Decoupling of Rates of Protein Synthesis from Cell Expansion Leads to Supergrowth.

Cell systems Pub Date : 2019-11-27 Epub Date: 2019-11-06 DOI:10.1016/j.cels.2019.10.001
Benjamin D Knapp, Pascal Odermatt, Enrique R Rojas, Wenpeng Cheng, Xiangwei He, Kerwyn Casey Huang, Fred Chang
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Abstract

Cell growth is a complex process in which cells synthesize cellular components while they increase in size. It is generally assumed that the rate of biosynthesis must somehow be coordinated with the rate of growth in order to maintain intracellular concentrations. However, little is known about potential feedback mechanisms that could achieve proteome homeostasis or the consequences when this homeostasis is perturbed. Here, we identify conditions in which fission yeast cells are prevented from volume expansion but nevertheless continue to synthesize biomass, leading to general accumulation of proteins and increased cytoplasmic density. Upon removal of these perturbations, this biomass accumulation drove cells to undergo a multi-generational period of "supergrowth" wherein rapid volume growth outpaced biosynthesis, returning proteome concentrations back to normal within hours. These findings demonstrate a mechanism for global proteome homeostasis based on modulation of volume growth and dilution.

蛋白质合成速率与细胞扩增的解耦导致超生长。
细胞生长是一个复杂的过程,在这个过程中,细胞在体积增加的同时合成细胞成分。通常认为生物合成速率必须以某种方式与生长速率协调,以保持细胞内浓度。然而,人们对可能实现蛋白质组稳态的潜在反馈机制或这种稳态受到干扰时的后果知之甚少。在这里,我们确定了裂变酵母细胞被阻止体积膨胀但仍继续合成生物质的条件,导致蛋白质的普遍积累和细胞质密度的增加。在消除这些扰动后,这种生物量的积累驱动细胞经历多代的“超生长”期,其中快速的体积生长超过了生物合成,使蛋白质组浓度在数小时内恢复正常。这些发现证明了一种基于体积生长和稀释调节的全球蛋白质组稳态机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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