Lee S B, Bailey J E
Plasmid. 1984 Mar;11(2):151-65. doi: 10.1016/0147-619x(84)90020-9.
A mathematical model for lambda dv plasmid replication in a growing single cell of Escherichia coli has been formulated and solved numerically. Quantitative description of the molecular control mechanism for initiation of lambda dv replication presumes regulatory functions of repressor and initiator proteins and transcriptional activation of the origin region. Random selection of a single plasmid for activation and replication is assumed, as is regular plasmid segregation to daughter cells. The model is capable of simulating the periodic changes in each regulatory element and the plasmid copy number during the cell cycle. The calculated average copy number, repressor concentration, and timing of plasmid replication agree well with experimental data. The simulated lambda dv plasmid replication rate is controlled primarily by transcription frequency. Initiation of plasmid replication is not related to variations in the levels of repressor or initiator proteins during the cell cycle. Simulation studies of perturbations in plasmid and repressor segregation indicate that replication regulation of the lambda dv plasmid compensates to readjust copy number to normal values in a few generations. Implications of these studies relative to the molecular mechanisms of replication control are discussed.
已构建并通过数值求解了一个用于描述λdv质粒在生长中的大肠杆菌单细胞中复制的数学模型。对λdv复制起始的分子控制机制进行定量描述,假定阻遏蛋白和起始蛋白具有调控功能,且起始区域存在转录激活。假定单个质粒被随机选择进行激活和复制,并且质粒会定期分配到子细胞中。该模型能够模拟细胞周期中每个调控元件和质粒拷贝数的周期性变化。计算得到的平均拷贝数、阻遏蛋白浓度和质粒复制时间与实验数据吻合良好。模拟的λdv质粒复制速率主要受转录频率控制。质粒复制的起始与细胞周期中阻遏蛋白或起始蛋白水平的变化无关。对质粒和阻遏蛋白分配扰动的模拟研究表明,λdv质粒的复制调控会在几代内进行补偿,将拷贝数重新调整到正常值。讨论了这些研究对复制控制分子机制的意义。