昆虫学报 ›› 2016, Vol. 59 ›› Issue (11): 1189-1198.doi: 10.16380/j.kcxb.2016.11.006

• 研究论文 • 上一篇    下一篇

橘小实蝇nAChR α9亚基基因的鉴定及其时空表达

袁国瑞1, 杨文佳1,2, 许抗抗1,2, 王进军1,*   

  1. (1. 西南大学植物保护学院, 昆虫学及害虫控制工程重庆市市级重点实验室, 重庆 400716; 2. 贵阳学院生物与环境工程学院, 贵阳 550005)
  • 出版日期:2016-11-20 发布日期:2016-11-20

Identification and expression profiling of nicotinic acetylcholine receptor α9 subunit gene in Bactrocera dorsalis (Diptera: Tephritidae)

YUAN Guo-Rui1, YANG Wen-Jia1,2, XU Kang-Kang1,2, WANG Jin-Jun1,*   

  1. (1. Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400716, China; 2. College of Biology and Environment Engineering, Guiyang University, Guiyang 550005, China)
  • Online:2016-11-20 Published:2016-11-20

摘要: 【目的】橘小实蝇Bactrocera dorsalis是世界性分布的危害果蔬的重要检疫性农业害虫,目前已对包括新烟碱类在内的多种杀虫剂产生了抗性。本研究在克隆鉴定橘小实蝇烟碱型乙酰胆碱受体(nAChR)α9亚基基因cDNA的基础上,对其分子特性和系统发育进行生物信息学分析,并检测了该基因在橘小实蝇不同发育阶段及成虫不同组织中的表达模式,为进一步研究其潜在功能及在抗药性中的作用奠定基础。【方法】通过高通量测序技术对橘小实蝇进行转录组测序,对高质量序列拼接组装、基因鉴定及同源性比对分析,预测橘小实蝇烟碱型乙酰胆碱受体候选基因。采用RT-PCR和RACE(rapid-amplification of cDNA ends)技术克隆该基因的cDNA全长序列,利用生物信息学分析软件分析其基本生物信息;以α-tubulin为内参基因,利用qPCR研究该基因mRNA在橘小实蝇不同发育阶段及成虫头、胸、腹等组织中的表达模式。【结果】根据预测的基因序列,设计特异性引物进行RACE扩增,从橘小实蝇中克隆获得一条烟碱型乙酰胆碱受体基因的全长序列,cDNA全长1 486 bp,完整开放阅读框1 281 bp,编码426个氨基酸,推测其蛋白质分子量为49.1 kD,理论等电点6.56。该基因经序列比对命名为Bdα9,GenBank登录号为JQ178254。氨基酸同源性及系统进化树分析显示,该基因的编码蛋白具有nAChR α亚基的典型特征,并与Agα9和Dmβ3聚类在一起,与其他昆虫nAChR α9亚基具有22%~27%的氨基酸序列一致性。qPCR结果表明,Bdα9 mRNA在橘小实蝇整个发育阶段均有表达,成虫期的表达量显著高于卵、2龄幼虫、3龄幼虫和蛹期;Bdα9在橘小实蝇成虫头部中表达量最高,且显著高于胸部和腹部中的表达量。【结论】鉴定了橘小实蝇烟碱型乙酰胆碱受体基因Bdα9,明确了该基因在橘小实蝇不同发育阶段及成虫不同组织中的表达模式。根据qPCR的结果,推测Bdα9可能在橘小实蝇成虫期具有重要功能。

关键词: 橘小实蝇; 烟碱型乙酰胆碱受体; 基因克隆; 序列分析; 表达谱, 实时定量PCR

Abstract: 【Aim】 The oriental fruit fly, Bactrocera dorsalis, is an important worldwide quarantine pest that damages many fruits and vegetables and has developed resistance to many insecticide classes including neonicotinoids. In this study, based on the identification of the cDNA of nicotinic acetylcholine receptor α9 subunit gene in B. dorsalis, we analyzed its molecular characterization and polygenetic relationship, and detected its expression pattern in different developmental stages and adult tissues of B. dorsalis, which will lay the foundation for further understanding the potential function properties and the role of Bdα9 in insecticide resistance in B. dorsalis. 【Methods】 Based on the transcriptome data of B. dorsalis by next-generation sequencing, nicotinic acetylcholine receptor gene sequence was successfully screened, assembled and identified by homologous blast. The full-length cDNA sequence was cloned by using RT-PCR and RACE technology, and bioinformatics analysis software package was used to predict its general biological information. Quantitative real-time polymerase chain reaction was used to investigate the expression profiles of this gene in different developmental stages of the fly and the head, thorax and abdomen of adult B. dorsalis. 【Results】 The nicotinic acetylcholine receptor α9 subunit gene was cloned from B. dorsalis by specific primers designed based on the predicted gene sequence. The full-length cDNA contains 1 486 bp with 1 281 bp of open reading frame encoding 426 amino acids with a predicted molecular weight of 49.1 kD and an isoelectric point of 6.56. The gene was named Bdα9 with the GenBank accession number of JQ178254. The amino acid sequence homology and phylogenetic tree analysis indicated that Bdα9 possesses the typical characteristics of nAChR α subunit, clusters together with Agα9 and Dmβ3, and shares 22%-27% amino acid sequence identity with nAChR α9 subunits from other insects. The qPCR results showed that Bdα9 was expressed in all developmental stages of B. dorsalis. The relative expression level of Bdα9 in the adult was significantly higher than those in the egg, the 2nd instar larva, the 3rd instar larva and the pupa. The expression level of Bdα9 in adult head was the highest and significantly higher than those in adult thorax and abdomen. 【Conclusion】 The nicotinic acetylcholine receptor gene, Bdα9, was identified, and its expression profiles in different developmental stages and adult tissues of B. dorsalis were examined, with the highest expression level in adults and the adult head, respectively, implying that it may play a critical role in the central nervous system of adult.  

Key words: Bactrocera dorsalis; nicotinic acetylcholine receptor, gene cloning, sequence analysis, expression profile, qPCR