Huang Chunmeng, Zhang Yongjun, Yu Huilin, Chen Xiuping, Xie Jiajian
Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Key Laboratory of Safety Assessment of Genetically Modified Organisms (Environment), Ministry of Agriculture and Rural Affairs, Beijing 100193, China.
Plants (Basel). 2024 Aug 15;13(16):2276. doi: 10.3390/plants13162276.
Genetically modified maize ( L.) MON810 was approved for importation into China for feed use in 2004; however, the localization data concerning exogenous insertion sequences, which confer insect resistance, have been questionable. MON810 maize plants discovered in northeastern China were used to analyze the molecular characteristics of the exogenous insertion. Using PacBio-HiFi sequencing and PCR assays, we found the insertion was located in chromosome 8, and there was a promoter, intron, and insecticide gene , except for genome sequence insertion in the MON810 event. Importantly, the 5' and 3' flanking sequences were located in the region of 55869747-55879326 and 68416240-68419152 on chromosome 5, respectively. The results of this study correct previous results on the genomic localization of the insertion structure for the MON810 event. We also found a single-nucleotide polymorphism (SNP) in the intron, which is most likely the first SNP found in a transgenic insertion sequence. PCR amplification in conjunction with Sanger sequencing, allele-specific PCR (AS-PCR), and blocker displacement amplification (BDA) assays were all effective at detecting the base variance. The integrated strategy used in this study can serve as a model for other cases when facing similar challenges involving partially characterized genetic modification events or SNPs.
转基因玉米(L.)MON810于2004年被批准进口到中国用于饲料;然而,关于赋予抗虫性的外源插入序列的本地化数据一直存在疑问。利用在中国东北地区发现的MON810玉米植株来分析外源插入的分子特征。通过PacBio-HiFi测序和PCR检测,我们发现该插入位于8号染色体上,除了MON810事件中的基因组序列插入外,还有一个启动子、一个内含子和一个杀虫基因。重要的是,5'和3'侧翼序列分别位于5号染色体上55869747 - 55879326和68416240 - 68419152区域。本研究结果纠正了先前关于MON810事件插入结构基因组定位的结果。我们还在内含子中发现了一个单核苷酸多态性(SNP),这很可能是在转基因插入序列中首次发现的SNP。PCR扩增结合桑格测序、等位基因特异性PCR(AS-PCR)和阻断剂置换扩增(BDA)检测在检测碱基变异方面均有效。本研究中使用的综合策略可作为面对涉及部分特征化的转基因事件或SNP的类似挑战时其他案例的模型。