Targeted disruption of exogenous EGFP gene in medaka using zinc-finger nucleases

被引:32
作者
Ansai, Satoshi [1 ]
Ochiai, Hiroshi [2 ]
Kanie, Yuta [3 ]
Kamei, Yasuhiro [3 ]
Gou, Yuki [4 ]
Kitano, Takeshi [4 ]
Yamamoto, Takashi [2 ]
Kinoshita, Masato [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Appl Biosci, Sakyo Ku, Kyoto 6068502, Japan
[2] Hiroshima Univ, Dept Math & Life Sci, Grad Sch Sci, Higashihiroshima 7398526, Japan
[3] Natl Inst Nat Sci, Spectrog & Bioimaging Facil, Okazaki, Aichi 4448585, Japan
[4] Kumamoto Univ, Grad Sch Sci & Technol, Kumamoto 8608555, Japan
关键词
gene knock-out; germ-line transmission; green fluorescent protein; medaka; zinc-finger nucleases; ORYZIAS-LATIPES; KNOCKOUT RATS; GERM-CELLS; ZEBRAFISH; GENOME; MUTAGENESIS; GENERATION; FLUORESCENCE; TRANSLATION; EXPRESSION;
D O I
10.1111/j.1440-169X.2012.01357.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zinc-finger nucleases (ZFNs) are artificial enzymes that create site-specific double-strand breaks and thereby induce targeted genome editing. Here, we demonstrated successful gene disruption in somatic and germ cells of medaka (Oryzias latipes) using ZFN to target exogenous EGFP genes. Embryos that were injected with an RNA sequence pair coding for ZFNs showed mosaic loss of green fluorescent protein fluorescence in skeletal muscle. A number of mutations that included both deletions and insertions were identified within the ZFN target site in each embryo, whereas no mutations were found at the non-targeted sites. In addition, ZFN-induced mutations were introduced in germ cells and efficiently transmitted to the next generation. The mutation frequency varied (6100%) in the germ cells from each founder, and a founder carried more than two types of mutation in germ cells. Our results have introduced the possibility of targeted gene disruption and reverse genetics in medaka.
引用
收藏
页码:546 / 556
页数:11
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