Zenklusen Daniel, Singer Robert H
Department of Anatomy and Structural Biology and The Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, New York, USA.
Methods Enzymol. 2010;470:641-59. doi: 10.1016/S0076-6879(10)70026-4. Epub 2010 Mar 1.
As the product of transcription and the blueprint for translation, mRNA is the main intermediate product of the gene expression pathway. The ability to accurately determine mRNA levels is, therefore, a major requirement when studying gene expression. mRNA is also a target of different regulatory steps, occurring in different subcellular compartments. To understand the different steps of gene expression regulation, it is therefore essential to analyze mRNA in the context of a single cell, maintaining spatial information. Here, we describe a stepwise protocol for fluorescent in situ hybridization (FISH) that allows detection of individual mRNAs in single yeast cells. This method allows quantitative analysis of mRNA expression in single cells, permitting "absolute" quantification by simply counting mRNAs. It further allows us to study many aspects of mRNA metabolism, from transcription to processing, localization, and mRNA degradation.
作为转录产物和翻译蓝图,mRNA是基因表达途径的主要中间产物。因此,在研究基因表达时,准确测定mRNA水平的能力是一项主要要求。mRNA也是发生在不同亚细胞区室的不同调控步骤的靶点。因此,为了理解基因表达调控的不同步骤,在保持空间信息的单细胞背景下分析mRNA至关重要。在这里,我们描述了一种用于荧光原位杂交(FISH)的逐步方案,该方案允许在单个酵母细胞中检测单个mRNA。这种方法允许对单细胞中的mRNA表达进行定量分析,通过简单地计数mRNA实现“绝对”定量。它还使我们能够研究mRNA代谢从转录到加工、定位和mRNA降解的许多方面。