家蚕中H3K9me3/H3K9ac修饰引起的基因表达水平变化与BmCPV感染有关。

IF 5.4 1区 农林科学 Q1 IMMUNOLOGY
Virulence Pub Date : 2025-12-01 Epub Date: 2025-05-26 DOI:10.1080/21505594.2025.2510535
Qunnan Qiu, Xinyu Tong, Min Zhu, Zhe Liu, Huilin Pang, Liuyang Li, Yongjie Feng, Xiaolong Hu, Chengliang Gong
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引用次数: 0

摘要

组蛋白修饰引起的染色质可及性改变调节基因转录。然而,关于组蛋白修饰引起的基因表达变化与病毒感染之间的关系知之甚少。采用CUT&Tag-seq和RNA-seq技术,对感染家蚕拟虫病毒(BmCPV) 48 h和96 h的家蚕内脏(CPV48和CPV96)和未感染家蚕内脏(GUT48和GUT96)进行了检测。我们报道了H3K9me3、H3K9ac和基因表达谱在全基因组水平上随着BmCPV感染而改变。差异H3K9me3峰相关基因主要富集于MAPK、Wnt和Hippo信号通路;H3K9ac差异峰相关基因主要富集于Hippo信号通路、凋亡通路和柠檬酸循环通路;差异表达基因(DEGs)主要富集于碳代谢、内质网蛋白质加工和糖酵解/糖异生途径。H3K9me3/H3K9ac峰值与基因表达的整合分析显示,基因表达谱的变化与H3K9me3/H3K9ac启动子的改变有关;基因表达与基因体内相应的H3K9me3信号呈负相关,与转录起始位点相应的H3K9ac信号呈正相关。筛选CUT&Tag-seq峰和RNA-seq FPKM > 1同时发生log2倍变化的交叉基因并进行标注。差异H3K9me3峰相关基因和deg共享的基因富集在昆虫激素生物合成、MAPK信号通路和tgf - β信号通路中,差异H3K9ac峰相关基因和deg共享的基因富集在糖酵解/糖异生、tgf - β信号通路和线粒体自噬通路中。这些结果表明BmCPV通过H3K9me3/H3K9ac调控基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in gene expression levels caused by H3K9me3/H3K9ac modifications are associated with BmCPV infection in Bombyx mori.

Changes in chromatin accessibility caused by histone modifications regulate gene transcription. However, little is known about associations between gene expression changes caused by histone modifications and viral infections. We investigate the midguts of silkworms infected with Bombyx mori cypovirus (BmCPV) at 48 h and 96 h post infection (CPV48 and CPV96), and corresponding midguts of uninfected silkworms (GUT48 and GUT96) using CUT&Tag-seq and RNA-seq. We report H3K9me3, H3K9ac, and gene expression profiles at the genome-wide level to change with BmCPV infection. Differential H3K9me3 peak-related genes were mainly enriched in MAPK, Wnt, and Hippo signalling pathways; Differential H3K9ac peaks-related genes were mainly enriched in the Hippo signalling, apoptosis, and citrate cycle pathways; and differentially expressed genes (DEGs) were mainly enriched in carbon metabolism, protein processing in endoplasmic reticulum, and glycolysis/gluconeogenesis pathways. Integration analysis between H3K9me3/H3K9ac peaks and gene expression revealed changes in gene expression profiles to be associated with alteration of H3K9me3/H3K9ac at promoters; gene expression correlates negatively with corresponding H3K9me3 signals in gene bodies, and positively with corresponding H3K9ac signals at the transcription start site. Intersection genes with log2foldchange of both CUT&Tag-seq peak and RNA-seq FPKM > 1 were screened and annotated. Genes shared by differential H3K9me3 peak-related genes and DEGs were enriched in insect hormone biosynthesis, MAPK signalling, and TGF-beta signalling pathways, and genes shared by differential H3K9ac peak-related genes and DEGs were enriched in glycolysis/gluconeogenesis, TGF-beta signalling, and mitophagy pathways. These results indicate that BmCPV regulates gene expression through H3K9me3/H3K9ac.

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来源期刊
Virulence
Virulence IMMUNOLOGY-MICROBIOLOGY
CiteScore
9.20
自引率
1.90%
发文量
123
审稿时长
6-12 weeks
期刊介绍: Virulence is a fully open access peer-reviewed journal. All articles will (if accepted) be available for anyone to read anywhere, at any time immediately on publication. Virulence is the first international peer-reviewed journal of its kind to focus exclusively on microbial pathogenicity, the infection process and host-pathogen interactions. To address the new infectious challenges, emerging infectious agents and antimicrobial resistance, there is a clear need for interdisciplinary research.
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