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Philos Trans R Soc Lond B Biol Sci. 2014 Sep 26;369(1652). pii: 20130504. doi: 10.1098/rstb.2013.0504.

The RNA-centred view of the synapse: non-coding RNAs and synaptic plasticity.

Author information

1
Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612, USA neils@uic.edu.

Abstract

If mRNAs were the only RNAs made by a neuron, there would be a simple mapping of mRNAs to proteins. However, microRNAs and other non-coding RNAs (ncRNAs; endo-siRNAs, piRNAs, BC1, BC200, antisense and long ncRNAs, repeat-related transcripts, etc.) regulate mRNAs via effects on protein translation as well as transcriptional and epigenetic mechanisms. Not only are genes ON or OFF, but their ability to be translated can be turned ON or OFF at the level of synapses, supporting an enormous increase in information capacity. Here, I review evidence that ncRNAs are expressed pervasively within dendrites in mammalian brain; that some are activity-dependent and highly enriched near synapses; and that synaptic ncRNAs participate in plasticity responses including learning and memory. Ultimately, ncRNAs can be viewed as the post-it notes of the neuron. They have no literal meaning of their own, but derive their functions from where (and to what) they are stuck. This may explain, in part, why ncRNAs differ so dramatically from protein-coding genes, both in terms of the usual indicators of functionality and in terms of evolutionary constraints. ncRNAs do not appear to be direct mediators of synaptic transmission in the manner of neurotransmitters or receptors, yet they orchestrate synaptic plasticity-and may drive species-specific changes in cognition.

KEYWORDS:

microRNAs; non-coding RNAs; synaptic plasticity; transposable elements

PMID:
25135965
PMCID:
PMC4142025
DOI:
10.1098/rstb.2013.0504
[Indexed for MEDLINE]
Free PMC Article

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