A transposon-mediated gene trap approach identifies developmentally regulated genes in zebrafish

被引:684
作者
Kawakami, K
Takeda, H
Kawakami, N
Kobayashi, M
Matsuda, N
Mishina, M
机构
[1] Natl Inst Genet, Div Mol & Dev Biol, Shizuoka 4118540, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Mol Neurobiol & Pharmacol, Tokyo 1130033, Japan
[3] Japan Sci & Technol Corp, SORST, Tokyo 1130033, Japan
[4] Univ Tsukuba, Inst Basic Med Sci, Tsukuba, Ibaraki 3058577, Japan
[5] Univ Tsukuba, Ctr Tsukuba Adv Res Alliance, Tsukuba, Ibaraki 3058577, Japan
关键词
D O I
10.1016/j.devcel.2004.06.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We report here development of a novel gene trap method in zebrafish using the Tol2 transposon system. First, we established a highly efficient transgenesis method in which a plasmid DNA containing the Tol2 transposon vector and the transposase mRNA synthesized in vitro were coinjected into one-cell stage embryos. The transposon vector inserted in the genome could be transmitted to the F1 progeny at high frequencies, and regulated gene expression by a specific promoter could be recapitulated in transgenic fish. Then we constructed a transposon-based gene trap vector containing a splice acceptor and the GFP gene, performed a pilot screen for gene trapping, and obtained fish expressing GFP in temporally and spatially restricted patterns. We confirmed the endogenous transcripts were indeed trapped by the insertions, and the insertion could interfere with expression of the trapped gene. We propose our gene trap approach should facilitate studies of vertebrate development and organogenesis.
引用
收藏
页码:133 / 144
页数:12
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