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Generation of gene-modified goats targeting MSTN and FGF5 via zygote injection of CRISPR/Cas9 system

机译:通过CRISPR / Cas9系统的合子注射产生针对 MSTN 和 FGF5 的基因修饰山羊

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Recent advances in the study of the CRISPR/Cas9 system have provided a precise and versatile approach for genome editing in various species. However, the applicability and efficiency of this method in large animal models, such as the goat, have not been extensively studied. Here, by co-injection of one-cell stage embryos with Cas9?mRNA and sgRNAs targeting two functional genes ( MSTN and FGF5 ), we successfully produced gene-modified goats with either one or both genes disrupted. The targeting efficiency of MSTN and FGF5 in cultured primary fibroblasts was as high as 60%, while the efficiency of disrupting MSTN and FGF5 in 98 tested animals was 15% and 21% respectively, and 10% for double gene modifications. The on- and off-target mutations of the target genes in fibroblasts, as well as in somatic tissues and testis of founder and dead animals, were carefully analyzed. The results showed that simultaneous editing of several sites was achieved in large animals, demonstrating that the CRISPR/Cas9 system has the potential to become a robust and efficient gene engineering tool in farm animals, and therefore will be critically important and applicable for breeding.
机译:CRISPR / Cas9系统研究的最新进展为各种物种的基因组编辑提供了一种精确而通用的方法。但是,这种方法在大型动物模型(例如山羊)中的适用性和效率尚未得到广泛研究。在这里,通过将单细胞期胚胎与靶向两个功能基因(MSTN和FGF5)的Cas9?mRNA和sgRNA一起注射,我们成功地生产了一个或两个基因都被破坏的基因修饰山羊。在培养的原代成纤维细胞中,MSTN和FGF5的靶向效率高达60%,而在98只试验动物中破坏MSTN和FGF5的效率分别为15%和21%,而双基因修饰的破坏效率为10%。仔细分析了成纤维细胞中以及创始和死亡动物的体细胞组织和睾丸中靶基因的靶标和靶标外突变。结果表明,在大型动物中可以同时编辑多个位点,这表明CRISPR / Cas9系统有潜力成为家畜中强大而有效的基因工程工具,因此将至关重要,并适用于育种。

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