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首页> 外文期刊>藥學雜誌 >Visualization and evaluation of the promoter activities of genes for stress-inducible proteins in response to environmental pollutants
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Visualization and evaluation of the promoter activities of genes for stress-inducible proteins in response to environmental pollutants

机译:可视化和评估应激诱导蛋白响应环境污染物的基因启动子活性

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We examined the systematic assay of the reporter gene for the assessment of heavy metals and organic chemical pollutants using the reporter plasmids carrying stress-responsive elements fused to the green fluorescence protein (GFP) gene as follows: metallothionein (MTIIA), heme oxigenase-1 (HO-1), quinone reductase (ARE), and c-fos genes. The treatment of COS7 cells in which the c-fos gene promoter-, ARE-, or HO-1 enhancer-fused GFP with a low concentration of NaAsO(2) was introduced led to the detection of the fluorescent cells, and an agrichemical paraquat enhanced the fluorescence of ARE or HO-1 enhancer-transfected cells. The cells in which the plasmid carrying the MT-IIA gene promoter (the -765 bp upstream from the transcription initiation site) was introduced highly expressed GFP on treatment with CdCl(2), ZnSO(4), or CuCl(2). The plasmid carrying seven metal-responsive elements of the MT-IIA gene increased the response of the fluorescence intensity to these heavy metals. These results indicated that the use of the gene promoters and enhancers of the stress-responsive genes fused to GFP contributes to the visualization of pollutant-responsive mammalian cells and can be applied to biomonitoring of environmental pollution.
机译:我们使用携带与绿色荧光蛋白(GFP)基因融合的胁迫响应元件的报告质粒检查了报告基因的系统分析,以评估重金属和有机化学污染物,具体如下:金属硫蛋白(MTIIA),血红素产氧酶-1 (HO-1),醌还原酶(ARE)和c-fos基因。引入了具有低浓度NaAsO(2)的c-fos基因启动子,ARE-或HO-1增强子融合的GFP的COS7细胞的治疗导致了荧光细胞和农用百草枯的检测增强了ARE或HO-1增强子转染细胞的荧光。引入带有MT-IIA基因启动子(转录起始位点上游-765 bp)的质粒的细胞在用CdCl(2),ZnSO(4)或CuCl(2)处理后被高度表达GFP。带有MT-IIA基因的七个金属响应元件的质粒增加了荧光强度对这些重金属的响应。这些结果表明,与GFP融合的应激反应基因的基因启动子和增强子的使用有助于可视化污染物反应性哺乳动物细胞,并可用于环境污染的生物监测。

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