Betteridge T, Yang J, Pittard A J, Praszkier J
Department of Microbiology and Immunology, The University of Melbourne, Melbourne, Victoria 3010, Australia.
J Bacteriol. 2003 Apr;185(7):2210-8. doi: 10.1128/JB.185.7.2210-2218.2003.
The replication initiator protein RepA of the IncB plasmid pMU720 was purified and used in DNase I protection assays in vitro. RepA protected a 68-bp region of the origin of replication of pMU720. This region, which lies immediately downstream of the DnaA box, contains four copies of the sequence motif 5'AANCNGCAA3'. Mutational analyses identified this sequence as the binding site specifically recognized by RepA (the RepA box). Binding of RepA to the RepA boxes was ordered and sequential, with the box closest to the DnaA binding site (box 1) occupied first and the most distant boxes (boxes 3 and 4) occupied last. However, only boxes 1, 2, and 4 were essential for origin activity, with box 3 playing a lesser role. Changing the spacing between box 1 and the other three boxes affected binding of RepA in vitro and origin activity in vivo, indicating that the RepA molecules bound to ori(B) interact with one another.
对IncB质粒pMU720的复制起始蛋白RepA进行了纯化,并用于体外DNase I保护试验。RepA保护了pMU720复制起点的一个68bp区域。该区域位于DnaA框的紧邻下游,包含四个5'AANCNGCAA3'序列基序拷贝。突变分析确定该序列为RepA特异性识别的结合位点(RepA框)。RepA与RepA框的结合是有序且连续的,最靠近DnaA结合位点的框(框1)首先被占据,最远的框(框3和框4)最后被占据。然而,只有框1、2和4对起点活性至关重要,框3的作用较小。改变框1与其他三个框之间的间距会影响RepA在体外的结合以及体内的起点活性,这表明与ori(B)结合的RepA分子相互作用。