Ryu Junghyun, Lee Kiho
Department of Animal and Poultry Sciences, Virginia Tech, 175 W. Campus Dr., Blacksburg, VA, 24061, USA.
Methods Mol Biol. 2017;1605:231-244. doi: 10.1007/978-1-4939-6988-3_16.
Ability to disrupt genes is essential in elucidating gene function. Unlike rodents or amphibians, it has been difficult to generate gene-targeted embryos in large animals. Therefore, studies of early embryo development have been hampered in large animals. A recent technology suggests that targeted mutations can be successfully introduced during embryogenesis, thus by-passing the need of breeding to produce gene-targeted embryos. This is particularly important in large animal models because of longer gestation period and higher animal cost. Here, we describe a specific approach to disrupt up to two genes simultaneously during embryogenesis using the CRISPR/Cas9 technology in swine. The approach can help understand the mechanism of zygotic genome activation in large animals.
破坏基因的能力对于阐明基因功能至关重要。与啮齿动物或两栖动物不同,在大型动物中生成基因靶向胚胎一直很困难。因此,大型动物的早期胚胎发育研究受到了阻碍。最近的一项技术表明,可以在胚胎发生过程中成功引入靶向突变,从而无需通过繁殖来产生基因靶向胚胎。由于妊娠期较长且动物成本较高,这在大型动物模型中尤为重要。在此,我们描述了一种在猪胚胎发生过程中使用CRISPR/Cas9技术同时破坏多达两个基因的具体方法。该方法有助于了解大型动物中合子基因组激活的机制。