库蚊脂肪体中的 H3K27me2 水平降低。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xueyan Wei, Prabin Dhungana, Cheolho Sim
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引用次数: 0

摘要

北方家蚊库蚊是西尼罗河病毒的主要传播媒介。为了度过严冬,成蚊会进入休眠期。寿命延长和脂质储存增加是休眠的关键指标。组蛋白的翻译后修饰会影响基因的表达,并与许多昆虫的寿命和能量利用有关。在这里,我们研究了表观遗传学改变在启动该蚊子物种休眠中的潜在作用。来自其他昆虫物种的 H3 序列的多重序列比对表明,在整个进化过程中,H3 组蛋白在 Cx.然后,我们用 Western 印迹法比较了舒缓期和非舒缓期喙蚊卵巢和脂肪体组织中组蛋白甲基化的水平。我们的数据表明,蝰蛇卵巢中的组蛋白甲基化水平在休眠期没有变化。相反,相对于非休眠期的蚊子,休眠期蚊子脂肪体中的 H3K27me2 水平下降了两倍多。在许多昆虫物种的发育过程中,H3K27甲基化对染色体的激活和失活起着至关重要的作用。这主要是由多角体抑制复合体 2(polycomb repressor complex 2)控制的。耐人寻味的是,之前的一项 ChIP-seq 研究表明,转录因子 FOXO(叉头盒 O)的靶标是组成该复合体的基因。此外,H3K27me2 在 Cx. pipiens 的整个休眠程序中表现出动态丰度,表明它在休眠程序的初始激活过程中可能发挥作用。这项研究拓展了我们对表观遗传调控改变与暂停之间关系的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The diapausing mosquito Culex pipiens exhibits reduced levels of H3K27me2 in the fat body

The diapausing mosquito Culex pipiens exhibits reduced levels of H3K27me2 in the fat body

Culex pipiens, the northern house mosquito, is a major vector of West Nile virus. To survive the severe winter, adult mosquitoes enter a diapause programme. Extended lifespan and an increase in lipid storage are key indicators of diapause. Post-translational modifications to histone proteins impact the expression of genes and have been linked to the lifespan and energy utilisation of numerous insects. Here, we investigated the potential contribution of epigenetic alterations in initiating diapause in this mosquito species. Multiple sequence alignment of H3 sequences from other insect species demonstrates a high conservation of the H3 histone in Cx. pipiens throughout evolution. We then compared the levels of histone methylation in the ovaries and fat body tissues of diapausing and non-diapausing Cx. pipiens using western blots. Our data indicate that histone methylation levels in the ovaries of Cx. pipiens do not change during diapause. In contrast, H3K27me2 levels decrease more than twofold in the fat body of diapausing mosquitoes relative to non-diapausing counterparts. H3K27 methylation plays a crucial role in chromosome activation and inactivation during development in many insect species. This is predominantly governed by polycomb repressor complex 2. Intriguingly, a previous ChIP-seq study demonstrated that the transcription factor FOXO (Forkhead box O) targets the genes that comprise this complex. In addition, H3K27me2 exhibits dynamic abundance throughout the diapause programme in Cx. pipiens, suggesting its potential role in the initial activation of the diapause programme. This study expands our understanding of the relationship between alterations in epigenetic regulation and diapause.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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