Study on the haplotypes of MICA and MICB microsatellite and HLA-B locus in the Guangzhou Han population

:  The purpose of this study was to investigate the genetic polymorphisms and haplotypes of microsatellite locus in exon 5 of the MICA gene and intron 1 of the MICB gene and human leukocyte antigen‐B (HLA‐B) gene based on 106 samples of the Guangzhou Han population through means of polymerase chain...

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Veröffentlicht in:Tissue antigens 2004-09, Vol.64 (3), p.281-285
Hauptverfasser: Feng, M.-L., Guo, X.-J., Zhang, J.-Y., Xie, J.-H., Chen, L., Lu, Q., Yang, J.-H., Ji, Y., Qian, K.-C.
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container_end_page 285
container_issue 3
container_start_page 281
container_title Tissue antigens
container_volume 64
creator Feng, M.-L.
Guo, X.-J.
Zhang, J.-Y.
Xie, J.-H.
Chen, L.
Lu, Q.
Yang, J.-H.
Ji, Y.
Qian, K.-C.
description :  The purpose of this study was to investigate the genetic polymorphisms and haplotypes of microsatellite locus in exon 5 of the MICA gene and intron 1 of the MICB gene and human leukocyte antigen‐B (HLA‐B) gene based on 106 samples of the Guangzhou Han population through means of polymerase chain reaction and the fluorescent technique (6‐FAM). The corresponding haplotype frequencies, linkage disequilibrium values and relative linkage disequilibrium values were estimated based on population data. The results show that the genotype distributions of MICA and MICB microsatellite and HLA‐B satisfy the Hardy–Weinberg equilibrium. In total, five alleles of MICA microsatellite locus and 14 alleles of MICB microsatellite locus were observed. MICA A5 was the most common allele (0.2877), whereas A4 was the least common (0.1321). MICB CA14 was the most common allele (0.3255), and CA19 and CA28 were the two least common (0.0047). CA27 was not observed at all. Five kinds of MICA–MICB haplotypes, 18 kinds of MICA–HLA‐B haplotypes and 12 kinds of MICB–HLA‐B haplotypes occurred at frequencies of more than 1%. The common haplotypes of MICA–MICB, MICA–HLA‐B and MICB–HLA‐B were A5‐CA14, A5.1‐CA18, A4‐CA26, A9‐CA15, A5‐B*15(62), A5.1‐B*1301/1302, A4‐B*1301/1302, A6‐B*51, A6‐B*4403, A9‐B*3802, CA14‐B*4601, CA18‐B*1301/1302 and CA26‐B*1301/1302, and these haplotypes showed strong linkage disequilibrium. The polymorphisms and haplotype distributions of MICA and MICB microsatellite and HLA‐B locus in the Guangzhou Han population have their own distinct genetic characteristics. The microsatellite locus of exon 5 of the MICA gene and intron 1 of the MICB gene could therefore be used as genetic markers in the studies of anthropology, gene linkage analysis in genetic diseases, individual identification and paternity testing in forensic medicine.
