Impact of MicroRNA Levels, Target-Site Complementarity, and Cooperativity on Competing Endogenous RNA-Regulated Gene Expression

Expression changes of competing endogenous RNAs (ceRNAs) have been proposed to influence microRNA (miRNA) activity and thereby regulate other transcripts containing miRNA-binding sites. Here, we find that although miRNA levels define the extent of repression, they have little effect on the magnitude...

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Bibliographic Details
Main Authors: Denzler, Rémy, Title, Alexandra C., Stoffel, Markus, McGeary, Sean Edward, Agarwal, Vikram, Bartel, David
Other Authors: Massachusetts Institute of Technology. Computational and Systems Biology Program
Format: Article
Published: Elsevier BV 2018
Online Access:http://hdl.handle.net/1721.1/116299
https://orcid.org/0000-0001-5343-6447
https://orcid.org/0000-0001-8148-952X
https://orcid.org/0000-0002-3872-2856
Description
Summary:Expression changes of competing endogenous RNAs (ceRNAs) have been proposed to influence microRNA (miRNA) activity and thereby regulate other transcripts containing miRNA-binding sites. Here, we find that although miRNA levels define the extent of repression, they have little effect on the magnitude of the ceRNA expression change required to observe derepression. Canonical 6-nt sites, which typically mediate modest repression, can nonetheless compete for miRNA binding, with potency ∼20% of that observed for canonical 8-nt sites. In aggregate, low-affinity/background sites also contribute to competition. Sites with extensive additional complementarity can appear as more potent, but only because they induce miRNA degradation. Cooperative binding of proximal sites for the same or different miRNAs does increase potency. These results provide quantitative insights into the stoichiometric relationship between miRNAs and target abundance, target-site spacing, and affinity requirements for ceRNA-mediated gene regulation, and the unusual circumstances in which ceRNA-mediated gene regulation might be observed. Keywords: competing endogenous RNA; miRNA; target abundance; cooperatively; gene regulation; base pair complementarity; miRNA degradation