利用表观遗传修饰因子揭示高静水压力下互交菌mapk介导的调控机制。

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Qingqing Peng, Qifei Wei, Xi Yu
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引用次数: 0

摘要

高静水压力(HHP)可以显著调节微生物代谢,而化学表观遗传修饰剂可以重新激活沉默的生物合成基因簇并诱导新的天然产物。然而,这些表观遗传修饰因子在差压条件下调节真菌反应的机制,以及这种调节如何影响天然产物的生物合成,仍然完全未被探索。本文研究了从马里亚纳海沟7332 m沉积物中分离到的赤潮真菌Alternaria alternata CIEL23,并对其进行了表观遗传修饰剂处理(0.1 MPa和40 MPa)。我们的研究结果表明,表观遗传扰动和高压显著改变了真菌表型、基因表达和次级代谢物组成。在0.1 MPa和40 MPa两种压力条件下,表观遗传修饰因子对表观遗传调控机制的转录组水平分析表明,表观遗传修饰因子的加入调节了环境刺激下MAPK通路相关基因的表达。在双重应激条件下,MAPK通路的IG、CWI和HOG分支的活动模式发生了显著改变。这些变化与菌丝生长、细胞壁重塑、细胞周期进程和渗透物合成相关基因的差异调控有关,表明多种细胞过程的协调调节。这些发现提供了表观遗传修饰诱导hahp反应变化和调控之间的机制联系。我们的研究不仅促进了对双胁迫源hadal真菌反应的理解,而且为利用其应激驱动的代谢多样性进行生物技术应用开辟了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing Epigenetic Modifiers Reveals MAPK-Mediated Regulation Mechanisms in Hadal Fungi of Alternaria alternata Under High Hydrostatic Pressure.

High hydrostatic pressure (HHP) significantly modulates microbial metabolism, while chemical epigenetic modifiers are known to reactivate silent biosynthetic gene clusters and induce novel natural products. However, the mechanisms by which these epigenetic modifiers regulate fungal responses under differential pressure conditions, and how such regulation affects natural product biosynthesis, remain completely unexplored. Here, we investigated the hadal fungus Alternaria alternata CIEL23 isolated from 7332 m sediments in the Mariana Trench under epigenetic modifier treatment with contrasting pressures (0.1 MPa vs. 40 MPa). Our results revealed that epigenetic perturbations and high pressure significantly altered fungal phenotypes, gene expression, and secondary metabolite composition. Transcriptome-level analysis of epigenetic regulatory mechanisms under epigenetic modifiers in both pressure conditions (0.1 MPa and 40 MPa) demonstrated that the addition of epigenetic modifiers regulated MAPK pathway-related gene expression in response to the environment stimuli. Under dual stress conditions, the IG, CWI, and HOG branches of the MAPK pathway showed significantly altered activity patterns. These changes were associated with differential the regulation of genes related to hyphal growth, cell wall remodeling, cell cycle progression, and osmolyte synthesis, suggesting the coordinated modulation of multiple cellular processes. These findings provide the mechanistic link between epigenetic modification induced HHP-response changes and regulation in hadal fungi. Our study not only advances understanding of hadal fungal response to dual stressors but also unlocks new possibilities for harnessing their stress-driven metabolic versatility for biotechnological applications.

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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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