中国农业科学 ›› 2013, Vol. 46 ›› Issue (18): 3793-3799.doi: 10.3864/j.issn.0578-1752.2013.18.007

• 植物保护 • 上一篇    下一篇

斜纹夜蛾受翻译控制肿瘤蛋白基因的克隆及表达

 卢梦玲, 闫超, 毛根林, 徐汉虹   

  1. 华南农业大学亚热带农业生物资源保护与利用国家重点实验室/天然农药与化学生物学教育部重点实验室,广州 510642
  • 收稿日期:2013-03-18 出版日期:2013-09-15 发布日期:2013-05-09
  • 通讯作者: menglinglu88@gmail.com。通信作者徐汉虹,Tel:020-85285127;E-mail:hhxu@scau.edu.cn
  • 作者简介:卢梦玲,Tel:020-85285127;E-mail:menglinglu88@gmail.com
  • 基金资助:

    农业部行业专项(200903052)、广东省科技基础条件建设项目(20110608)

Molecular Cloning and Expression of Translationally Controlled Tumor Protein of Spodoptera litura (Fab.)

 LU  Meng-Ling, YAN  Chao, MAO  Gen-Lin, XU  Han-Hong   

  1. State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources/Key Laboratory of Natural Pesticide and Chemical Biology, Ministry of Education, South China Agricultural University, Guangzhou 510642
  • Received:2013-03-18 Online:2013-09-15 Published:2013-05-09

摘要: 【目的】克隆斜纹夜蛾受翻译控制肿瘤蛋白(TCTP)基因,分析其序列特征,为深入研究该基因奠定基础。【方法】利用RACE末端快速扩增技术,在斜纹夜蛾卵巢细胞中克隆TCTP基因的全长。根据不同物种间TCTP基因的同源性来构建进化树,并在原核细胞中对斜纹夜蛾TCTP进行表达。【结果】克隆得到斜纹夜蛾TCTP基因全长cDNA,登录号为HQ896486.1。序列分析表明,该基因cDNA全长829 bp,开放阅读框长519 bp,编码含172个氨基酸的蛋白,蛋白分子质量19.67 kD。生物信息学分析表明,斜纹夜蛾TCTP基因属于受翻译控制肿瘤蛋白家族,与其它物种TCTP基因有很高相似性。构建重组质粒 pET32a(+)-TCTP,在大肠杆菌中表达重组蛋白,确定了1 mmol•L-1 IPTG诱导4 h为重组蛋白表达的最佳条件,在短期内能得到大量稳定性好的TCTP蛋白。【结论】从斜纹夜蛾卵巢细胞中克隆得到斜纹夜蛾TCTP基因全长cDNA,并且成功在原核细胞中进行表达。本研究为深入研究斜纹夜蛾TCTP的功能以及针对斜纹夜蛾TCTP基因RNAi干扰的生物防控提供了理论依据和技术支持。

关键词: 斜纹夜蛾 , TCTP基因 , 克隆和表达 , 序列分析

Abstract: 【Objective】 The objective of this study is to clone the full-length cDNA of TCTP from Spodoptera litura cells, as well as to analyze its sequence.【Method】The full-length cDNA of TCTP was obtained by RACE-PCR. A phylogenetic tree of TCTP protein in different species was constructed. TCTP was cloned in pET-32a (+) and was expressed as fusion protein in Escherichia coli BL21(DE3) cells.【Result】The full-length cDNA of SLTCTP (GenBank accession number: HQ896486.1) was 829 bp with an open reading frame of 519 and encodes 172 amino acids. According to Protparam on-line tools, the deduced protein was predicted to have a computed molecular mass of 19.67 kD. TCTP cloned in pET-32a (+) was expressed as fusion protein in E. coli BL21 (DE3) cells. In order to obtain much target protein of TCTP, optimal culture conditions of pET-32a (+)-TCTP were studied. Induced by 1mmol•L-1 IPTG for 4 h was the best optimized condition for recombinant protein expression. TCTP gene belonged to the TCTP protein family and had a high similarity with other species.【Conclusion】This study has provided a basis of method for further research on the function of SLTCTP and pest control.

Key words: Spodoptera litura , translationally controlled transcription proteins (TCTP) gene , gene clone and expression , sequence analysis