Fuller R S, Funnell B E, Kornberg A
Cell. 1984 Oct;38(3):889-900. doi: 10.1016/0092-8674(84)90284-8.
Specific binding of dnaA protein to the E. coli origin of replication (oriC) is essential for initiation of chromosomal replication. Based on binding of plasmid DNA fragments, dnaA protein recognizes in addition to oriC a number of specific sites: within or near the replication origins of pSC101, pBR322, and ColE1; within the regulatory regions of the dnaA and "X-protein" genes; and in IRL-Tn5. All strong binding sites share a common 9 bp sequence, 5'-TTATCACACAA, repeated at four conserved positions within oriC. As shown by DNAase I footprinting, dnaA protein binding is highly cooperative, covering 250 bp at oriC and 100 bp at single 9 bp sequence sites. Consistent with filter-binding and nuclease-protection studies, complexes of 20 to 30 dnaA monomers are visualized at oriC and other sites by electron microscopy. The functions of dnaA complexes and 9 bp sequences at these sites are discussed.
DnaA蛋白与大肠杆菌复制起点(oriC)的特异性结合对于染色体复制的起始至关重要。基于质粒DNA片段的结合情况,DnaA蛋白除了能识别oriC外,还能识别许多特定位点:在pSC101、pBR322和ColE1的复制起点内或附近;在dnaA和“X蛋白”基因的调控区域内;以及在IRL-Tn5中。所有强结合位点都共享一个9bp的共同序列5'-TTATCACACAA,该序列在oriC内的四个保守位置重复出现。如DNA酶I足迹分析所示,DnaA蛋白的结合具有高度协同性,在oriC处覆盖250bp,在单个9bp序列位点处覆盖100bp。与滤膜结合和核酸酶保护研究一致,通过电子显微镜在oriC和其他位点观察到20至30个DnaA单体的复合物。本文讨论了这些位点上DnaA复合物和9bp序列的功能。