Post-transcriptional Regulation of α-Synuclein Expression by mir-7 and mir-153

被引:392
作者
Doxakis, Epaminondas [1 ]
机构
[1] Acad Athens, Basic Neurosci Div, Biomed Res Fdn, Athens 11527, Greece
关键词
PARKINSONS-DISEASE; GENE-EXPRESSION; MESSENGER-RNAS; MICRORNAS; TARGET; AGGREGATION; DEGRADATION; AUTOPHAGY; INSIGHTS; MONKEYS;
D O I
10.1074/jbc.M109.086827
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genetic and biochemical studies have established a central role for alpha-synuclein accumulation in the pathogenesis of Parkinson disease. Here, two microRNAs, namely mir-7 and mir-153, have been identified to regulate alpha-synuclein levels post-transcriptionally. These microRNAs bind specifically to the 3'-untranslated region of alpha-synuclein and down-regulate its mRNA and protein levels, with their effect being additive. They are expressed predominantly in the brain with a pattern that mirrors synuclein expression in different tissues as well as during neuronal development, indicating that they play a tuning role in the amount of alpha-synuclein produced. Overexpression of mir-7 and mir-153 significantly reduces endogenous alpha-synuclein levels, whereas inhibition of mir-7 and mir-153 enhances translation of a luciferase construct bearing the alpha-synuclein 3'-untranslated region in primary neurons. These findings reveal a significant additional mechanism by which alpha-synuclein is regulated and point toward new therapeutic regimes for lowering endogenous alpha-synuclein levels in patients with familial or sporadic Parkinson disease.
引用
收藏
页码:12726 / 12734
页数:9
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