| Literature DB >> 27180071 |
Aron Kos1,2, Teun Klein-Gunnewiek1,2, Julia Meinhardt1,2, Nikkie F M Olde Loohuis1,2, Hans van Bokhoven1,2,3, Barry B Kaplan4, Gerard J Martens2,5, Sharon M Kolk2,5, Armaz Aschrafi6,7.
Abstract
MicroRNAs (miRs) are small non-coding RNAs that confer robustness to gene networks through post-transcriptional gene regulation. Previously, we identified miR-338 as a modulator of axonal outgrowth in sympathetic neurons. In the current study, we examined the role of miR-338 in the development of cortical neurons and uncovered its downstream mRNA targets. Long-term inhibition of miR-338 during neuronal differentiation resulted in reduced dendritic complexity and altered dendritic spine morphology. Furthermore, monitoring axon outgrowth in cortical cells revealed that miR-338 overexpression decreased, whereas inhibition of miR-338 increased axonal length. To identify gene targets mediating the observed phenotype, we inhibited miR-338 in cortical neurons and performed whole-transcriptome analysis. Pathway analysis revealed that miR-338 modulates a subset of transcripts involved in the axonal guidance machinery by means of direct and indirect gene targeting. Collectively, our results implicate miR-338 as a novel regulator of cortical neuronal maturation by fine-tuning the expression of gene networks governing cortical outgrowth.Entities:
Keywords: Cortex; MicroRNA; Neurite development; Neurodevelopment; Robo2
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Year: 2016 PMID: 27180071 PMCID: PMC5658782 DOI: 10.1007/s12035-016-9925-z
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590