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Gene Editing with Helper-Dependent Adenovirus Can Efficiently Introduce Multiple Changes Simultaneously over a Large Genomic Region

机译:辅助依赖腺病毒的基因编辑可以有效地在一个大的基因组区域内同时引入多个变化。

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摘要

Helper-dependent adenoviral vectors (HDAds) possess long homology arms that mediate high-efficiency gene editing. These long homology arms may permit simultaneous introduction of multiple modifications into a large genomic region or may permit a single HDAd to correct many different individual mutations spread widely across a gene. We investigated this important potential using an HDAd bearing 13 genetic markers in the region of homology to the target CFTR locus in human iPSCs and found that all markers can be simultaneously introduced into the target locus, with the two farthest markers being 22.2 kb apart. We found that genetic markers closer to the HDAd’s selectable marker are more efficiency introduced into the target locus; a marker located 208 bp from the selectable marker was introduced with 100% efficiency. However, even markers 11 kb from the selectable marker were introduced at a relatively high frequency of 21.7%. Our study also revealed extensive heteroduplex DNA formation of up to 10 kb with no bias toward vector or chromosomal repair. However, mismatches escape repair at a frequency of up to 15%, leading to a genetically mixed colony and emphasizing the need for caution, especially if the donor and target sequences are not 100% homologous.
机译:依赖助手的腺病毒载体(HDAds)具有长的同源臂,可介导高效基因编辑。这些长的同源臂可以允许将多个修饰同时引入一个大的基因组区域,或者可以允许单个HDAd纠正跨基因广泛分布的许多不同的个体突变。我们使用在人类iPSC中与目标CFTR基因座同源的区域中带有13个遗传标记的HDAd,研究了这一重要潜力,并发现可以同时将所有标记引入目标基因座,两个最远的标记相距22.2 kb。我们发现,更接近HDAd选择标记的遗传标记可以更有效地引入目标基因座。距离选择标记208 bp处的标记以100%的效率引入。但是,即使是来自选择标记的11 kb标记也以21.7%的较高频率被引入。我们的研究还揭示了高达10 kb的广泛异源双链DNA形成,对载体或染色体修复无偏见。但是,错配以高达15%的频率逃避修复,从而导致了遗传上混合的菌落,并强调了谨慎的需要,尤其是在供体和靶序列不是100%同源的情况下。

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