Even Dan Y, Kedmi Adi, Ideses Diana, Juven-Gershon Tamar
The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Life Sciences Building (212) Room 102, Ramat-Gan, Israel.
Methods Mol Biol. 2017;1651:77-91. doi: 10.1007/978-1-4939-7223-4_7.
The core promoter is the DNA sequence that recruits the basal transcription machinery and directs accurate initiation of transcription. It is an active contributor to gene expression that can be rationally designed to manipulate the levels of expression. Core promoter function can be analyzed using different experimental approaches. Here, we describe the qualitative and quantitative analysis of engineered core promoter functions using the EGFP reporter gene that is driven by distinct core promoters. Expression plasmids are transfected into different mammalian cell lines, and the resulting fluorescence is monitored by live cell imaging , as well as by flow cytometry. In order to verify that the transcriptional activity of the examined core promoters is indeed a function of their activity, as opposed to differences in DNA uptake, real-time quantitative PCR analysis is performed. Importantly, the described methodology for functional screening of core promoter activity has enabled the analysis of engineered potent core promoters for extended time periods.
核心启动子是招募基础转录机制并指导准确转录起始的DNA序列。它是基因表达的积极贡献者,可通过合理设计来操纵表达水平。核心启动子功能可使用不同的实验方法进行分析。在此,我们描述了使用由不同核心启动子驱动的EGFP报告基因对工程化核心启动子功能进行定性和定量分析。将表达质粒转染到不同的哺乳动物细胞系中,并通过活细胞成像以及流式细胞术监测产生的荧光。为了验证所检测核心启动子的转录活性确实是其活性的函数,而非DNA摄取差异,进行实时定量PCR分析。重要的是,所描述的核心启动子活性功能筛选方法能够长时间分析工程化的强效核心启动子。