Green Center for Systems Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Mol Syst Biol. 2011 Dec 6;7:557. doi: 10.1038/msb.2011.88.
Multipotent differentiation, where cells adopt one of several possible fates, occurs in diverse systems ranging from bacteria to mammals. This decision-making process is driven by multiple differentiation programs that operate simultaneously in the cell. How these programs interact to govern cell fate choice is poorly understood. To investigate this issue, we simultaneously measured activities of the competing sporulation and competence programs in single Bacillus subtilis cells. This approach revealed that these competing differentiation programs progress independently without cross-regulation before the decision point. Cells seem to arrive at a fate choice through differences in the relative timing between the two programs. To test this proposed dynamic mechanism, we altered the relative timing by engineering artificial cross-regulation between the sporulation and competence circuits. Results suggest a simple model that does not require a checkpoint or intricate cross-regulation before cellular decision-making. Rather, cell fate choice appears to be the outcome of a 'molecular race' between differentiation programs that compete in time, providing a simple dynamic mechanism for decision-making.
多能分化,即细胞采用几种可能的命运之一,发生在从细菌到哺乳动物等多种系统中。这个决策过程是由多个分化程序驱动的,这些程序在细胞中同时运行。这些程序如何相互作用来控制细胞命运选择还知之甚少。为了研究这个问题,我们同时测量了单个枯草芽孢杆菌细胞中竞争的孢子形成和感受态程序的活性。这种方法表明,在决策点之前,这些竞争的分化程序在没有交叉调节的情况下独立进行。细胞似乎通过两个程序之间的相对时间差异来做出命运选择。为了验证这个提出的动态机制,我们通过工程改造孢子形成和感受态回路之间的人工交叉调节来改变相对时间。结果表明了一个简单的模型,该模型不需要在细胞决策之前进行检查点或复杂的交叉调节。相反,细胞命运选择似乎是分化程序之间时间竞争的“分子竞赛”的结果,为决策提供了一个简单的动态机制。