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解析10-羟基癸酸生物合成的分子机制:酰基辅酶A Δ(11) 去饱和酶和转录调节因子在蜜蜂下颚腺中的作用

Dissecting the Molecular Mechanism of 10-HDA Biosynthesis: Role of Acyl-CoA Delta(11) Desaturase and Transcriptional Regulators in Honeybee Mandibular Glands.

作者信息

Li Yunchang, Zhang Xiaojing, Xia Zhenyu, Hao Yue

机构信息

Institute of Apicultural Research, Chinese Academy of Agricultural Sciences, Beijing 100093, China.

出版信息

Insects. 2025 May 26;16(6):563. doi: 10.3390/insects16060563.

Abstract

10-Hydroxy-2-decenoic acid (10-HDA), a major fatty acid (FA) component of royal jelly, is synthesized in the mandibular glands (MGs) of worker honeybees. Despite its well-documented nutritional and therapeutic significance, the biosynthetic pathway and regulatory mechanisms of 10-HDA production remain largely unresolved. In this study, the molecular basis of 10-HDA biosynthesis and regulation in the MGs of newly emerged bees (NEBs), nurse bees (NBs), and forager bees (FBs) were investigated using RNA sequencing and weighted gene co-expression network analysis (WGCNA). A five-step biosynthetic pathway for 10-HDA was proposed, and cross-species analysis of and revealed the conserved expression patterns of 15 key enzymes involved. Functional validation via RNA interference (RNAi) demonstrated that knockdown of acyl-CoA Delta(11) desaturase (, LOC551527), a key enzyme in FA desaturation, led to a 50% reduction in 10-HDA levels. Protein-protein interaction (PPI) network analysis further identified transcriptional regulators Kay and Drep-2 as potential modulators of 10-HDA metabolism. This study provides the first comprehensive mechanistic model of 10-HDA biosynthesis in honeybee MGs and highlights the labor-specific regulation of FA metabolism. These findings offer promising genetic targets for improving the royal jelly quality through genetic technology.

摘要

10-羟基-2-癸烯酸(10-HDA)是蜂王浆的主要脂肪酸(FA)成分,由工蜂的下颌腺(MGs)合成。尽管其营养和治疗意义已得到充分证明,但10-HDA产生的生物合成途径和调控机制仍 largely 未得到解决。在本研究中,使用RNA测序和加权基因共表达网络分析(WGCNA)研究了新出现的蜜蜂(NEBs)、哺育蜂(NBs)和采集蜂(FBs)的MGs中10-HDA生物合成和调控的分子基础。提出了10-HDA的五步生物合成途径,跨物种分析揭示了15种关键酶的保守表达模式。通过RNA干扰(RNAi)进行的功能验证表明,敲低FA去饱和关键酶酰基辅酶A Delta(11)去饱和酶(,LOC551527)会导致10-HDA水平降低50%。蛋白质-蛋白质相互作用(PPI)网络分析进一步确定转录调节因子Kay和Drep-2为10-HDA代谢的潜在调节因子。本研究提供了蜜蜂MGs中10-HDA生物合成的第一个全面机制模型,并突出了FA代谢的劳动特异性调节。这些发现为通过基因技术提高蜂王浆质量提供了有前景的遗传靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e0/12193250/4dea553fbfd2/insects-16-00563-g001.jpg

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