Neuronal dark matter: the emerging role of microRNAs in neurodegeneration

被引:152
作者
Goodall, Emily F. [1 ]
Heath, Paul R. [1 ]
Bandmann, Oliver [1 ]
Kirby, Janine [1 ]
Shaw, Pamela J. [1 ]
机构
[1] Univ Sheffield, Sheffield Inst Translat Neurosci, Dept Neurosci, Sheffield S10 2HQ, S Yorkshire, England
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
microRNA; neurodegeneration; Alzheimer's disease; Parkinson's disease; amyotrophic lateral sclerosis; Huntington's disease; AMYOTROPHIC-LATERAL-SCLEROSIS; ALPHA-SYNUCLEIN EXPRESSION; AMYLOID PRECURSOR PROTEIN; MEDIATED TRANSLATIONAL REPRESSION; ALZHEIMERS-DISEASE BRAIN; HUNTINGTONS-DISEASE; PARKINSONS-DISEASE; MESSENGER-RNAS; POSTTRANSCRIPTIONAL REGULATION; MICROPROCESSOR COMPLEX;
D O I
10.3389/fncel.2013.00178
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
MicroRNAs (miRNAs) are small, abundant RNA molecules that constitute part of the cell's non-coding RNA "dark matter." In recent years, the discovery of miRNAs has revolutionised the traditional view of gene expression and our understanding of miRNA biogenesis and function has expanded. Altered expression of miRNAs is increasingly recognized as a feature of many disease states, including neurodegeneration. Here, we review the emerging role for miRNA dysfunction in Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS) and Huntington's disease pathogenesis. We emphasize the complex nature of gene regulatory networks and the need for systematic studies, with larger sample cohorts than have so far been reported, to reveal the most important miRNA regulators in disease. Finally, miRNA diversity and their potential to target multiple pathways, offers novel clinical applications for miRNAs as biomarkers and therapeutic agents in neurodegenerative diseases.
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页数:16
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