[HTML][HTML] Relief of microRNA-mediated translational repression in human cells subjected to stress

SN Bhattacharyya, R Habermacher, U Martine… - Cell, 2006 - cell.com
SN Bhattacharyya, R Habermacher, U Martine, EI Closs, W Filipowicz
Cell, 2006cell.com
In metazoans, most microRNAs imperfectly base-pair with the 3′ untranslated region (3′
UTR) of target mRNAs and prevent protein accumulation by either repressing translation or
inducing mRNA degradation. Examples of specific mRNAs undergoing microRNA-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 its 3′ UTR can be relieved from the microRNA miR-122-induced inhibition in …
Summary
In metazoans, most microRNAs imperfectly base-pair with the 3′ untranslated region (3′UTR) of target mRNAs and prevent protein accumulation by either repressing translation or inducing mRNA degradation. Examples of specific mRNAs undergoing microRNA-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 its 3′UTR can be relieved from the microRNA miR-122-induced inhibition in human hepatocarcinoma cells subjected to different stress conditions. The derepression of CAT-1 mRNA is accompanied by its release from cytoplasmic processing bodies and its recruitment to polysomes. The derepression requires binding of HuR, an AU-rich-element binding 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.
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