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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of human genetics 2004-11, Vol.75 (5), p.862-872
Hauptverfasser: Hodgkinson, Colin A., Goldman, David, Jaeger, Judith, Persaud, Shalini, Kane, John M., Lipsky, Robert H., Malhotra, Anil K.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 872
container_issue 5
container_start_page 862
container_title American journal of human genetics
container_volume 75
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
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1182115</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0002929707637914</els_id><sourcerecordid>66924810</sourcerecordid><originalsourceid>FETCH-LOGICAL-c433t-ac72483f1b50062a911ec86dac35574ff02683909d245e899434140c55766afe3</originalsourceid><addsrcrecordid>eNpdkU9v1DAQxS0EossCHwH5AgKpgbGdeBMOSGXLn0qVOBTOluuM2UFZO9jZRfDpcbVRl3KyxvPTm6f3GHsq4LWAVr-pZdO0-h5biEatKq2huc8WACCrTnarE_Yo5x8AQrSgHrKTArVaCrlg0znltBsn7DkFfuU29CeOm4SBLBf85fnF1Vq8esvPco6O7EQx8F80be6Sp_NovUc30R55UY2px3TKbej5exrjYNPt72P2wNsh45P5XbJvHz98XX-uLr98ulifXVauVmqqrFvJulVeXDcAWtpOCHSt7q1TTbOqvQepW9VB18u6wbbralWLGlxZam09qiV7d9Add9db7B2GKdnBjIm2Nv020ZK5uwm0Md_j3pScpCghLdmLWSDFnzvMk9lSdjgMNmDcZaN1VxwKOIIuxZwT-tsjAsxNQeZQUAGf_WvpiM2NFOD5DNjs7OCTDY7ykStQafjGGhw4LAHuCZPJjjA47CmVEkwf6f_bfwGrKKec</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>66924810</pqid></control><display><type>article</type><title>Disrupted in Schizophrenia 1 (DISC1): Association with Schizophrenia, Schizoaffective Disorder, and Bipolar Disorder</title><source>MEDLINE</source><source>Cell Press Free Archives</source><source>Access via ScienceDirect (Elsevier)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Hodgkinson, Colin A. ; Goldman, David ; Jaeger, Judith ; Persaud, Shalini ; Kane, John M. ; Lipsky, Robert H. ; Malhotra, Anil K.</creator><creatorcontrib>Hodgkinson, Colin A. ; Goldman, David ; Jaeger, Judith ; Persaud, Shalini ; Kane, John M. ; Lipsky, Robert H. ; Malhotra, Anil K.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0002-9297
ispartof American journal of human genetics, 2004-11, Vol.75 (5), p.862-872
issn 0002-9297
1537-6605
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1182115
source MEDLINE; Cell Press Free Archives; Access via ScienceDirect (Elsevier); EZB-FREE-00999 freely available EZB journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T09%3A58%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Disrupted%20in%20Schizophrenia%201%20(DISC1):%20Association%20with%20Schizophrenia,%20Schizoaffective%20Disorder,%20and%20Bipolar%20Disorder&rft.jtitle=American%20journal%20of%20human%20genetics&rft.au=Hodgkinson,%20Colin%20A.&rft.date=2004-11-01&rft.volume=75&rft.issue=5&rft.spage=862&rft.epage=872&rft.pages=862-872&rft.issn=0002-9297&rft.eissn=1537-6605&rft.coden=AJHGAG&rft_id=info:doi/10.1086/425586&rft_dat=%3Cproquest_pubme%3E66924810%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=66924810&rft_id=info:pmid/15386212&rft_els_id=S0002929707637914&rfr_iscdi=true