利用金属毒性与植物DNA甲基化之间的相互作用。

IF 2.7 4区 环境科学与生态学 Q2 ECOLOGY
Alistar Moy, Kabwe Nkongolo
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引用次数: 0

摘要

研究植物如何通过遗传和表观遗传机制适应胁迫是一个快速发展的领域,表观遗传灵活性是在重污染、高金属环境中生存的关键因素。尖端技术,特别是全基因组亚硫酸氢盐测序(WGBS)和减少代表性亚硫酸氢盐测序(RRBS),通过超越广泛的全基因组调查,精确定位由金属胁迫引起的特定基因水平的改变,彻底改变了这一领域。这些高通量的方法从根本上改变了环境植物研究的格局。对文献的批判性分析表明,暴露于金属应激源会引发植物DNA甲基化的快速、随时间变化,通常在几分钟内发生。这些表观遗传反应高度依赖于物种和遗传背景,以及所涉及的特定金属应激源,在不改变潜在DNA序列的情况下促进位点特异性基因调控。这种灵活性允许植物主要通过超甲基化(70%)而不是低甲基化(30%)来调节基因表达,以维持体内平衡并发展遗传的应激记忆。这些修饰主要针对与金属运输相关的基因(60%),如HMA、ZIP和ABC转运蛋白,其次是固存(20%)和其他代谢功能(20%)。最终,利用这些表观遗传机制为开发作物品种提供了一条途径,这些作物品种不仅在受污染的环境中表现出更高的耐受性和生产力,而且还限制有毒金属在可食用组织中的积累,从而提高食品安全和支持bednarek边缘土地的可持续农业。尽管有重大的分析突破,但DNA甲基化在调节基因对金属毒性反应中的确切作用仍然是研究中一个关键的、未解决的挑战。本文综述了DNA甲基化机制,并概述了植物基因在金属暴露下的修饰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing the interplay between metal toxicity and DNA methylation in plants.

Research into how plants adapt to stress through genetic and epigenetic mechanisms is a rapidly evolving field, with epigenetic flexibility serving as a critical factor for survival in heavily contaminated, high-metal environments. Cutting-edge technologies, specifically Whole Genome Bisulfite Sequencing (WGBS) and Reduced Representation Bisulfite Sequencing (RRBS), have revolutionized this area by moving beyond broad, genome-wide surveys to pinpoint specific, gene-level alterations induced by metal stress. These high-throughput methods have fundamentally transformed the landscape of environmental plant research. Critical analysis of the literature revealed that exposure to metal stressors triggers rapid, time-dependent shifts in plant DNA methylation, often occurring within minutes. These epigenetic responses are highly contingent on species and genetic background, and the specific metal stressor involved, facilitating site-specific gene regulation without altering the underlying DNA sequence. This flexibility allows plants to modulate gene expression primarily through hypermethylation (70%) rather than hypomethylation (30%) to maintain homeostasis and develop heritable stress memory. These modifications predominantly target genes associated with metal transport (60%), such as HMA, ZIP, and ABC transporters, followed by sequestration (20%) and other metabolic functions (20%). Ultimately, harnessing these epigenetic mechanisms offers a pathway to developing crop cultivars that not only exhibit enhanced tolerance and productivity in contaminated environments but also restrict the accumulation of toxic metals in edible tissues, thereby improving food safety and supporting sustainable agriculture on Bednarekmarginal lands. Despite major analytical breakthroughs, the precise role of DNA methylation in regulating gene responses to metal toxicity remains a critical, unresolved challenge in research. This review provides an overview of DNA methylation mechanisms and outlines the plant genes that are modified in response to metal exposure.

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来源期刊
Ecotoxicology
Ecotoxicology 环境科学-毒理学
CiteScore
5.30
自引率
3.70%
发文量
107
审稿时长
4.7 months
期刊介绍: Ecotoxicology is an international journal devoted to the publication of fundamental research on the effects of toxic chemicals on populations, communities and terrestrial, freshwater and marine ecosystems. It aims to elucidate mechanisms and processes whereby chemicals exert their effects on ecosystems and the impact caused at the population or community level. The journal is not biased with respect to taxon or biome, and papers that indicate possible new approaches to regulation and control of toxic chemicals and those aiding in formulating ways of conserving threatened species are particularly welcome. Studies on individuals should demonstrate linkage to population effects in clear and quantitative ways. Laboratory studies must show a clear linkage to specific field situations. The journal includes not only original research papers but technical notes and review articles, both invited and submitted. A strong, broadly based editorial board ensures as wide an international coverage as possible.
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