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

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...

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Detalles Bibliográficos
Autores principales: Sung, Young Hoon, Kim, Jong Min, Kim, Hyun-Taek, Lee, Jaehoon, Jeon, Jisun, Jin, Young, Choi, Jung-Hwa, Ban, Young Ho, Ha, Sang-Jun, Kim, Cheol-Hee, Lee, Han-Woong, Kim, Jin-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3875853/
https://www.ncbi.nlm.nih.gov/pubmed/24253447
http://dx.doi.org/10.1101/gr.163394.113
Descripción
Sumario: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.