Jiang Yan, Hu Jingsong, Li Yaohui, Tang Xiangyou, Peng Xiaomei, Xie Linxuan, Song Huali, Zhou Zeyang, Xu Jinshan
College of Life Sciences, Chongqing Normal University, Chongqing, China.
Key Laboratory of Pollinator Resources Conservation and Utilization of the Upper Yangtze River, Ministry of Agriculture and Rural Affairs, Chongqing, China.
Mol Biol Evol. 2025 Apr 1;42(4). doi: 10.1093/molbev/msaf074.
The honeybee (Apis mellifera) is a highly social insect whose caste differentiation is regulated by epigenetic mechanisms, representing a classic example of phenotypic plasticity in social insects. Although the importance of transposable elements (TEs) in epigenetic research is well recognized, their specific role in honeybee caste differentiation has not been fully explored. This study reveals a novel regulatory mechanism where the microRNA (miRNA) ame-mir-3721-3p, derived from ApME (Apis miniature inverted-repeat TEs), suppresses DNA methyltransferase gene DNMT3, promoting queen-like development in honeybee larvae. Genome-wide analysis identified 43 ApME elements in Apis, with ApMETm15 being particularly abundant and species-specific. These elements gave rise to 6 miRNAs, including ame-mir-3721-3p which showed notable regulatory potential. Target gene prediction and luciferase reporter assays confirmed that ame-mir-3721-3p binds to and suppresses DNMT3 expression. Spatiotemporal expression analysis indicated that ame-mir-3721-3p is significantly upregulated during the critical L3 larval stage, exhibiting a similar expression pattern to DNMT3. Larval feeding experiments with agomir demonstrated that ame-mir-3721-3p suppresses DNMT3 expression and significantly impacts the expression of genes related to the juvenile hormone and ecdysone pathways. Further physiological evidence showed that when larvae were treated with agomir-3721 during the critical caste differentiation window (L3-L4 stage), the emerging adult bees exhibited increased body size, doubled ovarian area, and significantly higher frequency of ovary development, with significant upregulation of ovarian-specific marker genes. These findings provide direct evidence for ame-mir-3721-3p's role in promoting queen-like developmental trajectories during caste differentiation, uncovering a new regulatory pathway in honeybee development and offering insights into epigenetic mechanisms in social insects.
蜜蜂(西方蜜蜂)是一种高度社会化的昆虫,其等级分化受表观遗传机制调控,是社会昆虫表型可塑性的经典例子。尽管转座元件(TEs)在表观遗传研究中的重要性已得到充分认识,但其在蜜蜂等级分化中的具体作用尚未得到充分探索。本研究揭示了一种新的调控机制,即源自ApME(蜜蜂微型反向重复转座元件)的微小RNA(miRNA)ame-mir-3721-3p抑制DNA甲基转移酶基因DNMT3,促进蜜蜂幼虫向蜂王样发育。全基因组分析在蜜蜂中鉴定出43个ApME元件,其中ApMETm15特别丰富且具有物种特异性。这些元件产生了6种miRNA,包括具有显著调控潜力的ame-mir-3721-3p。靶基因预测和荧光素酶报告基因检测证实ame-mir-3721-3p与DNMT3结合并抑制其表达。时空表达分析表明,ame-mir-3721-3p在关键的L3幼虫阶段显著上调,呈现出与DNMT3相似的表达模式。用agomir进行的幼虫喂养实验表明,ame-mir-3721-3p抑制DNMT3表达,并显著影响与保幼激素和蜕皮激素途径相关基因的表达。进一步的生理学证据表明,在关键的等级分化窗口(L3-L4阶段)用agomir-3721处理幼虫时,羽化出的成年蜜蜂体型增大,卵巢面积翻倍,卵巢发育频率显著更高,卵巢特异性标记基因显著上调。这些发现为ame-mir-3721-3p在等级分化过程中促进蜂王样发育轨迹的作用提供了直接证据,揭示了蜜蜂发育中的一条新调控途径,并为社会昆虫中的表观遗传机制提供了见解。