Gene cloning and expression analysis of the Nilaparvata lugens (Hemiptera:Delphacidae) BphMIF1 gene
Author of the article:YE Sui;FENG Pei;ZHONG Xiao;MA Qi-Qi;ZENG Man;QI Jing-Wen; WANG Xiang-Ping;YANG Ya-Zhen;ZHANG Jian-Min
Author's Workplace:College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;College of Agriculture, Yangtze University;
Key Words:Nilaparvata lugens; BphMIF1; qPCR; prokaryotic expression
Abstract:
[Objectives] To investigate the expression profile of the
saliva protein BphMIF1 gene of the
brown planthopper, Nilaparvata lugens,
an important insect pest of rice, in response to the feeding activity of this species. [Methods] BphMIF1 was cloned by RT-PCR and sequenced for bioinformatic analysis. The expression
levels of BphMIF1 in nymphs (1st-5th instars), adults and different adult body parts, were analyzed with real-time
fluorescent quantitative PCR (qPCR), and the prokaryotic expression of BphMIF1 was also quantified. [Results]
The BphMIF1 gene was cloned and found to encode 119 amino acids. qPCR results showed that BphMIF1 was rapidly up-regulated in 4th instar nymphs. BphMIF1 was expressed
in the head, thorax and abdomen of adults, but was most highly expressed in the
abdomen. Prokaryotic expression analysis showed that the BphMIF1 gene was expressed at an induced concentration of 0.5
mmol/L IPTG for 4 h. [Conclusion] The BphMIF1 gene is differentially
expressed in different age groups and body parts of N. lugens. These results provide a theoretical basis for the
functional study of BphMIF1 in response to the feeding process of N. lugens.