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通过 CRISPR/Cas9 的多重基因编辑可实现理想的肌肉肥大,而在绵羊中未检测到脱靶效应。

Multiplex gene editing via CRISPR/Cas9 exhibits desirable muscle hypertrophy without detectable off-target effects in sheep.

机构信息

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

MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center of Nanjing University, National Resource Center for Mutant Mice, Nanjing 210061, China.

出版信息

Sci Rep. 2016 Aug 26;6:32271. doi: 10.1038/srep32271.

Abstract

The CRISPR/Cas9 system provides a flexible approach for genome engineering of genetic loci. Here, we successfully achieved precise gene targeting in sheep by co-injecting one-cell-stage embryos with Cas9 mRNA and RNA guides targeting three genes (MSTN, ASIP, and BCO2). We carefully examined the sgRNAs:Cas9-mediated targeting effects in injected embryos, somatic tissues, as well as gonads via cloning and sequencing. The targeting efficiencies in these three genes were within the range of 27-33% in generated lambs, and that of simultaneously targeting the three genes was 5.6%, which demonstrated that micro-injection of zygotes is an efficient approach for generating gene-modified sheep. Interestingly, we observed that disruption of the MSTN gene resulted in the desired muscle hypertrophy that is characterized by enlarged myofibers, thereby providing the first detailed evidence supporting that gene modifications had occurred at both the genetic and morphological levels. In addition, prescreening for the off-target effect of sgRNAs was performed on fibroblasts before microinjection, to ensure that no detectable off-target mutations from founder animals existed. Our findings suggested that the CRISPR/Cas9 method can be exploited as a powerful tool for livestock improvement by simultaneously targeting multiple genes that are responsible for economically significant traits.

摘要

CRISPR/Cas9 系统为基因座的基因组工程提供了一种灵活的方法。在这里,我们通过将 Cas9 mRNA 和靶向三个基因(MSTN、ASIP 和 BCO2)的 RNA 向导共注射到单细胞期胚胎中,成功地实现了绵羊的精确基因靶向。我们仔细检查了 sgRNA:Cas9 介导的靶向效应,包括注射胚胎、体细胞组织以及性腺,通过克隆和测序进行分析。在这些基因中,靶向效率在产生的羔羊中为 27-33%,同时靶向三个基因的效率为 5.6%,这表明微注射受精卵是一种有效的方法,可以用于产生基因修饰绵羊。有趣的是,我们观察到 MSTN 基因的破坏导致了所需的肌肉肥大,其特征是肌纤维增大,从而提供了第一个详细的证据,支持基因修饰已经在遗传和形态水平上发生。此外,在微注射前对成纤维细胞进行了 sgRNA 的脱靶效应预筛选,以确保不存在可检测的来自起始动物的脱靶突变。我们的研究结果表明,CRISPR/Cas9 方法可以通过同时靶向多个负责经济重要性状的基因,作为一种强大的工具用于家畜改良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a9d/4999810/fd5d8ea64970/srep32271-f1.jpg

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