Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population

We describe for the first time extended haplotypes in a Croatian population. The present study gives the HLA‐A, ‐B, ‐DRB1, ‐DQA1 and ‐DQB1 allele and haplotype frequencies in 105 families with at least two offspring. All individuals were studied by conventional serology for HLA class I antigens (A a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of immunogenetics 2000-02, Vol.27 (1), p.47-51
Hauptverfasser: Grubic, Z., Zunec, R., Cec uk-Jelic ic, E., Kerhin-Brkljacic, V., Kastelan, A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 51
container_issue 1
container_start_page 47
container_title European journal of immunogenetics
container_volume 27
creator Grubic, Z.
Zunec, R.
Cec uk-Jelic ic, E.
Kerhin-Brkljacic, V.
Kastelan, A.
description We describe for the first time extended haplotypes in a Croatian population. The present study gives the HLA‐A, ‐B, ‐DRB1, ‐DQA1 and ‐DQB1 allele and haplotype frequencies in 105 families with at least two offspring. All individuals were studied by conventional serology for HLA class I antigens (A and B), while class II alleles (DRB1, DQA1, DQB1) were typed using the PCR–SSOP method. HLA genotyping was performed by segregation in all 105 families. For extended haplotype analysis, 420 independent parental haplotypes were included. Fourteen HLA‐A, 18 HLA‐B, 28 DRB1, 9 DQA1 and 11 DQB1 alleles were found in the studied population. Most of the DRB1 alleles in our population had an exclusive association with one specific DQA1‐DQB1 combination. This strong linkage disequilibrium within the HLA class II region is often extended to the HLA‐B locus. A total of 10 HLA‐A, ‐B, ‐DRB1, ‐DQA1, ‐DQB1 haplotypes were observed with a frequency ≤ 1.0%. The three most frequent haplotypes were HLA‐A1, B8, DRB1*0301, DQA1*0501, DQB1*0201; HLA‐A3, B7, DRB1*1501, DQA1*0102, DQB1*0602 and HLA‐A24, B44, DRB1*0701, DQA1*0201, DQB1*02. These results should provide a useful reference for further anthropological studies, transplantation studies, and studies of associations between HLA and diseases.
doi_str_mv 10.1046/j.1365-2370.2000.00193.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70915672</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17499712</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4333-3920381607d7cf2f14cb92f5237c723c243b74750bffef013120bc4dbcb559923</originalsourceid><addsrcrecordid>eNqNkMtu2zAQRYmgReI8fiHgqqtKHZIiaQLd2E4aO3DzQoIsCYomEbmSqIg2av99pCoIumsXxAzAc2cGByFMICWQiW_rlDDBE8okpBQAUgCiWLo7QKOPj09oBEpAIjMKR-g4xnUHMaLEIToiIDgZczJCT3eh3FehbV6KWOHg8Xw5SSZfcTLt3sXDlPTlfkKwqVd9NyX4xTRl2OwbF3FRY4NnbTCbwtS4Cc227NpQn6LP3pTRnb3XE_T04_JxNk-Wt1eL2WSZ2IwxljBFgY2JALmS1lNPMpsr6nl3vpWUWZqxXGaSQ-698_31FHKbrXKbc64UZSfoyzC3acPr1sWNropoXVma2oVt1BIU4UL-GyQyU0qSHhwPoG1DjK3zummLyrR7TUD37vVa94p1r1j37vUf93rXRc_fd2zzyq3-Cg6yO-D7APwuSrf_78F6cb3omi6eDPEibtzuI27aX1pIJrl-vrnS148385-CcS3YG256m_s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17499712</pqid></control><display><type>article</type><title>Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Grubic, Z. ; Zunec, R. ; Cec uk-Jelic ic, E. ; Kerhin-Brkljacic, V. ; Kastelan, A.</creator><creatorcontrib>Grubic, Z. ; Zunec, R. ; Cec uk-Jelic ic, E. ; Kerhin-Brkljacic, V. ; Kastelan, A.</creatorcontrib><description>We describe for the first time extended haplotypes in a Croatian population. The present study gives the HLA‐A, ‐B, ‐DRB1, ‐DQA1 and ‐DQB1 allele and haplotype frequencies in 105 families with at least two offspring. All individuals were studied by conventional serology for HLA class I antigens (A and B), while class II alleles (DRB1, DQA1, DQB1) were typed using the PCR–SSOP method. HLA genotyping was performed by segregation in all 105 families. For extended haplotype analysis, 420 independent parental haplotypes were included. Fourteen HLA‐A, 18 HLA‐B, 28 DRB1, 9 DQA1 and 11 DQB1 alleles were found in the studied population. Most of the DRB1 alleles in our population had an exclusive association with one specific DQA1‐DQB1 combination. This strong linkage disequilibrium within the HLA class II region is often extended to the HLA‐B locus. A total of 10 HLA‐A, ‐B, ‐DRB1, ‐DQA1, ‐DQB1 haplotypes were observed with a frequency ≤ 1.0%. The three most frequent haplotypes were HLA‐A1, B8, DRB1*0301, DQA1*0501, DQB1*0201; HLA‐A3, B7, DRB1*1501, DQA1*0102, DQB1*0602 and HLA‐A24, B44, DRB1*0701, DQA1*0201, DQB1*02. These results should provide a useful reference for further anthropological studies, transplantation studies, and studies of associations between HLA and diseases.