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DNA oligonucleotides and plasmids perform equally as donors for targeted gene conversion.

机译:DNA寡核苷酸和质粒的作用等同于目标基因转化的供体。

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摘要

Site-specific gene modifications in cells are initiated by the introduction of exogenous DNA. We used a recently established cell assay to compare the ability of DNA donors to induce a single point mutation that converts a target gene encoding blue fluorescent protein (BFP) into expressing green fluorescent protein (GFP). In a chromosomal assay with cells stably expressing BFP, we showed that fluorescently labeled single-stranded oligonucleotides and a donor plasmid cotranscribing a red fluorescent protein provide similar efficiencies in triggering BFP-GFP conversions. In transient cotransfections, an isogenic donor plasmid comprising a nonfunctional GFP gene yielded a greater efficiency for the conversion of the BFP target gene than a nonisogenic donor, and all plasmid donors were superior to oligonucleotides.
机译:细胞中的位点特异性基因修饰是通过引入外源DNA引发的。我们使用最近建立的细胞测定法来比较DNA供体诱导单点突变的能力,该突变将编码蓝色荧光蛋白(BFP)的靶基因转变为表达绿色荧光蛋白(GFP)的靶基因。在使用稳定表达BFP的细胞进行的染色体测定中,我们显示了荧光标记的单链寡核苷酸和共转录红色荧光蛋白的供体质粒在触发BFP-GFP转化方面提供了相似的效率。在瞬时共转染中,与非等基因供体相比,包含非功能性GFP基因的等基因供体质粒对BFP靶基因的转化效率更高,并且所有质粒供体均优于寡核苷酸。

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