaA蛋白结合位点的螺旋相位对起点功能很重要。在最右侧两个结合位点之间插入或缺失一圈螺旋不会改变复制起始效率,而距离改变少于或多于一圈螺旋的所有修饰都会导致oriC失活。无论其在体内的功能如何,富含AT区域以及起始位点区域中的DnaA结合和螺旋扭曲在距离突变体中均不受影响。我们提出了起始复合物的一种特定紧密核蛋白结构。