Cell integrity limits ploidy in budding yeast.

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
Juliet Barker, Andrew Murray, Stephen P Bell
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引用次数: 0

Abstract

Evidence suggests that increases in ploidy have occurred frequently in the evolutionary history of organisms and can serve adaptive functions to specialized somatic cells in multicellular organisms. However, the sudden multiplication of all chromosome content may present physiological challenges to the cells in which it occurs. Experimental studies have associated increases in ploidy with reduced cell survival and proliferation. To understand the physiological challenges that suddenly increased chromosome content imposes on cells, we used S. cerevisiae to ask how much chromosomal DNA cells may contain and what determines this limit. We generated polyploid cells using 2 distinct methods causing cells to undergo endoreplication and identified the maximum ploidy of these cells, 32-64C. We found that physical determinants that alleviate or exacerbate cell surface stress increase and decrease the limit to ploidy, respectively. We also used these cells to investigate gene expression changes associated with increased ploidy and identified the repression of genes involved in ergosterol biosynthesis. We propose that ploidy is inherently limited by the impacts of growth in size, which accompany whole-genome duplication, to cell surface integrity.

细胞完整性限制了出芽酵母的倍性。
有证据表明,在生物进化的历史中,染色体倍性的增加经常发生,并能为多细胞生物中的特化体细胞提供适应功能。然而,所有染色体含量的突然增加可能会给其中的细胞带来生理挑战。实验研究表明,染色体倍性的增加与细胞存活率和增殖率的降低有关。为了了解染色体含量突然增加给细胞带来的生理挑战,我们利用 S. cerevisiae 来探究细胞可能含有多少染色体 DNA 以及决定这一限制的因素。我们采用两种不同的方法生成多倍体细胞,使细胞进行内复制,并确定了这些细胞的最大倍性(32-64C)。我们发现,缓解或加剧细胞表面应力的物理决定因素会分别增加和减少多倍体的极限。我们还利用这些细胞研究了与多倍体增加相关的基因表达变化,并确定了参与麦角甾醇生物合成的基因受到抑制。我们认为,伴随全基因组复制而来的体积增长会对细胞表面完整性产生影响,从而使倍性受到内在限制。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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