Referral Centre for Molecular Diagnosis of Transgenic Planting Materials, National Research Centre on DNA Fingerprinting, National Bureau of Plant Genetic Resources, Pusa Campus, New Delhi 110012, India.
J Agric Food Chem. 2010 Sep 22;58(18):9875-81. doi: 10.1021/jf100466n.
The genetically modified (GM) Bt crops expressing delta-endotoxins from Bacillus thuringiensis provide protection against a wide range of lepidopteron insect pests throughout the growing season of the plant. Bt cotton is the only commercialized crop in India that is planted on an area of 7.6 million hectares. With the increase in development and commercialization of transgenic crops, it is necessary to develop appropriate qualitative and quantitative methods for detection of different transgenic events. The present study reports on the development of a decaplex polymerase chain reaction (PCR) assay for simultaneous detection of transgene sequences, specific transgene constructs, and endogenous stearoyl acyl desaturase (Sad1) gene in two events of Bt cotton, i.e., MON531 and MON15985. The decaplex PCR assay is an efficient tool to identify and discriminate the two major commercialized events of Bt cotton, i.e., MON531 and MON15985, in India. Real-time PCR assays were also developed for quantification of cry1Ac and cry2Ab genes being employed in these two events. The quantitative method was developed using seven serial dilutions containing different levels of Bt cotton DNA mixed with a non-Bt counterpart ranging from 0.01 to 100%. The results revealed that the biases from the true value and the relative standard deviations were all within the range of ±20%. The limit of quantification (LOQ) of the developed real-time PCR method has also been established up to 0.01%.
表达苏云金芽孢杆菌δ-内毒素的基因改良(GM)抗虫作物为植物整个生长季节提供了对鳞翅目昆虫的广泛保护。Bt 棉花是印度唯一商业化种植的面积达 760 万公顷的作物。随着转基因作物的不断发展和商业化,有必要开发适当的定性和定量方法来检测不同的转基因事件。本研究报告了一种十重聚合酶链反应(PCR)检测方法的开发,用于同时检测两种 Bt 棉花事件,即 MON531 和 MON15985 中的转基因序列、特定转基因构建体和内源性硬脂酰酰基去饱和酶(Sad1)基因。十重 PCR 检测方法是一种有效的工具,可以识别和区分印度的两种主要商业化 Bt 棉花事件,即 MON531 和 MON15985。还开发了用于定量分析这两个事件中使用的 cry1Ac 和 cry2Ab 基因的实时 PCR 检测方法。该定量方法使用包含不同水平的 Bt 棉花 DNA 与非 Bt 对照物(从 0.01 到 100%)的 7 个系列稀释物进行开发。结果表明,偏差与真实值和相对标准偏差均在±20%范围内。所开发的实时 PCR 方法的定量限(LOQ)也已确定高达 0.01%。