DOI: 10.1007/s13311-017-0556-5 Pages: 623-629
Article Type: Review

Role of DISC1 in Neuronal Trafficking and its Implication in Neuropsychiatric Manifestation and Neurotherapeutics

1. University of Toronto, Centre for Addiction and Mental Health

2. Osaka University, Laboratory for Advanced Brain Functions, Institute for Protein Research

3. Kyoto University Graduate School of Medicine, Medical Innovation Center

Correspondence to:
Toshifumi Tomoda
Email: ttomoda1@gmail.com

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Abstract

Disrupted-in-schizophrenia 1 (DISC1) was initially identified as a gene disrupted by a translocation mutation co-segregating with a variety of psychotic and mood disorders in a Scottish pedigree. In agreement with this original finding, mouse models that perturb Disc1 display deficits of behaviors in specific dimensions, such as cognition and emotion, but not a motor dimension. Although DISC1 is not a risk gene for sporadic cases of specific psychiatric disorders defined by categorical diagnostic criteria (e.g., schizophrenia and major depressive disorder), DISC1 is now regarded as an important molecular lead to decipher molecular pathology for specific dimensions relevant to major mental illnesses. Emerging evidence points to the role of DISC1 in the regulation of intracellular trafficking of a wide range of neuronal cargoes. We will review recent progress in this aspect of DISC1 biology and discuss how we could utilize this body of knowledge to better understand the pathophysiology of mental illnesses.

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  • Online: Jun 29, 2017

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