A quantitative analysis of the kinetics of Gal4 activator and effector gene expression in the zebrafish

被引:61
作者
Scheer, N
Riedl, I
Warren, JT
Kuwada, JY
Campos-Ortega, JA [1 ]
机构
[1] Univ Cologne, Inst Entwicklungsbiol, D-50923 Cologne, Germany
[2] Univ Michigan, Dept Biol, Ann Arbor, MI 48109 USA
关键词
Gal4-UAS technique; kinetics; gene expression; zebrafish;
D O I
10.1016/S0925-4773(01)00621-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Using a temperature-inducible hsp70:Gal4 activator and UAS:myc-notch1a-intra as effector, we determined quantitatively the kinetics of expression of both transgenes and analysed the effects of varying their expressivity on several phenotypic traits in the developing zebrafish. hsp70:Gal4 is transcribed within 15 min after temperature-mediated induction, but Gal4 RNA decays rapidly. The Gal4 protein was found to be quite stable, as functional Gal4, which was detectable 1.5 h after heat shock HS, persisted for at least 13 h, myc-notch1a-intra RNA is expressed approximately 1.5 h after HS, but unlike the Gal4 RNA, it was found to be very stable; it continues to accumulate during the succeeding 17 h after HS. Fully penetrant phenotypic effects are obtained after a relatively long activator induction with a 30-min HS. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 14
页数:6
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