Park H M, Okumura J, Muramatsu T
Laboratory of Animal Nutrition, School of Agricultural Sciences, Nagoya University, Japan.
Biochem Mol Biol Int. 1995 Jul;36(4):811-6.
With primary cultures of chicken oviduct cells, we tested functional roles in the ovalbumin gene transcription of NF-1 like factor binding element, half estrogen-response-element direct repeat, and chicken ovalbumin upstream promoter residing in the 5'-flanking region of the chicken ovalbumin gene. The three putative regulatory elements were fused upstream to the chloramphencol acetyltransferase reporter gene driven by the chicken ovalbumin gene promoters, and transient gene expression was measured in primary cultured oviduct cells. The results indicated that neither the NF1 binding element nor the ovalbumin upstream promoter showed any enhancer-like activity. In addition, although the half estrogen response element direct repeat enhanced transcriptional activity of the ovalbumin gene promoter, it completely deprived the ovalbumin promoter of estrogen dependency. We concluded, therefore, that the biological significance of these three putative regulatory elements in the homologous chicken oviduct cell system might be different from those previously reported in heterologous systems.
利用鸡输卵管细胞的原代培养物,我们测试了鸡卵清蛋白基因5′侧翼区域中类NF-1因子结合元件、半雌激素反应元件直接重复序列以及鸡卵清蛋白上游启动子在卵清蛋白基因转录中的功能作用。将这三个假定的调控元件融合到由鸡卵清蛋白基因启动子驱动的氯霉素乙酰转移酶报告基因的上游,并在原代培养的输卵管细胞中测量瞬时基因表达。结果表明,NF1结合元件和卵清蛋白上游启动子均未显示出任何增强子样活性。此外,虽然半雌激素反应元件直接重复序列增强了卵清蛋白基因启动子的转录活性,但它完全剥夺了卵清蛋白启动子的雌激素依赖性。因此,我们得出结论,在同源鸡输卵管细胞系统中,这三个假定调控元件的生物学意义可能与先前在异源系统中报道的不同。