Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression
Epigenetic mechanisms are an important heritable and dynamic means of regulating various genomic functions, including gene expression, to orchestrate brain development, adult neurogenesis, and synaptic plasticity. These processes when perturbed are thought to contribute to schizophrenia pathophysiol...
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Veröffentlicht in: | American journal of medical genetics. Part B, Neuropsychiatric genetics Neuropsychiatric genetics, 2016-12, Vol.171B (8), p.1170-1179 |
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creator | Whitton, Laura Cosgrove, Donna Clarkson, Christopher Harold, Denise Kendall, Kimberley Richards, Alex Mantripragada, Kiran Owen, Michael J. O'Donovan, Michael C. Walters, James Hartmann, Annette Konte, Betina Rujescu, Dan Gill, Michael Corvin, Aiden Rea, Stephen Donohoe, Gary Morris, Derek W. |
description | Epigenetic mechanisms are an important heritable and dynamic means of regulating various genomic functions, including gene expression, to orchestrate brain development, adult neurogenesis, and synaptic plasticity. These processes when perturbed are thought to contribute to schizophrenia pathophysiology. A core feature of schizophrenia is cognitive dysfunction. For genetic disorders where cognitive impairment is more severe such as intellectual disability, there are a disproportionally high number of genes involved in the epigenetic regulation of gene transcription. Evidence now supports some shared genetic aetiology between schizophrenia and intellectual disability. GWAS have identified 108 chromosomal regions associated with schizophrenia risk that span 350 genes. This study identified genes mapping to those loci that have epigenetic functions, and tested the risk alleles defining those loci for association with cognitive deficits. We developed a list of 350 genes with epigenetic functions and cross‐referenced this with the GWAS loci. This identified eight candidate genes: BCL11B, CHD7, EP300, EPC2, GATAD2A, KDM3B, RERE, SATB2. Using a dataset of Irish psychosis cases and controls (n = 1235), the schizophrenia risk SNPs at these loci were tested for effects on IQ, working memory, episodic memory, and attention. Strongest associations were for rs6984242 with both measures of IQ (P = 0.001) and episodic memory (P = 0.007). We link rs6984242 to CHD7 via a long range eQTL. These associations were not replicated in independent samples. Our study highlights that a number of genes mapping to risk loci for schizophrenia may function as epigenetic regulators of gene expression but further studies are required to establish a role for these genes in cognition. © 2016 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/ajmg.b.32503 |
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These processes when perturbed are thought to contribute to schizophrenia pathophysiology. A core feature of schizophrenia is cognitive dysfunction. For genetic disorders where cognitive impairment is more severe such as intellectual disability, there are a disproportionally high number of genes involved in the epigenetic regulation of gene transcription. Evidence now supports some shared genetic aetiology between schizophrenia and intellectual disability. GWAS have identified 108 chromosomal regions associated with schizophrenia risk that span 350 genes. This study identified genes mapping to those loci that have epigenetic functions, and tested the risk alleles defining those loci for association with cognitive deficits. We developed a list of 350 genes with epigenetic functions and cross‐referenced this with the GWAS loci. This identified eight candidate genes: BCL11B, CHD7, EP300, EPC2, GATAD2A, KDM3B, RERE, SATB2. Using a dataset of Irish psychosis cases and controls (n = 1235), the schizophrenia risk SNPs at these loci were tested for effects on IQ, working memory, episodic memory, and attention. Strongest associations were for rs6984242 with both measures of IQ (P = 0.001) and episodic memory (P = 0.007). We link rs6984242 to CHD7 via a long range eQTL. These associations were not replicated in independent samples. Our study highlights that a number of genes mapping to risk loci for schizophrenia may function as epigenetic regulators of gene expression but further studies are required to establish a role for these genes in cognition. © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 1552-4841</identifier><identifier>EISSN: 1552-485X</identifier><identifier>DOI: 10.1002/ajmg.b.32503</identifier><identifier>PMID: 27762073</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Adult ; Alleles ; Brain - metabolism ; cognition ; Cognition - physiology ; Cognition Disorders - genetics ; Cognition Disorders - psychology ; Epigenesis, Genetic - genetics ; epigenetics ; Epigenomics ; Female ; gene ; Gene Expression Regulation - genetics ; Gene Frequency ; Genetic Predisposition to Disease ; Genetics ; Genome-Wide Association Study ; GWAS ; Humans ; Ireland ; Male ; Memory, Short-Term - physiology ; Middle Aged ; Polymorphism, Single Nucleotide - genetics ; Psychotic Disorders - genetics ; Risk Factors ; schizophrenia ; Schizophrenia - genetics ; Schizophrenic Psychology</subject><ispartof>American journal of medical genetics. 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Part B, Neuropsychiatric genetics</title><addtitle>Am. J. Med. Genet</addtitle><description>Epigenetic mechanisms are an important heritable and dynamic means of regulating various genomic functions, including gene expression, to orchestrate brain development, adult neurogenesis, and synaptic plasticity. These processes when perturbed are thought to contribute to schizophrenia pathophysiology. A core feature of schizophrenia is cognitive dysfunction. For genetic disorders where cognitive impairment is more severe such as intellectual disability, there are a disproportionally high number of genes involved in the epigenetic regulation of gene transcription. Evidence now supports some shared genetic aetiology between schizophrenia and intellectual disability. GWAS have identified 108 chromosomal regions associated with schizophrenia risk that span 350 genes. This study identified genes mapping to those loci that have epigenetic functions, and tested the risk alleles defining those loci for association with cognitive deficits. We developed a list of 350 genes with epigenetic functions and cross‐referenced this with the GWAS loci. This identified eight candidate genes: BCL11B, CHD7, EP300, EPC2, GATAD2A, KDM3B, RERE, SATB2. Using a dataset of Irish psychosis cases and controls (n = 1235), the schizophrenia risk SNPs at these loci were tested for effects on IQ, working memory, episodic memory, and attention. Strongest associations were for rs6984242 with both measures of IQ (P = 0.001) and episodic memory (P = 0.007). We link rs6984242 to CHD7 via a long range eQTL. These associations were not replicated in independent samples. Our study highlights that a number of genes mapping to risk loci for schizophrenia may function as epigenetic regulators of gene expression but further studies are required to establish a role for these genes in cognition. © 2016 Wiley Periodicals, Inc.</description><subject>Adult</subject><subject>Alleles</subject><subject>Brain - metabolism</subject><subject>cognition</subject><subject>Cognition - physiology</subject><subject>Cognition Disorders - genetics</subject><subject>Cognition Disorders - psychology</subject><subject>Epigenesis, Genetic - genetics</subject><subject>epigenetics</subject><subject>Epigenomics</subject><subject>Female</subject><subject>gene</subject><subject>Gene Expression Regulation - genetics</subject><subject>Gene Frequency</subject><subject>Genetic Predisposition to Disease</subject><subject>Genetics</subject><subject>Genome-Wide Association Study</subject><subject>GWAS</subject><subject>Humans</subject><subject>Ireland</subject><subject>Male</subject><subject>Memory, Short-Term - physiology</subject><subject>Middle Aged</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Psychotic Disorders - genetics</subject><subject>Risk Factors</subject><subject>schizophrenia</subject><subject>Schizophrenia - genetics</subject><subject>Schizophrenic Psychology</subject><issn>1552-4841</issn><issn>1552-485X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0c1v0zAYBnALMbExuO2MLHHZYSl2_JnjVrEO1IGEQONmOe6b1l0aZ3YCK389ybr1sAPiZMv-vY8sPwidUDKhhOQf7HqznJQTlgvCXqAjKkSecS1-vtzvOT1Er1NaE8KIUOoVOsyVkjlR7AitpmHZ-M7_AmwbW2-TTzhUOLmV_xPaVYTGWxx9usVLaCDhbmU7XPWN63xosE0YWj_edN7hCMu-tl2IDxHjKYb7NkJKg32DDipbJ3j7uB6jH5cfv0-vsvnX2afp-TxzXDGWqQJAFk5yZstKSUJcJTgIJoA70LbQpcsZFwBisWBaF5oUWvGSUueo5NqxY3S6y21juOshdWbjk4O6tg2EPhmqBVGy0Dr_D8rEiLkY6PtndB36OHzYqPj4cqrloM52ysWQUoTKtNFvbNwaSsxYlhnLMqV5KGvg7x5D-3IDiz1-amcAfAd--xq2_wwz55-vZxdPudluzKcO7vdjNt4aqZgS5ubLzHyb3VzJ-YU2mv0FC8SwIA</recordid><startdate>201612</startdate><enddate>201612</enddate><creator>Whitton, Laura</creator><creator>Cosgrove, Donna</creator><creator>Clarkson, Christopher</creator><creator>Harold, Denise</creator><creator>Kendall, Kimberley</creator><creator>Richards, Alex</creator><creator>Mantripragada, Kiran</creator><creator>Owen, Michael J.</creator><creator>O'Donovan, Michael C.</creator><creator>Walters, James</creator><creator>Hartmann, Annette</creator><creator>Konte, Betina</creator><creator>Rujescu, Dan</creator><creator>Gill, Michael</creator><creator>Corvin, Aiden</creator><creator>Rea, Stephen</creator><creator>Donohoe, Gary</creator><creator>Morris, Derek W.