昆虫学报 ›› 2025, Vol. 68 ›› Issue (4): 397-406.doi: 10.16380/j.kcxb.2025.04.003

• 研究论文 • 上一篇    下一篇

西方蜜蜂lncRNA13922的时空表达谱与潜在调控作用分析

董舒楠1,#, 曹瑞华1,#, 陈颖1, 荆欣1, 臧贺1, 孙恺玥1, 刘锋2徐细建2, 骆群2, 陈大福1,3,4, 邱剑丰1,3,4,*, 郭睿1,2,3,*   

  1. (1. 福建农林大学蜂学与生物医药学院, 福州 350002; 2. 江西省养蜂研究所, 南昌 330000; 3. 天然生物毒素国家地方联合工程实验室, 福州 350002; 4. 福建农林大学蜂疗研究所, 福州 350002)
  • 出版日期:2025-04-20 发布日期:2025-05-22

Spatiotemporal expression profiles and potential regulatory roles of lncRNA13922 in Apis mellifera

DONG Shu-Nan1,#, CAO Rui-Hua1,#, CHEN Ying1, JING Xin1, ZANG He1, SUN Kai-Yue1, LIU Feng2, XU Xi-Jian2, LUO Qun2, CHEN Da-Fu1,3,4, QIU Jian-Feng1,3,4,*, GUO Rui1,3,4,*    

  1. (1. College of Bee Science and Biomedicine, Fujian Agriculture and Forestry University, Fuzhou 350002, China; 2. Apicultural Research Institute of Jiangxi Province, Nanchang 330000, China; 3. National & Local United Engineering Laboratory of Natural Biotoxin, Fuzhou 350002, China; 4. Apitherapy Research Institute of Fujian Agriculture and Forestry University, Fuzhou 350002, China)
  • Online:2025-04-20 Published:2025-05-22

摘要: 【目的】通过测定lncRNA13922在西方蜜蜂Apis mellifera工蜂不同发育阶段和成虫组织的表达谱,并解析lncRNA13922的调控方式和作用,为进一步探究lncRNA13922的调控功能和机制提供科学依据。【方法】通过RT-PCR验证lncRNA13922在西方蜜蜂工蜂成虫不同组织(触角、毒腺、脑、中肠、脂肪体、表皮和咽下腺)中的表达量;采用RT-qPCR检测lncRNA13922在西方蜜蜂工蜂不同发育阶段(卵、幼虫、预蛹、蛹和成虫)和工蜂成虫组织(触角、毒腺、脑、中肠、脂肪体、表皮和咽下腺)中的相对表达量;通过Pearson相关性分析预测与西方蜜蜂lncRNA13922共表达的mRNA;利用miRDeep2将lncRNA13922的核苷酸序列比对到miRBase数据库,再通过miRPara来预测miRNA前体;联用Miranda, RNAhybrid和TargetScan软件分别预测lncRNA13922靶向的miRNA及miRNA靶向的mRNA,取交集作为可靠的靶标集合;根据靶向关系构建竞争性内源RNA(competing endogenous RNA, ceRNA)调控网络, 进而利用相关软件对靶mRNA进行GO和KEGG数据库注释。【结果】lncRNA13922在西方蜜蜂工蜂成虫的触角、脑、中肠、脂肪体、咽下腺、表皮和毒腺均能被扩增出符合预期大小(约127 bp)的目的片段。lncRNA13922在西方蜜蜂卵、 3日龄幼虫、 1和2日龄预蛹及4日龄蛹中差异表达,在卵中的表达量最高,且显著高于3日龄幼虫及1和2日龄预蛹中的表达量; lncRNA13922在1, 2, 6, 12, 15和17日龄成虫体内均有表达,但表达量存在差异; lncRNA13922在2日龄成虫体内的表达量最高且显著高于1和17日龄成虫体内的表达量。lncRNA13922在西方蜜蜂工蜂成虫上述7种组织中差异表达,在毒腺中的表达量最高,且显著高于脑、中肠、脂肪体和咽下腺中的表达量。lncRNA13922与29条mRNA潜在共表达且它们的表达量具有正相关关系,与12条mRNA潜在共表达且它们的表达量具有负相关关系。lncRNA13922可作为2个miRNA的潜在前体。lncRNA13922可靶向75个miRNA进而靶向1 833条mRNA。上述靶mRNA涉及细胞部分和细胞等603个GO条目与内吞作用和嘌呤代谢等56条KEGG通路。【结论】西方蜜蜂lncRNA13922在工蜂的不同发育阶段和成虫不同组织中动态差异表达,并通过反式作用、miRNA前体和ceRNA作用网络潜在参与调控发育过程。

