高等学校化学学报

高等学校化学学报

• 研究论文 • 上一篇    下一篇

转基因玉米的多重PCR-毛细管电泳-激光诱导荧光检测方法研究

周颖, 黎源倩, 裴晓方   

  1. 四川大学华西公共卫生学院, 成都 610041
  • 收稿日期:2006-11-13 修回日期:1900-01-01 出版日期:2007-08-10 发布日期:2007-08-10
  • 通讯作者: 黎源倩

Rapid and Sensitive Analysis of Genetically Modified Maize by Multiplex PCR and Capillary Electrophoresis with Laser-induced Fluorescence Detection

ZHOU Ying, LI Yuan-Qian*, PEI Xiao-Fang   

  1. School of Huaxi Public Health, Sichuan University, Chengdu 610041, China
  • Received:2006-11-13 Revised:1900-01-01 Online:2007-08-10 Published:2007-08-10
  • Contact: LI Yuan-Qian

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被引次数

37

摘要： 采用三重PCR反应, 同时扩增CaMV 35S启动子、 hsp70 intron1和CryIA(b)基因之间序列以及Invertase基因, 扩增产物用无胶筛分毛细管电泳-激光诱导荧光检测, 从而建立了多重PCR-毛细管电泳-激光诱导荧光快速检测转基因玉米的新方法. 对影响多重PCR扩增和毛细管电泳的因素进行了优化. 在优化的条件下, 本方法可以同时检测转基因玉米样品中3种外源基因. 经序列测试证实, 三重PCR 扩增产物的序列与原基因完全一致, 表明扩增结果可靠. 该方法能检出0.05% MON810转基因玉米成分, 远低于欧盟对转基因食品规定标识的质量分数阈值(1％). 该方法对玉米及其制品的检测结果与实时荧光PCR方法的检测结果一致, 与传统的琼脂糖凝胶电泳法相比, 具有特异性高\, 快速及灵敏等优点, 适用于玉米中转基因成分以及转基因玉米MON810品系的快速筛选、 鉴定和检测, 能满足我国实施转基因食品标签法规的要求.

关键词: 多重PCR, 无胶筛分毛细管电泳, 激光诱导荧光检测, 转基因玉米

Abstract: A rapid method for detection of genetically modified maize by multiplex polymerase chain reaction(PCR) followed by capillary electrophoresis with laser-induced fluorescence was developed. The triplex PCR procedure was applied to simultaneously amplify CaMV 35S promoter and the junction between hsp70 intron 1 and CryIA(b) gene as well as Invertase gene. The amplified products were analyzed by capillary sieving electrophoresis with laser-induced fluorescence detection. The parameters of multiplex PCR and capillary sieving electrophoresis were optimized. Under the optimal conditions, the proposed method was able to simultaneously detect the three heterogenous genes existing in genetically modified maize. The amplified DNA fragments were sequenced and showed the good agreement with original gene, which indicated the reliability of the amplification reaction. The limit of detection was 0.05%, which is much lower than 1% threshold for labeling genetically modified food required by the European Community. There was a good agreement in the determined results of maize and its products by using this method and real-time quantitative PCR method. Compared with conventional agarose gel electrophoresis, the proposed method offered a more specific and sensitive procedure to rapid screening, identification and detection of genetically modified maize.

Key words: Multiplex polymerase chain reaction, Capillary sieving electrophoresis, Laser-induced fluorescence detection, Genetically modified maize

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