Abstract
Targeted gene expression is a powerful tool for understanding gene function in vivo. In zebrafish, over-expression of gene products is typically accomplished ubiquitously, without temporal and spatial specificity. However, the yeast Gal4/UAS system can be used for targeted gene expression in zebrafish. Here we describe the generation and characterization of Tg[gsc: Gal4-VP16] transgenic zebrafish lines that harbor a construct encoding Gal4-VP16 transcriptional activator under the control of a fragment of the goosecoid gene promoter. Tg[gsc:Gal4-VP16] embryos express Gal4-VP16 RNA in presumptive prechordal plate mesendoderm during late blastula and throughout gastrulation. By crossing these fish to Tg[UAS-GFP] transgenic fish, we show that the gsc:Gal4-VP16 transgene is capable of driving strong expression of a target gene in the prechordal plate and its derivatives during gastrulation and segmentation. Thus, the use of Tg[gsc:Gal4-VP16] fish can help in understanding gene function in the prechordal plate, an embryonic structure that is crucial for normal neural patterning.
Original language | English (US) |
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Pages (from-to) | 584-588 |
Number of pages | 5 |
Journal | Genesis |
Volume | 44 |
Issue number | 12 |
DOIs | |
State | Published - Dec 2006 |
Keywords
- GFP
- Gal4-VP16
- Goosecoid
- UAS
ASJC Scopus subject areas
- Genetics
- Endocrinology
- Cell Biology