Abstract

The transcriptome at the synapse consists of thousands of messengers encoding several cellular functions, including a significant number of receptors and ion channels and associated proteins. The concerted translational regulation of all these molecules contributes to the dynamic control of synaptic strength. Cumulative evidence supports that dendritic RNA granules and mRNA-silencing foci play an important role in translational regulation. Several relevant RBPs – FMRP; FUS/TLS; TDP-43; Staufen; Smaug; Pumilio; CPEB; HuD; ZBP1; and DDX6 among others – form granules that contain dormant mRNAs repressed by multiple pathways. Recent reports indicate that dendritic granules may contain stalled polysomes, and furthermore, active translation may occur in association with RNA granules. Here, we discuss the molecules and pathways involved in this continuum of RNA granules that contain masked mRNAs, mRNAs trapped in inactive polysomes or mRNAs engaged in translation.

Highlights

  • The transcriptome at the synapse comprises thousands of messengers encoding highly diverse proteins, which include an important proportion of the receptors and ion channels that modulate synaptic plasticity

  • The processing bodies (PBs) are ubiquitous mRNA-silencing foci and specialized assemblies are formed under specific conditions, as for example the stress granules (SGs), which are induced upon cellular stress (Mitchell and Parker, 2014; Thomas et al, 2014)

  • Recent work identified a novel type of mRNA silencing foci that contain the repressor Smaug1/Samd4a and that are different from PBs

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Summary

Introduction

The transcriptome at the synapse comprises thousands of messengers encoding highly diverse proteins, which include an important proportion of the receptors and ion channels that modulate synaptic plasticity. Dendritic RNA granules may contain stalled polysomes, allowing a fast resuming of protein production RNA granules may dissolve completely to release transcripts or restructure to allow mRNA translation at their periphery, as discussed below (Figure 1).

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Conclusion

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