Literature DB >> 20946829

Analyzing mRNA expression using single mRNA resolution fluorescent in situ hybridization.

Daniel Zenklusen1, Robert H Singer.   

Abstract

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.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20946829      PMCID: PMC3162037          DOI: 10.1016/S0076-6879(10)70026-4

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


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  28 in total

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10.  Protein aggregation behavior regulates cyclin transcript localization and cell-cycle control.

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