MicroRNA degradation by a conserved target RNA regulates animal behavior

microRNAs (miRNAs) repress target transcripts through partial complementarity. By contrast, highly complementary miRNA-binding sites within viral and artificially engineered transcripts induce miRNA degradation in vitro and in cell lines. Here, we show that a genome-encoded transcript harboring a ne...

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Veröffentlicht in:Nature structural & molecular biology 2018-03, Vol.25 (3), p.244-251
Hauptverfasser: Bitetti, Angelo, Mallory, Allison C., Golini, Elisabetta, Carrieri, Claudia, Carreño Gutiérrez, Héctor, Perlas, Emerald, Pérez-Rico, Yuvia A., Tocchini-Valentini, Glauco P., Enright, Anton J., Norton, William H. J., Mandillo, Silvia, O’Carroll, Dónal, Shkumatava, Alena
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Sprache:eng
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Zusammenfassung:microRNAs (miRNAs) repress target transcripts through partial complementarity. By contrast, highly complementary miRNA-binding sites within viral and artificially engineered transcripts induce miRNA degradation in vitro and in cell lines. Here, we show that a genome-encoded transcript harboring a near-perfect and deeply conserved miRNA-binding site for miR-29 controls zebrafish and mouse behavior. This transcript originated in basal vertebrates as a long noncoding RNA (lncRNA) and evolved to the protein-coding gene NREP in mammals, where the miR-29-binding site is located within the 3′ UTR. We show that the near-perfect miRNA site selectively triggers miR-29b destabilization through 3′ trimming and restricts its spatial expression in the cerebellum. Genetic disruption of the miR-29 site within mouse Nrep results in ectopic expression of cerebellar miR-29b and impaired coordination and motor learning. Thus, we demonstrate an endogenous target-RNA-directed miRNA degradation event and its requirement for animal behavior. RNA-directed miRNA degradation triggered by a brain-specific genome-encoded transcript regulates explorative and anxiety-like behavior in zebrafish and affects balance and motor learning in mice.
ISSN:1545-9993
1545-9985
DOI:10.1038/s41594-018-0032-x