The DISC locus in psychiatric illness
- PMID: 17912248
- DOI: 10.1038/sj.mp.4002106
The DISC locus in psychiatric illness
Abstract
The DISC locus is located at the breakpoint of a balanced t(1;11) chromosomal translocation in a large and unique Scottish family. This translocation segregates in a highly statistically significant manner with a broad diagnosis of psychiatric illness, including schizophrenia, bipolar disorder and major depression, as well as with a narrow diagnosis of schizophrenia alone. Two novel genes were identified at this locus and due to the high prevalence of schizophrenia in this family, they were named Disrupted-in-Schizophrenia-1 (DISC1) and Disrupted-in-Schizophrenia-2 (DISC2). DISC1 encodes a novel multifunctional scaffold protein, whereas DISC2 is a putative noncoding RNA gene antisense to DISC1. A number of independent genetic linkage and association studies in diverse populations support the original linkage findings in the Scottish family and genetic evidence now implicates the DISC locus in susceptibility to schizophrenia, schizoaffective disorder, bipolar disorder and major depression as well as various cognitive traits. Despite this, with the exception of the t(1;11) translocation, robust evidence for a functional variant(s) is still lacking and genetic heterogeneity is likely. Of the two genes identified at this locus, DISC1 has been prioritized as the most probable candidate susceptibility gene for psychiatric illness, as its protein sequence is directly disrupted by the translocation. Much research has been undertaken in recent years to elucidate the biological functions of the DISC1 protein and to further our understanding of how it contributes to the pathogenesis of schizophrenia. These data are the main subject of this review; however, the potential involvement of DISC2 in the pathogenesis of psychiatric illness is also discussed. A detailed picture of DISC1 function is now emerging, which encompasses roles in neurodevelopment, cytoskeletal function and cAMP signalling, and several DISC1 interactors have also been defined as independent genetic susceptibility factors for psychiatric illness. DISC1 is a hub protein in a multidimensional risk pathway for major mental illness, and studies of this pathway are opening up opportunities for a better understanding of causality and possible mechanisms of intervention.
Similar articles
-
DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness.Ann Med. 2004;36(5):367-78. doi: 10.1080/07853890410033603. Ann Med. 2004. PMID: 15478311 Review.
-
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.Mol Psychiatry. 2014 Jun;19(6):668-75. doi: 10.1038/mp.2013.68. Epub 2013 Jun 4. Mol Psychiatry. 2014. PMID: 23732877 Free PMC article.
-
Disruption of two novel genes by a translocation co-segregating with schizophrenia.Hum Mol Genet. 2000 May 22;9(9):1415-23. doi: 10.1093/hmg/9.9.1415. Hum Mol Genet. 2000. PMID: 10814723
-
Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia.Mol Psychiatry. 2001 Mar;6(2):173-8. doi: 10.1038/sj.mp.4000784. Mol Psychiatry. 2001. PMID: 11317219
-
DISC1 in schizophrenia: genetic mouse models and human genomic imaging.Schizophr Bull. 2011 Jan;37(1):14-20. doi: 10.1093/schbul/sbq135. Epub 2010 Dec 13. Schizophr Bull. 2011. PMID: 21149852 Free PMC article. Review.
Cited by
-
Mouse Genetic Models of Human Brain Disorders.Front Genet. 2016 Mar 23;7:40. doi: 10.3389/fgene.2016.00040. eCollection 2016. Front Genet. 2016. PMID: 27047540 Free PMC article. Review.
-
Mutation of the 3-Phosphoinositide-Dependent Protein Kinase 1 (PDK1) Substrate-Docking Site in the Developing Brain Causes Microcephaly with Abnormal Brain Morphogenesis Independently of Akt, Leading to Impaired Cognition and Disruptive Behaviors.Mol Cell Biol. 2016 Nov 14;36(23):2967-2982. doi: 10.1128/MCB.00230-16. Print 2016 Dec 1. Mol Cell Biol. 2016. PMID: 27644329 Free PMC article.
-
Schizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models.Front Psychiatry. 2015 Feb 18;6:13. doi: 10.3389/fpsyt.2015.00013. eCollection 2015. Front Psychiatry. 2015. PMID: 25762938 Free PMC article. Review.
-
What is complex about complex disorders?Genome Biol. 2012 Jan 23;13(1):237. doi: 10.1186/gb-2012-13-1-237. Genome Biol. 2012. PMID: 22269335 Free PMC article.
-
Astrocytes in schizophrenia.Brain Neurosci Adv. 2021 Apr 27;5:23982128211009148. doi: 10.1177/23982128211009148. eCollection 2021 Jan-Dec. Brain Neurosci Adv. 2021. PMID: 33997293 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases