Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder
Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and variable phenotypes. The Disrupted in Schizophrenia 1 ( DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a...
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Veröffentlicht in: | American journal of human genetics 2004-11, Vol.75 (5), p.862-872 |
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creator | Hodgkinson, Colin A. Goldman, David Jaeger, Judith Persaud, Shalini Kane, John M. Lipsky, Robert H. Malhotra, Anil K. |
description | Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and variable phenotypes. The
Disrupted in Schizophrenia 1 (
DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a balanced translocation that disrupts
DISC1 and
DISC2. More recently, DISC1 was linked to schizophrenia, broadly defined, in the general Finnish population, through the undertransmission to affected women of a common haplotype from the region of intron 1/exon 2. We present data from a case-control study of a North American white population, confirming the underrepresentation of a common haplotype of the intron 1/exon 2 region in individuals with schizoaffective disorder. Multiple haplotypes contained within four haplotype blocks extending between exon 1 and exon 9 are associated with schizophrenia, schizoaffective disorder, and bipolar disorder. We also find overrepresentation of the exon 9 missense allele Phe607 in schizoaffective disorder. These data support the idea that these apparently distinct disorders have at least a partially convergent etiology and that variation at the
DISC1 locus predisposes individuals to a variety of psychiatric disorders. |
doi_str_mv | 10.1086/425586 |
format | Article |
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Disrupted in Schizophrenia 1 (
DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a balanced translocation that disrupts
DISC1 and
DISC2. More recently, DISC1 was linked to schizophrenia, broadly defined, in the general Finnish population, through the undertransmission to affected women of a common haplotype from the region of intron 1/exon 2. We present data from a case-control study of a North American white population, confirming the underrepresentation of a common haplotype of the intron 1/exon 2 region in individuals with schizoaffective disorder. Multiple haplotypes contained within four haplotype blocks extending between exon 1 and exon 9 are associated with schizophrenia, schizoaffective disorder, and bipolar disorder. We also find overrepresentation of the exon 9 missense allele Phe607 in schizoaffective disorder. These data support the idea that these apparently distinct disorders have at least a partially convergent etiology and that variation at the
DISC1 locus predisposes individuals to a variety of psychiatric disorders.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1086/425586</identifier><identifier>PMID: 15386212</identifier><identifier>CODEN: AJHGAG</identifier><language>eng</language><publisher>Chicago, IL: Elsevier Inc</publisher><subject>Adult ; Adult and adolescent clinical studies ; Biological and medical sciences ; Bipolar Disorder - genetics ; Chromosomes, Human, Pair 1 - genetics ; European Continental Ancestry Group ; Female ; General aspects. Genetic counseling ; Genetic Markers - genetics ; Genotype ; Haplotypes - genetics ; Humans ; Male ; Medical genetics ; Medical sciences ; Nerve Tissue Proteins - genetics ; North America ; Polymorphism, Single Nucleotide - genetics ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; Psychotic Disorders - genetics ; Schizophrenia ; Schizophrenia - genetics</subject><ispartof>American journal of human genetics, 2004-11, Vol.75 (5), p.862-872</ispartof><rights>2004 The American Society of Human Genetics</rights><rights>2005 INIST-CNRS</rights><rights>2004 by The American Society of Human Genetics. All rights reserved. 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-ac72483f1b50062a911ec86dac35574ff02683909d245e899434140c55766afe3</citedby><cites>FETCH-LOGICAL-c433t-ac72483f1b50062a911ec86dac35574ff02683909d245e899434140c55766afe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182115/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1086/425586$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,3551,27926,27927,45997,53793,53795</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16215375$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15386212$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hodgkinson, Colin A.</creatorcontrib><creatorcontrib>Goldman, David</creatorcontrib><creatorcontrib>Jaeger, Judith</creatorcontrib><creatorcontrib>Persaud, Shalini</creatorcontrib><creatorcontrib>Kane, John M.</creatorcontrib><creatorcontrib>Lipsky, Robert H.</creatorcontrib><creatorcontrib>Malhotra, Anil K.</creatorcontrib><title>Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and variable phenotypes. The
Disrupted in Schizophrenia 1 (
DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a balanced translocation that disrupts
DISC1 and
DISC2. More recently, DISC1 was linked to schizophrenia, broadly defined, in the general Finnish population, through the undertransmission to affected women of a common haplotype from the region of intron 1/exon 2. We present data from a case-control study of a North American white population, confirming the underrepresentation of a common haplotype of the intron 1/exon 2 region in individuals with schizoaffective disorder. Multiple haplotypes contained within four haplotype blocks extending between exon 1 and exon 9 are associated with schizophrenia, schizoaffective disorder, and bipolar disorder. We also find overrepresentation of the exon 9 missense allele Phe607 in schizoaffective disorder. These data support the idea that these apparently distinct disorders have at least a partially convergent etiology and that variation at the
