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通过向受精卵注射CRISPR/Cas9系统生成靶向肌肉生长抑制素(MSTN)和成纤维细胞生长因子5(FGF5)的基因编辑山羊。

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

作者信息

Wang Xiaolong, Yu Honghao, Lei Anmin, Zhou Jiankui, Zeng Wenxian, Zhu Haijing, Dong Zhiming, Niu Yiyuan, Shi Bingbo, Cai Bei, Liu Jinwang, Huang Shuai, Yan Hailong, Zhao Xiaoe, Zhou Guangxian, He Xiaoling, Chen Xiaoxu, Yang Yuxin, Jiang Yu, Shi Lei, Tian Xiue, Wang Yongjun, Ma Baohua, Huang Xingxu, Qu Lei, Chen Yulin

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China.

Shaanxi Provincial Engineering and Technology Research Center of Cashmere Goats, Yulin University, Yulin 719000, China.

出版信息

Sci Rep. 2015 Sep 10;5:13878. doi: 10.1038/srep13878.

Abstract

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.

摘要

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且通用的方法。然而,该方法在大型动物模型(如山羊)中的适用性和效率尚未得到广泛研究。在此,通过将Cas9 mRNA和靶向两个功能基因(MSTN和FGF5)的sgRNAs共同注射到单细胞期胚胎中,我们成功培育出了一个或两个基因被破坏的基因修饰山羊。MSTN和FGF5在培养的原代成纤维细胞中的靶向效率高达60%,而在98只受试动物中破坏MSTN和FGF5的效率分别为15%和21%,双基因修饰的效率为10%。我们仔细分析了原代成纤维细胞以及奠基动物和死亡动物的体细胞组织与睾丸中靶基因的靶向和脱靶突变情况。结果表明,在大型动物中实现了多个位点的同时编辑,这表明CRISPR/Cas9系统有潜力成为家畜中强大而高效的基因工程工具,因此对于育种至关重要且具有实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6524/4564737/0f7d77a44f89/srep13878-f1.jpg

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