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Comparison of DNA fragments as donor DNAs upon sequence conversion of cleaved target DNA

机译:DNA片段在切割靶DNA序列转化时作为供体DNA的比较

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摘要

Pinpoint sequence alteration (genome editing) by the combination of the site-specific cleavage of a target DNA and a donor nucleic acid has attracted much attention and the sequence of the target DNA is expected to be changed to that of a donor nucleic acid. In most cases, oligodeoxyribonucleotides (ODNs) and plasmid DNAs have been used as donors. However, a several hundred-base single-stranded (ss) DNA fragment and a 5'-tailed duplex (TD) accomplished the desired sequence changes without DNA cleavage, and might serve as better donors for the cleaved target DNA than ODNs and plasmid DNAs. In this study, sequence conversion efficiencies were compared with various donor DNAs in model sequence alteration experiments, using episomal DNA. The efficiencies with the ss and TD fragments were higher than those with the ODN and plasmid DNA. The sequence change by the TD seemed somewhat less efficient but slightly more accurate than that by the ss DNA fragment. These results suggested that the ss and TD fragments are better donors for targeted sequence alteration.
机译:通过靶DNA的位点特异性切割和供体核酸的组合,针尖序列改变(基因组编辑)引起了许多关注,并且预期靶DNA的序列将改变为供体核酸的序列。在大多数情况下,寡脱氧氧核糖核苷酸(ODNS)和质粒DNA已被用作供体。然而,几百个碱单链(SS)DNA片段和5'尾双链体(TD)完成所需的序列变化,没有DNA切割,并且可以作为切割靶DNA的更好的供体,而不是ODN和质粒DNA 。在该研究中,将序列转化效率与各种供体DNA进行比较,在模型序列改变实验中,使用异构DNA。 SS和TD片段的效率高于ODN和质粒DNA的效率。 TD的序列变化似乎有效,但比SS DNA片段略微更准确。这些结果表明,SS和TD片段是针对目标序列变化的更好的供体。

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