昆虫学报 ›› 2025, Vol. 68 ›› Issue (3): 271-281.doi: 10.16380/j.kcxb.2025.03.003

• 研究论文 • 上一篇    下一篇

中华蜜蜂幼虫肠道体液免疫通路相关基因及其剪接异构体鉴定

李坤泽1,#, 杜丽婷1,#, 王梦怡1, 胡艳雯1, 吴函雨1, 邱剑丰1,2,3严提珍2,4, 卢兆辉4, 陈大福1,2,3, 骆庆明2,4,*, 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. 天然生物毒素国家地方联合工程实验室, 福州 350002; 3. 福建农林大学蜂疗研究所, 福州 350002; 4. 东莞市妇幼保健院, 东莞 523000)
  • 出版日期:2025-03-20 发布日期:2025-04-21

Identification of humoral immune pathway-associated genes and their splice variants in the larval guts of Apis cerana cerana (Hymenoptera: Apidae)

LI Kun-Ze1,#, DU Li-Ting1,#, WANG Meng-Yi1, HU Yan-Wen1, WU Han-Yu1, QIU Jian-Feng1,2,3, YAN Ti-Zhen2,4, LU Zhao-Hui4, CHEN Da-Fu1,2,3, LUO Qing-Ming2,4,*, GUO Rui1,2,3,*   

  1. (1. College of Bee Science and Biomedicine, Fujian Agriculture and Forestry University, Fuzhou 350002, China; 2. National & Local United Engineering Laboratory of Natural Biotoxin, Fuzhou 350002, China; 3. Apitherapy Research Institute of Fujian Agriculture and Forestry University, Fuzhou 350002, China; 4. Dongguan Maternal and Children Health Hospital, Dongguan 523000, China)
  • Online:2025-03-20 Published:2025-04-21

摘要: 【目的】本研究旨在鉴定中华蜜蜂Apis cerana cerana幼虫肠道中体液免疫通路相关基因及其剪接异构体,为持续开展中华蜜蜂体液免疫通路相关基因和剪接异构体的分子克隆与功能研究提供资源和基础。【方法】通过Blast将前期基于中华蜜蜂工蜂幼虫肠道转录组的纳米孔(nanopore)测序数据鉴定到的所有全长转录本分别比对到KEGG和Nr数据库,筛选出体液免疫信号通路相关基因及其剪接异构体。利用GffCompare软件将鉴定到的体液免疫信号通路相关基因比对到东方蜜峰A. cerana参考基因组(版本号: ACSNU-2.0),以优化已注释基因的结构。使用Astalavista软件鉴定体液免疫信号通路相关基因的可变剪接(alternative splicing, AS)事件类型,再统计不同类型的AS事件数目;采用RT-PCR验证AS事件的真实性。利用TAPIS pipeline软件预测体液免疫信号通路相关基因所含可变多聚腺苷酸化(alternative polyadenylation, APA)位点,并通过MEME软件鉴定APA位点上游50 bp的基序(motif);通过3′RACE验证APA位点的真实性。【结果】共鉴定到JNK-p38-MAPK信号通路相关的23个基因及135条剪接异构体,Toll信号通路相关的21个基因和130条剪接异构体,JAK/STAT信号通路相关12个基因和53条剪接异构体, IMD信号通路相关10个基因和46条剪接异构体。注释到东方蜜蜂参考基因组上体液免疫通路相关的18个基因的5′UTR被延长, 19个基因的3′UTR被延长, 8个基因的5′UTR和3′UTR同时被延长。共鉴定到体液免疫信号通路相关的16个基因的60次AS事件,其中最丰富的类型是可变5′端剪接(alternative 5′splice site, A5SS)(26次)。通过RT-PCR证实了随机选择的3个基因的AS事件的真实性。共鉴定到体液免疫信号通路相关的47个基因含有1个及以上的APA位点,其中含有1个APA位点的基因最多。在APA位点上游鉴定到3条一致性序列: ATATAWAWWTATATRWATNYD, HVVN VNNDBDNBHNDDDNWNNNNNWNNH和BSHDVWDRDBDDDKKNVWDRDKHHVKHDVNNVWDND BHWHB。3′RACE结果证实了随机选择的2个基因所含APA位点的真实性。【结论】首次鉴定到中华蜜蜂幼虫肠道体液免疫信号通路相关的66个基因和364条剪接异构体,优化了东方蜜蜂参考基因组上注释到体液免疫通路的29个基因结构,挖掘出体液免疫相关的60次AS事件和139个APA位点,并证实了体液免疫相关基因的AS事件和APA位点的真实性。

关键词: 中华蜜蜂, 纳米孔测序, 体液免疫通路, 基因结构优化;可变剪接, 可变多聚腺苷酸化

Abstract: 【Aim】This study aims to identify the humoral immune pathway-associated genes and their splice variants in the larval guts of Apis cerana cerana, so as to provide the resource and basis for the molecular cloning and functional study of genes and splice variants related to the humoral immune pathways in A. c. cerana. 【Methods】All of the identified full-length transcripts based on previous nanopore sequencing data of the gut transcriptome of A. c. cerana worker larvae were respectively aligned to the KEGG and Nr databases to screen out the genes and their splice variants related to the humoral immune signaling pathway by Blast. The identified humoral immune signaling pathway-associated genes were mapped to the A. cerana reference genome (version number: ACSNU-2.0) to optimize the structure of annotated genes using GffCompare software. Astalavista software was used to identify the types of alternative splicing (AS) events of the humoral immune signaling pathway-associated genes, followed by calculation of the numbers of different types of AS events. RT-PCR was employed to verify the authenticity of AS events. TAPIS pipeline software was utilized to predict the alternative polyadenylation (APA) sites contained in the genes related to the humoral immune signaling pathways, and the motifs of 50 bp upstream of the APA sites were identified by MEME software. The authenticity of the APA site was validated through 3′RACE. 【Results】 A total of 23 genes and 135 splice variants related to JNK-p38-MAPK signaling pathway, 21 genes and 130 splice variants related to Toll signaling pathway, 12 genes and 53 splice variants related to JAK/STAT signaling pathway, and 10 genes and 46 splice variants related to IMD signaling pathway were identified. The 5′UTRs of 18 genes related to the humoral immune pathways on the reference genome of A. cerana were extended, the 3′UTRs of 19 genes were extended, and the 5′UTRs and 3′UTRs of 8 genes were simultaneously extended. A total of 60 AS events of 16 genes related to humoral immune signaling pathways were identified, of which the most abundant type was alternative 5′splice site (A5SS) (26 events). The authenticity of the AS events of the randomly selected three genes was confirmed by RT-PCR. A total of 47 genes associated with humoral immune signaling pathways were detected to contain one or more APA sites, of which the genes containing one APA site were the largest group. Three consensus sequences were identified upstream of the APA sites: ATATA WAWWTATATRWATNYD, HVVNVNNDBDNBHNDDDNWNNNWNNHH and BSHDVWDRDBDDDKK NVWDRDKHHVKHDVNNVWDNDBHWHB. The results of 3′RACE confirmed the authenticity of the APA sites contained in two randomly selected genes. 【Conclusion】 For the first time, 66 genes and 364 splice variants related to humoral immune signaling pathways of A. c. cerana larval gut were identified. The structures of 29 genes annotated to humoral immune pathways on the A. cerana reference genome were optimized. Sixty AS events and 139 APA sites associated with humoral immune were discovered. The authenticity of AS events and APA sites of humoral immune genes was confirmed.

Key words: Apis cerana cerana, nanopore sequencing, humoral immune pathway, gene structure optimization, alternative splicing, alternative polyadenylation