Noncoding RNAs and neurobehavioral mechanisms in psychiatric disease

被引:67
作者
Kocerha, J. [1 ]
Dwivedi, Y. [2 ]
Brennand, K. J. [3 ,4 ]
机构
[1] Georgia So Univ, Dept Chem, Statesboro, GA 30458 USA
[2] Univ Alabama Birmingham, Dept Psychiat & Behav Neurobiol, Birmingham, AL 35294 USA
[3] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
关键词
NUCLEAR RECEPTOR TLX; NATURAL ANTISENSE TRANSCRIPT; SEROTONIN TRANSPORTER; NEURONAL DEVELOPMENT; MICRORNA EXPRESSION; CELL-PROLIFERATION; EARLY NEUROGENESIS; REGULATORY ROLES; BRAIN; SCHIZOPHRENIA;
D O I
10.1038/mp.2015.30
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
The human genome project has revolutionized our understanding of the underlying mechanisms in psychiatric disease. It is now abundantly clear that neurobehavioral phenotypes are epigenetically controlled by noncoding RNAs (ncRNAs). The microRNA (miRNA) class of ncRNAs are ubiquitously expressed throughout the brain and govern all major neuronal pathways. The attractive therapeutic potential of miRNAs is underscored by their pleiotropic capacities, putatively targeting multiple pathways within a single neuron. Many psychiatric diseases stem from a multifactorial origin, thus conventional drug targeting of single proteins may not prove most effective. In this exciting post-genome sequencing era, many new epigenetic targets are emerging for therapeutic investigation. Here we review the reported roles of miRNAs, as well as other ncRNA classes, in the pathology of psychiatric disorders; there are both common and unique ncRNA mechanisms that influence the various diagnoses. Collectively, these potent epigenetic regulators may clarify the disrupted signaling networks in psychiatric phenotypes.
引用
收藏
页码:677 / 684
页数:8
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