| Literature DB >> 31706948 |
Benjamin D Knapp1, Pascal Odermatt2, Enrique R Rojas3, Wenpeng Cheng4, Xiangwei He4, Kerwyn Casey Huang5, Fred Chang6.
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.Entities:
Keywords: Schizosaccharomyces pombe; brefeldin A; cell cycle; cell growth; cell size; cytoplasmic density; homeostasis; osmotic stress
Year: 2019 PMID: 31706948 PMCID: PMC6911364 DOI: 10.1016/j.cels.2019.10.001
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304