Highly efficient gene knockout in mice and zebrafish with RNA-guided endonucleases

被引:226
作者
Sung, Young Hoon [1 ]
Kim, Jong Min [2 ,3 ]
Kim, Hyun-Taek [4 ]
Lee, Jaehoon [1 ]
Jeon, Jisun [1 ]
Jin, Young [1 ]
Choi, Jung-Hwa [4 ]
Ban, Young Ho [1 ]
Ha, Sang-Jun [1 ]
Kim, Cheol-Hee [4 ]
Lee, Han-Woong [1 ,5 ]
Kim, Jin-Soo [2 ,3 ]
机构
[1] Yonsei Univ, Coll Life Sci & Biotechnol, Dept Biochem, Seoul 120749, South Korea
[2] Seoul Natl Univ, Natl Creat Res Initiat Ctr Genome Engn, Seoul 151747, South Korea
[3] Seoul Natl Univ, Dept Chem, Seoul 151747, South Korea
[4] Chungnam Natl Univ, Dept Biol, Taejon 305764, South Korea
[5] Yonsei Univ, Anim Res Ctr, Yonsei Lab, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
ZINC-FINGER NUCLEASES; CRISPR-CAS SYSTEMS; HUMAN GENOME; HUMAN-CELLS; SPECIFICITY; MUTAGENESIS; GENERATION; TALENS;
D O I
10.1101/gr.163394.113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA-guided endonucleases (RGENs), derived from the prokaryotic Type II CRISPR-Cas system, enable targeted genome modification in cells and organisms. Here we describe the establishment of gene-knockout mice and zebrafish by the injection of RGENs as Cas9 protein: guide RNA complexes or Cas9 mRNA plus guide RNA into one-cell-stage embryos of both species. RGENs efficiently generated germline transmittable mutations in up to 93% of newborn mice with minimal toxicity. RGEN-induced mutations in the mouse Prkdc gene that encodes an enzyme critical for DNA double-strand break repair resulted in immunodeficiency both in F-0 and F-1 mice. We propose that RGEN-mediated mutagenesis in animals will greatly expedite the creation of genetically engineered model organisms, accelerating functional genomic research.
引用
收藏
页码:125 / 131
页数:7
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