二聚体西兰花在活细菌和哺乳动物细胞中的RNA成像

Q3 Biochemistry, Genetics and Molecular Biology
Grigory S. Filonov, Samie R. Jaffrey
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引用次数: 41

摘要

RNA空间动力学在细胞生理学中起着至关重要的作用,因此监测活细胞中RNA定位的能力可以为重要的生物学问题提供见解。本单元着重于使用GFP的RNA模拟物对RNA进行成像。这种方法依赖于一种叫做二聚体西兰花的RNA适体,它结合并打开DFHBI的荧光,DFHBI是一种模仿绿色荧光蛋白中的荧光团的小分子。二聚体西兰花被标记到异源表达的rna上,在与DFHBI结合后,二聚体西兰花的荧光信号报告了转录物在细胞中的定位。本方案描述了在体外和细胞中验证二聚体西兰花标记转录本的荧光,流式细胞术分析以确定细胞中的总体荧光水平,以及细菌和哺乳动物细胞的荧光成像过程。总的来说,该方案对于寻求高丰度rna成像的研究人员应该是有用的,例如那些从细菌中的T7启动子转录的rna或从哺乳动物细胞中的Pol III -依赖性启动子转录的rna。©2016 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA Imaging with Dimeric Broccoli in Live Bacterial and Mammalian Cells

RNA spatial dynamics play a crucial role in cell physiology, and thus the ability to monitor RNA localization in live cells can provide insight into important biological problems. This unit focuses on imaging RNAs using an RNA mimic of GFP. This approach relies on an RNA aptamer called dimeric Broccoli, which binds to and switches on the fluorescence of DFHBI, a small molecule mimicking the fluorophore in GFP. Dimeric Broccoli is tagged to heterologously expressed RNAs and, upon DFHBI binding, the fluorescent signal of dimeric Broccoli reports the transcript's localization in cells. This protocol describes the process of validating the fluorescence of dimeric Broccoli−labeled transcripts in vitro and in cells, flow cytometry analysis to determine overall fluorescence levels in cells, and fluorescence imaging in bacterial and mammalian cells. Overall, the protocol should be useful for researchers seeking to image high-abundance RNAs, such as those transcribed off the T7 promoter in bacteria or off Pol III−dependent promoters in mammalian cells. © 2016 by John Wiley & Sons, Inc.

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Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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