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Activity of the medaka translation elongation factor 1α-A promoter examined using the GFP gene as a reporter
Article first published online: 25 DEC 2001
Development, Growth & Differentiation
Volume 42, Issue 5, pages 469–478, October 2000
How to Cite
Kinoshita, M., Kani, S., Ozato, K. and Wakamatsu, Y. (2000), Activity of the medaka translation elongation factor 1α-A promoter examined using the GFP gene as a reporter. Development, Growth & Differentiation, 42: 469–478. doi: 10.1046/j.1440-169x.2000.00530.x
- Issue published online: 25 DEC 2001
- Article first published online: 25 DEC 2001
- green fluorescent protein;
- maternal factors;
The translation elongation factor 1α (EF-1α) is known to have several isoforms, which are expressed in a tissue- and stage-specific manner. Two genes encoding EF-1α exist per haploid genome in the medaka. In the present study, the promoter activity of the 5′-flanking region of the medaka EF-1α-A gene, an isoform of EF-1α, was characterized using transgenic techniques. First, using CAT gene as a reporter, it was revealed that about 1.8 kbp 5′-flanking sequence from the transcription initiation site of EF-1α-A was sufficient for high-level promoter activity. Second, the green fluorescent protein (GFP) gene fused to this region was introduced into medaka eggs using the microinjection method. Three germline transgenic individuals (one male and two female) were mated with non-transgenic medaka to obtain F1 offspring. In the case of embryonic and adult F1 transgenic individuals, GFP fluorescence was observed in almost all the tissues examined (e.g. kidney, liver, heart, gill, ovary, and testis), except for the skeletal muscle. In the case of F2 transgenic embryos derived from F1 transgenic males and non-transgenic females, the fluorescence was observed from the early gastrula stage. On the other hand, in the case of F2 transgenic embryos derived from F1 transgenic females and non-transgenic males, the fluorescence was observed even at the 1-cell stage, suggesting that this region is transcriptionally active during oogenesis. The usefulness of the EF-1α-A promoter as a tool for introducing foreign proteins into oocytes is discussed.