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Detection of recombinant DNA segments introduced to genetically modified maize (Zea mays)

机译:检测转基因玉米(Zea mays)中引入的重组DNA片段

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Polymerase Chain Reaction (PCR) techniques are increasingly used for the detection of genetically modified (GM) crops in foods. In this paper, recombinant DNAs introduced into the seven lines of GM maize, such as Event 176, Bt11, T25, MON810, GA21, DLL25, and MON802, are sequenced. On the basis of the obtained sequence, 14 primer pairs for the detection of the segments, such as promoter, terminator regions, and construct genes, were designed. To confirm the specificities of the designed primer pairs, PCR was performed on genomic DNAs extracted from GM and non-GM maize, GM and non-GM soy, and other cereal crops. Because the presence of the corresponding DNA segments was specifically detected in GM crops by the designed primer pairs, it was concluded that this method is useful for fast and easy screening of GM crops including unauthorized ones.
机译:聚合酶链反应(PCR)技术越来越多地用于检测食品中的基因改造(GM)作物。在本文中,对导入到GM玉米的七个品系中的重组DNA进行了测序,例如事件176,Bt11,T25,MON810,GA21,DLL25和MON802。根据获得的序列,设计了14对用于检测片段的引物对,例如启动子,终止子区域和构建基因。为了确认设计引物对的特异性,对从转基因和非转基因玉米,转基因和非转基因大豆以及其他谷物中提取的基因组DNA进行了PCR。由于通过设计的引物对在转基因作物中特异性检测到了相应的DNA片段,因此得出结论,该方法可用于快速简便地筛选包括未经授权的转基因作物。

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