Querido Emmanuelle, Chartrand Pascal
Département de Biochimie, Université de Montréal, 2900 Edouard-Montpetit, Montréal, Québec H3C 3J7, Canada.
Methods Cell Biol. 2008;85:273-92. doi: 10.1016/S0091-679X(08)85012-1.
This chapter presents the MS2-GFP system, a method to study the trafficking of RNA molecules in living cells. This system is based on two components: a fusion of the MS2 coat protein to a fluorescent protein and a reporter mRNA containing multimers of the RNA stem-loop recognized by the MS2 coat protein. The MS2-GFP protein bound to the RNA stem-loops acts as a beacon that allows the detection of this mRNA within a cell by epifluorescence or confocal microscopy. This chapter focuses on the use of this system in mammalian fibroblast cells and in yeast cells, and discusses several technical considerations of the MS2-GFP system. Detailed protocols for validating the MS2-GFP signal in fixed cells by fluorescent in situ hybridization of the target RNA using fluorophore-labeled oligonucleotide probes are also provided.
本章介绍了MS2-GFP系统,这是一种研究活细胞中RNA分子运输的方法。该系统基于两个组件:MS2外壳蛋白与荧光蛋白的融合体,以及含有被MS2外壳蛋白识别的RNA茎环多聚体的报告mRNA。与RNA茎环结合的MS2-GFP蛋白充当信标,通过落射荧光或共聚焦显微镜在细胞内检测该mRNA。本章重点介绍该系统在哺乳动物成纤维细胞和酵母细胞中的应用,并讨论了MS2-GFP系统的几个技术要点。还提供了使用荧光团标记的寡核苷酸探针通过靶RNA的荧光原位杂交在固定细胞中验证MS2-GFP信号的详细方案。