Camara Johanna E, Breier Adam M, Brendler Therese, Austin Stuart, Cozzarelli Nicholas R, Crooke Elliott
Department of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, District of Columbia 20007, USA.
EMBO Rep. 2005 Aug;6(8):736-41. doi: 10.1038/sj.embor.7400467.
Initiation of DNA replication from the Escherichia coli chromosomal origin is highly regulated, assuring that replication occurs precisely once per cell cycle. Three mechanisms for regulation of replication initiation have been proposed: titration of free DnaA initiator protein by the datA locus, sequestration of newly replicated origins by SeqA protein and regulatory inactivation of DnaA (RIDA), in which active ATP-DnaA is converted to the inactive ADP-bound form. DNA microarray analyses showed that the level of initiation in rapidly growing cells that lack datA was indistinguishable from that in wild-type cells, and that the absence of SeqA protein caused only a modest increase in initiation, in agreement with flow-cytometry data. In contrast, cells lacking Hda overinitiated replication twofold, implicating RIDA as the predominant mechanism preventing extra initiation events in a cell cycle.
大肠杆菌染色体复制起点处的DNA复制起始受到严格调控,确保每个细胞周期精确复制一次。目前已提出三种复制起始调控机制:datA位点对游离DnaA起始蛋白的滴定作用、SeqA蛋白对新复制起点的隔离作用以及DnaA的调节性失活(RIDA),即活性ATP-DnaA转化为无活性的ADP结合形式。DNA微阵列分析表明,缺乏datA的快速生长细胞中的起始水平与野生型细胞中的起始水平没有区别,并且SeqA蛋白的缺失仅导致起始水平适度增加,这与流式细胞术数据一致。相比之下,缺乏Hda的细胞复制起始过量两倍,这表明RIDA是防止细胞周期中额外起始事件的主要机制。