俄勒冈白蜡(Fraxinus latifolia)基因组学监测为保护和eab抗性育种提供信息。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anthony E Melton, Trevor M Faske, Richard A Sniezko, Tim Thibault, Wyatt Williams, Thomas Parchman, Jill A Hamilton
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引用次数: 0

摘要

了解大范围基因组变异背后的进化过程对于设计有效的保护和恢复策略至关重要。评估连通性、人口变化和环境适应对濒危物种的影响,对于积极保护进化潜力具有不可估量的价值。在这项研究中,我们评估了大叶曲霉(Fraxinus latifolia)的基因组变异,大叶曲霉是一种原产于北美西部的基础河岸树木,最近暴露于入侵的祖母绿灰螟(Agrilus planipennis;EAB)。利用减少代表性(ddRAD-seq)对61个种群的1000多个个体进行了测序。种群结构沿纬度梯度明显,种群连通性在很大程度上保持在中央山谷河流系统,遗传多样性中心与物种范围中心的主要河流系统一致。尽管存在连通性的证据,但对所有种群的核苷酸多样性和有效种群规模的估计都很低,这表明麻风种群的斑块分布可能影响其长期进化潜力。在物种分布范围内,对基因组偏移的估计(表明适应未来气候预测所需的基因组变化)在东部最大,在南部最低,这表明基因组变异的区域分布可能会长期影响进化潜力。为了保护种群间的进化能力,以发展繁殖和恢复计划为目的,优先保护大范围的基因组多样性将为长期的物种管理提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomics-Driven Monitoring of Fraxinus latifolia (Oregon Ash) to Inform Conservation and EAB-Resistance Breeding.

Understanding the evolutionary processes underlying range-wide genomic variation is critical to designing effective conservation and restoration strategies. Evaluating the influence of connectivity, demographic change and environmental adaptation for threatened species can be invaluable to proactive conservation of evolutionary potential. In this study, we assessed genomic variation across the range of Fraxinus latifolia, a foundational riparian tree native to western North America recently exposed to the invasive emerald ash borer (Agrilus planipennis; EAB). Over 1000 individuals from 61 populations were sequenced using reduced representation (ddRAD-seq) across the species' range. Strong population structure was evident along a latitudinal gradient, with population connectivity largely maintained along central valley river systems, and a centre of genetic diversity coinciding with major river systems central to the species' range. Despite evidence of connectivity, estimates of nucleotide diversity and effective population size were low across all populations, suggesting the patchy distribution of F. latifolia populations may impact its long-term evolutionary potential. Range-wide estimates of genomic offset, which indicate genomic change required to adjust to future climate projections, were greatest in the eastern and lowest in the southern portions of the species' range, suggesting the regional distribution of genomic variation may impact evolutionary potential longer-term. To preserve evolutionary capacity across populations needed for the development of breeding and restoration programmes, prioritising conservation of range-wide genomic diversity will provide a foundation for long-term species management.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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