关键词: 西方蜜蜂, 长链非编码RNA, 反式作用, 内源性竞争RNA, 时空表达谱

Abstract:  【Aim】This study aims to offer a scientific basis for investigating the regulatory function and mechanism of lncRNA13922 in Apis mellifera by determining its expression profiles in different developmental stages and adult tissues of workers and analyzing its manipulation modes and function. 【Methods】The expression levels of lncRNA13922 in different tissues (antennae, venom gland, brain, midgut, fat body, cuticle and hypopharyngeal gland) of adult workers of A. mellifera were validated using RT-PCR. The expression levels of lncRNA13922 in different developmental stages (egg, larva, prepupa, pupa and adult) and tissues (antennae, venom gland, brain, midgut, fat body, cuticle and hypopharyngeal gland) of adult workers of A. mellifera were determined using RT-qPCR. The Pearson correlation analysis was used to predict the co-expressed mRNAs of lncRNA13922 of A. mellifera. The nucleotide sequence of lncRNA13922 was aligned to the miRBase database using miRDeep2 software, and miRNA precursors were predicted through miRPara software. Miranda, RNAhybrid, and TargetScan software was respectively utilized to predict miRNAs targeted by lncRNA13922 and mRNAs targeted by miRNAs, the intersection was adopted as the high-confidence target candidate set, and then the competitive endogenous RNA (ceRNA) regulatory network was constructed based on the targeting relationships. GO and KEGG database functional annotation of target mRNAs was performed by using related software. 【Results】The target fragment with expected size (about 127 bp) of lncRNA13922 was amplified in the antennae, brain, midgut, fat body, hypopharyngeal gland, cuticle and venom gland of adult workers of A. mellifera. lncRNA13922 was differentially expressed in the eggs, 3-day-old larvae, 1- and 2-day-old prepupae and 4-day-old pupae of A. mellifera, and its expression level in the eggs was the highest and significantly higher than those in the 3-day-old larvae and 1- and 2-day-old prepupae. lncRNA13922 was expressed in the 1-, 2-, 6-, 12-, 15- and 17-day-old adults, with differential expression levels, and the expression level of lncRNA13922 in the 2-day-old adult was the highest and significantly higher than those in the 1- and 17-day-old adults. lncRNA13922 was differentially expressed in the above-mentioned seven tissues of adult workers of A. mellifera, and its expression level in the venom gland was the highest and significantly higher than those in the brain, midgut, fat body and hypopharyngeal gland. lncRNA13922 was potentially co-expressed with 29 mRNAs, with their expression levels showing positive correlation relationships, while lncRNA13922 was potentially co-expressed with 12 mRNAs, with their expression levels showing negative correlation relationships. lncRNA13922 was predicted to be the precursors for two miRNAs. lncRNA13922 could target 75 miRNAs, further targeting 1 833 mRNAs. These target mRNAs were involved in 603 GO terms such as cell part and cell, as well as 56 KEGG pathways such as endocytosis and purine metabolism. 【Conclusion】lncRNA13922 is dynamically and differentially expressed in different developmental stages and adult tissues of A. mellifera workers, and potentially participates in the regulation of developmental process through trans-acting, miRNA precursor, and ceRNA network.

Key words: Apis mellifera, long non-coding RNA; trans-action, endogenous competitive RNA, spatiotemporal expression profile