细胞生长导致的基因组稀释推动了哺乳动物和酵母细胞中类似饥饿的蛋白质组重塑

Michael C. Lanz, Shuyuan Zhang, Matthew P. Swaffer, Inbal Ziv, Luisa Hernández Götz, Jacob Kim, Frank McCarthy, Daniel F. Jarosz, Joshua E. Elias, Jan M. Skotheim
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引用次数: 0

摘要

细胞大小在健康组织和单细胞生物体中受到严格控制,但细胞大小如何影响生理机能仍不清楚。最近的研究表明,细胞体积的增大会重塑培养人体细胞的蛋白质组,这表明同一类型的大细胞和小细胞在组成上可能是不同的。在本研究中,我们利用肝细胞倍性和酵母遗传学的天然异质性,确定倍性与细胞大小比是蛋白质组组成的一个高度保守的决定因素。在哺乳动物和酵母细胞中,细胞生长造成的基因组稀释会引发类似饥饿的表型,这表明大细胞的生长受到基因组浓度的限制,其方式类似于限制性营养物质。此外,基因组稀释还能解释酵母衰老引起的一些蛋白质组变化。总之,我们的数据表明,基因组浓度驱动细胞组成的变化与外部环境线索无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genome dilution by cell growth drives starvation-like proteome remodeling in mammalian and yeast cells

Genome dilution by cell growth drives starvation-like proteome remodeling in mammalian and yeast cells

Cell size is tightly controlled in healthy tissues and single-celled organisms, but it remains unclear how cell size influences physiology. Increasing cell size was recently shown to remodel the proteomes of cultured human cells, demonstrating that large and small cells of the same type can be compositionally different. In the present study, we utilize the natural heterogeneity of hepatocyte ploidy and yeast genetics to establish that the ploidy-to-cell size ratio is a highly conserved determinant of proteome composition. In both mammalian and yeast cells, genome dilution by cell growth elicits a starvation-like phenotype, suggesting that growth in large cells is restricted by genome concentration in a manner that mimics a limiting nutrient. Moreover, genome dilution explains some proteomic changes ascribed to yeast aging. Overall, our data indicate that genome concentration drives changes in cell composition independently of external environmental cues.

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