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Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23
We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive heterogeneity of linkage for genetic subtypes of schizophrenia. Our strategy consisted of selecting 13 kindreds containing multiple affected cases in three or more genera...
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Published in: | American journal of human genetics 2001-03, Vol.68 (3), p.661-673 |
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creator | Gurling, Hugh M.D. Kalsi, Gursharan Brynjolfson, Jon Sigmundsson, Thordur Sherrington, Robin Mankoo, Baljinder S. Read, Timothy Murphy, Patrice Blaveri, Ekaterina McQuillin, Andrew Petursson, Hannes Curtis, David |
description | We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive heterogeneity of linkage for genetic subtypes of schizophrenia. Our strategy consisted of selecting 13 kindreds containing multiple affected cases in three or more generations, an absence of bipolar affective disorder, and a single progenitor source of schizophrenia with unilineal transmission into the branch of the kindred sampled. DNA samples from these families were genotyped with 365 microsatellite markers spaced at ∼10-cM intervals across the whole genome. We observed LOD scores >3.0 at five distinct loci, either in the sample as a whole or within single families, strongly suggesting etiological heterogeneity. Heterogeneity LOD scores >3.0 in the sample as a whole were found at 1q33.2 (LOD score 3.2;
P=.0003), 5q33.2 (LOD score 3.6;
P=.0001), 8p22.1-22 (LOD score 3.6;
P=.0001), and 11q21 (LOD score 3.1;
P=.0004). LOD scores >3.0 within single pedigrees were found at 4q13-31 (LOD score 3.2;
P=.0003) and at 11q23.3-24 (LOD score 3.2;
P=.0003). A LOD score of 2.9 was also found at 20q12.1-11.23 within in a single family. The fact that other studies have also detected LOD scores >3.0 at 1q33.2, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci. We believe that the weight of evidence for linkage to the chromosome 1q22, 5q33.2, and 8p21-22 loci is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium. Such studies will soon allow the identification of mutations having a direct effect on susceptibility to schizophrenia. |
doi_str_mv | 10.1086/318788 |
format | article |
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P=.0003), 5q33.2 (LOD score 3.6;
P=.0001), 8p22.1-22 (LOD score 3.6;
P=.0001), and 11q21 (LOD score 3.1;
P=.0004). LOD scores >3.0 within single pedigrees were found at 4q13-31 (LOD score 3.2;
P=.0003) and at 11q23.3-24 (LOD score 3.2;
P=.0003). A LOD score of 2.9 was also found at 20q12.1-11.23 within in a single family. The fact that other studies have also detected LOD scores >3.0 at 1q33.2, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci. We believe that the weight of evidence for linkage to the chromosome 1q22, 5q33.2, and 8p21-22 loci is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium. Such studies will soon allow the identification of mutations having a direct effect on susceptibility to schizophrenia.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>DOI: 10.1086/318788</identifier><identifier>PMID: 11179014</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Chromosome Aberrations ; Chromosome Mapping ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 11 ; Chromosomes, Human, Pair 20 ; Chromosomes, Human, Pair 5 ; Chromosomes, Human, Pair 8 ; Family ; Female ; Genetic Linkage ; Genetic Markers ; Genetic Predisposition to Disease - genetics ; Genome, Human ; Genotype ; Humans ; Lod Score ; Male ; Microsatellite Repeats ; Pedigree ; Schizophrenia - genetics</subject><ispartof>American journal of human genetics, 2001-03, Vol.68 (3), p.661-673</ispartof><rights>2001 The American Society of Human Genetics</rights><rights>2001 by The American Society of Human Genetics. All rights reserved. 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-ff27b0411bfb086e1e1678de48d4174ebd117f37cacb499863473770a0a0f6243</citedby><cites>FETCH-LOGICAL-c500t-ff27b0411bfb086e1e1678de48d4174ebd117f37cacb499863473770a0a0f6243</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/PMC1274479/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1274479/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11179014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gurling, Hugh M.D.