Identification of the Tol2 transposase of the medaka fish Oryzias latipes that catalyzes excision of a nonautonomous Tol2 element in zebrafish Danio rerio

被引:149
作者
Kawakami, K
Shima, A
机构
[1] Univ Tokyo, Inst Med Sci, Dept Tumor Biol, Tokyo 1080071, Japan
[2] Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Tokyo 1130033, Japan
基金
日本学术振兴会;
关键词
insertional mutagenesis; transgenesis; transposase; transposon; vertebrate;
D O I
10.1016/S0378-1119(99)00444-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Tol2 element is found in the genome of the medaka fish, Oryzias latipes, and contains DNA sequences similar to those of transposons of the hAT family. Previously, we have developed a transient embryonic excision assay in zebrafish, in which zebrafish embryos were injected with a plasmid DNA harboring the Tol2 element, and have shown that the Tol2 element is excisable from the injected plasmid DNA (Kawakami, K., Koga, A., Hori, H., Shima, A., 1998. Excision of the Tol2 transposable element of the medaka fish, Oryzias latipes, in zebrafish, Danio rerio. Gene 225, 17-22). Although the Tol2 element is thought to be autonomous, an active transposase encoded by the Tol2 element has not been identified. Here we report the identification and analysis of mRNA transcribed from the Tol2 element in zebrafish embryos. The Tol2 transcript has the capacity to encode a protein of 649 amino acids, whose amino acid sequence is similar to those of transposases of the hAT family. To determine whether the transcript encodes an active enzyme, we developed a novel transient embryonic excision assay in which zebrafish fertilized eggs were co-injected with RNA transcribed in vitro using the Tol2 cDNA as a template and a plasmid DNA harboring a nonautonomous Tol2 element, which has a deletion in the transposase coding region. The nonautonomous Tol2 element could be efficiently excised in the zebrafsh only when co-injected with the Tol2 RNA. This result indicates that the Tol2 transcript encodes an active enzyme, a probable transposase, that can catalyze the excision reaction in trans. Further, by the co-injection analysis, we found that the Tol2 sequence lacking the first intron sequence of the transposase gene could not be excised, suggesting that it may contain essential cis-elements. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:239 / 244
页数:6
相关论文
共 19 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
Amsterdam A, 1997, COLD SPRING HARB SYM, V62, P437, DOI 10.1101/SQB.1997.062.01.052
[3]   EVIDENCE FOR A COMMON EVOLUTIONARY ORIGIN OF INVERTED REPEAT TRANSPOSONS IN DROSOPHILA AND PLANTS - HOBO, ACTIVATOR, AND TAM3 [J].
CALVI, BR ;
HONG, TJ ;
FINDLEY, SD ;
GELBART, WM .
CELL, 1991, 66 (03) :465-471
[4]  
Driever W, 1996, DEVELOPMENT, V123, P37
[5]   Transposition of the mariner element from Drosophila mauritiana in zebrafish [J].
Fadool, JM ;
Hartl, DL ;
Dowling, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5182-5186
[6]   Insertional mutagenesis and rapid cloning of essential genes In zebrafish [J].
Gaiano, N ;
Amsterdam, A ;
Kawakami, K ;
Allende, M ;
Becker, T ;
Hopkins, N .
NATURE, 1996, 383 (6603) :829-832
[7]  
Haffter P, 1996, DEVELOPMENT, V123, P1
[8]   Molecular reconstruction of Sleeping beauty, a Tc1-like transposon from fish, and its transposition in human cells [J].
Ivics, Z ;
Hackett, PB ;
Plasterk, RH ;
Izsvak, Z .
CELL, 1997, 91 (04) :501-510
[9]   Short inverted-repeat transposable elements in teleost fish and implications for a mechanism of their amplification [J].
Izsvák, Z ;
Ivics, Z ;
Shimoda, N ;
Mohn, D ;
Okamoto, H ;
Hackett, PB .
JOURNAL OF MOLECULAR EVOLUTION, 1999, 48 (01) :13-21
[10]   Excision of the Tol2 transposable element of the medaka fish, Oryzias latipes, in zebrafish, Danio rerio [J].
Kawakami, K ;
Koga, A ;
Hori, H ;
Shima, A .
GENE, 1998, 225 (1-2) :17-22