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首页> 外文期刊>PLoS One >Identification of genomic insertion and flanking sequences of the transgenic drought-tolerant maize line “SbSNAC1-382” using the single-molecule real-time (SMRT) sequencing method
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Identification of genomic insertion and flanking sequences of the transgenic drought-tolerant maize line “SbSNAC1-382” using the single-molecule real-time (SMRT) sequencing method

机译:使用单分子实时(SMRT)测序法鉴定转基因干旱耐受玉米“SBSNAC1-382”的基因组插入和侧翼序列

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摘要

Safety assessment of genetically modified (GM) crops is crucial at the product-development phase before GM crops are placed on the market. Determining characteristics of sequences flanking exogenous insertion sequences is essential for the safety assessment and marketing of transgenic crops. In this study, we used genome walking and whole-genome sequencing (WGS) to identify the flanking sequence characteristics of the SbSNAC1 transgenic drought-tolerant maize line “SbSNAC1-382”, but both of the two methods failed. Then, we constructed a genomic fosmid library of the transgenic maize line, which contained 4.18×10 5 clones with an average insertion fragment of 35 kb, covering 5.85 times the maize genome. Subsequently, three positive clones were screened by pairs of specific primers, and one of the three positive clones was sequenced by using single-molecule real-time (SMRT) sequencing technology. More than 1.95 Gb sequence data (~10 5 × coverage) for the sequenced clone were generated. The junction reads mapped to the boundaries of T-DNA, and the flanking sequences in the transgenic line were identified by comparing all sequencing reads with the maize reference genome and the sequence of the transgenic vector. Furthermore, the putative insertion loci and flanking sequences were confirmed by PCR amplification and Sanger sequencing. The results indicated that two copies of the exogenous T-DNA fragments were inserted at the same genomic site, and the exogenous T-DNA fragments were integrated at the position of Chromosome 5 from 177155650 to 177155696 in the transgenic line 382. In this study, we demonstrated the successful application of the SMRT technology for the characterization of genomic insertion and flanking sequences.
机译:基因改性(GM)作物的安全评估对于转基因作物置于市场上的产品显影阶段至关重要。确定序列侧翼外源插入序列的序列特征对于转基因作物的安全评估和营销至关重要。在这项研究中,我们使用基因组行走和全基因组测序(WGS)来鉴定SBSNAC1转基因干旱含量玉米“SBSNAC1-382”的侧翼序列特征,但两种方法两种失效。然后,我们构建了转基因玉米系的基因组Fosmid文库,其含有4.18×10 5克隆,平均插入片段为35kb,覆盖玉米基因组的5.85倍。随后,通过比对筛选三个阳性克隆,通过使用单分子实时(SMRT)测序技术对三种阳性克隆中的一种进行测序。产生了用于测序克隆的超过1.95GB的序列数据(〜10 5×覆盖率)。通过将所有测序读数与转基因载体的序列进行比较,通过比较γ读取的所有测序和转基因载体的序列来鉴定成映射到T-DNA的边界的结读数,以及转基因系中的侧翼序列。此外,通过PCR扩增和Sanger测序确认推定的插入基因座和侧面序列。结果表明,外源T-DNA片段的两份在同一基因组位点插入,并且外源T-DNA片段在转基因线382中从177155650至177155696中整合到染色体5中的位置。在本研究中,我们展示了SMRT技术的成功应用,以表征基因组插入和侧翼序列。

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