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Unique Reporter-Based Sensor Platforms to Monitor Signalling in Cells

机译:独特的基于报告器的传感器平台,用于监控单元中的信号

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摘要

Introduction: In recent years much progress has been made in the development of tools for systems biology to study the levels of mRNA and protein, and their interactions within cells. However, few multiplexed methodologies are available to study cell signalling directly at the transcription factor level. Methods: Here we describe a sensitive, plasmid-based RNA reporter methodology to study transcription factor activation in mammalian cells, and apply this technology to profiling 60 transcription factors in parallel. The methodology uses two robust and easily accessible detection platforms; quantitative real-time PCR for quantitative analysis and DNA microarrays for parallel, higher throughput analysis. Findings: We test the specificity of the detection platforms with ten inducers and independently validate the transcription factor activation. Conclusions: We report a methodology for the multiplexed study of transcription factor activation in mammalian cells that is direct and not theoretically limited by the number of available reporters.
机译:简介:近年来,在开发用于研究mRNA和蛋白质水平及其在细胞内相互作用的系统生物学工具方面已取得了很大进展。但是,很少有多重方法可用于直接在转录因子水平上研究细胞信号传导。方法:在这里,我们描述了一种敏感的,基于质粒的RNA报告基因方法,用于研究哺乳动物细胞中的转录因子激活,并将这项技术应用于并行分析60个转录因子。该方法使用两个强大且易于访问的检测平台;用于定量分析的定量实时PCR和用于并行,更高通量分析的DNA微阵列。发现:我们用十种诱导剂测试检测平台的特异性,并独立验证转录因子的激活。结论:我们报道了一种在哺乳动物细胞中对转录因子激活进行多重研究的方法,该方法是直接的,并且在理论上不受可用报道分子数量的限制。

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