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首页> 外文期刊>Frontiers in Genetics >Programmable Base Editing of the Sheep Genome Revealed No Genome-Wide Off-Target Mutations
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Programmable Base Editing of the Sheep Genome Revealed No Genome-Wide Off-Target Mutations

机译:绵羊基因组的可编程基础编辑显示没有全基因组的脱靶突变。

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Since its emergence, CRISPR/Cas9-mediated base editors (BEs) with cytosine deaminase activity have been used to precisely and efficiently introduce single-base mutations in genomes, including those of human cells, mice, and crop species. Most production traits in livestock are induced by point mutations, and genome editing using BEs without homology-directed repair of double-strand breaks can directly alter single nucleotides. The p.96R & C variant of Suppressor cytokine signaling 2 (SOCS2) has profound effects on body weight, body size, and milk production in sheep. In the present study, we successfully obtained lambs with defined point mutations resulting in a p.96R & C substitution in SOCS2 by the co-injection of BE3 mRNA and a single guide RNA (sgRNA) into sheep zygotes. The observed efficiency of the single nucleotide exchange in newborn animals was as high as 25%. Observations of body size and body weight in the edited group showed that gene modification contributes to enhanced growth traits in sheep. Moreover, targeted deep sequencing and unbiased family trio-based whole genome sequencing revealed undetectable off-target mutations in the edited animals. This study demonstrates the potential for the application of BE-mediated point mutations in large animals for the improvement of production traits in livestock species.
机译:自从出现以来,具有胞嘧啶脱氨酶活性的CRISPR / Cas9介导的碱基编辑器(BEs)已被用于精确,高效地在基因组中引入单碱基突变,包括人类细胞,小鼠和农作物物种的基因组。牲畜的大多数生产性状都是由点突变诱导的,使用BE进行基因组编辑而没有同源性指导的双链断裂修复可直接改变单个核苷酸。 p.96R&抑制细胞因子信号传导2(SOCS2)的C变体对绵羊的体重,体型和产奶量具有深远的影响。在本研究中,我们成功地获得了具有确定的点突变的羔羊,从而导致p.96R> pR。通过将BE3 mRNA和单个向导RNA(sgRNA)共注入绵羊合子,在SOCS2中进行C取代。在新生动物中观察到的单核苷酸交换效率高达25%。对编辑组的体重和体重的观察表明,基因修饰有助于增强绵羊的生长性状。此外,针对性的深度测序和基于无偏见家族三重基因的全基因组测序揭示了在编辑过的动物中无法检测到的脱靶突变。这项研究证明了BE介导的点突变在大型动物中的应用潜力,可以改善牲畜物种的生产性状。

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