种子库改变枯草芽孢杆菌的分子进化动力学

IF 3.3 3区 生物学
Genetics Pub Date : 2022-05-31 DOI:10.1093/genetics/iyac071
William R Shoemaker, Evgeniya Polezhaeva, Kenzie B Givens, Jay T Lennon
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引用次数: 0

摘要

资源可用性的波动限制了个体的生长和繁殖,从而影响了各自种群的进化。许多生物体通过进入代谢活性降低的可逆状态来应对这种波动,这种现象被称为休眠。这种休眠个体库(即种子库)不会繁殖,预计将作为进化缓冲区,尽管很难在延长的进化时间尺度上直接观察到这种影响。通过基因操作,我们分析了枯草芽孢杆菌种群在存在和不存在种子库的情况下700多天的分子进化动力学。这些细菌进入休眠状态的能力随着时间的推移增加了遗传多样性的积累,并改变了突变的轨迹,这些发现通过基于进化动力学数学模型的模拟进行了重述。虽然形成种子库的能力并没有改变负选择的程度,但我们发现它始终改变了跨基因的分子进化方向。总之,这些结果表明,在延长的进化时间尺度上,形成种子库的能力可以影响分子进化的方向和速度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seed banks alter the molecular evolutionary dynamics of Bacillus subtilis.

Fluctuations in the availability of resources constrain the growth and reproduction of individuals, which subsequently affects the evolution of their respective populations. Many organisms contend with such fluctuations by entering a reversible state of reduced metabolic activity, a phenomenon known as dormancy. This pool of dormant individuals (i.e. a seed bank) does not reproduce and is expected to act as an evolutionary buffer, though it is difficult to observe this effect directly over an extended evolutionary timescale. Through genetic manipulation, we analyze the molecular evolutionary dynamics of Bacillus subtilis populations in the presence and absence of a seed bank over 700 days. The ability of these bacteria to enter a dormant state increased the accumulation of genetic diversity over time and altered the trajectory of mutations, findings that were recapitulated using simulations based on a mathematical model of evolutionary dynamics. While the ability to form a seed bank did not alter the degree of negative selection, we found that it consistently altered the direction of molecular evolution across genes. Together, these results show that the ability to form a seed bank can affect the direction and rate of molecular evolution over an extended evolutionary timescale.

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来源期刊
Genetics
Genetics 生物-遗传学
CiteScore
6.20
自引率
6.10%
发文量
177
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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