(Epi)genomic adaptation driven by fine geographical scale environmental heterogeneity after recent biological invasions

Ecol Appl. 2024 Jan;34(1):e2772. doi: 10.1002/eap.2772. Epub 2022 Dec 26.

Abstract

Elucidating processes and mechanisms involved in rapid local adaptation to varied environments is a poorly understood but crucial component in management of invasive species. Recent studies have proposed that genetic and epigenetic variation could both contribute to ecological adaptation, yet it remains unclear on the interplay between these two components underpinning rapid adaptation in wild animal populations. To assess their respective contributions to local adaptation, we explored epigenomic and genomic responses to environmental heterogeneity in eight recently colonized ascidian (Ciona intestinalis) populations at a relatively fine geographical scale. Based on MethylRADseq data, we detected strong patterns of local environment-driven DNA methylation divergence among populations, significant epigenetic isolation by environment (IBE), and a large number of local environment-associated epigenetic loci. Meanwhile, multiple genetic analyses based on single nucleotide polymorphisms (SNPs) showed genomic footprints of divergent selection. In addition, for five genetically similar populations, we detected significant methylation divergence and local environment-driven methylation patterns, indicating the strong effects of local environments on epigenetic variation. From a functional perspective, a majority of functional genes, Gene Ontology (GO) terms, and biological pathways were largely specific to one of these two types of variation, suggesting partial independence between epigenetic and genetic adaptation. The methylation quantitative trait loci (mQTL) analysis showed that the genetic variation explained only 18.67% of methylation variation, further confirming the autonomous relationship between these two types of variation. Altogether, we highlight the complementary interplay of genetic and epigenetic variation involved in local adaptation, which may jointly promote populations' rapid adaptive capacity and successful invasions in different environments. The findings here provide valuable insights into interactions between invaders and local environments to allow invasive species to rapidly spread, thus contributing to better prediction of invasion success and development of management strategies.

阐明入侵生物快速环境适应的过程和机制对于入侵生物管控至关重要,然而目前相关研究仍存在不足。近期研究表明,遗传和表观遗传变异均可在生物环境适应中发挥重要作用,但是关于两者在野外动物群体快速环境适应中的关系尚不明晰。为了阐明遗传和表观遗传变异在局域适应中的相对贡献,本研究以小地理尺度获得的8个玻璃海鞘群体为研究对象,分别开展了表观基因组和基因组学研究。利用简化甲基化组测序技术,我们发现当地环境驱动的不同地理群体DNA甲基化分化特征,环境距离与表观遗传分化显著相关模式以及大量环境关联的表观遗传位点。同时,在遗传层面,基于单核苷酸多态性(SNP)的多种分析方法,我们揭示了环境选择作用在基因组上留下了印记。我们发现遗传相近的5个群体之间存在显著的甲基化分化,并且这种分化模式是由当地环境因子驱动的,这进一步表明当地环境对表观遗传变异产生了显著影响。从功能角度出发,我们发现大部分的适应性基因和生物学通路是表观遗传或遗传两种变异类型各自特有的,表明两者在功能上存在一定独立性和互补性。此外,甲基化数量性状位点分析结果显示,遗传变异仅能解释18.67%的表观遗传变异,这进一步验证了两种变异类型的独立性。本研究揭示了表观遗传与遗传变异之间的功能互补关系,两者相互协作,共同促进了玻璃海鞘快速环境适应能力并成功入侵至不同环境。本研究有助于我们更好的理解入侵生物与当地环境之间互作是如何促进入侵生物快速地域扩张,为入侵生物的地理分布预测和管控策略制定提供科学依据。.

Keywords: epigenetic variation; genetic variation; independent relationship; invasive species; local adaptation; tunicate.

MeSH terms

  • Adaptation, Biological / genetics
  • Adaptation, Physiological* / genetics
  • Animals
  • Environment*
  • Genomics
  • Geography