Honda Arata, Hirose Michiko, Sankai Tadashi, Yasmin Lubna, Yuzawa Kazuaki, Honsho Kimiko, Izu Haruna, Iguchi Atsushi, Ikawa Masahito, Ogura Atsuo
Organization for Promotion of Tenure Track, University of Miyazaki, 5200 Kibara, Kiyotake 889-1692; RIKEN BioResource Center, Tsukuba, Ibaraki 305-0074, Japan.
Exp Anim. 2015;64(1):31-7. doi: 10.1538/expanim.14-0034. Epub 2014 Sep 8.
Targeted genome editing of nonrodent mammalian species has provided the potential for highly accurate interventions into gene function in humans and the generation of useful animal models of human diseases. Here we show successful clustered regularly interspaced short palindromic repeat (CRISPR) and CRISPR-associated (Cas)-mediated gene targeting via circular plasmid injection in rabbits. The rabbit tyrosinase gene (TYR) was effectively disrupted, and we confirmed germline transmission by pronuclear injection of a circular plasmid expressing humanized Cas9 (hCas9) and single-guide RNA. Direct injection into pronuclear stage zygotes was possible following an in vitro validation assay. Neither off-target mutagenesis nor hCas9 transgenesis was detected in any of the genetically targeted pups and embryos examined. Gene targeting with this rapid and simplified strategy will help accelerate the development of translational research using other nonrodent mammalian species.
对非啮齿类哺乳动物物种进行靶向基因组编辑,为在人类中对基因功能进行高度精确干预以及生成有用的人类疾病动物模型提供了可能。在此,我们展示了通过在兔中注射环状质粒成功实现成簇规律间隔短回文重复序列(CRISPR)和CRISPR相关蛋白(Cas)介导的基因靶向。兔酪氨酸酶基因(TYR)被有效破坏,并且我们通过向原核注射表达人源化Cas9(hCas9)和单向导RNA的环状质粒证实了种系传递。经过体外验证试验后,可以直接向原核期受精卵进行注射。在所检测的任何基因靶向幼崽和胚胎中均未检测到脱靶诱变或hCas9转基因现象。采用这种快速且简化的策略进行基因靶向,将有助于加速利用其他非啮齿类哺乳动物物种开展转化研究的进程。