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

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dc.contributor.authorSung, Young Hoon-
dc.contributor.authorKim, Jong Min-
dc.contributor.authorKim, Hyun-Taek-
dc.contributor.authorLee, Jaehoon-
dc.contributor.authorJeon, Jisun-
dc.contributor.authorJin, Young-
dc.contributor.authorChoi, Jung-Hwa-
dc.contributor.authorBan, Young Ho-
dc.contributor.authorHa, Sang-Jun-
dc.contributor.authorKim, Cheol-Hee-
dc.contributor.authorLee, Han-Woong-
dc.contributor.authorKim, Jin-Soo-
dc.date.accessioned2020-04-27T12:41:40Z-
dc.date.available2020-04-27T12:41:40Z-
dc.date.created2018-01-10-
dc.date.created2018-01-10-
dc.date.issued2014-01-
dc.identifier.citationGenome Research, Vol.24 No.1, pp.125-131-
dc.identifier.issn1088-9051-
dc.identifier.other12257-
dc.identifier.urihttps://hdl.handle.net/10371/165645-
dc.description.abstractRNA-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.-
dc.language영어-
dc.publisherCold Spring Harbor Laboratory Press-
dc.titleHighly efficient gene knockout in mice and zebrafish with RNA-guided endonucleases-
dc.typeArticle-
dc.contributor.AlternativeAuthor김진수-
dc.identifier.doi10.1101/gr.163394.113-
dc.citation.journaltitleGenome Research-
dc.identifier.wosid000329163500012-
dc.identifier.scopusid2-s2.0-84891704542-
dc.citation.endpage131-
dc.citation.number1-
dc.citation.startpage125-
dc.citation.volume24-
dc.identifier.sci000329163500012-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Jin-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusZINC-FINGER NUCLEASES-
dc.subject.keywordPlusCRISPR-CAS SYSTEMS-
dc.subject.keywordPlusHUMAN GENOME-
dc.subject.keywordPlusHUMAN-CELLS-
dc.subject.keywordPlusSPECIFICITY-
dc.subject.keywordPlusMUTAGENESIS-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusTALENS-
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Biology and Biochemistry

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