Canadian Food Inspection Agency (CFIA), Ottawa, Ontario, Canada.
Plant Biotechnol J. 2024 Apr;22(4):904-914. doi: 10.1111/pbi.14232. Epub 2023 Dec 5.
Glyphosate-resistant wheat plants were discovered in southern Alberta in 2017, representing an unauthorized GM release in Canada. The Canadian Food Inspection Agency undertook a series of experiments to characterize and identify this unknown GM wheat, as well as to develop and validate construct-specific and event-specific qPCR assays. Results of PCR-based assays and Sanger sequencing indicated the presence of CaMV 35S promoter (p35S), Rice Actin 1 intron (RactInt1), CP4-EPSPS gene and nopaline synthase terminator (tNOS) elements in the unknown GM wheat. Genome walking and bead capture strategies, combined with high-throughput sequencing, were used to identify the 5' and 3' wheat junctions and the subsequent mapping of the insert to chromosome 3B of the wheat genome. A probable transformation vector, pMON25497, was recognized, and further testing identified the unknown GM wheat as MON71200 event, one of two events obtained with the pMON25497 vector. The two construct-specific assays targeted the junctions of the RactInt1 and the CP4-EPSPS elements and the CP4-EPSPS and tNOS elements, while the event-specific assay was located at the 3' junction into the wheat genome. Both construct-specific and event-specific assays had limits of detection of 0.10% of MON71200 in a seed pool. As expected, the two construct-specific assays cross-reacted with other wheat and corn events containing the same elements in the same order. No cross-reactivity was observed for the event-specific assay. The integrated strategy employed in this study can serve as a model for other cases when facing similar challenges involving unknown GM events.
2017 年,在阿尔伯塔省南部发现了抗草甘膦的小麦植株,这代表加拿大未经授权的转基因释放。加拿大食品检验局(Canadian Food Inspection Agency)进行了一系列实验,以表征和鉴定这种未知的转基因小麦,并开发和验证构建体特异性和事件特异性 qPCR 检测方法。基于 PCR 的检测方法和 Sanger 测序的结果表明,未知的转基因小麦中存在 CaMV 35S 启动子(p35S)、水稻肌动蛋白 1 内含子(RactInt1)、CP4-EPSPS 基因和胭脂碱合成酶终止子(tNOS)元件。利用基因组步移和珠子捕获策略,结合高通量测序,鉴定了未知 GM 小麦的 5'和 3'小麦接头,随后将插入物映射到小麦基因组的第 3B 染色体上。识别出一个可能的转化载体 pMON25497,并进一步测试鉴定未知的 GM 小麦为 MON71200 事件,这是使用 pMON25497 载体获得的两个事件之一。两种构建体特异性检测方法针对 RactInt1 和 CP4-EPSPS 元件以及 CP4-EPSPS 和 tNOS 元件的接头,而事件特异性检测方法位于进入小麦基因组的 3'接头处。两种构建体特异性和事件特异性检测方法在种子库中 MON71200 的检测限均为 0.10%。如预期的那样,两种构建体特异性检测方法与含有相同元件的其他小麦和玉米事件发生交叉反应,而事件特异性检测方法则没有发生交叉反应。本研究中采用的集成策略可以作为其他类似情况下面临未知 GM 事件的模型。