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Cold Spring Harbor Laboratory Press, RNA, 11(15), p. 2063-2071, 2009

DOI: 10.1261/rna.1678209

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In vivo detection of RNA-binding protein interactions with cognate RNA sequences by fluorescence resonance energy transfer

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Expression of the nascent RNA transcript is regulated by its interaction with a number of proteins. The misregulation of such interactions can often result in impaired cellular functions that can lead to cancer and a number of diseases. Thus, our understanding of RNA–protein interactions within the cellular context is essential for the development of novel diagnostic and therapeutic tools. While there are many in vitro methods that analyze RNA–protein interactions in vivo approaches are scarce. Here we established a method based on fluorescence resonance energy transfer (FRET), which we term RNA-binding mediated FRET (RB-FRET), which determines RNA–protein interaction inside cells and tested it on hnRNP H protein binding to its cognate RNA. Using two different approaches, we provide evidence that RB-FRET is sensitive enough to detect specific RNA–protein interactions in the cell, providing a powerful tool to study spatial and temporal localization of specific RNA–protein complexes.