Histone acetyltransferase p300/CBP regulates reproductive diapause via the juvenile hormone pathway in the cabbage beetle, Colaphellus bowringi.

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hao-Min An, Yi-Ke Zhang, Qian-Lu Bai, Wen Liu, Xiao-Ping Wang
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引用次数: 0

Abstract

Juvenile hormone (JH) serves as a pivotal endocrine regulator of reproductive diapause (also known as adult diapause) in insects, though the molecular mechanisms underlying JH signalling remain poorly characterised. In this study, we investigate the roles of the histone acetyltransferase p300/CBP in regulating reproductive diapause through JH signalling in the cabbage beetle Colaphellus bowringi. RNA interference-mediated knockdown of p300/CBP in reproductive females induced diapause-like phenotypes, including arrested ovarian maturation, suppressed vitellogenesis, increased lipid accumulation and upregulation of diapause-associated genes. These effects were accompanied by downregulation of key JH biosynthetic enzymes and signalling components. Although exogenous JH application decreased lipid accumulation, it failed to rescue ovarian development. Similar results were observed in diapause females following p300/CBP knockdown: JH analog treatment reduced lipid accumulations but did not restore ovarian development. Collectively, these findings demonstrate that p300/CBP regulates photoperiodic reproductive diapause by modulating both JH biosynthesis and signal transduction pathways in C. bowringi. Our results establish p300/CBP as a critical epigenetic mediator of JH-mediated reproductive diapause and provide new insights into the molecular mechanisms underlying environmental adaptation in insects.

组蛋白乙酰转移酶p300/CBP通过幼体激素途径调控白菜甲虫的生殖滞育。
幼虫激素(JH)是昆虫生殖滞育(也称为成虫滞育)的关键内分泌调节剂,尽管JH信号传导的分子机制尚不清楚。在这项研究中,我们研究了组蛋白乙酰转移酶p300/CBP在白菜甲虫JH信号传导中调节生殖滞育的作用。RNA干扰介导的p300/CBP敲低在生殖雌性中诱导了滞育样表型,包括卵巢成熟阻滞、卵黄生成抑制、脂质积累增加和滞育相关基因上调。这些影响伴随着关键的JH生物合成酶和信号成分的下调。虽然外源性JH降低了脂质积累,但未能挽救卵巢发育。在p300/CBP敲除后的滞育雌性中观察到类似的结果:JH类似物治疗减少了脂质积累,但没有恢复卵巢发育。综上所述,这些发现表明p300/CBP通过调节弓形虫JH生物合成和信号转导途径来调节光周期生殖滞育。我们的研究结果表明p300/CBP是jh介导的生殖滞育的关键表观遗传介质,并为昆虫环境适应的分子机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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