Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

Although DISC1 has been implicated in many psychiatric disorders, including schizophrenia, bipolar disorder, schizoaffective disorder and major depression, its biological role in these disorders is unclear. To better understand this gene and its role in psychiatric disease, we conducted transcriptio...

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Main Authors: Carless, M.A., Glahn, D.C., Johnson, M.P., Curran, J.E., Bozaoglu, K., Dyer, T.D., Winkler, A.M., Cole, S.A., Almasy, L., MacCluer, J.W., Duggirala, R., Moses, E.K., Göring, H.H.H., Blangero, J.
Format: Online
Language:English
Published: 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135724/
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spelling pubmed-31357242012-05-01 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes Carless, M.A. Glahn, D.C. Johnson, M.P. Curran, J.E. Bozaoglu, K. Dyer, T.D. Winkler, A.M. Cole, S.A. Almasy, L. MacCluer, J.W. Duggirala, R. Moses, E.K. Göring, H.H.H. Blangero, J. Article Although DISC1 has been implicated in many psychiatric disorders, including schizophrenia, bipolar disorder, schizoaffective disorder and major depression, its biological role in these disorders is unclear. To better understand this gene and its role in psychiatric disease, we conducted transcriptional profiling and genome-wide association analysis in 1 232 pedigreed Mexican American individuals for whom we have neuroanatomic images, neurocognitive assessments and neuropsychiatric diagnoses. SOLAR was used to determine heritability, identify gene expression patterns and perform association analyses on 188 quantitative brain-related phenotypes. We found that the DISC1 transcript is highly heritable (h2=0.50; p=1.97 × 10−22), and that gene expression is strongly cis-regulated (cis-LOD=3.89) but is also influenced by trans-effects. We identified several DISC1 polymorphisms that were associated with cortical gray-matter thickness within the parietal, temporal and frontal lobes. Associated regions affiliated with memory included the entorhinal cortex (rs821639, p=4.11 × 10−5; rs2356606, p=4.71 × 10−4), cingulate cortex (rs16856322, p=2.88 × 10−4) and parahippocampal gyrus (rs821639, p=4.95 × 10−4); those affiliated with executive and other cognitive processing included the transverse temporal gyrus (rs9661837, p=5.21 × 10−4; rs17773946, p=6.23 × 10−4), anterior cingulate cortex (rs2487453, p=; 4.79 × 10−4; rs3738401, p= 5.43 × 10−4) and medial orbitofrontal cortex (rs9661837; p=7.40 × 10−4). Cognitive measures of working memory (rs2793094, p=3.38 × 10−4), as well as lifetime history of depression (rs4658966, p=4.33 × 10−4; rs12137417, p=4.93 × 10−4) and panic (rs12137417, p=7.41 × 10−4) were associated with DISC1 sequence variation. DISC1 has well-defined genetic regulation and clearly influences important phenotypes related to psychiatric disease. 2011-04-12 2011-11 /pmc/articles/PMC3135724/ /pubmed/21483430 http://dx.doi.org/10.1038/mp.2011.37 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Carless, M.A.
Glahn, D.C.
Johnson, M.P.
Curran, J.E.
Bozaoglu, K.
Dyer, T.D.
Winkler, A.M.
Cole, S.A.
Almasy, L.
MacCluer, J.W.
Duggirala, R.
Moses, E.K.
Göring, H.H.H.
Blangero, J.
spellingShingle Carless, M.A.
Glahn, D.C.
Johnson, M.P.
Curran, J.E.
Bozaoglu, K.
Dyer, T.D.
Winkler, A.M.
Cole, S.A.
Almasy, L.
MacCluer, J.W.
Duggirala, R.
Moses, E.K.
Göring, H.H.H.
Blangero, J.
Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
author_facet Carless, M.A.
Glahn, D.C.
Johnson, M.P.
Curran, J.E.
Bozaoglu, K.
Dyer, T.D.
Winkler, A.M.
Cole, S.A.
Almasy, L.
MacCluer, J.W.
Duggirala, R.
Moses, E.K.
Göring, H.H.H.
Blangero, J.
author_sort Carless, M.A.
title Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
title_short Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
title_full Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
title_fullStr Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
title_full_unstemmed Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
title_sort impact of disc1 variation on neuroanatomical and neurocognitive phenotypes
description Although DISC1 has been implicated in many psychiatric disorders, including schizophrenia, bipolar disorder, schizoaffective disorder and major depression, its biological role in these disorders is unclear. To better understand this gene and its role in psychiatric disease, we conducted transcriptional profiling and genome-wide association analysis in 1 232 pedigreed Mexican American individuals for whom we have neuroanatomic images, neurocognitive assessments and neuropsychiatric diagnoses. SOLAR was used to determine heritability, identify gene expression patterns and perform association analyses on 188 quantitative brain-related phenotypes. We found that the DISC1 transcript is highly heritable (h2=0.50; p=1.97 × 10−22), and that gene expression is strongly cis-regulated (cis-LOD=3.89) but is also influenced by trans-effects. We identified several DISC1 polymorphisms that were associated with cortical gray-matter thickness within the parietal, temporal and frontal lobes. Associated regions affiliated with memory included the entorhinal cortex (rs821639, p=4.11 × 10−5; rs2356606, p=4.71 × 10−4), cingulate cortex (rs16856322, p=2.88 × 10−4) and parahippocampal gyrus (rs821639, p=4.95 × 10−4); those affiliated with executive and other cognitive processing included the transverse temporal gyrus (rs9661837, p=5.21 × 10−4; rs17773946, p=6.23 × 10−4), anterior cingulate cortex (rs2487453, p=; 4.79 × 10−4; rs3738401, p= 5.43 × 10−4) and medial orbitofrontal cortex (rs9661837; p=7.40 × 10−4). Cognitive measures of working memory (rs2793094, p=3.38 × 10−4), as well as lifetime history of depression (rs4658966, p=4.33 × 10−4; rs12137417, p=4.93 × 10−4) and panic (rs12137417, p=7.41 × 10−4) were associated with DISC1 sequence variation. DISC1 has well-defined genetic regulation and clearly influences important phenotypes related to psychiatric disease.
publishDate 2011
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3135724/
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