Kou Wang, Yu-Lian Zhao, Yan-Zi Jiang, Wen Liu, Xiao-Ping Wang
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RNA interference-mediated knockdown of Svp in SD females induced typical diapause phenotypes, including ovarian arrest and lipid accumulation. The application of methoprene (ME), a JH receptor agonist, reversed these diapause phenotypes and restored reproduction, indicating that Svp's regulation of reproductive diapause is dependent on JH signaling. Additionally, Svp knockdown led to the downregulation of JH pathway genes and a reduction in JH titers. Further evidence suggested that Svp regulates the expression of JHAMT1, a critical gene in JH biosynthesis, which determines diapause entry in C. bowringi. These findings suggest that diapause-inducing photoperiods suppress Svp expression, blocking JH production and triggering diapause. 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引用次数: 0
摘要
生殖滞育是昆虫为应对不利的环境变化而暂时停止繁殖的一种生存策略。这个过程的特点是卵巢发育受阻和脂质积累在女性。已知幼崽激素(JH)生物合成的减少可启动生殖滞育,但其调节机制尚不清楚。7 up (Svp)是核受体家族的转录因子,在昆虫的各种发育过程中起着至关重要的作用。本研究以大白菜甲虫(colaphelus bowringi)为模型,观察到在生殖光周期条件(short day [SD])下,Svp在雌性成虫头部的表达高于滞育条件(长day [LD])。RNA干扰介导的Svp敲低在SD雌性中诱导了典型的滞育表型,包括卵巢停滞和脂质积累。应用甲基戊二烯(methoprene, ME),一种JH受体激动剂,逆转了这些滞育表型并恢复了生殖,这表明Svp对生殖滞育的调节依赖于JH信号。此外,Svp敲低导致JH途径基因下调和JH滴度降低。进一步的证据表明,Svp调控JHAMT1的表达,而JHAMT1是JH生物合成的关键基因,决定了弓形虫滞育的进入。这些结果表明,诱导滞育的光周期抑制了Svp的表达,阻断了JH的产生并触发了滞育。这项工作揭示了一个关键的转录因子,通过调节JH的产生来调节生殖滞育的启动,为控制能够进入生殖滞育的害虫提供了一个潜在的靶点。
Seven up regulates reproductive diapause initiation via juvenile hormone biosynthesis in the cabbage beetle Colaphellus bowringi.
Reproductive diapause is an insect survival strategy in which reproduction temporarily halts in response to adverse environmental changes. This process is characterized by arrested ovarian development and lipid accumulation in females. A reduction in juvenile hormone (JH) biosynthesis is known to initiate reproductive diapause, but its regulatory mechanism remains unclear. Seven up (Svp), a transcription factor from the nuclear receptor family, plays a crucial role in various developmental processes in insects. In this study, using the cabbage beetle Colaphellus bowringi as a model, we observed higher expression of Svp in the heads of female adults under reproductive photoperiodic conditions (short-day [SD]) compared to diapause conditions (long-day [LD]). RNA interference-mediated knockdown of Svp in SD females induced typical diapause phenotypes, including ovarian arrest and lipid accumulation. The application of methoprene (ME), a JH receptor agonist, reversed these diapause phenotypes and restored reproduction, indicating that Svp's regulation of reproductive diapause is dependent on JH signaling. Additionally, Svp knockdown led to the downregulation of JH pathway genes and a reduction in JH titers. Further evidence suggested that Svp regulates the expression of JHAMT1, a critical gene in JH biosynthesis, which determines diapause entry in C. bowringi. These findings suggest that diapause-inducing photoperiods suppress Svp expression, blocking JH production and triggering diapause. This work reveals a critical transcription factor that regulates reproductive diapause initiation through modulating JH production, providing a potential target for controlling pests capable of entering reproductive diapause.
期刊介绍:
Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.