doi_str_mv 10.1111/j.0001-2815.2004.00293.x
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The corresponding haplotype frequencies, linkage disequilibrium values and relative linkage disequilibrium values were estimated based on population data. The results show that the genotype distributions of MICA and MICB microsatellite and HLA‐B satisfy the Hardy–Weinberg equilibrium. In total, five alleles of MICA microsatellite locus and 14 alleles of MICB microsatellite locus were observed. MICA A5 was the most common allele (0.2877), whereas A4 was the least common (0.1321). MICB CA14 was the most common allele (0.3255), and CA19 and CA28 were the two least common (0.0047). CA27 was not observed at all. Five kinds of MICA–MICB haplotypes, 18 kinds of MICA–HLA‐B haplotypes and 12 kinds of MICB–HLA‐B haplotypes occurred at frequencies of more than 1%. The common haplotypes of MICA–MICB, MICA–HLA‐B and MICB–HLA‐B were A5‐CA14, A5.1‐CA18, A4‐CA26, A9‐CA15, A5‐B*15(62), A5.1‐B*1301/1302, A4‐B*1301/1302, A6‐B*51, A6‐B*4403, A9‐B*3802, CA14‐B*4601, CA18‐B*1301/1302 and CA26‐B*1301/1302, and these haplotypes showed strong linkage disequilibrium. The polymorphisms and haplotype distributions of MICA and MICB microsatellite and HLA‐B locus in the Guangzhou Han population have their own distinct genetic characteristics. The microsatellite locus of exon 5 of the MICA gene and intron 1 of the MICB gene could therefore be used as genetic markers in the studies of anthropology, gene linkage analysis in genetic diseases, individual identification and paternity testing in forensic medicine.</description><identifier>ISSN: 0001-2815</identifier><identifier>EISSN: 1399-0039</identifier><identifier>DOI: 10.1111/j.0001-2815.2004.00293.x</identifier><identifier>PMID: 15304009</identifier><language>eng</language><publisher>Oxford, UK; Malden, USA: Munksgaard International Publishers</publisher><subject>Asian Continental Ancestry Group - genetics ; Gene Frequency ; Genetic Markers ; Guangzhou Han population ; haplotype ; Haplotypes ; Histocompatibility Antigens Class I - genetics ; HLA-B ; HLA-B Antigens - genetics ; Humans ; Linkage Disequilibrium ; MICA ; MICB ; microsatellite ; Microsatellite Repeats ; Polymorphism, Genetic</subject><ispartof>Tissue antigens, 2004-09, Vol.64 (3), p.281-285</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4993-77d511b5264c0b8e681a0522d4298b635d47f8b5e4a238fde12e34de2af496563</citedby><cites>FETCH-LOGICAL-c4993-77d511b5264c0b8e681a0522d4298b635d47f8b5e4a238fde12e34de2af496563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.0001-2815.2004.00293.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.0001-2815.2004.00293.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15304009$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, M.-L.</creatorcontrib><creatorcontrib>Guo, X.-J.</creatorcontrib><creatorcontrib>Zhang, J.-Y.</creatorcontrib><creatorcontrib>Xie, J.-H.</creatorcontrib><creatorcontrib>Chen, L.</creatorcontrib><creatorcontrib>Lu, Q.</creatorcontrib><creatorcontrib>Yang, J.-H.</creatorcontrib><creatorcontrib>Ji, Y.</creatorcontrib><creatorcontrib>Qian, K.-C.</creatorcontrib><title>Study on the haplotypes of MICA and MICB microsatellite and HLA-B locus in the Guangzhou Han population</title><title>Tissue antigens</title><addtitle>Tissue Antigens</addtitle><description>:  The purpose of this study was to investigate the genetic polymorphisms and haplotypes of microsatellite locus in exon 5 of the MICA gene and intron 1 of the MICB gene and human leukocyte antigen‐B (HLA‐B) gene based on 106 samples of the Guangzhou Han population through means of polymerase chain reaction and the fluorescent technique (6‐FAM). The corresponding haplotype frequencies, linkage disequilibrium values and relative linkage