Exploring the proteins and metabolites associated with male antennae responses to female exposure of Antheraea pernyi (Lepidoptera: Saturniidae) moths.

IF 2.2 2区 农林科学 Q1 ENTOMOLOGY
Guobao Wang, Xiang Ji, Lei Nie, Ruirui Xu
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引用次数: 0

Abstract

Detection of sex pheromones of insects relies on the antennae. The female pheromone signal transmission in the male antennae ultimately initiates the courtship and mating behaviors of males. To investigate the proteins and metabolites involved in this neural transduction, integrative proteomics and metabolomics analysis including tandem mass tag (TMT) proteomic quantification and liquid chromatography tandem mass spectrometry (LC/MS)-based metabolomics was adopted for comparing proteomic and metabolic changes between the antennae of male moths following stimulation by females and the non-stimulated males of Antheraea pernyi (Guérin-Méneville, Lepidoptera: Saturniidae) in this study. A total of 92 differentially expressed proteins (DEPs) containing 52 upregulated and 40 downregulated proteins and 545 differentially expressed metabolites (DEMs) including 218 upregulated and 327 downregulated metabolites were identified from the antennae of female-stimulated male moths based on the proteome and metabolome data, respectively. Bioinformatics analysis was performed for the 45 DEPs and 160 DEMs, including Gene Ontology (GO), Clusters of Orthologous Groups (COG), and Kyoto Encylopaedia of Genes and Genomes (KEGG) enrichment analysis and Human Metabolome Database (HMDB) annotation. A number of DEPs and DEMs related to neural transmission of female pheromone signals in the male antennae of A. pernyi were screened, including tyrosine hydroxylase, cryptochrome-1, tachykinin, arylalkylamine N-acetyltransferase, cadherin-23, glutathione S-transferase delta 3, tyramine, tryptamine, n-oleoyl dopamine, n-stearoyl dopamine, and n-stearoyl tyrosine. The altered expression levels of those proteins or metabolites were speculated involved in regulating the neuron activity for enhanced transmission of neural impulses and continuous perception, reception, and transduction of female pheromone signals. Our findings yielded novel insights into the potential mechanisms in the antennae of male A. pernyi responding to female attraction.

探讨柞蚕(鳞翅目:桑科)蛾雄触角对雌触角暴露反应的相关蛋白质和代谢产物。
昆虫性信息素的检测依赖于触角。雌性信息素信号在雄性触角中的传递最终启动了雄性的求偶和交配行为。为了研究参与这种神经转导的蛋白质和代谢产物,采用串联质谱(TMT)蛋白质组学定量和液相色谱-串联质谱(LC/MS)代谢组学相结合的蛋白质组学和代谢组学分析方法,比较了柞蚕雌蛾和未受刺激雄蛾触角的蛋白质组和代谢变化(Guérin-Méneville,鳞翅目:金龟子科)。基于蛋白质组和代谢组数据,从雌性刺激雄蛾的触角中分别鉴定出92种差异表达蛋白(DEP)和545种差异表达代谢产物(DEM),其中包括52种上调和40种下调蛋白,包括218种上调和327种下调代谢产物。对45个DEP和160个DEM进行了生物信息学分析,包括基因本体论(GO)、同源群簇(COG)、京都基因和基因组百科全书(KEGG)富集分析和人类代谢组数据库(HMDB)注释。筛选了许多与柞蚕雄性触角中雌性信息素信号的神经传递有关的DEP和DEMs,包括酪氨酸羟化酶、隐花色素-1、速激肽、芳烷基胺N-乙酰基转移酶、钙粘蛋白-23、谷胱甘肽S-转移酶delta 3、酪胺、色胺、N-亮氨酸多巴胺、N-硬脂酰多巴胺和N-硬脂酰酪氨酸。据推测,这些蛋白质或代谢产物表达水平的改变与调节神经元活性有关,以增强神经冲动的传递以及女性信息素信号的持续感知、接收和转导。我们的研究结果为雄性A.pernyi触角对雌性吸引力的潜在机制提供了新的见解。
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来源期刊
CiteScore
4.60
自引率
9.10%
发文量
198
审稿时长
3-6 weeks
期刊介绍: Journal of Economic Entomology the most-cited entomological journal – publishes articles on the economic significance of insects and other arthropods and includes sections on apiculture & social insects, insecticides, biological control, household & structural insects, crop protection, forest entomology, and more. In addition to research papers, Journal of Economic Entomology publishes Reviews, interpretive articles in a Forum section, Short Communications, and Letters to the Editor. The journal is published bimonthly in February, April, June, August, October, and December.
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