</creatorcontrib><creatorcontrib>Kalsi, Gursharan</creatorcontrib><creatorcontrib>Brynjolfson, Jon</creatorcontrib><creatorcontrib>Sigmundsson, Thordur</creatorcontrib><creatorcontrib>Sherrington, Robin</creatorcontrib><creatorcontrib>Mankoo, Baljinder S.</creatorcontrib><creatorcontrib>Read, Timothy</creatorcontrib><creatorcontrib>Murphy, Patrice</creatorcontrib><creatorcontrib>Blaveri, Ekaterina</creatorcontrib><creatorcontrib>McQuillin, Andrew</creatorcontrib><creatorcontrib>Petursson, Hannes</creatorcontrib><creatorcontrib>Curtis, David</creatorcontrib><title>Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive heterogeneity of linkage for genetic subtypes of schizophrenia. Our strategy consisted of selecting 13 kindreds containing multiple affected cases in three or more generations, an absence of bipolar affective disorder, and a single progenitor source of schizophrenia with unilineal transmission into the branch of the kindred sampled. DNA samples from these families were genotyped with 365 microsatellite markers spaced at ∼10-cM intervals across the whole genome. We observed LOD scores >3.0 at five distinct loci, either in the sample as a whole or within single families, strongly suggesting etiological heterogeneity. Heterogeneity LOD scores >3.0 in the sample as a whole were found at 1q33.2 (LOD score 3.2;
P=.0003), 5q33.2 (LOD score 3.6;
P=.0001), 8p22.1-22 (LOD score 3.6;
P=.0001), and 11q21 (LOD score 3.1;
P=.0004). LOD scores >3.0 within single pedigrees were found at 4q13-31 (LOD score 3.2;
P=.0003) and at 11q23.3-24 (LOD score 3.2;
P=.0003). A LOD score of 2.9 was also found at 20q12.1-11.23 within in a single family. The fact that other studies have also detected LOD scores >3.0 at 1q33.2, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci. We believe that the weight of evidence for linkage to the chromosome 1q22, 5q33.2, and 8p21-22 loci is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium. Such studies will soon allow the identification of mutations having a direct effect on susceptibility to schizophrenia.</description><subject>Chromosome Aberrations</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 1</subject><subject>Chromosomes, Human, Pair 11</subject><subject>Chromosomes, Human, Pair 20</subject><subject>Chromosomes, Human, Pair 5</subject><subject>Chromosomes, Human, Pair 8</subject><subject>Family</subject><subject>Female</subject><subject>Genetic Linkage</subject><subject>Genetic Markers</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genome, Human</subject><subject>Genotype</subject><subject>Humans</subject><subject>Lod Score</subject><subject>Male</subject><subject>Microsatellite Repeats</subject><subject>Pedigree</subject><subject>Schizophrenia - genetics</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFks1u1DAUhSMEokOBR0BesWoGX9uJnQ1SNYKCNBKVCmsrcW46hsTO2JlBwzv3Her5gQKbyot7JR99Pjo-WfYa6ByoKt9xUFKpJ9kMCi7zsqTF02xGKWV5xSp5lr2I8TulAIry59kZAMiKgphld1fo_IA_bYskrThZQ5bW_ahvkVy6ut9FG8nCu86GIZJpheQ6YERnkPiO3GyiwXGyje3ttCNLbyzpfCA3ZmV_-XEV0Nn6gnhHFqvgBx_TU5HAmrM5uyDFmvP9rF1L1MggZ-ywXwe_TX5iwo-jD9MB-dvU5B-jw5rxOc-ZOMAYXQObQw4wZ_xl9qyr-4ivTvM8-_bxw9fFp3z55erz4nKZm4LSKe86JhsqAJquSeEiIJRStShUK0AKbNqUX8elqU0jqkqVXEguJa3T6Uom-Hn2_sgdN82ArUE3hbrXY7BDHXba11b_e-PsSt_6rQYmhZBVArw9AYJfbzBOerAp6r6vHfpN1JIWqkq_-6gQFC8qWtEHoQk-xoDdHzdA9b5C-lihJHzzt_cH2akzSUCPAkwJbi0GHY3dN6K1Ac2kW2__Z94Dgn7PcQ</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>Gurling, Hugh M.D.</creator><creator>Kalsi, Gursharan</creator><creator>Brynjolfson, Jon</creator><creator>Sigmundsson, Thordur</creator><creator>Sherrington, Robin</creator><creator>Mankoo, Baljinder S.