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首页> 外文期刊>Journal of biomolecular screening: The official journal of the Society for Biomolecular Screening >Development of a high-throughput gaussia luciferase reporter assay for the activation of the GADD45a gene by mutagens, promutagens, clastogens, and aneugens
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Development of a high-throughput gaussia luciferase reporter assay for the activation of the GADD45a gene by mutagens, promutagens, clastogens, and aneugens

机译:高通量高斯荧光素酶报告基因检测试剂盒的开发,可通过诱变剂,促突变素,clastogens和agengens激活GADD45a基因

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摘要

Exposure to genotoxic carcinogens leads to increased expression of the GADD45a gene in mammalian cells. This signature of genotoxic hazard has previously been exploited in the GreenScreen HC assay, in which GADD45a expression is linked to green fluorescent protein (GFP) expression in the human TK6 lymphoblastoid cell line. This article describes the development and validation of an alternative assay ("BlueScreen HC"), in which expression is linked to Gaussia luciferase (GLuc) expression, yielding a luminescent reporter, the preferred optical output in high-throughput screening. The coelentrazine substrate of GLuc is relatively unstable, and a new buffer is reported that improves its stability. A more sensitive method is demonstrated for the measurement of cell densities in the assay, using the fluorescent cyanine dye thiazole orange. A protocol amendment also allows the assessment of pro-genotoxicity using S9 liver extracts. Compounds from the European Centre for the Validation of Alternative Methods (ECVAM) recommended list for the assessment of new or improved genotoxicity assays were evaluated with and without S9 in the new assay. The new GLuc assay was as effective as the GFP assay in producing positive results for all classes of genotoxic carcinogen and negative results for all nongenotoxins tested.
机译:暴露于遗传毒性致癌物会导致GADD45a基因在哺乳动物细胞中的表达增加。这种遗传毒性危害的特征先前已在GreenScreen HC分析中得到了利用,其中GADD45a表达与人TK6淋巴母细胞系中的绿色荧光蛋白(GFP)表达相关。本文介绍了另一种测定方法(“ BlueScreen HC”)的开发和验证,该方法的表达与高斯荧光素酶(GLuc)的表达有关,从而产生发光的报告基因,这是高通量筛选中的首选光学输出。 GLuc的腔肠素底物相对不稳定,据报道有新的缓冲液可改善其稳定性。使用荧光花青染料噻唑橙,证明了一种更灵敏的方法可用于测定细胞密度。方案修正案还允许使用S9肝提取物评估前遗传毒性。来自欧洲替代方法验证中心(ECVAM)推荐的清单,用于评估新的或改良的遗传毒性试验,并在新试验中使用S9和不使用S9进行了评估。对于所有种类的遗传毒性致癌物,新的GLuc测定与GFP测定一样有效,而对于所有测试的非基因毒素,则产生阴性结果。

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