</description><identifier>ISSN: 0960-7420</identifier><identifier>EISSN: 1365-2370</identifier><identifier>DOI: 10.1046/j.1365-2370.2000.00193.x</identifier><identifier>PMID: 10651851</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Croatia ; Genetics, Population ; Haplotypes ; histocompatibility locus HLA ; HLA-A Antigens - genetics ; HLA-B Antigens - genetics ; HLA-DQ alpha-Chains ; HLA-DQ Antigens - genetics ; HLA-DQ beta-Chains ; HLA-DR Antigens - genetics ; HLA-DRB1 Chains ; Humans ; Linkage Disequilibrium ; Nucleic Acid Hybridization ; Polymorphism, Genetic</subject><ispartof>European journal of immunogenetics, 2000-02, Vol.27 (1), p.47-51</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4333-3920381607d7cf2f14cb92f5237c723c243b74750bffef013120bc4dbcb559923</citedby><cites>FETCH-LOGICAL-c4333-3920381607d7cf2f14cb92f5237c723c243b74750bffef013120bc4dbcb559923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-2370.2000.00193.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-2370.2000.00193.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10651851$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grubic, Z.</creatorcontrib><creatorcontrib>Zunec, R.</creatorcontrib><creatorcontrib>Cec uk-Jelic ic, E.</creatorcontrib><creatorcontrib>Kerhin-Brkljacic, V.</creatorcontrib><creatorcontrib>Kastelan, A.</creatorcontrib><title>Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population</title><title>European journal of immunogenetics</title><addtitle>Eur J Immunogenet</addtitle><description>We describe for the first time extended haplotypes in a Croatian population. The present study gives the HLA‐A, ‐B, ‐DRB1, ‐DQA1 and ‐DQB1 allele and haplotype frequencies in 105 families with at least two offspring. All individuals were studied by conventional serology for HLA class I antigens (A and B), while class II alleles (DRB1, DQA1, DQB1) were typed using the PCR–SSOP method. HLA genotyping was performed by segregation in all 105 families. For extended haplotype analysis, 420 independent parental haplotypes were included. Fourteen HLA‐A, 18 HLA‐B, 28 DRB1, 9 DQA1 and 11 DQB1 alleles were found in the studied population. Most of the DRB1 alleles in our population had an exclusive association with one specific DQA1‐DQB1 combination. This strong linkage disequilibrium within the HLA class II region is often extended to the HLA‐B locus. A total of 10 HLA‐A, ‐B, ‐DRB1, ‐DQA1, ‐DQB1 haplotypes were observed with a frequency ≤ 1.0%. The three most frequent haplotypes were HLA‐A1, B8, DRB1*0301, DQA1*0501, DQB1*0201; HLA‐A3, B7, DRB1*1501, DQA1*0102, DQB1*0602 and HLA‐A24, B44, DRB1*0701, DQA1*0201, DQB1*02. These results should provide a useful reference for further anthropological studies, transplantation studies, and studies of associations between HLA and diseases.</description><subject>Croatia</subject><subject>Genetics, Population</subject><subject>Haplotypes</subject><subject>histocompatibility locus HLA</subject><subject>HLA-A Antigens - genetics</subject><subject>HLA-B Antigens - genetics</subject><subject>HLA-DQ alpha-Chains</subject><subject>HLA-DQ Antigens - genetics</subject><subject>HLA-DQ beta-Chains</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DRB1 Chains</subject><subject>Humans</subject><subject>Linkage Disequilibrium</subject><subject>Nucleic Acid Hybridization</subject><subject>Polymorphism, Genetic</subject><issn>0960-7420</issn><issn>1365-2370</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtu2zAQRYmgReI8fiHgqqtKHZIiaQLd2E4aO3DzQoIsCYomEbmSqIg2av99pCoIumsXxAzAc2cGByFMICWQiW_rlDDBE8okpBQAUgCiWLo7QKOPj09oBEpAIjMKR-g4xnUHMaLEIToiIDgZczJCT3eh3FehbV6KWOHg8Xw5SSZfcTLt3sXDlPTlfkKwqVd9NyX4xTRl2OwbF3FRY4NnbTCbwtS4Cc227NpQn6LP3pTRnb3XE_T04_JxNk-Wt1eL2WSZ2IwxljBFgY2JALmS1lNPMpsr6nl3vpWUWZqxXGaSQ-698_31FHKbrXKbc64UZSfoyzC3acPr1sWNropoXVma2oVt1BIU4UL-GyQyU0qSHhwPoG1DjK3zummLyrR7TUD37vVa94p1r1j37vUf93rXRc_fd2zzyq3-Cg6yO-D7APwuSrf_78F6cb3omi6eDPEibtzuI27aX1pIJrl-vrnS148385-CcS3YG256m_s</recordid><startdate>200002</startdate><enddate>200002</enddate><creator>Grubic, Z.</creator><creator>Zunec, R.</creator><creator>Cec uk-Jelic ic, E.</creator><creator>Kerhin-Brkljacic, V.</creator><creator>Kastelan, A.