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A model freed from endogenous reference gene for quantification of genetically modified DNA by real-time PCR. 1. Quantification of DNA from genetically modified organisms in haplo-species materials

机译:一个没有内源参考基因的模型,用于通过实时PCR量化转基因DNA。 1.量化单倍材料中转基因生物的DNA

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摘要

This paper is the first part of a serial study investigating a quantification model freed from endogenous reference gene for genetically modified (GM) content by real-time polymerase chain reaction (PCR). The serial study involves two parts: (1) quantitative determination of GM DNA in haplo-species plant samples; (2) quantitative determination of GM DNA in multi-species plant samples. The paper describes a methodology to quantify the GM content in a DNA extract using on one hand real-time PCR to determine the amount of GM targets present and on the other hand absorbance reading at 260 nm to measure the total DNA present in sample. The ratio of both values is expressed as GM percentage. The most prominent dominance of the novel model is that the direct quantitative relation between the initial amount of target template in real-time PCR reaction (X 0) and the content of GM DNA in tested material (X SD) is established. Theoretical analysis indicates that the developed quantitative model relieved from the dependence on endogenous reference genes is suitable to quantify the GM content in haplo-species plant sample, in addition, it has the applicability in the quantitative detection of GM content in multi-species GM plant sample. A trail, in which 75 haplo-species GM plant samples were involved, was conducted to validate the suitability of the novel quantification model. The bias varied from 0.00 to 24.00% except a tested sample with lower level of GM content, and the precision expressed as coefficient of variation (CV) was from 2.81 to 25.00%. The limit of quantitation (LOQ) of the quantitative assay was as low as 0.1%. Compared with the previous papers and the performance requirements raised by European Network of GMO Laboratories (ENGL) for analytical methods of GMO testing, the results demonstrated that the established quantification model is a suitable alternative to the more traditional endogenous reference assay in the quantification of GM content in haplo-species plant sample.
机译:本文是系列研究的第一部分,该研究探讨了通过实时聚合酶链反应(PCR)去除内源参考基因的转基因(GM)含量的定量模型。该系列研究包括两个部分:(1)定量测定单倍种植物样品中的GM DNA; (2)定量测定多种植物样品中的GM DNA。该论文描述了一种方法,该方法定量DNA提取物中的GM含量,一方面使用实时PCR确定存在的GM靶标的数量,另一方面使用260 nm处的吸光度读数来测量样品中存在的总DNA。两个值的比率表示为GM百分比。该模型最突出的优势是实时PCR反应中目标模板的初始量(X 0 )与被测材料中GM DNA的含量(X SD )成立。理论分析表明,所建立的定量模型摆脱了对内源参考基因的依赖,适用于定量单倍体植物样品中的转基因含量,并且具有定量检测多物种转基因植物中转基因含量的适用性。样品。进行了一条涉及75个单倍种转基因植物样品的试验,以验证新型定量模型的适用性。除了测试样品中的GM含量较低外,偏差从0.00到24.00%不等,用变异系数(CV)表示的精度为2.81至25.00%。定量分析的定量限(LOQ)低至0.1%。与先前的论文以及欧洲GMO实验室网络(ENGL)对GMO测试的分析方法提出的性能要求相比,结果表明,所建立的量化模型是GM量化中更传统的内源参考测定的合适替代品单倍种植物样品中的含量。

著录项

  • 来源
    《European Food Research and Technology》 |2008年第5期|1485-1498|共14页
  • 作者单位

    Shenzhen Center for Disease Control and Prevention No. 21 1st Road of Tianbei 518020 Shenzhen People’s Republic of China;

    Shenzhen Center for Disease Control and Prevention No. 21 1st Road of Tianbei 518020 Shenzhen People’s Republic of China;

    Shenzhen Center for Disease Control and Prevention No. 21 1st Road of Tianbei 518020 Shenzhen People’s Republic of China;

    Shenzhen Center for Disease Control and Prevention No. 21 1st Road of Tianbei 518020 Shenzhen People’s Republic of China;

    College of Animal Science South China Agricultural University Wushan Road 510642 Guangzhou People’s Republic of China;

    Center for Quality Crop Seed of ShenZhen Municipality F3 213 Building 9th Tairan Road of Chegongmiao 518040 Shenzhen People’s Republic of China;

    Center for Quality Crop Seed of ShenZhen Municipality F3 213 Building 9th Tairan Road of Chegongmiao 518040 Shenzhen People’s Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Genetically modified; Quantification model; Haplo-species; Real-time PCR;

    机译:转基因定量模型单倍种实时荧光定量PCR;

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