RNA interference knockdown of the nuclear receptor HR3 suppresses vitellogenesis in Chilo suppressalis.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jingxuan Hu, Qingzhen He, Yang Cui, Wenbing Ding, Hualiang He, Hongshuai Gao, Qiao Gao, Lin Qiu, Youzhi Li
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引用次数: 0

Abstract

Background: Developmental and reproductive processes are the most critical physiological processes in insects, with the insect hormone 20-hydroxyecdysone (20E, the major active form of ecdysone) playing a central regulatory role in key developmental events such as embryonic development, larval molting, metamorphosis, and reproduction. As an early-late gene within the ecdysone-mediated genetic regulatory network, the orphan nuclear receptor HR3, which exhibits characteristics of both early and late genes, serves as a critical regulator of insect metamorphosis and development. However, the precise molecular mechanisms underlying HR3's function in the reproduction of non-model insects remain poorly understood.

Methods and results: We cloned Chilo suppressalis HR3 (CsHR3) and phylogenetic analysis demonstrates that CsHR3 shares the highest sequence homology with its ortholog in Ostrinia furnacalis. Spatiotemporal expression profiling revealed that CsHR3 expression peaked during day 4 of the female pupal stage, with the highest tissue-specific expression observed in the heads of female pupae. RNA-interference (RNAi) mediated silencing of CsHR3 resulted in delayed oocyte maturation, reduced yolk deposition, and decreased fecundity. Concurrently, transcriptional levels of key genes involved in yolk formation vitellogenin (Vg), 20E and juvenile hormones (JH) signaling pathways, including chitin synthase 1 (CHS1), were significantly downregulated in the CsHR3-knockdown group.

Conclusion: These findings collectively demonstrate that CsHR3 plays an essential role in the reproductive regulation of C. suppressalis, potentially mediating transcriptional control of 20E and JH pathway-related genes and chitin biosynthesis-related targets. This study not only advances the understanding of reproductive regulation in Lepidoptera but also highlights HR3 as a potential molecular target for pest management strategies.

核受体HR3的RNA干扰敲低抑制Chilo suppressalis的卵黄形成。
背景:发育和生殖过程是昆虫最关键的生理过程,昆虫激素20-羟基蜕皮激素(20E,蜕皮激素的主要活性形式)在胚胎发育、幼虫蜕皮、变态和繁殖等关键发育事件中起着核心调节作用。孤儿核受体HR3作为蜕皮激素介导的遗传调控网络中的一个早、晚基因,具有早、晚基因的双重特征,是昆虫变态发育的重要调控因子。然而,HR3在非模式昆虫繁殖中的精确分子机制仍然知之甚少。方法与结果:克隆了抑制Chilo suppressalis HR3 (CsHR3),系统发育分析表明,CsHR3与Ostrinia furnacalis同源基因序列同源性最高。时空表达谱显示,CsHR3的表达在雌蛹期第4天达到峰值,在雌蛹头部的组织特异性表达最高。rna干扰(RNAi)介导的CsHR3沉默导致卵母细胞成熟延迟、卵黄沉积减少和生殖力下降。同时,在cshr3敲低组中,参与蛋黄形成卵黄原蛋白(Vg)、卵黄原蛋白(20E)和幼体激素(JH)信号通路的关键基因,包括几丁质合成酶1 (CHS1)的转录水平显著下调。结论:综上所述,CsHR3在C. suppressalis的生殖调控中发挥重要作用,可能介导20E和JH通路相关基因的转录调控以及几丁质生物合成相关靶点。该研究不仅促进了对鳞翅目昆虫生殖调控的认识,而且突出了HR3作为害虫防治策略的潜在分子靶点。
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
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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