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Size control models of Saccharomyces cerevisiae cell proliferation.

机译:酿酒酵母细胞增殖的大小控制模型。

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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.
机译:通过使用延时显微镜,可以测量在特殊生长的幻灯片中在平衡生长条件下成指数增长的酿酒酵母细胞群体的芽萌出时的个体周期和大小。子代细胞和亲代细胞的参数均存在很大差异。分析了关于162对同胞兄弟姐妹的数据,以与酵母细胞增殖的转移概率假说和临界大小假说的预测相吻合,并与同时包含这两个假说的模型相一致。没有一个模型可以解释所有的实验数据,但是两个模型确实对所有数据都具有很好的一致性。摆动串联模型提出,细胞需要达到非常大的临界尺寸,从而使其能够进入起始状态,并以一级动力学从中退出。松散的大小控制模型表明,单元格随着大小的增加而具有每单位时间开始遍历的概率增加,达到的高平稳值小于1。两种模型都预测进入细胞分裂序列的动力学将在很大程度上取决于出生大小的变异性,因此对于不对称分裂的酵母细胞的女儿和父母而言,将有很大不同。讨论了这些模型的基础机制。

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