Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10870527 | FEBS Letters | 2015 | 7 Pages |
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 3â²-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 3â²-UTR of α-syn can increase α-syn expression, possibly contributing to PD pathogenesis.
Keywords
Related Topics
Life Sciences
Agricultural and Biological Sciences
Plant Science
Authors
Savan Kabaria, Doo Chul Choi, Amrita Datta Chaudhuri, M. Maral Mouradian, Eunsung Junn,