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201612</creationdate><title>Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression</title><author>Whitton, Laura ; Cosgrove, Donna ; Clarkson, Christopher ; Harold, Denise ; Kendall, Kimberley ; Richards, Alex ; Mantripragada, Kiran ; Owen, Michael J. ; O'Donovan, Michael C. ; Walters, James ; Hartmann, Annette ; Konte, Betina ; Rujescu, Dan ; Gill, Michael ; Corvin, Aiden ; Rea, Stephen ; Donohoe, Gary ; Morris, Derek W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4733-79ee69c643abf7600cf54e535e4ce8a98bc2345ee5dd3889809874b11cc1648c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Alleles</topic><topic>Brain - metabolism</topic><topic>cognition</topic><topic>Cognition - physiology</topic><topic>Cognition Disorders - genetics</topic><topic>Cognition Disorders - psychology</topic><topic>Epigenesis, Genetic - genetics</topic><topic>epigenetics</topic><topic>Epigenomics</topic><topic>Female</topic><topic>gene</topic><topic>Gene Expression Regulation - genetics</topic><topic>Gene Frequency</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetics</topic><topic>Genome-Wide Association Study</topic><topic>GWAS</topic><topic>Humans</topic><topic>Ireland</topic><topic>Male</topic><topic>Memory, Short-Term - physiology</topic><topic>Middle Aged</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Psychotic Disorders - genetics</topic><topic>Risk Factors</topic><topic>schizophrenia</topic><topic>Schizophrenia - genetics</topic><topic>Schizophrenic Psychology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Whitton, Laura</creatorcontrib><creatorcontrib>Cosgrove, Donna</creatorcontrib><creatorcontrib>Clarkson, Christopher</creatorcontrib><creatorcontrib>Harold, Denise</creatorcontrib><creatorcontrib>Kendall, Kimberley</creatorcontrib><creatorcontrib>Richards, Alex</creatorcontrib><creatorcontrib>Mantripragada, Kiran</creatorcontrib><creatorcontrib>Owen, Michael J.</creatorcontrib><creatorcontrib>O'Donovan, Michael C.</creatorcontrib><creatorcontrib>Walters, James</creatorcontrib><creatorcontrib>Hartmann, Annette</creatorcontrib><creatorcontrib>Konte, Betina</creatorcontrib><creatorcontrib>Rujescu, Dan</creatorcontrib><creatorcontrib>Gill, Michael</creatorcontrib><creatorcontrib>Corvin, Aiden</creatorcontrib><creatorcontrib>Rea, Stephen</creatorcontrib><creatorcontrib>Donohoe, Gary</creatorcontrib><creatorcontrib>Morris, Derek W.</creatorcontrib><creatorcontrib>WTCCC2</creatorcontrib><creatorcontrib>WTCCC2</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics. 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Genet</addtitle><date>2016-12</date><risdate>2016</risdate><volume>171B</volume><issue>8</issue><spage>1170</spage><epage>1179</epage><pages>1170-1179</pages><issn>1552-4841</issn><eissn>1552-485X</eissn><abstract>Epigenetic mechanisms are an important heritable and dynamic means of regulating various genomic functions, including gene expression, to orchestrate brain development, adult neurogenesis, and synaptic plasticity. These processes when perturbed are thought to contribute to schizophrenia pathophysiology. A core feature of schizophrenia is cognitive dysfunction. For genetic disorders where cognitive impairment is more severe such as intellectual disability, there are a disproportionally high number of genes involved in the epigenetic regulation of gene transcription. Evidence now supports some shared genetic aetiology between schizophrenia and intellectual disability. GWAS have identified 108 chromosomal regions associated with schizophrenia risk that span 350 genes. This study identified genes mapping to those loci that have epigenetic functions, and tested the risk alleles defining those loci for association with cognitive deficits. We developed a list of 350 genes with epigenetic functions and cross‐referenced this with the GWAS loci. This identified eight candidate genes: BCL11B, CHD7, EP300, EPC2, GATAD2A, KDM3B, RERE, SATB2. Using a dataset of Irish psychosis cases and controls (n = 1235), the schizophrenia risk SNPs at these loci were tested for effects on IQ, working memory, episodic memory, and attention. Strongest associations were for rs6984242 with both measures of IQ (P = 0.001) and episodic memory (P = 0.007). We link rs6984242 to CHD7 via a long range eQTL. These associations were not replicated in independent samples. 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subjects | Adult Alleles Brain - metabolism cognition Cognition - physiology Cognition Disorders - genetics Cognition Disorders - psychology Epigenesis, Genetic - genetics epigenetics Epigenomics Female gene Gene Expression Regulation - genetics Gene Frequency Genetic Predisposition to Disease Genetics Genome-Wide Association Study GWAS Humans Ireland Male Memory, Short-Term - physiology Middle Aged Polymorphism, Single Nucleotide - genetics Psychotic Disorders - genetics Risk Factors schizophrenia Schizophrenia - genetics Schizophrenic Psychology |
title | Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression |
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