EcR-JHAMT3 Axis Regulates Reproductive Plasticity in the Predatory Beetle Harmonia axyridis.

IF 3.7 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Li Zhu, Jia Lv, Zhen-Dong Huang, Zhan-Xu Pu, Lian-Ming Lu, Shuo Xu
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Abstract

Ecdysone (20-hydroxyecdysone, 20E) is a master regulator of insect development, but its function in adult reproduction-particularly in predatory species-remains poorly understood. We employed Harmonia axyridis to explore 20E signaling in reproduction regulation through RNAi, transcriptomic analysis, and hormone rescue assays. The results demonstrated that both JH and 20E biosynthesis were activated in aphid-fed females, whereas injection of 1.0 μg 20E effectively promoted ovarian development in artificial diet-fed individuals. Expression of the 20E receptor EcR was significantly upregulated in aphid-fed H. axyridis females. EcR silencing severely arrested ovarian development and reduced Vg expression. Transcriptomic analysis revealed that the insect hormone biosynthesis pathway (ko00981) serves as the crucial downstream pathway of EcR-mediated reproductive regulation, with JHAMT3 identified as the core effector. JHAMT3 silencing phenocopied the reproductive suppression observed in EcR-silenced beetles, while exogenous JHA and JH III treatment effectively rescued ovarian development in both cases. Furthermore, multiple high-confidence EcR binding motifs were predicted in the JHAMT3 promoter, and two binding sites (5'-AACTACACTGCCATC-3', 5'-AAGATCCTTGAATTT-3') were verified through EMSA and dual-luciferase reporter assays. These findings establish an EcR-JHAMT3-reproduction regulatory axis in H. axyridis, offering a mechanistic framework for understanding reproductive plasticity in predatory insects.

EcR-JHAMT3轴调控捕食甲虫生殖可塑性。
蜕皮激素(20-羟基蜕皮激素,20E)是昆虫发育的主要调节因子,但其在成虫繁殖中的作用——尤其是在掠食性物种中——仍然知之甚少。我们利用毛缕草(Harmonia axyridis)通过RNAi、转录组学分析和激素拯救试验来探索20E信号在生殖调节中的作用。结果表明,在蚜虫喂养的雌性中,JH和20E的生物合成均被激活,而在人工饲料喂养的雌性中,注射1.0 μg的20E可有效促进卵巢发育。20E受体EcR的表达在蚜虫喂养的雌鼠中显著上调。EcR沉默严重阻碍卵巢发育,降低Vg表达。转录组学分析显示,昆虫激素生物合成通路(ko00981)是ecr介导的生殖调控的关键下游通路,JHAMT3被确定为核心效应体。JHAMT3沉默表现了在ecr沉默的甲虫中观察到的生殖抑制,而外源JHA和JH III处理有效地挽救了这两种情况下的卵巢发育。此外,在JHAMT3启动子中预测了多个高置信度的EcR结合基序,并通过EMSA和双荧光素酶报告基因检测验证了两个结合位点(5'-AACTACACTGCCATC-3', 5'-AAGATCCTTGAATTT-3')。这些发现建立了食蚜鼠的ecr - jhamt3生殖调控轴,为了解食蚜虫的生殖可塑性提供了一个机制框架。
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来源期刊
CiteScore
7.40
自引率
5.30%
发文量
105
审稿时长
40 days
期刊介绍: This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.
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