Dysfunctional Gene Splicing as a Potential Contributor to Neuropsychiatric Disorders

被引:41
作者
Glatt, Stephen J. [1 ,2 ,3 ]
Cohen, Ori S. [1 ,2 ,3 ]
Faraone, Stephen V. [1 ,2 ,3 ]
Tsuang, Ming T. [4 ,5 ,6 ,7 ]
机构
[1] SUNY Upstate Med Univ, Psychiat Genet Epidemiol & Neurobiol Lab, Dept Psychiat & Behav Sci, Med Genet Res Ctr, Syracuse, NY 13210 USA
[2] SUNY Upstate Med Univ, Dept Neurosci, Med Genet Res Ctr, Syracuse, NY 13210 USA
[3] SUNY Upstate Med Univ, Dept Physiol, Med Genet Res Ctr, Syracuse, NY 13210 USA
[4] Univ Calif San Diego, Dept Psychiat, Inst Genom Med, Ctr Behav Genom, San Diego, CA 92103 USA
[5] Vet Affairs San Diego Healthcare Syst, San Diego, CA USA
[6] Harvard Inst Psychiat Epidemiol & Genet, Harvard Dept Epidemiol, Boston, MA USA
[7] Harvard Inst Psychiat Epidemiol & Genet, Harvard Dept Psychiat, Boston, MA USA
基金
美国国家卫生研究院;
关键词
alternative splicing; mRNA; pre-mRNA; RNA processing; spliceosome; NMDA RECEPTOR SUBUNIT; MESSENGER-RNA; BIPOLAR DISORDER; MAMMALIAN NUMB; SYNAPTIC PLASTICITY; FUNCTIONAL VARIANTS; PREFRONTAL CORTEX; MOLECULAR-CLONING; PROTEIN ISOFORMS; MOOD DISORDERS;
D O I
10.1002/ajmg.b.31181
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Alternative pre-mRNA splicing is a major mechanism by which the proteomic diversity of eukaryotic genomes is amplified. Much akin to neuropsychiatric disorders themselves, alternative splicing events can be influenced by genetic, developmental, and environmental factors. Here, we review the evidence that abnormalities of splicing may contribute to the liability toward these disorders. First, we introduce the phenomenon of alternative splicing and describe the processes involved in its regulation. We then review the evidence for specific splicing abnormalities in a wide range of neuropsychiatric disorders, including psychotic disorders (schizophrenia), affective disorders (bipolar disorder and major depressive disorder), suicide, substance abuse disorders (cocaine abuse and alcoholism), and neurodevelopmental disorders (autism). Next, we provide a theoretical reworking of the concept of "gene-focused" epidemiologic and neurobiologic investigations. Lastly, we suggest potentially fruitful lines for future research that should illuminate the nature, extent, causes, and consequences of alternative splicing abnormalities in neuropsychiatric disorders. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:382 / 392
页数:11
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