Affinity purification of binding miRNAs for messenger RNA fused with a common tag

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Abstract

Prediction of microRNA-mRNA interaction typically relies on bioinformatic methods, but these methods only suggest the possibility of microRNA binding and may miss important interactions as well as falsely predict others. A major obstacle to the miRNA research has been the lack of experimental procedures for the identification of miRNA-mRNA interactions. Recently, a few studies have attempted to explore experimental methods to isolate and identify miRNA targets or miRNAs targeting a single gene. Here, we developed an more convenient experimental approach for the isolation and identification of miRNAs targeting a single gene by applying short biotinylated DNA anti-sense oligonucleotides mix to enhanced green fluorescent protein (EGFP) mRNA which was fused to target gene mRNA. This method does not require a design of differentanti-sense oligonucleotides to any mRNA. This is a simple and an efficient method to potentially identify miRNAs targeting specific gene mRNA combined with chip screen. © 2014 by the authors; licensee MDPI, Basel, Switzerland.

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Wei, K., Yan, F., Xiao, H., Yang, X., Xie, G., Xiao, Y., … Xiang, S. (2014). Affinity purification of binding miRNAs for messenger RNA fused with a common tag. International Journal of Molecular Sciences, 15(8), 14753–14765. https://doi.org/10.3390/ijms150814753

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