Genetic analysis of α-synuclein 3′ untranslated region and its corresponding microRNAs in relation to Parkinson's disease compared to dementia with Lewy bodies

被引:25
作者
Tagliafierro, Lidia [1 ,2 ]
Glenn, Omolara-Chinue [1 ,2 ]
Zamora, Madison E. [1 ,2 ]
Beach, Thomas G. [3 ]
Woltjer, Randy L. [4 ]
Lutz, Michael W. [1 ]
Chiba-Falek, Ornit [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Dept Neurol, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Ctr Genom & Computat Biol, Durham, NC 27708 USA
[3] Banner Sun Hlth Res Inst, Sun City, AZ USA
[4] Oregon Hlth & Sci Univ, Dept Pathol, Layton Aging & Alzheimers Dis Ctr, Portland, OR 97201 USA
基金
美国国家卫生研究院;
关键词
SNCA; DLB; PD; miRNA; iPSC-derived neurons; SNCA 3 ' UTR; ALZHEIMERS-DISEASE; COMMON VARIANTS; BASAL FOREBRAIN; EXPRESSION; SNCA; PATHOLOGY; DYSFUNCTION; BINDING; RISK; NEURODEGENERATION;
D O I
10.1016/j.jalz.2017.03.001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The alpha-synuclein (SNCA) gene has been implicated in the etiology of Parkinson's disease (PD) and dementia with Lewy bodies (DLB). Methods: A computational analysis of SNCA 3' untranslated region to identify potential microRNA (miRNA) binding sites and quantitative real-time polymerase chain reaction (PCR) to determine their expression in isogenic induced pluripotent stem cell-derived dopaminergic and cholinergic neurons as a model of PD and DLB, respectively, were performed. In addition, we performed a deep sequencing analysis of the SNCA 3' untranslated region of autopsy-confirmed cases of PD, DLB, and normal controls, followed by genetic association analysis of the identified variants. Results: We identified four miRNA binding sites and observed a neuronal-type-specific expression profile for each miRNA in the different isogenic induced pluripotent stem cell-derived dopaminergic and cholinergic neurons. Furthermore, we found that the short structural variant rs777296100-polyT was moderately associated with DLB but not with PD. Discussion: We suggest that the regulation of SNCA expression through miRNAs is neuronal-type-specific and possibly plays a part in the phenotypic heterogeneity of synucleinopathies. Furthermore, genetic variability in the SNCA gene may contribute to synucleinopathies in a pathology-specific manner. (C) 2017 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1237 / 1250
页数:14
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