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“Adder 现象源于出芽酵母细胞周期的起始前期和起始后期的独立控制。”

The Adder Phenomenon Emerges from Independent Control of Pre- and Post-Start Phases of the Budding Yeast Cell Cycle.

机构信息

Department of Biology, Stanford University, Stanford, CA 94305, USA.

Department of Biology, Stanford University, Stanford, CA 94305, USA.

出版信息

Curr Biol. 2017 Sep 25;27(18):2774-2783.e3. doi: 10.1016/j.cub.2017.08.015. Epub 2017 Sep 7.

DOI:10.1016/j.cub.2017.08.015
PMID:28889980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5679121/
Abstract

Although it has long been clear that cells actively regulate their size, the molecular mechanisms underlying this regulation have remained poorly understood. In budding yeast, cell size primarily modulates the duration of the cell-division cycle by controlling the G1/S transition known as Start. We have recently shown that the rate of progression through Start increases with cell size, because cell growth dilutes the cell-cycle inhibitor Whi5 in G1. Recent phenomenological studies in yeast and bacteria have shown that these cells add an approximately constant volume during each complete cell cycle, independent of their size at birth. These results seem to be in conflict, as the phenomenological studies suggest that cells measure the amount they grow, rather than their size, and that size control acts over the whole cell cycle, rather than specifically in G1. Here, we propose an integrated model that unifies the adder phenomenology with the molecular mechanism of G1/S cell-size control. We use single-cell microscopy to parameterize a full cell-cycle model based on independent control of pre- and post-Start cell-cycle periods. We find that our model predicts the size-independent amount of cell growth during the full cell cycle. This suggests that the adder phenomenon is an emergent property of the independent regulation of pre- and post-Start cell-cycle periods rather than the consequence of an underlying molecular mechanism measuring a fixed amount of growth.

摘要

虽然细胞主动调节其大小这一点早已明确,但这一调节背后的分子机制仍知之甚少。在出芽酵母中,细胞大小主要通过控制 G1/S 转换来调节细胞分裂周期的持续时间,这种转换被称为起始(Start)。我们最近发现,通过起始的进展速度随细胞大小而增加,因为细胞生长会在 G1 期稀释细胞周期抑制剂 Whi5。最近在酵母和细菌中的现象学研究表明,这些细胞在每个完整的细胞周期中都会添加一个大约恒定的体积,而与它们出生时的大小无关。这些结果似乎存在冲突,因为现象学研究表明细胞测量的是它们的生长量,而不是它们的大小,并且大小控制作用于整个细胞周期,而不是专门在 G1 期。在这里,我们提出了一个整合模型,将加法器现象学与 G1/S 细胞大小控制的分子机制统一起来。我们使用单细胞显微镜,根据对起始前和起始后细胞周期时期的独立控制,对完整的细胞周期模型进行参数化。我们发现,我们的模型预测了整个细胞周期中与大小无关的细胞生长量。这表明加法器现象是起始前和起始后细胞周期时期独立调控的一个突现性质,而不是测量固定生长量的潜在分子机制的结果。

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Characterization of dependencies between growth and division in budding yeast.芽殖酵母生长与分裂之间的依赖性特征
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