disequilibrium values were estimated based on population data. The results show that the genotype distributions of MICA and MICB microsatellite and HLA‐B satisfy the Hardy–Weinberg equilibrium. In total, five alleles of MICA microsatellite locus and 14 alleles of MICB microsatellite locus were observed. MICA A5 was the most common allele (0.2877), whereas A4 was the least common (0.1321). MICB CA14 was the most common allele (0.3255), and CA19 and CA28 were the two least common (0.0047). CA27 was not observed at all. Five kinds of MICA–MICB haplotypes, 18 kinds of MICA–HLA‐B haplotypes and 12 kinds of MICB–HLA‐B haplotypes occurred at frequencies of more than 1%. The common haplotypes of MICA–MICB, MICA–HLA‐B and MICB–HLA‐B were A5‐CA14, A5.1‐CA18, A4‐CA26, A9‐CA15, A5‐B*15(62), A5.1‐B*1301/1302, A4‐B*1301/1302, A6‐B*51, A6‐B*4403, A9‐B*3802, CA14‐B*4601, CA18‐B*1301/1302 and CA26‐B*1301/1302, and these haplotypes showed strong linkage disequilibrium. The polymorphisms and haplotype distributions of MICA and MICB microsatellite and HLA‐B locus in the Guangzhou Han population have their own distinct genetic characteristics. The microsatellite locus of exon 5 of the MICA gene and intron 1 of the MICB gene could therefore be used as genetic markers in the studies of anthropology, gene linkage analysis in genetic diseases, individual identification and paternity testing in forensic medicine.</description><subject>Asian Continental Ancestry Group - genetics</subject><subject>Gene Frequency</subject><subject>Genetic Markers</subject><subject>Guangzhou Han population</subject><subject>haplotype</subject><subject>Haplotypes</subject><subject>Histocompatibility Antigens Class I - genetics</subject><subject>HLA-B</subject><subject>HLA-B Antigens - genetics</subject><subject>Humans</subject><subject>Linkage Disequilibrium</subject><subject>MICA</subject><subject>MICB</subject><subject>microsatellite</subject><subject>Microsatellite Repeats</subject><subject>Polymorphism, Genetic</subject><issn>0001-2815</issn><issn>1399-0039</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUV1P2zAUtdAQdGx_YfLT3lL8GdsSL21F26ECQjDt0XISh6akcYgT0e7Xz2kq9gh-8b3WOef6ngMAxGiMw7ncjBFCOCIS8zFBiIWWKDrenYARpkpFCFH1BYzeQefgq_eb0DGh1Bk4x5wihpAagefHtsv20FWwXVu4NnXp2n1tPXQ5vP01m0BTZX0xhdsibZw3rS3LorWH9-VqEk1h6dLOw2JQWHSmev67dh1cmgrWru5K0xau-gZOc1N6-_14X4Df8-un2TJa3S_CmFWUMqVoJETGMU44iVmKEmljiQ3ihGSMKJnElGdM5DLhlhlCZZ5ZTCxlmSUmZyrmMb0APwfdunGvnfWt3hY-DX82lXWd13EshJKCfgjEAkmMSA-UA7Bf3zc213VTbE2z1xjpPg290b3Rujda92noQxp6F6g_jjO6ZGuz_8Sj_QFwNQDeitLuPy2snyZ3oQj0aKAXvrW7d7ppXnQsqOD6z91Cy7l8uAlr6wX9B0OTpPM</recordid><startdate>200409</startdate><enddate>200409</enddate><creator>Feng, M.-L.</creator><creator>Guo, X.-J.</creator><creator>Zhang, J.-Y.</creator><creator>Xie, J.-H.</creator><creator>Chen, L.</creator><creator>Lu, Q.</creator><creator>Yang, J.-H.</creator><creator>Ji, Y.</creator><creator>Qian, K.-C.</creator><general>Munksgaard International Publishers</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>200409</creationdate><title>Study on the haplotypes of MICA and MICB microsatellite and HLA-B locus in the Guangzhou Han population</title><author>Feng, M.-L. ; Guo, X.-J. ; Zhang, J.-Y. ; Xie, J.-H. ; Chen, L. ; Lu, Q. ; Yang, J.-H. ; Ji, Y. ; Qian, K.-C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4993-77d511b5264c0b8e681a0522d4298b635d47f8b5e4a238fde12e34de2af496563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Asian Continental Ancestry Group - genetics</topic><topic>Gene Frequency</topic><topic>Genetic Markers</topic><topic>Guangzhou Han population</topic><topic>haplotype</topic><topic>Haplotypes</topic><topic>Histocompatibility Antigens Class I - genetics</topic><topic>HLA-B</topic><topic>HLA-B Antigens - genetics</topic><topic>Humans</topic><topic>Linkage Disequilibrium</topic><topic>MICA</topic><topic>MICB</topic><topic>microsatellite</topic><topic>Microsatellite Repeats</topic><topic>Polymorphism, Genetic</topic><toplevel>online_resources</toplevel><creatorcontrib>Feng, M.