rDNA拷贝数变异影响酵母对不同环境的适应性。

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-05-03 DOI:10.1093/genetics/iyaf075
Kevin Thornton, Elizabeth X Kwan, Kerry Bubb, Luana Paleologu, M K Raghuraman, Bonita J Brewer, Josh T Cuperus, Christine Queitsch
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引用次数: 0

摘要

真核生物的核糖体DNA (rDNA)以数百个拷贝的形式存在,同一物种内不同个体的rDNA拷贝数差异很大。芽殖酵母(Saccharomyces cerevisiae)的rDNA拷贝数在90 ~ 300个拷贝之间。先前的研究表明,35个rDNA拷贝足以在这种酵母中进行核糖体生物发生,并在标准的实验室生长条件下实现野生型生长。我们解决了关于该酵母rDNA拷贝数变异的两个主要问题:(1)在标准实验室生长条件下,rDNA拷贝数变异在自然范围外和范围内的适应度后果是什么?(2)在不同的生长条件下,这些适应度效应是否会发生变化?我们采用生长竞争的方法比较了rDNA拷贝数在35 ~ 200之间的非等基因菌株的rDNA拷贝数变化的适合度效应。在标准生长条件下,我们发现适应度从35个rDNA拷贝逐渐增加,直到达到98到160个rDNA拷贝的平稳期,完全在自然范围内。然而,rDNA拷贝数依赖的适应度在不同的环境中有所不同。在标准生长条件下,随着rDNA拷贝数的增加,适应度逐渐增加,在这两种胁迫条件下,拷贝数低于自然范围的菌株的适应度明显降低。这些结果表明,选择压力使这种酵母的rDNA拷贝数至少达到100拷贝,更高的拷贝数可能会缓冲环境胁迫。葡萄球菌的rDNA拷贝数范围与秀丽隐杆线虫、黑葡萄球菌和人类的相似表明,在这些高度多样化的物种中,保守的选择压力维持了自然rDNA拷贝数的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
rDNA copy number variation affects yeast fitness in response to different environments.

Ribosomal DNA (rDNA) in eukaryotes is maintained in hundreds of copies with rDNA copy number varying greatly among individuals within a species. In the budding yeast Saccharomyces cerevisiae, the rDNA copy number across wild isolates ranges from 90 to 300 copies. Previous studies showed that 35 rDNA copies are sufficient for ribosome biogenesis in this yeast and enable wild-type-like growth in standard laboratory growth conditions. We addressed two major questions concerning rDNA copy number variation in this yeast: (1) What are the fitness consequences of rDNA copy number variation outside and within the natural range in standard laboratory growth conditions? (2) Do these fitness effects change in different growth conditions? We used growth competitions to compare the fitness effects of rDNA copy number variation in otherwise isogenic strains whose rDNA copy number ranged from 35 to 200. In standard growth conditions, we found that fitness gradually increases from 35 rDNA copies until reaching a plateau that spans from 98 to 160 rDNA copies, well within the natural range. However, rDNA copy number-dependent fitness differed across environments. The gradual fitness increase with increasing rDNA copy number in standard growth conditions gave way to a markedly lower fitness of strains with copy numbers below the natural range in these two stress conditions. These results suggest that selective pressures drive rDNA copy number in this yeast to at least ∼100 copies and that a higher number of copies might buffer against environmental stress. The similarity of the S. cerevisiae rDNA copy number range to the ranges reported in C. elegans, D. melanogaster, and humans points to conserved selective pressures maintaining the range of natural rDNA copy number in these highly diverse species.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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