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• W2052108496 abstract "RNA-protein interactions are pivotal in fundamental cellular processes such as translation, mRNA processing, early development, and infection by RNA viruses. However, in spite of the central importance of these interactions, few approaches are available to analyze them rapidly in vivo. We describe a yeast genetic method to detect and analyze RNA-protein interactions in which the binding of a bifunctional RNA to each of two hybrid proteins activates transcription of a reporter gene in vivo. We demonstrate that this three-hybrid system enables the rapid, phenotypic detection of specific RNA-protein interactions. As examples, we use the binding of the iron regulatory protein 1 (IRP1) to the iron response element (IRE), and of HIV trans-activator protein (Tat) to the HIV trans-activation response element (TAR) RNA sequence. The three-hybrid assay we describe relies only on the physical properties of the RNA and protein, and not on their natural biological activities; as a result, it may have broad application in the identification of RNA-binding proteins and RNAs, as well as in the detailed analysis of their interactions." @default.
• W2052108496 created "2016-06-24" @default.
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• W2052108496 date "1996-08-06" @default.
• W2052108496 modified "2023-10-16" @default.
• W2052108496 title "A three-hybrid system to detect RNA-protein interactions in vivo." @default.
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• W2052108496 doi "https://doi.org/10.1073/pnas.93.16.8496" @default.
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