-L.</creatorcontrib><creatorcontrib>Guo, X.-J.</creatorcontrib><creatorcontrib>Zhang, J.-Y.</creatorcontrib><creatorcontrib>Xie, J.-H.</creatorcontrib><creatorcontrib>Chen, L.</creatorcontrib><creatorcontrib>Lu, Q.</creatorcontrib><creatorcontrib>Yang, J.-H.</creatorcontrib><creatorcontrib>Ji, Y.</creatorcontrib><creatorcontrib>Qian, K.-C.</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>Tissue antigens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, M.-L.</au><au>Guo, X.-J.</au><au>Zhang, J.-Y.</au><au>Xie, J.-H.</au><au>Chen, L.</au><au>Lu, Q.</au><au>Yang, J.-H.</au><au>Ji, Y.</au><au>Qian, K.-C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study on the haplotypes of MICA and MICB microsatellite and HLA-B locus in the Guangzhou Han population</atitle><jtitle>Tissue antigens</jtitle><addtitle>Tissue Antigens</addtitle><date>2004-09</date><risdate>2004</risdate><volume>64</volume><issue>3</issue><spage>281</spage><epage>285</epage><pages>281-285</pages><issn>0001-2815</issn><eissn>1399-0039</eissn><abstract>:  The purpose of this study was to investigate the genetic polymorphisms and haplotypes of microsatellite locus in exon 5 of the MICA gene and intron 1 of the MICB gene and human leukocyte antigen‐B (HLA‐B) gene based on 106 samples of the Guangzhou Han population through means of polymerase chain reaction and the fluorescent technique (6‐FAM). The corresponding haplotype frequencies, linkage disequilibrium values and relative linkage disequilibrium values were estimated based on population data. The results show that the genotype distributions of MICA and MICB microsatellite and HLA‐B satisfy the Hardy–Weinberg equilibrium. In total, five alleles of MICA microsatellite locus and 14 alleles of MICB microsatellite locus were observed. MICA A5 was the most common allele (0.2877), whereas A4 was the least common (0.1321). MICB CA14 was the most common allele (0.3255), and CA19 and CA28 were the two least common (0.0047). CA27 was not observed at all. Five kinds of MICA–MICB haplotypes, 18 kinds of MICA–HLA‐B haplotypes and 12 kinds of MICB–HLA‐B haplotypes occurred at frequencies of more than 1%. The common haplotypes of MICA–MICB, MICA–HLA‐B and MICB–HLA‐B were A5‐CA14, A5.1‐CA18, A4‐CA26, A9‐CA15, A5‐B*15(62), A5.1‐B*1301/1302, A4‐B*1301/1302, A6‐B*51, A6‐B*4403, A9‐B*3802, CA14‐B*4601, CA18‐B*1301/1302 and CA26‐B*1301/1302, and these haplotypes showed strong linkage disequilibrium. The polymorphisms and haplotype distributions of MICA and MICB microsatellite and HLA‐B locus in the Guangzhou Han population have their own distinct genetic characteristics. The microsatellite locus of exon 5 of the MICA gene and intron 1 of the MICB gene could therefore be used as genetic markers in the studies of anthropology, gene linkage analysis in genetic diseases, individual identification and paternity testing in forensic medicine.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Munksgaard International Publishers</pub><pmid>15304009</pmid><doi>10.1111/j.0001-2815.2004.00293.x</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Asian Continental Ancestry Group - genetics
Gene Frequency
Genetic Markers
Guangzhou Han population
haplotype
Haplotypes
Histocompatibility Antigens Class I - genetics
HLA-B
HLA-B Antigens - genetics
Humans
Linkage Disequilibrium
MICA
MICB
microsatellite
Microsatellite Repeats
Polymorphism, Genetic
title Study on the haplotypes of MICA and MICB microsatellite and HLA-B locus in the Guangzhou Han population
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