Desaturase 11 responds to the pheromone biosynthesis activating neuropeptide signal to regulate the biosynthesis of sex pheromones and oviposition in Helicoverpa armigera
Wenhui Lu, Huan Guo, Mengdan Dai, Qing Zhai, Xingtu Wei, Heng Wang, Shiheng An, Xiang Li
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引用次数: 0
Abstract
The sex pheromones of moths consist of multiple components that serve as chemical signals emitted by female individuals to attract male counterparts for mating purposes. Desaturases, which are key enzymes involved in creating unsaturated bonds on fatty acid chains, play a critical role in producing specific sex pheromone components. In this study, the Old World bollworm, Helicoverpa armigera Hübner (Lepidoptera: Noctuidae), was used as a model to identify a desaturase gene called Hades11, which showed a high level of expression in the pheromone glands. RNA interference-mediated knockdown of Hades11 led to a significant decrease in the production of the main sex pheromone components (Z11-16:Ald and Z9-16:Ald). However, the ratio of sex pheromone components remained unchanged, indicating that Hades11 specifically affects sex pheromonal compound biosynthesis rather than their release ratio. Furthermore, inhibiting the expression of Hades11 also caused a notable reduction in the total number of eggs laid by female moths, without affecting the hatching rate. Importantly, it was found that the expression level of Hades11 may be indirectly regulated by pheromone biosynthesis activating neuropeptide (PBAN) and PBAN receptors in H. armigera.
飞蛾的性信息素由多种成分组成,作为雌性个体发出的化学信号,以吸引雄性个体进行交配。去饱和酶是脂肪酸链上产生不饱和键的关键酶,在产生特定的性信息素成分中起着关键作用。本研究以东半球棉铃虫Helicoverpa armigera h bner(鳞翅目:夜蛾科)为模型,鉴定了一种名为Hades11的去饱和酶基因,该基因在信息素腺体中表达水平较高。RNA干扰介导的Hades11的敲低导致主要性信息素成分(Z11-16:Ald和Z9-16:Ald)的产生显著减少。然而,性信息素成分的比例保持不变,表明Hades11特异性影响性信息素化合物的生物合成而不是其释放比例。此外,抑制Hades11的表达也能显著降低雌蛾产卵总数,但不影响孵化率。重要的是,我们发现Hades11的表达水平可能受到棉铃虫信息素生物合成激活神经肽(PBAN)和PBAN受体的间接调节。
期刊介绍:
Entomologia Experimentalis et Applicata publishes top quality original research papers in the fields of experimental biology and ecology of insects and other terrestrial arthropods, with both pure and applied scopes. Mini-reviews, technical notes and media reviews are also published. Although the scope of the journal covers the entire scientific field of entomology, it has established itself as the preferred medium for the communication of results in the areas of the physiological, ecological, and morphological inter-relations between phytophagous arthropods and their food plants, their parasitoids, predators, and pathogens. Examples of specific areas that are covered frequently are:
host-plant selection mechanisms
chemical and sensory ecology and infochemicals
parasitoid-host interactions
behavioural ecology
biosystematics
(co-)evolution
migration and dispersal
population modelling
sampling strategies
developmental and behavioural responses to photoperiod and temperature
nutrition
natural and transgenic plant resistance.