TY - JOUR
T1 - Targeted disruption of exogenous EGFP gene in medaka using zinc-finger nucleases
AU - Ansai, Satoshi
AU - Ochiai, Hiroshi
AU - Kanie, Yuta
AU - Kamei, Yasuhiro
AU - Gou, Yuki
AU - Kitano, Takeshi
AU - Yamamoto, Takashi
AU - Kinoshita, Masato
PY - 2012/6
Y1 - 2012/6
N2 - 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 (6-100%) 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.
AB - 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 (6-100%) 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.
KW - Gene knock-out
KW - Germ-line transmission
KW - Green fluorescent protein
KW - Medaka
KW - Zinc-finger nucleases
UR - http://www.scopus.com/inward/record.url?scp=84862682521&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862682521&partnerID=8YFLogxK
U2 - 10.1111/j.1440-169X.2012.01357.x
DO - 10.1111/j.1440-169X.2012.01357.x
M3 - Article
C2 - 22642582
AN - SCOPUS:84862682521
SN - 0012-1592
VL - 54
SP - 546
EP - 556
JO - Development Growth and Differentiation
JF - Development Growth and Differentiation
IS - 5
ER -