文献类型： 外文期刊

作者： Deng, Tingting ¹ ; Huang, Wensheng ² ; Ren, Junan ³ ; Ma, Xiuli ¹ ; Ge, Yiqiang ¹ ; Chen, Ying ² ;

作者机构： 1.China Agr Univ, Coll Food Sci & Nutr Engn, Beijing 100083, Peoples R China

2.Chinese Acad Inspect & Quarantine, Agroprod Safety Res Ctr, Beijing 100123, Peoples R China

3.Beijing Acad Agr & Forestry Sci, Beijing Res Ctr Agr Stand & Testing, Beijjing 100097, Peoples R China

4.China Rural Technol Dev Ctr, Beijing 100045, Peoples R China

关键词： Endogenous reference gene; Oryza sativa; Droplet digital PCR; Genetically modified detection

期刊名称：ANALYTICAL BIOCHEMISTRY （ 影响因子：3.365； 五年影响因子：3.049 ）

ISSN： 0003-2697

年卷期： 2019 年 587 卷

页码：

收录情况： SCI

摘要： To standardize the rice-specific quantification methods, the criteria of six genes of rice (gos9, PLD, SPS, RBE4, ppi-PPF and oriazain) were compared and evaluated by ddPCR. The results revealed that SPS, RBE4 and ppi-PPF were single copy genes per haploid genome and species specificity and stable among different rice cultivars, by employing Lectin gene of soybean as internal reference gene. The established ddPCR systems were precise and reliable with an absolute LOQ of 10-20 copies/reaction. Furthermore, the robustness of these three assays was verified by performing an infra-laboratory repeatability validation and the results showed that the three endogenous genes of rice could be quantitated repeatedly and precisely above the LOQ. These ddPCR methods can reliably quantified the GM content even if the content was low to 0.1%, which were much more reliable than the results from real-time PCR using the same primers and probes.