生物技术通报 ›› 2014, Vol. 0 ›› Issue (6): 128-133.

• 研究报告 • 上一篇    下一篇

草鱼细胞系CIK酵母双杂交cDNA文库的构建及 初步应用

闫秀英1, 谢吉国1, 李杰1, 丁燏1, 吴灶和2, 鲁义善1, 简纪常1   

  1. (1. 广东海洋大学水产学院 广东省水产经济动物病原生物学及流行病学重点实验室暨广东省高等学校水产经济动物病害控制重点实验室,湛江 524088;2. 仲恺农业工程学院,广州 510225)
  • 收稿日期:2013-11-26 出版日期:2014-06-25 发布日期:2014-06-25
  • 作者简介:闫秀英,女,博士,讲师,研究方向:水产动物病害防控;E-mail:yanxiuying1201@126.com
  • 基金资助:
    国家“973”计划项目(2009CB118704)

Construction and Preliminary Application of the Yeast Two-hybrid cDNA Library from Grass Carp CIK Cells

Yan Xiuying1,Xie Jiguo1,Li Jie1,Ding Yu1,Wu Zaohe2,Lu Yishan1,Jian Jichang1   

  1. (1. Guangdong Key Laboratory of Pathogenic Biology and Epidemiology for Aquatic Economic Animals,Fisheries College of Guangdong Ocean University, Zhanjiang 524088;2. Zhongkai University of Agriculture and Engineering, Guangzhou 510225)
  • Received:2013-11-26 Published:2014-06-25 Online:2014-06-25

摘要: 旨在探索草鱼呼肠孤病毒与宿主细胞蛋白质间的相互作用,运用SMART技术构建了草鱼肾组织细胞系CIK(Ctenopharyngodon idellus kidney)的酵母双杂交cDNA文库。提取CIK细胞总RNA后,分离纯化mRNA,然后以mRNA为模板,反转录合成cDNA第一链,再在DNA聚合酶作用下,通过长距离PCR,扩增双链cDNA。利用SMART技术,通过同源重组的方法,在酵母株Y187中构建了草鱼CIK细胞全长cDNA文库。经检测,未扩增文库的转化率为1.6×105,文库容量为2.4×106,插入的双链cDNA片段的长度为250-2 000 bp,文库滴度为7×107 CFU/mL,重组率为98%,此文库具有良好的cDNA片段多态性和完整性。利用构建的CIK酵母双杂交文库,以草鱼呼肠孤病毒的VP7和VP5蛋白作为诱饵进行筛选试验,得到VP7相互作用蛋白的阳性菌落,未得到VP5相互作用蛋白的阳性菌落。草鱼CIK细胞酵母双杂交cDNA文库的构建为研究草鱼呼肠孤病毒与宿主细胞间的互作机制提供了重要研究工具。

关键词: 草鱼肾组织细胞系, 酵母双杂交, cDNA文库, 蛋白质互作

Abstract: In order to explore the interactions between grass carp reovirus and the host cell proteins, the yeast two-hybrid cDNA library from grass carp CIK(Ctenopharyngodon idellus kidney) was constructed by SMART technology. Total RNA of the CIK cells was extracted and mRNA was purified. Then, mRNA as the template, the first strand of cDNA was synthesized by reverse transcription. The double-stranded cDNA was amplified through the long-distance PCR with the DNA polymerase. The cDNA library from grass carp CIK cells was constructed in the yeast strain 187, using SMART technology and the homologous recombination method. After testing, the conversion rate and the capacity of the original library was 1.6×105 and 2.4×106, respectively. The length of the inserted double-stranded cDNA fragments were 250-2 000 bp. The titer of the library was 7×107 CFU/mL and the recombination rate was 98%. This library had the well polymorphism and the integrity of the cDNA fragments. Using the constructed yeast two-hybrid from the CIK cells, the VP7 and VP5 protein in grass carp reovirus were as the baits for the screening experiment. The positive colonies of the interacting proteins of VP7 had been acquired, without the positive colony of the interacting protein of VP5. The construction of the yeast two-hybrid cDNA library from the grass carp CIK cells provided an important research tool for the study on the interaction mechanism of grass carp reovirus with the host cell.

Key words: Ctenopharyngodon idellus kidney(CIK), Yeast two-hybrid cDNA library, Protein interaction