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Efficiency to Discovery Transgenic Loci in GM Rice Using Next Generation Sequencing Whole Genome Re-sequencing

机译:利用下一代测序全基因组重测序技术发现转基因水稻中转基因位点的效率

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摘要

Molecular characterization technology in genetically modified organisms, in addition to how transgenic biotechnologies are developed now require full transparency to assess the risk to living modified and non-modified organisms. Next generation sequencing (NGS) methodology is suggested as an effective means in genome characterization and detection of transgenic insertion locations. In the present study, we applied NGS to insert transgenic loci, specifically the epidermal growth factor (EGF) in genetically modified rice cells. A total of 29.3 Gb (~72× coverage) was sequenced with a 2 × 150 bp paired end method by Illumina HiSeq2500, which was consecutively mapped to the rice genome and T-vector sequence. The compatible pairs of reads were successfully mapped to 10 loci on the rice chromosome and vector sequences were validated to the insertion location by polymerase chain reaction (PCR) amplification. The EGF transgenic site was confirmed only on chromosome 4 by PCR. Results of this study demonstrated the success of NGS data to characterize the rice genome. Bioinformatics analyses must be developed in association with NGS data to identify highly accurate transgenic sites.
机译:除如何开发转基因生物技术外,转基因生物中的分子表征技术现在还要求完全透明,以评估对改性活生物体和非改性活生物体的风险。下一代测序(NGS)方法被认为是基因组表征和转基因插入位置检测的有效手段。在本研究中,我们应用NGS在转基因水稻细胞中插入转基因位点,特别是表皮生长因子(EGF)。通过Illumina HiSeq2500的2×150 bp配对末端方法对29.3 Gb(约72倍覆盖)的总序列进行了测序,并将其连续定位到水稻基因组和T-载体序列上。兼容的读对被成功地定位到水稻染色体上的10个位点,并通过聚合酶链反应(PCR)扩增将载体序列验证到插入位置。通过PCR仅在4号染色体上证实了EGF转基因位点。这项研究的结果证明了NGS数据成功地表征了水稻基因组。必须结合NGS数据进行生物信息学分析,以鉴定高度准确的转基因位点。

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