Method

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

    • 1Department of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul 120-749, Republic of Korea;
    • 2National Creative Research Initiatives Center for Genome Engineering and Department of Chemistry, Seoul National University, Seoul 151-747, Republic of Korea;
    • 3Department of Biology, Chungnam National University, Daejeon 305-764, Republic of Korea;
    • 4Yonsei Laboratory Animal Research Center, Yonsei University, Seoul 120-749, Republic of Korea
Published November 19, 2013. Vol 24 Issue 1, pp. 125-131. https://doi.org/10.1101/gr.163394.113
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Abstract

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 F0 and F1 mice. We propose that RGEN-mediated mutagenesis in animals will greatly expedite the creation of genetically engineered model organisms, accelerating functional genomic research.

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