PBAN regulates sex pheromone biosynthesis by Ca2+/CaN/ACC and Ca2+/PKC/HK2 signal pathways in Spodoptera litura.

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yao Zhang, Ruolan He, Zelong She, Xinming Yin, Xiang Li, Shuangyan Yao, Mengfang Du, Shiheng An
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引用次数: 0

Abstract

Sex pheromones emitted by female moths play important roles in mate attraction. The molecular mechanism underlying pheromone biosynthesis activating neuropeptide (PBAN)-regulated sex pheromone biosynthesis has been well elucidated in many moth species, although this mechanism is species-dependent. Spodoptera litura, an important pest, has caused serious economic losses to agricultural production, yet the mechanism for its sex pheromone biosynthesis has not been fully identified. The present study investigates in detail mechanism underlying PBAN-regulated sex pheromone biosynthesis in S. litura. The transcriptome sequencing of S. litura pheromone glands (PGs) was analysed to identify a serial of candidate genes potentially involved in sex pheromone biosynthesis. Further investigation revealed a bimodal pattern in both sex pheromone release and mating frequency. PBAN was found to regulate sex pheromone biosynthesis via its receptor by using Ca2+ as a secondary messenger, as demonstrated by RNA interference and the application of pharmacological inhibitors. Furthermore, PBAN/Ca2+ signalling activated calcineurin (CaN) and acetyl-CoA carboxylase (ACC), which mediated sex pheromone biosynthesis in response to PBAN stimulation. Mostly importantly, hexokinase 2 (HK2) was confirmed to be activated by PBAN/PBANR /Ca2+/PKC signalling via phosphorylation at two specific sites (ser423 and ser434 sites of HK2). Overall, our findings shed light on the intricate processes involved in sex pheromone production in S. litura, in which PBAN regulates sex pheromone biosynthesis through PBAN/PBANR/Ca2+/CaN/ACC and PBAN/PBANR/Ca2+/PKC/HK2 signalling pathways. These insights significantly contribute to our comprehension of the specific mechanisms underlying sex pheromone biosynthesis in this moth species.

PBAN通过Ca2+/CaN/ACC和Ca2+/PKC/HK2信号途径调控鞘翅目昆虫性信息素的生物合成。
雌蛾释放的性信息素在配偶吸引中发挥着重要作用。在许多蛾类物种中,费洛蒙生物合成激活神经肽(PBAN)调控性费洛蒙生物合成的分子机制已经被很好地阐明,尽管这种机制是物种依赖性的。斑翅蛾(Spodoptera litura)是一种重要害虫,给农业生产造成了严重的经济损失,但其性信息素的生物合成机制尚未完全确定。本研究详细探究了 PBAN 调控光翅目鞘翅目昆虫性信息素生物合成的机制。通过分析 S. litura 信息素腺体(PGs)的转录组测序,确定了一系列可能参与性信息素生物合成的候选基因。进一步研究发现,性信息素的释放和交配频率均呈双峰模式。通过 RNA 干扰和药物抑制剂的应用,发现 PBAN 可通过其受体利用 Ca2+ 作为次级信使来调节性信息素的生物合成。此外,PBAN/Ca2+ 信号激活了钙调神经蛋白(CaN)和乙酰-CoA 羧化酶(ACC),它们在 PBAN 的刺激下介导了性信息素的生物合成。最重要的是,已证实己糖激酶 2(HK2)通过两个特定位点(HK2 的 ser423 和 ser434 位点)的磷酸化被 PBAN/PBANR /Ca2+/PKC 信号激活。总之,我们的研究结果揭示了 S. litura 性信息素产生的复杂过程,其中 PBAN 通过 PBAN/PBANR/Ca2+/CaN/ACC 和 PBAN/PBANR/Ca2+/PKC/HK2 信号通路调控性信息素的生物合成。这些发现大大有助于我们理解该蛾类性费洛蒙生物合成的具体机制。
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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