Stress-induced Reversal of microRNA repression and mRNA P-body localization in human cells

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Abstract

In metazoa, microRNAs (miRNAs) imperfectly base-pair with the 3′-untranslated region (3′UTR) of mRNAs and prevent protein accumulation by either repressing translation or inducing mRNA degradation. Examples of specific mRNAs undergoing miRNA-mediated repression are numerous, but whether the repression is a reversible process remains largely unknown. Here, we show that cationic amino acid transporter 1 (CAT-1) mRNA and reporters bearing the CAT-1 3′UTR or its fragments can be relieved from the miRNA miR-122-induced inhibition in human hepatoma cells in response to different stress conditions. The derepression of CAT-1 mRNA is accompanied by its release from cytoplasmic processing bodies (P bodies) and its recruitment to polysomes, indicating that P bodies act as storage sites for mRNAs inhibited by miRNAs. The derepression requires binding of HuR, an AU-rich-element-binding ELAV family protein, to the 3′UTR of CAT-1 mRNA. We propose that proteins interacting with the 3′UTR will generally act as modifiers altering the potential of miRNAs to repress gene expression. © 2006 Cold Spring Harbor Laboratory Press.

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Bhattacharyya, S. N., Habermacher, R., Martine, U., Closs, E. I., & Filipowicz, W. (2006). Stress-induced Reversal of microRNA repression and mRNA P-body localization in human cells. In Cold Spring Harbor Symposia on Quantitative Biology (Vol. 71, pp. 513–521). https://doi.org/10.1101/sqb.2006.71.038

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