一种极度濒危软体动物突变率的直接测量及其进化后果。

IF 6.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular biology and evolution Pub Date : 2025-01-06 DOI:10.1093/molbev/msae266
T Brock Wooldridge, Sarah M Ford, Holland C Conwell, John Hyde, Kelley Harris, Beth Shapiro
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摘要

突变发生的速度是生物学的一个基本参数。尽管在测量不同分类群的生殖系突变率方面取得了进展,但地球上的大部分生物多样性都缺乏这样的估计。在这里,我们提出了对软体动物门的种系突变率的首次估计。我们对长寿命、体型庞大、极度濒危的白鲍鱼(Haliotis sorenseni)的三个纯种家族进行了测序,估计每一代每个位点的新生突变率为8.60 × 10-9个单核苷酸突变。这一突变率与在与鲍鱼具有相当世代时间和寿命的脊椎动物中测量到的突变率相似,并且高于在繁殖速度更快的无脊椎动物中测量到的突变率。新生突变的频谱也与脊椎动物物种相似,尽管野生个体中过量的罕见C > A多态性表明,修饰等位基因或环境暴露可能曾经增加了C > A突变率。我们使用我们的比率来推断多个太平洋鲍鱼的基线有效种群规模(Ne),并发现鲍鱼在其进化史的大部分时间里都保持着庞大而稳定的种群,与最近历史上的极端波动和今天的小人口普查规模形成鲜明对比。然后,我们使用我们的突变率来推断鲍属Haliotis的进化时间和模式,这在以前是未知的,因为很少有化石校准。我们的发现是理解突变率进化的重要一步,它们为软体动物的保护和进化基因组学研究建立了一个关键参数。
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Direct Measurement of the Mutation Rate and Its Evolutionary Consequences in a Critically Endangered Mollusk.

The rate at which mutations arise is a fundamental parameter of biology. Despite progress in measuring germline mutation rates across diverse taxa, such estimates are missing for much of Earth's biodiversity. Here, we present the first estimate of a germline mutation rate from the phylum Mollusca. We sequenced three pedigreed families of the white abalone Haliotis sorenseni, a long-lived, large-bodied, and critically endangered mollusk, and estimated a de novo mutation rate of 8.60 × 10-9 single nucleotide mutations per site per generation. This mutation rate is similar to rates measured in vertebrates with comparable generation times and longevity to abalone, and higher than mutation rates measured in faster-reproducing invertebrates. The spectrum of de novo mutations is also similar to that seen in vertebrate species, although an excess of rare C > A polymorphisms in wild individuals suggests that a modifier allele or environmental exposure may have once increased C > A mutation rates. We use our rate to infer baseline effective population sizes (Ne) across multiple Pacific abalone and find that abalone persisted over most of their evolutionary history as large and stable populations, in contrast to extreme fluctuations over recent history and small census sizes in the present day. We then use our mutation rate to infer the timing and pattern of evolution of the abalone genus Haliotis, which was previously unknown due to few fossil calibrations. Our findings are an important step toward understanding mutation rate evolution and they establish a key parameter for conservation and evolutionary genomics research in mollusks.

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来源期刊
Molecular biology and evolution
Molecular biology and evolution 生物-进化生物学
CiteScore
19.70
自引率
3.70%
发文量
257
审稿时长
1 months
期刊介绍: Molecular Biology and Evolution Journal Overview: Publishes research at the interface of molecular (including genomics) and evolutionary biology Considers manuscripts containing patterns, processes, and predictions at all levels of organization: population, taxonomic, functional, and phenotypic Interested in fundamental discoveries, new and improved methods, resources, technologies, and theories advancing evolutionary research Publishes balanced reviews of recent developments in genome evolution and forward-looking perspectives suggesting future directions in molecular evolution applications.
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