DISC1 locus predisposes individuals to a variety of psychiatric disorders.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Biological and medical sciences</subject><subject>Bipolar Disorder - genetics</subject><subject>Chromosomes, Human, Pair 1 - genetics</subject><subject>European Continental Ancestry Group</subject><subject>Female</subject><subject>General aspects. Genetic counseling</subject><subject>Genetic Markers - genetics</subject><subject>Genotype</subject><subject>Haplotypes - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>North America</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Psychotic Disorders - genetics</subject><subject>Schizophrenia</subject><subject>Schizophrenia - genetics</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU9v1DAQxS0EossCHwH5AgKpgbGdeBMOSGXLn0qVOBTOluuM2UFZO9jZRfDpcbVRl3KyxvPTm6f3GHsq4LWAVr-pZdO0-h5biEatKq2huc8WACCrTnarE_Yo5x8AQrSgHrKTArVaCrlg0znltBsn7DkFfuU29CeOm4SBLBf85fnF1Vq8esvPco6O7EQx8F80be6Sp_NovUc30R55UY2px3TKbej5exrjYNPt72P2wNsh45P5XbJvHz98XX-uLr98ulifXVauVmqqrFvJulVeXDcAWtpOCHSt7q1TTbOqvQepW9VB18u6wbbralWLGlxZam09qiV7d9Add9db7B2GKdnBjIm2Nv020ZK5uwm0Md_j3pScpCghLdmLWSDFnzvMk9lSdjgMNmDcZaN1VxwKOIIuxZwT-tsjAsxNQeZQUAGf_WvpiM2NFOD5DNjs7OCTDY7ykStQafjGGhw4LAHuCZPJjjA47CmVEkwf6f_bfwGrKKec</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Hodgkinson, Colin A.</creator><creator>Goldman, David</creator><creator>Jaeger, Judith</creator><creator>Persaud, Shalini</creator><creator>Kane, John M.</creator><creator>Lipsky, Robert H.</creator><creator>Malhotra, Anil K.</creator><general>Elsevier Inc</general><general>University of Chicago Press</general><general>The American Society of Human Genetics</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20041101</creationdate><title>Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder</title><author>Hodgkinson, Colin A. ; Goldman, David ; Jaeger, Judith ; Persaud, Shalini ; Kane, John M. ; Lipsky, Robert H. ; Malhotra, Anil K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-ac72483f1b50062a911ec86dac35574ff02683909d245e899434140c55766afe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Biological and medical sciences</topic><topic>Bipolar Disorder - genetics</topic><topic>Chromosomes, Human, Pair 1 - genetics</topic><topic>European Continental Ancestry Group</topic><topic>Female</topic><topic>General aspects. Genetic counseling</topic><topic>Genetic Markers - genetics</topic><topic>Genotype</topic><topic>Haplotypes - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>North America</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Psychotic Disorders - genetics</topic><topic>Schizophrenia</topic><topic>Schizophrenia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hodgkinson, Colin A.</creatorcontrib><creatorcontrib>Goldman, David</creatorcontrib><creatorcontrib>Jaeger, Judith</creatorcontrib><creatorcontrib>Persaud, Shalini</creatorcontrib><creatorcontrib>Kane, John M.</creatorcontrib><creatorcontrib>Lipsky, Robert H.</creatorcontrib><creatorcontrib>Malhotra, Anil K.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hodgkinson, Colin A.</au><au>Goldman, David</au><au>Jaeger, Judith</au><au>Persaud, Shalini</au><au>Kane, John M.</au><au>Lipsky, Robert H.</au><au>Malhotra, Anil K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>75</volume><issue>5</issue><spage>862</spage><epage>872</epage><pages>862-872</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><coden>AJHGAG</coden><abstract>Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and variable phenotypes. The
Disrupted in Schizophrenia 1 (
DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a balanced translocation that disrupts
DISC1 and
DISC2. More recently, DISC1 was linked to schizophrenia, broadly defined, in the general Finnish population, through the undertransmission to affected women of a common haplotype from the region of intron 1/exon 2. We present data from a case-control study of a North American white population, confirming the underrepresentation of a common haplotype of the intron 1/exon 2 region in individuals with schizoaffective disorder. Multiple haplotypes contained within four haplotype blocks extending between exon 1 and exon 9 are associated with schizophrenia, schizoaffective disorder, and bipolar disorder. We also find overrepresentation of the exon 9 missense allele Phe607 in schizoaffective disorder. These data support the idea that these apparently distinct disorders have at least a partially convergent etiology and that variation at the
DISC1 locus predisposes individuals to a variety of psychiatric disorders.</abstract><cop>Chicago, IL</cop><pub>Elsevier Inc</pub><pmid>15386212</pmid><doi>10.1086/425586</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Biological and medical sciences Bipolar Disorder - genetics Chromosomes, Human, Pair 1 - genetics European Continental Ancestry Group Female General aspects. Genetic counseling Genetic Markers - genetics Genotype Haplotypes - genetics Humans Male Medical genetics Medical sciences Nerve Tissue Proteins - genetics North America Polymorphism, Single Nucleotide - genetics Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Psychotic Disorders - genetics Schizophrenia Schizophrenia - genetics |
title | Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder |
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