Kerr Rex A, Levine Herbert, Sejnowski Terrence J, Rappel Wouter-Jan
Computational Neurobiology Laboratory and Howard Hughes Medical Institute, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 2006 Jan 10;103(2):347-52. doi: 10.1073/pnas.0505825102. Epub 2005 Dec 30.
Accurate cell division in Escherichia coli requires the Min proteins MinC, MinD, and MinE as well as the presence of nucleoids. MinD and MinE exhibit spatial oscillations, moving from pole to pole of the bacterium, resulting in an average MinD concentration that is low at the center of the cell and high at the poles. This concentration minimum is thought to signal the site of cell division. Deterministic models of the Min oscillations reproduce many observed features of the system, including the concentration minimum of MinD. However, there are only a few thousand Min proteins in a bacterium, so stochastic effects are likely to play an important role. Here, we show that Monte Carlo simulations with a large number of proteins agree well with the results from a deterministic treatment of the equations. The location of minimum local MinD concentration is too variable to account for cell division accuracy in wild-type, but is consistent with the accuracy of cell division in cells without nucleoids. This finding confirms the need to include additional mechanisms, such as reciprocal interactions with the cell division ring or positioning of the nucleoids, to explain wild-type accuracy.
大肠杆菌中精确的细胞分裂需要Min蛋白MinC、MinD和MinE以及类核的存在。MinD和MinE表现出空间振荡,从细菌的一极移动到另一极,导致细胞中心的平均MinD浓度较低,而两极的浓度较高。这种浓度最小值被认为是细胞分裂位点的信号。Min振荡的确定性模型再现了该系统许多观察到的特征,包括MinD的浓度最小值。然而,细菌中只有几千个Min蛋白,因此随机效应可能起着重要作用。在这里,我们表明,对大量蛋白质进行的蒙特卡罗模拟与对方程进行确定性处理的结果非常吻合。野生型中局部MinD浓度最小值的位置变化太大,无法解释细胞分裂的准确性,但与没有类核的细胞中细胞分裂的准确性一致。这一发现证实,需要纳入其他机制,如与细胞分裂环的相互作用或类核的定位,来解释野生型的准确性。