Review of the technology used for structural characterization of the GMO genome using NGS data.

Kahee Moon, Prakash Basnet, Taeyoung Um, Ik-Young Choi
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Abstract

The molecular characterization of genetically modified organisms (GMOs) is essential for ensuring safety and gaining regulatory approval for commercialization. According to CODEX standards, this characterization involves evaluating the presence of introduced genes, insertion sites, copy number, and nucleotide sequence structure. Advances in technology have led to the increased use of next-generation sequencing (NGS) over traditional methods such as Southern blotting. While both methods provide high reproducibility and accuracy, Southern blotting is labor-intensive and time-consuming due to the need for repetitive probe design and analyses for each target, resulting in low throughput. Conversely, NGS facilitates rapid and comprehensive analysis by mapping whole-genome sequencing (WGS) data to plasmid sequences, accurately identifying T-DNA insertion sites and flanking regions. This advantage allows for efficient detection of T-DNA presence, copy number, and unintended gene insertions without additional probe work. This paper reviews the current status of GMO genome characterization using NGS and proposes more efficient strategies for this purpose.

回顾利用 NGS 数据对转基因生物基因组进行结构表征的技术。
转基因生物(GMO)的分子特征描述对于确保安全和获得商业化监管批准至关重要。根据 CODEX 标准,这种表征包括评估引入基因的存在、插入位点、拷贝数和核苷酸序列结构。随着技术的进步,下一代测序(NGS)的使用已超过 Southern 印迹等传统方法。虽然这两种方法都具有较高的可重复性和准确性,但 Southern 印迹法需要对每个靶点进行重复探针设计和分析,耗费大量人力和时间,因此通量较低。相反,NGS 通过将全基因组测序(WGS)数据映射到质粒序列,准确识别 T-DNA 插入位点和侧翼区域,有助于进行快速、全面的分析。这一优势可有效检测 T-DNA 的存在、拷贝数和非预期基因插入,而无需额外的探针工作。本文回顾了利用 NGS 进行转基因生物基因组鉴定的现状,并为此提出了更有效的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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