Konieczny I, Doran K S, Helinski D R, Blasina A
Department of Biology, Center for Molecular Genetics, University of California, San Diego, La Jolla, California 92093-0634, USA.
J Biol Chem. 1997 Aug 8;272(32):20173-8. doi: 10.1074/jbc.272.32.20173.
The Escherichia coli protein DnaA and the plasmid RK2-encoded TrfA protein are required for initiation of replication of the broad host range plasmid RK2. The TrfA protein has been shown to bind to five 17-base pair repeat sequences, referred to as iterons, at the minimal replication origin (oriV). Using DNase I footprinting and a gel mobility shift assay, purified DnaA protein was found to bind to four DnaA consensus binding sequences immediately upstream of the five iterons at the RK2 origin of replication. Binding of the TrfA protein to the iterons results in localized strand opening within the A+T-rich region of the replication origin as determined by reactivity of the top and bottom strands to potassium permanganate (KMnO4). The presence of either the E. coli DnaA or HU protein is required for the TrfA-mediated strand opening. Although the DnaA protein itself did not produce an RK2 open complex, it did enhance and/or stabilize the TrfA-induced strand opening.
大肠杆菌蛋白DnaA和质粒RK2编码的TrfA蛋白是广泛宿主范围质粒RK2复制起始所必需的。TrfA蛋白已被证明能与最小复制起点(oriV)处的五个17碱基对重复序列(称为迭代子)结合。通过DNA酶I足迹法和凝胶迁移率变动分析,发现纯化的DnaA蛋白能与RK2复制起点处五个迭代子上游紧邻的四个DnaA共有结合序列结合。TrfA蛋白与迭代子的结合导致复制起点富含A+T区域内的局部链打开,这是通过上链和下链对高锰酸钾(KMnO4)的反应性确定的。TrfA介导的链打开需要大肠杆菌DnaA或HU蛋白的存在。尽管DnaA蛋白本身不会产生RK2开放复合物,但它确实增强和/或稳定了TrfA诱导的链打开。