Enhancer trapping with a red fluorescent protein reporter in Drosophila

被引:12
作者
Akimoto, A
Wada, H
Hayashi, S
机构
[1] RIKEN, Ctr Dev Biol, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Kobe Univ, Grad Sch Sci & Technol, Dept Life Sci, Kobe, Hyogo 657, Japan
关键词
enhancer trap; DsRed; Drosophila;
D O I
10.1002/dvdy.20439
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
Enhancer trapping allows the detection of genomic transcriptional enhancers and provides a rich source of cell- and region-specific markers in Drosophila. We report here the development of a P-element-based enhancer-trap vector with a nuclear red fluorescent protein (DsRed) reporter for enhancer detection. We demonstrate that this vector can be used for a standard enhancer-trap screen as well as for targeted replacement of previously characterized P-element insertions. We isolated DsRed insertion strains of hedgehog, patched, apterous, teashirt, and dachshund that label specific regions of imaginal discs. The time required for red fluorescence maturation in the eye imaginal disc was estimated to be 22.5 hr. The DsRed markers can be combined with green fluorescent protein markers for double labeling of living Drosophila tissues. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:993 / 997
页数:5
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