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当前位置: 首页 > 文章 > 棉铃虫转录因子c-Myc基因在滞育和非滞育蛹脑中的表达分析及多克隆抗体制备 昆虫学报 2015,58 (2) 115-121
Position: Home > Articles > Gene expression profiling and polyclonal antibody preparation of the transcription factor c-Myc in the brain of diapause and non-diapause pupae of the cotton bollworm, Helicoverpa armigera (Lepidoptera:Noctuiadae) Acta Entomologica Sinica 2015,58 (2) 115-121

棉铃虫转录因子c-Myc基因在滞育和非滞育蛹脑中的表达分析及多克隆抗体制备

作  者：
陈伟;徐卫华
单  位：
广东药学院生命科学与生物制药学院;中山大学生命科学学院
关键词：
棉铃虫;滞育;转录因子;c-Myc;多克隆抗体;Wnt/β-catenin信号通路
摘  要：
【目的】c-Myc是近年来研究较多的转录因子,也是受Wnt/β-catenin信号通路调节的重要靶标。本研究旨在克隆棉铃虫Helicoverpa armigera c-Myc基因,从核酸水平初步调查c-myc在滞育和非滞育蛹脑中的表达情况,同时制备其蛋白的多克隆抗体。【方法】通过RACE方法克隆棉铃虫c-myc基因的c DNA,运用RT-PCR方法比较滞育和非滞育蛹脑中Har-c-myc基因的表达情况。根据获取的序列构建原核表达载体,在大肠杆菌Escherichia coli中进行表达,纯化后免疫新西兰兔,制备了多克隆抗体。【结果】克隆了棉铃虫c-myc基因,核酸水平的研究表明滞育蛹脑中c-myc表达水平明显低于非滞育蛹脑。成功地在大肠杆菌中表达了c-Myc部分肽段并通过镍柱纯化获得了较纯的重组蛋白。制备的c-Myc抗体效价达到了1∶125 000。【结论】滞育蛹脑中Har-c-myc的表达下调。获得了抗棉铃虫c-Myc的多克隆抗体。本研究的成果为后续进一步深入研究棉铃虫Wnt/β-catenin信号通路在棉铃虫发育中的作用奠定了基础。
译  名：
Gene expression profiling and polyclonal antibody preparation of the transcription factor c-Myc in the brain of diapause and non-diapause pupae of the cotton bollworm, Helicoverpa armigera (Lepidoptera:Noctuiadae)
作  者：
CHEN Wei;XU Wei-Hua;Guangdong Province Key Laboratory for Biotechnology Drug Candidates, School of Biosciences and Biopharmaceutics, Guangdong Pharmaceutical University;State Key Laboratory of Biocontrol and Institute of Entomology,School of Life Sciences,Sun Yat-Sen University;
关键词：
Helicoverpa aimigera;;diapause;;transcription factor;;c-Myc;;polyclonal antibody;;Wnt/β-catenin signaling pathway
摘  要：
【Aim】c-Myc is an intensively studied transcription factor and also an important downstream target of Wnt / β-catenin signaling pathway. The objective of this research was to clone the c-myc c DNA from Helicoverpa armigera,to investigate the expression of Har-c-myc in mRNA level,and to prepare polyclonal antibody against Har-c-Myc. 【Methods】Har-c-myc was cloned by RACE. The mRNA levels of Har-c-myc in the brain of non-diapause and diapause pupae were investigated by RT-PCR. Prokaryotic expression vector of Har-c-myc was constructed and the recombinant protein was expressed in Escherichia coli. The purified recombinant protein was injected into a New Zealand rabbit to generate polyclonal antibody. The antibody titer was determined by ELISA. 【Results 】 Har-c-myc c DNA was cloned successfully from H. armigera. The mRNA levels of Har-c-Myc were significantly lower in the brain of diapause pupae than in the brain of non-diapause pupae. Recombinant Har-c-Myc was successfully expressed in E. coli and purified by Ni-NTA agarose column. The titer of the antibody against Har-c-Myc was estimated by ELISA as high as 1 ∶ 125 000. 【Conclusion】The expression of Har-c-myc is downregulated in the brain of diapause pupae. Antibody against Har-c-Myc was obtained. This study lays a foundation for further investigating the function of Wnt / β-catenin in the diapause of H. armigera.

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