| Literature DB >> 25541488 |
Savan Kabaria1, Doo Chul Choi1, Amrita Datta Chaudhuri1, M Maral Mouradian1, Eunsung Junn2.
Abstract
Mounting evidence suggests that microRNA (miR) dysregulation contributes to neurodegenerative disorders including Parkinson's disease (PD). MiR-34b and miR-34c have been previously shown to be down-regulated in the brains of patients with PD. Here, we demonstrate that miR-34b and miR-34c repress the expression of α-synuclein (α-syn), a key protein in PD pathogenesis. Inhibition of miR-34b and miR-34c expression in human dopaminergic SH-SY5Y cells increased α-syn levels and stimulated aggregate formation. Additionally, a single nucleotide polymorphism (SNP) in the 3'-UTR of α-syn was found to lower the miR-34b-mediated repression of the protein. Our results suggest that down-regulation of miR-34b and miR-34c in the brain, as well as an SNP in the 3'-UTR of α-syn can increase α-syn expression, possibly contributing to PD pathogenesis.Entities:
Keywords: Parkinson’s disease; microRNA-34b; microRNA-34c; α-Synuclein
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Year: 2014 PMID: 25541488 PMCID: PMC4306645 DOI: 10.1016/j.febslet.2014.12.014
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124