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International Collaborative Study of the Endogenous Reference Gene, Sucrose Phosphate Synthase (SPS), Used for Qualitative and Quantitative Analysis of Genetically Modified Rice

机译:内源参考基因蔗糖磷酸合酶(SPS)的国际合作研究,用于转基因水稻的定性和定量分析

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One rice (Oryza sativa) gene, sucrose phosphate synthase (SPSS), has been proven to be a suitable endogenous reference gene for genetically modified (GM) rice detection in a previous study. Herein are the reported results of an international collaborative ring trial for validation of the SPS gene as an endogenous reference gene and its optimized qualitative and quantitative polymerase chain reaction (PCR) systems. A total of 12 genetically modified organism (GMO) detection laboratories from seven countries participated in the ring trial and returned their results. The validated results confirmed the species specificity of the method through testing 10 plant genomic DNAs, low heterogeneity, and a stable single-copy number of the rice SPS gene among 7 indica varieties and 5 japonica varieties. The SPS qualitative PCR assay was validated with a limit of detection (LOD) of 0.1 %, which corresponded to about 230 copies of haploid rice genomic DNA, while the limit of quantification (LOQ) for the quantitative PCR system was about 23 copies of haploid rice genomic DNA, with acceptable PCR efficiency and linearity. Furthermore, the bias between the test and true values of eight blind samples ranged from 5.22 to 26.53%. Thus, we believe that the SPS gene is suitable for use as an endogenous reference gene for the identification and quantification of GM rice and its derivates.
机译:在以前的研究中,一种水稻(Oryza sativa)基因蔗糖磷酸合酶(SPSS)已被证明是检测转基因(GM)水稻的合适内源参考基因。本文是一项国际协作环试验的报道结果,该试验用于验证SPS基因作为内源参考基因及其优化的定性和定量聚合酶链反应(PCR)系统。来自七个国家的总共12个转基因生物(GMO)检测实验室参加了环试验,并返回了结果。通过测试10个植物基因组DNA,低异质性和7个in稻和5个粳稻品种的水稻SPS基因单拷贝数稳定,该方法的物种特异性得到了证实。验证SPS定性PCR分析的检出限(LOD)为0.1%,相当于约230份单倍体水稻基因组DNA拷贝,而定量PCR系统的定量限(LOQ)约为23份单倍体。水稻基因组DNA,具有可接受的PCR效率和线性。此外,八个盲样本的测试值与真实值之间的偏差范围为5.22%至26.53%。因此,我们认为SPS基因适合用作内源参考基因,用于转基因水稻及其衍生物的鉴定和定量。

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