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首页> 外文期刊>Transgenic research >Mosaicism diminishes the value of pre-implantation embryo biopsies for detecting CRISPR/Cas9 induced mutations in sheep
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Mosaicism diminishes the value of pre-implantation embryo biopsies for detecting CRISPR/Cas9 induced mutations in sheep

机译:马赛克主义减少了预注入胚胎活检的价值,用于检测绵羊中的CRISPR / CAS9诱导突变

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摘要

The production of knock-out (KO) livestock models is both expensive and time consuming due to their long gestational interval and low number of offspring. One alternative to increase efficiency is performing a genetic screening to select pre-implantation embryos that have incorporated the desired mutation. Here we report the use of sheep embryo biopsies for detecting CRISPR/Cas9-induced mutations targeting the gene PDX1 prior to embryo transfer. PDX1 is a critical gene for pancreas development and the target gene required for the creation of pancreatogenesis-disabled sheep. We evaluated the viability of biopsied embryos in vitro and in vivo, and we determined the mutation efficiency using PCR combined with gel electrophoresis and digital droplet PCR(ddPCR). Next, we determined the presence of mosaicism in similar to 50% of the recovered fetuses employing a clonal sequencing methodology. While the use of biopsies did not compromise embryo viability, the presence of mosaicism diminished the diagnostic value of the technique. If mosaicism could be overcome, pre-implantation embryo biopsies for mutation screening represents a powerful approach that will streamline the creation of KO animals.
机译:由于其长的妊娠间隔和低位后代,敲除(KO)畜牧业模型的生产既昂贵又耗时。提高效率的一种替代方案正在进行遗传筛选以选择已掺入所需突变的预注入胚胎。在这里,我们报告使用绵羊胚胎活组织检查以在胚胎转移之前检测靶向基因PDX1的CRISPR / CAS9诱导突变。 PDX1是胰腺癌发育的关键基因和产生胰腺发生禁用绵羊所需的靶基因。我们在体外和体内评估了活检胚胎的可行性,并使用PCR结合凝胶电泳和数字液滴PCR(DDPCR)确定突变效率。接下来,我们确定了类似于采用克隆测序方法的回收胎儿的50%的马赛克主义的存在。虽然使用活组织检查没有损害胚胎活力,但是马赛克的存在减少了该技术的诊断价值。如果可以克服马赛主义,突变筛查的预注入胚胎活组织检查代表了一种强大的方法,可以简化KO动物的创造。

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