The effect of nitrosative stress on histone H3 and H4 acetylation in Phytophthora infestans life cycle

IF 6.1 2区 生物学 Q1 PLANT SCIENCES Plant Physiology and Biochemistry Pub Date : 2024-09-14 DOI:10.1016/j.plaphy.2024.109129
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Abstract

The oomycete Phytophthora infestans is one of the most destructive phytopathogens globally. It has a proven ability to adapt to changing environments rapidly; however, molecular mechanisms responsible for host invasion and adaptation to new environmental conditions still need to be explored. The study aims to understand the epigenetic mechanisms exploited by P. infestans in response to nitrosative stress conditions created by the (micro)environment and the host plant. To characterize reactive nitrogen species (RNS)-dependent acetylation profiles in avirulent/virulent (avr/vr) P. infestans, a transient gene expression, ChIP and immunoblot analyses, and nitric oxide (NO) emission by chemiluminescence were used in combination with the pharmacological approach. Nitrosative stress increased total H3/H4 acetylation and some histone acetylation marks, mainly in sporulating hyphae of diverse (avr/vr) isolates and during potato colonization. These results correlated with transcriptional up-regulation of acetyltransferases PifHAC3 and PifHAM1, catalyzing H3K56 and H4K16 acetylation, respectively. NO or peroxynitrite–mediated changes were also associated with H3K56 and H4K16 mark deposition on the critical pathogenicity-related gene promoters (CesA1, CesA2, CesA3, sPLD-like1, Hmp1, and Avr3a) elevating their expression. Our study highlights RNS-dependent transcriptional reprogramming via histone acetylation of essential gene expression in the sporulating and biotrophic phases of plant colonization by P. infestans as a tool promoting its evolutionary plasticity.

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亚硝基胁迫对根瘤蚜生命周期中组蛋白 H3 和 H4 乙酰化的影响
卵菌 Phytophthora infestans 是全球最具破坏性的植物病原体之一。事实证明,它有能力迅速适应不断变化的环境;然而,宿主入侵和适应新环境条件的分子机制仍有待探索。本研究旨在了解 P. infestans 在应对由(微)环境和寄主植物造成的亚硝酸胁迫条件时所利用的表观遗传学机制。为了描述无病毒/有病毒(avr/vr)P. infestans中依赖于活性氮物种(RNS)的乙酰化特征,研究人员结合药理学方法,使用了瞬时基因表达、ChIP和免疫印迹分析以及化学发光一氧化氮(NO)发射。亚硝基胁迫增加了总的 H3/H4 乙酰化和一些组蛋白乙酰化标记,主要是在不同(avr/vr)分离株的孢子菌丝中和马铃薯定殖过程中。这些结果与分别催化 H3K56 和 H4K16 乙酰化的乙酰转移酶 PifHAC3 和 PifHAM1 的转录上调有关。氮氧化物或过亚硝酸盐介导的变化还与关键致病相关基因启动子(CesA1、CesA2、CesA3、sPLD-like1、Hmp1 和 Avr3a)上的 H3K56 和 H4K16 标记沉积有关,从而提高了它们的表达。我们的研究突出表明,在P. infestans定殖植物的孢子期和生物营养期,通过组蛋白乙酰化对重要基因表达进行依赖性转录重编程是促进其进化可塑性的一种工具。
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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
期刊介绍: Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement. Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB. Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.
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