Qin Qianyue, Zhang Bo, Fang Bin, Chang Yanpeng, Li Xiang, An Shiheng, Zhao Wenli
State Key Laboratory of Wheat and Maize Crop Science/College of Plant Protection, Henan Agricultural University, Zhengzhou, China.
Insect Mol Biol. 2025 Apr;34(2):249-262. doi: 10.1111/imb.12969. Epub 2024 Nov 6.
Trehalase (Treh) is crucial for ovarian development as it directly regulates the energy supply by hydrolyzing trehalose into glucose. Juvenile hormone (JH) is also essential for ovarian development, but how it affects Treh2 activity remains unclear. This study, which employed Helicoverpa armigera as a model, showed that HaTreh2 transcription and enzymatic activity peaks coincided with the peak of JH titers (the 2 and 3 days after emergence). Compared to the dsGFP control, knockdown of HaTreh2 transcription severely impaired ovarian development. LC-MS/MS and site mutation experiments demonstrated that JH triggered the serine 345 phosphorylation of HaTreh2 via the GPCR-cAMP-PKA pathway, thereby activating its enzymatic activity. Additionally, HaTreh2 is directly bound with trehalose transporter (HaTreT) under JH induction, thus controlling intracellular trehalose and glucose contents as well as the transcription of HaTreT. TreT controls the amount of trehalose, which serves as a substrate for Treh1, entering the cell. Treh2, on the other hand, uses extracellular trehalose as substrate, and the hydrolysis product glucose is further transported into the cell. Here, HaTreh2 regulated the substrate that HaTreh1 can act upon in the cell by directly binding with HaTreT during ovarian development when JH is induced. Therefore, JH systematically regulated trehalose metabolism during ovarian development through regulating the activity of HaTreh2. This study sheds light on the coordinated interplay between JH pathway and sugar metabolism in ovarian development.
海藻糖酶(Treh)对卵巢发育至关重要,因为它通过将海藻糖水解为葡萄糖直接调节能量供应。保幼激素(JH)对卵巢发育也必不可少,但其如何影响Treh2活性仍不清楚。本研究以棉铃虫为模型,结果表明,HaTreh2的转录和酶活性峰值与JH滴度峰值(羽化后第2天和第3天)一致。与dsGFP对照相比,敲低HaTreh2转录严重损害卵巢发育。液相色谱-串联质谱(LC-MS/MS)和位点突变实验表明,JH通过GPCR-cAMP-PKA途径触发HaTreh2的丝氨酸345磷酸化,从而激活其酶活性。此外,在JH诱导下,HaTreh2与海藻糖转运蛋白(HaTreT)直接结合,从而控制细胞内海藻糖和葡萄糖含量以及HaTreT的转录。TreT控制作为Treh1底物的海藻糖进入细胞的量。另一方面,Treh2以细胞外海藻糖为底物,水解产物葡萄糖进一步转运到细胞内。在此,在JH诱导的卵巢发育过程中,HaTreh2通过与HaTreT直接结合来调节HaTreh1在细胞中可作用的底物。因此,JH通过调节HaTreh2的活性在卵巢发育过程中系统性地调节海藻糖代谢。本研究揭示了JH途径与卵巢发育中糖代谢之间的协同相互作用。