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Development of a transient expression assay for detecting environmental oestrogens in zebrafish and medaka embryos

机译:开发用于检测斑马鱼和种子中环境雌激素的瞬时表达测定法的开发

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摘要

BackgroundOestrogenic contaminants are widespread in the aquatic environment and have been shown to induce adverse effects in both wildlife (most notably in fish) and humans, raising international concern. Available detecting and testing systems are limited in their capacity to elucidate oestrogen signalling pathways and physiological impacts. Here we developed a transient expression assay to investigate the effects of oestrogenic chemicals in fish early life stages and to identify target organs for oestrogenic effects. To enhance the response sensitivity to oestrogen, we adopted the use of multiple tandem oestrogen responsive elements (EREc38) in a Tol2 transposon mediated Gal4ff-UAS system. The plasmid constructed (pTol2_ERE-TATA-Gal4ff), contains three copies of oestrogen response elements (3ERE) that on exposure to oestrogen induces expression of Gal4ff which this in turn binds Gal4-responsive Upstream Activated Sequence (UAS) elements, driving the expression of a second reporter gene, EGFP (Enhanced Green Fluorescent Protein).
机译:背景雌激素污染物在水生环境中广泛存在,并已显示出对野生动植物(尤其是鱼类)和人类产生不利影响,引起了国际关注。可用的检测和测试系统阐明雌激素信号传导途径和生理影响的能力有限。在这里,我们开发了一种瞬时表达测定法,以研究鱼类中的雌激素化学物质在生命早期阶段的作用,并确定雌激素作用的靶器官。为了增强对雌激素的反应敏感性,我们在Tol2转座子介导的Gal4ff-UAS系统中采用了多个串联的雌激素反应元件(EREc38)。构建的质粒(pTol2_ERE-TATA-Gal4ff)包含三份雌激素反应元件(3ERE),暴露于雌激素时会诱导Gal4ff的表达,而后者又与Gal4反应上游激活序列(UAS)元件结合,从而驱动Gal4ff的表达第二个报告基因,EGFP(增强型绿色荧光蛋白)。

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