National Institute of Health Sciences, 1-18-1 Kamiyoga, Tokyo 158-8501, Japan.
Food Chem. 2013 Dec 1;141(3):2618-24. doi: 10.1016/j.foodchem.2013.05.005. Epub 2013 May 14.
Genetically modified (GM) rice (Oryza sativa) lines, such as insecticidal Kefeng and Kemingdao, have been developed and found unauthorised in processed rice products in many countries. Therefore, qualitative detection methods for the GM rice are required for the GM food regulation. A transgenic construct for expressing cowpea (Vigna unguiculata) trypsin inhibitor (CpTI) was detected in some imported processed rice products contaminated with Kemingdao. The 3' terminal sequence of the identified transgenic construct for expression of CpTI included an endoplasmic reticulum retention signal coding sequence (KDEL) and nopaline synthase terminator (T-nos). The sequence was identical to that in a report on Kefeng. A novel construct-specific real-time polymerase chain reaction (PCR) detection method for detecting the junction region sequence between the CpTI-KDEL and T-nos was developed. The imported processed rice products were evaluated for the contamination of the GM rice using the developed construct-specific real-time PCR methods, and detection frequency was compared with five event-specific detection methods. The construct-specific detection methods detected the GM rice at higher frequency than the event-specific detection methods. Therefore, we propose that the construct-specific detection method is a beneficial tool for screening the contamination of GM rice lines, such as Kefeng, in processed rice products for the GM food regulation.
转基因为表达豇豆胰蛋白酶抑制剂(CpTI)的构建体在一些受 Kemingdao 污染的进口加工稻米产品中被检测到。鉴定的表达 CpTI 的转基因构建体的 3'末端序列包括内质网保留信号编码序列(KDEL)和胭脂碱合成酶终止子(T-nos)。该序列与关于 Kefeng 的报告中的序列相同。开发了一种用于检测 CpTI-KDEL 和 T-nos 之间的连接区序列的新型构建体特异性实时聚合酶链反应(PCR)检测方法。使用开发的构建体特异性实时 PCR 方法评估了进口加工稻米产品对 GM 水稻的污染情况,并与五种事件特异性检测方法进行了检测频率比较。构建体特异性检测方法比事件特异性检测方法检测到 GM 水稻的频率更高。因此,我们建议该构建体特异性检测方法是用于筛选 GM 水稻品系(如 Kefeng)在 GM 食品监管中对加工稻米产品污染的有益工具。