</creator><general>Blackwell Science Ltd</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>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200002</creationdate><title>Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population</title><author>Grubic, Z. ; Zunec, R. ; Cec uk-Jelic ic, E. ; Kerhin-Brkljacic, V. ; Kastelan, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4333-3920381607d7cf2f14cb92f5237c723c243b74750bffef013120bc4dbcb559923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Croatia</topic><topic>Genetics, Population</topic><topic>Haplotypes</topic><topic>histocompatibility locus HLA</topic><topic>HLA-A Antigens - genetics</topic><topic>HLA-B Antigens - genetics</topic><topic>HLA-DQ alpha-Chains</topic><topic>HLA-DQ Antigens - genetics</topic><topic>HLA-DQ beta-Chains</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DRB1 Chains</topic><topic>Humans</topic><topic>Linkage Disequilibrium</topic><topic>Nucleic Acid Hybridization</topic><topic>Polymorphism, Genetic</topic><toplevel>online_resources</toplevel><creatorcontrib>Grubic, Z.</creatorcontrib><creatorcontrib>Zunec, R.</creatorcontrib><creatorcontrib>Cec uk-Jelic ic, E.</creatorcontrib><creatorcontrib>Kerhin-Brkljacic, V.</creatorcontrib><creatorcontrib>Kastelan, A.</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>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of immunogenetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grubic, Z.</au><au>Zunec, R.</au><au>Cec uk-Jelic ic, E.</au><au>Kerhin-Brkljacic, V.</au><au>Kastelan, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population</atitle><jtitle>European journal of immunogenetics</jtitle><addtitle>Eur J Immunogenet</addtitle><date>2000-02</date><risdate>2000</risdate><volume>27</volume><issue>1</issue><spage>47</spage><epage>51</epage><pages>47-51</pages><issn>0960-7420</issn><eissn>1365-2370</eissn><abstract>We describe for the first time extended haplotypes in a Croatian population. The present study gives the HLA‐A, ‐B, ‐DRB1, ‐DQA1 and ‐DQB1 allele and haplotype frequencies in 105 families with at least two offspring. All individuals were studied by conventional serology for HLA class I antigens (A and B), while class II alleles (DRB1, DQA1, DQB1) were typed using the PCR–SSOP method. HLA genotyping was performed by segregation in all 105 families. For extended haplotype analysis, 420 independent parental haplotypes were included. Fourteen HLA‐A, 18 HLA‐B, 28 DRB1, 9 DQA1 and 11 DQB1 alleles were found in the studied population. Most of the DRB1 alleles in our population had an exclusive association with one specific DQA1‐DQB1 combination. This strong linkage disequilibrium within the HLA class II region is often extended to the HLA‐B locus. A total of 10 HLA‐A, ‐B, ‐DRB1, ‐DQA1, ‐DQB1 haplotypes were observed with a frequency ≤ 1.0%. The three most frequent haplotypes were HLA‐A1, B8, DRB1*0301, DQA1*0501, DQB1*0201; HLA‐A3, B7, DRB1*1501, DQA1*0102, DQB1*0602 and HLA‐A24, B44, DRB1*0701, DQA1*0201, DQB1*02. These results should provide a useful reference for further anthropological studies, transplantation studies, and studies of associations between HLA and diseases.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>10651851</pmid><doi>10.1046/j.1365-2370.2000.00193.x</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0960-7420
ispartof European journal of immunogenetics, 2000-02, Vol.27 (1), p.47-51
issn 0960-7420
1365-2370
language eng
recordid cdi_proquest_miscellaneous_70915672
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Croatia
Genetics, Population
Haplotypes
histocompatibility locus HLA
HLA-A Antigens - genetics
HLA-B Antigens - genetics
HLA-DQ alpha-Chains
HLA-DQ Antigens - genetics
HLA-DQ beta-Chains
HLA-DR Antigens - genetics
HLA-DRB1 Chains
Humans
Linkage Disequilibrium
Nucleic Acid Hybridization
Polymorphism, Genetic
title Polymorphism of HLA-A, -B, -DRB1, -DQA1 and -DQB1 haplotypes in a Croatian population
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T02%3A01%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polymorphism%20of%20HLA-A,%20-B,%20-DRB1,%20-DQA1%20and%20-DQB1%20haplotypes%20in%20a%20Croatian%20population&rft.jtitle=European%20journal%20of%20immunogenetics&rft.au=Grubic,%20Z.&rft.date=2000-02&rft.volume=27&rft.issue=1&rft.spage=47&rft.epage=51&rft.pages=47-51&rft.issn=0960-7420&rft.eissn=1365-2370&rft_id=info:doi/10.1046/j.1365-2370.2000.00193.x&rft_dat=%3Cproquest_cross%3E17499712%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17499712&rft_id=info:pmid/10651851&rfr_iscdi=true