The miRNome of Alzheimer's disease: consistent downregulation of the miR-132/212 cluster

被引:88
|
作者
Pichler, Sabrina [1 ]
Gu, Wei [1 ,2 ]
Hartl, Daniela [1 ]
Gasparoni, Gilles [1 ]
Leidinger, Petra [3 ]
Keller, Andreas [4 ]
Meese, Eckart [3 ]
Mayhaus, Manuel [1 ]
Hampel, Harald [5 ,6 ,7 ,8 ]
Riemenschneider, Matthias [1 ,9 ]
机构
[1] Univ Saarland, Dept Psychiat & Psychotherapy, Neurobiol Lab, Kirrberger Str 1, D-66421 Homburg, Germany
[2] Univ Luxembourg, LCSB, Esch Belval, Luxembourg
[3] Univ Saarland, Dept Human Genet, Homburg, Germany
[4] Univ Saarland, Chair Clin Bioinformat, Saarbrucken, Germany
[5] AXA Res Fund, Paris, France
[6] UPMC Chair, Paris, France
[7] Univ Paris 06, Paris 06, Sorbonne Univ, IM2A, Paris, France
[8] Hop La Pitie Salpetriere, ICM, Dept Neurol, Paris, France
[9] Saarland Univ Hosp, Dept Psychiat & Psychotherapy, Homburg, Germany
关键词
Alzheimer's disease; Human cortical brain tissue; microRNA; mRNA; Hsa-miR-132; Hsa-miR-212; RECRUITMENT FACTOR; MESSENGER-RNA; MICRORNA-132; EXPRESSION; BRAIN; IDENTIFICATION; PREDICTION; PATHOLOGY; PATHWAYS; NETWORK;
D O I
10.1016/j.neurobiolaging.2016.09.019
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNA molecules, with essential functions in RNA silencing and post-transcriptional regulation of gene expression. miRNAs appear to regulate the development and function of the nervous system. Alterations of miRNA expression have been associated with Alzheimer's disease (AD). To characterize the AD miRNA signature, we examined genome-wide miRNA and mRNA expression patterns in the temporal cortex of AD and control samples. We validated our miRNA results by semiquantitative real-time polymerase chain reaction (PCR) in independent prefrontal cortex. Furthermore, we separated gray and white matter brain sections to identify the cellular origin of the altered miRNA expression. We observed genome-wide downregulation of hsa-miR-132-3p and hsa-miR-212-3p in AD with a stronger decrease in gray matter AD samples. We further identified 10 differently expressed transcripts achieving genome-wide levels of significance. Significantly deregulated miRNAs and mRNAs were correlated and examined for potential binding sites (in silico). This miRNome-wide study in AD provides supportive evidence and corroborates an important contribution of miR-132/212 and corresponding target mRNAs to the pathogenesis of AD. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:167.e1 / 167.e10
页数:10
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