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Dev Cell. 2011 Mar 15;20(3):388-96. doi: 10.1016/j.devcel.2011.02.008.

Target-mediated protection of endogenous microRNAs in C. elegans.

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1
Friedrich Miescher Institute for Biomedical Research, P.O. Box 2543, CH-4002 Basel, Switzerland.

Abstract

MicroRNAs (miRNAs) are tightly regulated through transcriptional and posttranscriptional mechanisms, including degradation by nucleases. Here, we report that in C. elegans, target mRNAs can protect their cognate miRNAs from degradation in vivo. We show that the let-7(n2853) mutation destabilizes the mature let-7 miRNA by impairing this protection. Moreover, presence of a cognate target or depletion of the xrn-1 (XRN1) or xrn-2 (XRN2/Rat1p) exoribonucleases enforces accumulation of certain miRNA passenger (miR(∗)) strands. Thus, following biased miRNA strand loading into Argonaute, elimination of nonfunctional RNAs can further refine miRNA strand selection. Conversely, by aligning the levels of miRNAs with those of their targets, the opposing activities of mature miRNA degradation and target-mediated miRNA protection (TMMP) may enable dynamic expression of either mature strand of a pre-miRNA, and evolution of miRNAs. Thus, it seems that mRNAs are more than inert targets and function with miRNAs in a network of mutual regulation.

PMID:
21397849
DOI:
10.1016/j.devcel.2011.02.008
[Indexed for MEDLINE]
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