华北农学报 ›› 2012, Vol. 27 ›› Issue (2): 12-18. doi: 10.3969/j.issn.1000-7091.2012.02.003

所属专题: 生物技术

• 论文 • 上一篇    下一篇

二价核酶基因构建及对PLRV负链靶序列的体外切割研究

张剑峰1, 张鹤龄2, 于嘉林3, 迟胜起1, 贺秀芳1, 郝文胜2, 杨静华2   

  1. 1. 青岛农业大学农学与植保学院, 山东青岛?266109;
    2. 内蒙古大学生命科学院, 内蒙古呼和浩特?010021;
    3. 中国农业大学农业生物技术国家重点实验室, 北京?100094
  • 收稿日期:2012-01-21 出版日期:2012-04-28
  • 作者简介:张剑峰(1964-), 男, 内蒙古呼和浩特人, 教授, 博士, 主要从事分子植物病理学研究。
  • 基金资助:
    国家科技支撑计划项目(2007BAD49B02-6);青岛农业大学人才基金(630915)

Construction of a Divalent Ribozyme Gene Specific to Potato Leafroll Virus Repelicase Gene and Cleavage of Negative Strand RNA in vitro by Ribozyme

ZHANG Jian-feng1, ZHANG He-ling2, YU Jia-lin3, CHI Sheng-qi1, HE Xiu-fang1, HAO Wen-sheng2, YANG Jing-hua2   

  1. 1. College of Agricultural and Plant Protection, Qingdao Agricultural University, Qindao 266109, China;
    2. Life Science College of Innermogolia University, Huhhot 010021, China;
    3. State Key Laboratory of Agrobiotechnology, China Agricultural University, Beijing 100094, China
  • Received:2012-01-21 Published:2012-04-28

摘要: 根据锤头状核酶的作用模式,设计、合成并克隆了特异性切割马铃薯卷叶病毒(Potato leaf roll virus,PLRV)中国分离株(PLRV-Ch)复制酶基因负链RNA的二价核酶序列。将该核酶基因克隆到pGEM-4Z中,构建成体外转录载体pGEM-4ZDR;同时将包含核酶切割识别位点的PLRV-Ch复制酶基因cDNA近5’端的874 bp片段反向插入到pGEM-4Z中,构建了体外转录载体pGEM-4ZR5。以线性化的重组质粒pGEM-4ZDR和pGEM-4ZR5为模板,在T7 RNA聚合酶的作用下,分别转录获得核酶RNA和PLRV-Ch复制酶基因5’端负链RNA底物片段。将以上2种RNA转录物混合并经37℃保温后,检测结果表明,所得核酶RNA对PLRV-Ch复制酶基因负链RNA在体外具有较强的特异切割活性。

关键词: 二价核酶, 马铃薯卷叶病毒, 复制酶基因, 体外切割

Abstract: Based on the functional model of the hammerhead RNAs,a divalent ribozyme was designed for cleavage of Potato leafroll virus(PLRV)RNA,targeting at two sites on the negative strand of PLRV Chinese isolate replicase gene and cloned in vector pGEM-4Z. The recombinant plasmid pGEM-4ZDR was useed for in vitro transcription of the ribozyme RNA. The plasmid pGEM-4ZR5 for in vitro transcription of the substrate viral RNA was synthesized by cDNA subcloning of a PLRV Chinese isolate(PLRV-Ch)into plasmid pGEM-4Z,in which an 874 bp cDNA fragment at the 5' end of PLRV-Ch replicase gene was reversely inserted downstream of the T7 promoter in pGEM-4Z. By using T7 DNA polymerase,the plasmids of pGEM-4ZDR and pGEM-4ZR5 were linearized with EcoR I and used as templates for in vitro transcription of the divalent ribozyme or the negative strand RNA of PLRV-Ch replicase gene,respectively. After mixture of the RNA transcripts and incubation at 37℃,results showed that the ribozyme has highly catalytic activity to the PLRV-Ch negative strand RNA in vitro.

Key words: Divalent ribozyme, Potato leaf roll virus(PLRV), Repilcase gene, in vitro cleavage

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引用本文

张剑峰, 张鹤龄, 于嘉林, 迟胜起, 贺秀芳, 郝文胜, 杨静华. 二价核酶基因构建及对PLRV负链靶序列的体外切割研究[J]. 华北农学报, 2012, 27(2): 12-18. doi: 10.3969/j.issn.1000-7091.2012.02.003.

ZHANG Jian-feng, ZHANG He-ling, YU Jia-lin, CHI Sheng-qi, HE Xiu-fang, HAO Wen-sheng, YANG Jing-hua. Construction of a Divalent Ribozyme Gene Specific to Potato Leafroll Virus Repelicase Gene and Cleavage of Negative Strand RNA in vitro by Ribozyme[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2012, 27(2): 12-18. doi: 10.3969/j.issn.1000-7091.2012.02.003.

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