Transgenic Xenopus laevis strain expressing Cre recombinase in muscle cells

被引:14
作者
Waldner, Christoph
Sakamaki, Kazuhiro
Ueno, Naoto
Turan, Gueluezar
Ryffel, Gerhart U.
机构
[1] Univ Klinikum Essen, Inst Zellbiol, D-45147 Essen, Germany
[2] Kyoto Univ, Grad Sch Biostudies, Dept Anim Dev & Physiol, Kyoto, Japan
[3] Natl Inst Basic Biol, Dept Dev Biol, Okazaki, Aichi 444, Japan
关键词
Cre recombinase; transgenic Xenopus laevis; conditional gene expression; FLUORESCENT PROTEIN; GENE-EXPRESSION; MOUSE; PROMOTER; RECEPTOR; MEDIATE; FLP;
D O I
10.1002/dvdy.20880
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
For reproducible analyses of gene function in Xenopus, the use of transgenic strains is a promising approach but has limitations when investigating factors interfering with development. Therefore, inducible systems are attractive alternatives, and a binary system based on recombinases is a most versatile approach. We have shown previously that Cre and FLP recombinases are active in Xenopus laevis and can induce a silent reporter gene in a corresponding reporter strain. Here, we describe the establishment of the transgenic Xenopus laevis strain A7 expressing Cre recombinase under the control of the muscle-specific cardiac actin promoter. Upon crossing to several distinct reporter strains, A7 is able to induce EYFP, DsRed2, or LacZ reporter genes in a muscle-specific manner. This first Cre-expressing strain allows conditional activation of any gene of interest in muscle cells and, thus, opens up the use of recombinases as a new experimental strategy in Xenopus.
引用
收藏
页码:2220 / 2228
页数:9
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