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Whole-Genome Analysis of Herbicide-Tolerant Mutant Rice Generated by Agrobacterium-Mediated Gene Targeting

机译:农杆菌介导的基因靶向产生耐除草剂突变水稻的全基因组分析

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摘要

Gene targeting (GT) is a technique used to modify endogenous genes in target genomes precisely via homologous recombination (HR). Although GT plants are produced using genetic transformation techniques, if the difference between the endogenous and the modified gene is limited to point mutations, GT crops can be considered equivalent to non-genetically modified mutant crops generated by conventional mutagenesis techniques. However, it is difficult to guarantee the non-incorporation of DNA fragments from Agrobacterium in GT plants created by Agrobacterium-mediated GT despite screening with conventional Southern blot and/or PCR techniques. Here, we report a comprehensive analysis of herbicide-tolerant rice plants generated by inducing point mutations in the rice ALS gene via Agrobacterium-mediated GT. We performed genome comparative genomic hybridization (CGH) array analysis and whole-genome sequencing to evaluate the molecular composition of GT rice plants. Thus far, no integration of Agrobacterium-derived DNA fragments has been detected in GT rice plants. However, >1,000 single nucleotide polymorphisms (SNPs) and insertion/deletion (InDels) were found in GT plants. Among these mutations, 20–100 variants might have some effect on expression levels and/or protein function. Information about additive mutations should be useful in clearing out unwanted mutations by backcrossing.
机译:基因靶向(GT)是一种用于通过同源重组(HR)精确修饰靶基因组中内源基因的技术。尽管GT植物是使用遗传转化技术生产的,但如果内源基因和修饰基因之间的差异仅限于点突变,则可以认为GT作物等同于通过常规诱变技术产生的非遗传修饰突变作物。然而,尽管用常规的Southern印迹和/或PCR技术进行了筛选,但仍难以保证在农杆菌介导的GT产生的GT植物中没有农杆菌DNA片段的掺入。在这里,我们报告了通过农杆菌介导的GT诱导水稻ALS基因中的点突变而产生的耐除草剂水稻植株的综合分析。我们进行了基因组比较基因组杂交(CGH)阵列分析和全基因组测序,以评估GT水稻植株的分子组成。迄今为止,在GT水稻植株中未检测到农杆菌来源的DNA片段的整合。但是,在GT植物中发现了> 1,000个单核苷酸多态性(SNP)和插入/缺失(InDels)。在这些突变中,20-100个变体可能对表达水平和/或蛋白质功能有一定影响。有关加性突变的信息应有助于通过回交清除不需要的突变。

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