Wheals A E
Mol Cell Biol. 1982 Apr;2(4):361-8. doi: 10.1128/mcb.2.4.361-368.1982.
By using time-lapse photomicroscopy, the individual cycle times and sizes at bud emergence were measured for a population of saccharomyces cerevisiae cells growing exponentially under balanced growth conditions in a specially constructed filming slide. There was extensive variability in both parameters for daughter and parent cells. The data on 162 pairs of siblings were analyzed for agreement with the predictions of the transition probability hypothesis and the critical-size hypothesis of yeast cell proliferation and also with a model incorporating both of these hypotheses in tandem. None of the models accounted for all of the experimental data, but two models did give good agreement to all of the data. The wobbly tandem model proposes that cells need to attain a critical size, which is very variable, enabling them to enter a start state from which they exit with first order kinetics. The sloppy size control model suggests that cells have an increasing probability per unit time of traversing start as they increase in size, reaching a high plateau value which is less than one. Both models predict that the kinetics of entry into the cell division sequence will strongly depend on variability in birth size and thus will be quite different for daughters and parents of the asymmetrically dividing yeast cells. Mechanisms underlying these models are discussed.
通过延时显微镜技术,在特制的拍摄载玻片上,对处于平衡生长条件下指数生长的酿酒酵母细胞群体,测量了出芽时的个体周期时间和大小。子细胞和母细胞的这两个参数都存在很大的变异性。分析了162对同胞细胞的数据,以检验其是否符合酵母细胞增殖的转变概率假说和临界大小假说的预测,以及一个将这两个假说串联起来的模型的预测。没有一个模型能够解释所有的实验数据,但有两个模型与所有数据都有很好的一致性。摇摆串联模型提出,细胞需要达到一个临界大小,这个临界大小变化很大,使它们能够进入一个起始状态,然后以一级动力学从该状态退出。宽松大小控制模型表明,细胞随着大小增加,单位时间内穿越起始点的概率也增加,达到一个小于1的高原值。两个模型都预测,进入细胞分裂序列的动力学将强烈依赖于出生时大小的变异性,因此对于不对称分裂的酵母细胞的子细胞和母细胞来说会有很大不同。文中讨论了这些模型背后的机制。