首页> 美国卫生研究院文献>Scientific Reports >Multiplex gene editing via CRISPR/Cas9 exhibits desirable muscle hypertrophy without detectable off-target effects in sheep
【2h】

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

机译:通过CRISPR / Cas9进行多重基因编辑显示出理想的肌肉肥大而在绵羊中没有可检测到的脱靶效应

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:CRISPR / Cas9系统为遗传基因座的基因组工程提供了灵活的方法。在这里,我们通过与Cas9 mRNA和靶向三个基因(MSTN,ASIP和BCO2)的RNA向导共同注射单细胞阶段胚胎,成功实现了绵羊的精确基因靶向。我们通过克隆和测序仔细检查了sgRNAs:Cas9介导的对注射的胚胎,体细胞组织以及性腺的靶向作用。这三个基因对羔羊的靶向效率在27-33%的范围内,同时对三个基因的靶向效率为5.6%,这表明显微注射合子是产生基因修饰绵羊的有效方法。有趣的是,我们观察到MSTN基因的破坏导致所需的肌肉肥大,其特征是肌纤维增大,从而提供了第一个详细的证据,证明基因修饰已在遗传和形态学水平上发生。此外,在显微注射之前,对成纤维细胞进行了sgRNA脱靶作用的预筛选,以确保不存在来自始祖动物的可检测到的脱靶突变。我们的研究结果表明,CRISPR / Cas9方法可同时靶向多个具有经济意义的性状的基因,因此可作为牲畜改良的强大工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号