</creator><creator>Read, Timothy</creator><creator>Murphy, Patrice</creator><creator>Blaveri, Ekaterina</creator><creator>McQuillin, Andrew</creator><creator>Petursson, Hannes</creator><creator>Curtis, David</creator><general>Elsevier Inc</general><general>The American Society of Human Genetics</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20010301</creationdate><title>Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23</title><author>Gurling, Hugh M.D. ; Kalsi, Gursharan ; Brynjolfson, Jon ; Sigmundsson, Thordur ; Sherrington, Robin ; Mankoo, Baljinder S. ; Read, Timothy ; Murphy, Patrice ; Blaveri, Ekaterina ; McQuillin, Andrew ; Petursson, Hannes ; Curtis, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-ff27b0411bfb086e1e1678de48d4174ebd117f37cacb499863473770a0a0f6243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Chromosome Aberrations</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Pair 1</topic><topic>Chromosomes, Human, Pair 11</topic><topic>Chromosomes, Human, Pair 20</topic><topic>Chromosomes, Human, Pair 5</topic><topic>Chromosomes, Human, Pair 8</topic><topic>Family</topic><topic>Female</topic><topic>Genetic Linkage</topic><topic>Genetic Markers</topic><topic>Genetic Predisposition to Disease - genetics</topic><topic>Genome, Human</topic><topic>Genotype</topic><topic>Humans</topic><topic>Lod Score</topic><topic>Male</topic><topic>Microsatellite Repeats</topic><topic>Pedigree</topic><topic>Schizophrenia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gurling, Hugh M.D.</creatorcontrib><creatorcontrib>Kalsi, Gursharan</creatorcontrib><creatorcontrib>Brynjolfson, Jon</creatorcontrib><creatorcontrib>Sigmundsson, Thordur</creatorcontrib><creatorcontrib>Sherrington, Robin</creatorcontrib><creatorcontrib>Mankoo, Baljinder S.</creatorcontrib><creatorcontrib>Read, Timothy</creatorcontrib><creatorcontrib>Murphy, Patrice</creatorcontrib><creatorcontrib>Blaveri, Ekaterina</creatorcontrib><creatorcontrib>McQuillin, Andrew</creatorcontrib><creatorcontrib>Petursson, Hannes</creatorcontrib><creatorcontrib>Curtis, David</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>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>Gurling, Hugh M.D.</au><au>Kalsi, Gursharan</au><au>Brynjolfson, Jon</au><au>Sigmundsson, Thordur</au><au>Sherrington, Robin</au><au>Mankoo, Baljinder S.</au><au>Read, Timothy</au><au>Murphy, Patrice</au><au>Blaveri, Ekaterina</au><au>McQuillin, Andrew</au><au>Petursson, Hannes</au><au>Curtis, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>68</volume><issue>3</issue><spage>661</spage><epage>673</epage><pages>661-673</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><abstract>We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive heterogeneity of linkage for genetic subtypes of schizophrenia. Our strategy consisted of selecting 13 kindreds containing multiple affected cases in three or more generations, an absence of bipolar affective disorder, and a single progenitor source of schizophrenia with unilineal transmission into the branch of the kindred sampled. DNA samples from these families were genotyped with 365 microsatellite markers spaced at ∼10-cM intervals across the whole genome. We observed LOD scores >3.0 at five distinct loci, either in the sample as a whole or within single families, strongly suggesting etiological heterogeneity. Heterogeneity LOD scores >3.0 in the sample as a whole were found at 1q33.2 (LOD score 3.2;
P=.0003), 5q33.2 (LOD score 3.6;
P=.0001), 8p22.1-22 (LOD score 3.6;
P=.0001), and 11q21 (LOD score 3.1;
P=.0004). LOD scores >3.0 within single pedigrees were found at 4q13-31 (LOD score 3.2;
P=.0003) and at 11q23.3-24 (LOD score 3.2;
P=.0003). A LOD score of 2.9 was also found at 20q12.1-11.23 within in a single family. The fact that other studies have also detected LOD scores >3.0 at 1q33.2, 5q33.2, 8p21-22 and 11q21 suggests that these regions do indeed harbor schizophrenia-susceptibility loci. We believe that the weight of evidence for linkage to the chromosome 1q22, 5q33.2, and 8p21-22 loci is now sufficient to justify intensive investigation of these regions by methods based on linkage disequilibrium. Such studies will soon allow the identification of mutations having a direct effect on susceptibility to schizophrenia.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11179014</pmid><doi>10.1086/318788</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Chromosome Aberrations Chromosome Mapping Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 5 Chromosomes, Human, Pair 8 Family Female Genetic Linkage Genetic Markers Genetic Predisposition to Disease - genetics Genome, Human Genotype Humans Lod Score Male Microsatellite Repeats Pedigree Schizophrenia - genetics |
title | Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23 |
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