Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population
In order to identify single nucleotide polymorphisms (SNPs) and haplotype frequencies of CYP3A4 in a Japanese population, the distal enhancer and proximal promoter regions, all exons, and the surrounding introns were sequenced from genomic DNA of 416 Japanese subjects. We found 24 SNPs, including 17...
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creator | Fukushima-Uesaka, Hiromi Saito, Yoshiro Watanabe, Hidemi Shiseki, Kisho Saeki, Mayumi Nakamura, Takahiro Kurose, Kouichi Sai, Kimie Komamura, Kazuo Ueno, Kazuyuki Kamakura, Shiro Kitakaze, Masafumi Hanai, Sotaro Nakajima, Toshiharu Matsumoto, Kenji Saito, Hirohisa Goto, Yu-ichi Kimura, Hideo Katoh, Masaaki Sugai, Kenji Minami, Narihiro Shirao, Kuniaki Tamura, Tomohide Yamamoto, Noboru Minami, Hironobu Ohtsu, Atsushi Yoshida, Teruhiko Saijo, Nagahiro Kitamura, Yutaka Kamatani, Naoyuki Ozawa, Shogo Sawada, Jun-ichi |
description | In order to identify single nucleotide polymorphisms (SNPs) and haplotype frequencies of CYP3A4 in a Japanese population, the distal enhancer and proximal promoter regions, all exons, and the surrounding introns were sequenced from genomic DNA of 416 Japanese subjects. We found 24 SNPs, including 17 novel ones: two in the distal enhancer, four in the proximal promoter, one in the 5′‐untranslated region (UTR), seven in the introns, and three in the 3′‐UTR. The most common SNP was c.1026+12G>A (IVS10+12G>A), with a 0.249 frequency. Four non‐synonymous SNPs, c.554C>G (p.T185S, CYP3A4*16), c.830_831insA (p.E277fsX8, *6), c.878T>C (p.L293P, *18), and c.1088 C>T (p.T363M, *11) were found with frequencies of 0.014, 0.001, 0.028, and 0.002, respectively. No SNP was found in the known nuclear transcriptional factor‐binding sites in the enhancer and promoter regions. Using these 24 SNPs, 16 haplotypes were unambiguously identified, and nine haplotypes were inferred by aid of an expectation‐maximization‐based program. In addition, using data from 186 subjects enabled a close linkage to be found between CYP3A4 and CYP3A5 SNPs, especially among the SNPs at c.1026+12 in CYP3A4 and c.219‐237 (IVS3‐237, a key SNP site for CYP3A5*3), c.865+77 (IVS9+77) and c.1523 in CYP3A5. This result suggested that CYP3A4 and CYP3A5 are within the same gene block. Haplotype analysis between CYP3A4 and CYP3A5 revealed several major haplotype combinations in the CYP3A4‐CYP3A5 block. Our findings provide fundamental and useful information for genotyping CYP3A4 (and CYP3A5) in the Japanese, and probably Asian populations. © 2003 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/humu.9210 |
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We found 24 SNPs, including 17 novel ones: two in the distal enhancer, four in the proximal promoter, one in the 5′‐untranslated region (UTR), seven in the introns, and three in the 3′‐UTR. The most common SNP was c.1026+12G>A (IVS10+12G>A), with a 0.249 frequency. Four non‐synonymous SNPs, c.554C>G (p.T185S, CYP3A4*16), c.830_831insA (p.E277fsX8, *6), c.878T>C (p.L293P, *18), and c.1088 C>T (p.T363M, *11) were found with frequencies of 0.014, 0.001, 0.028, and 0.002, respectively. No SNP was found in the known nuclear transcriptional factor‐binding sites in the enhancer and promoter regions. Using these 24 SNPs, 16 haplotypes were unambiguously identified, and nine haplotypes were inferred by aid of an expectation‐maximization‐based program. In addition, using data from 186 subjects enabled a close linkage to be found between CYP3A4 and CYP3A5 SNPs, especially among the SNPs at c.1026+12 in CYP3A4 and c.219‐237 (IVS3‐237, a key SNP site for CYP3A5*3), c.865+77 (IVS9+77) and c.1523 in CYP3A5. This result suggested that CYP3A4 and CYP3A5 are within the same gene block. Haplotype analysis between CYP3A4 and CYP3A5 revealed several major haplotype combinations in the CYP3A4‐CYP3A5 block. Our findings provide fundamental and useful information for genotyping CYP3A4 (and CYP3A5) in the Japanese, and probably Asian populations. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1059-7794</identifier><identifier>EISSN: 1098-1004</identifier><identifier>DOI: 10.1002/humu.9210</identifier><identifier>PMID: 14695543</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Cancer ; Childrens health ; CYP3A4 ; CYP3A5 ; Cytochrome ; Cytochrome P-450 CYP3A ; Cytochrome P-450 Enzyme System - genetics ; Gene Frequency ; Genetic Linkage ; Genetic testing ; haplotype ; Haplotypes ; Health sciences ; Hospitals ; Humans ; Japan ; Japanese ; Metabolism ; Mutation ; Oncology ; Polymorphism, Single Nucleotide ; Research centers ; SNP</subject><ispartof>Human mutation, 2004-01, Vol.23 (1), p.100-100</ispartof><rights>2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><rights>Copyright © 2004 Wiley-Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhumu.9210$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhumu.9210$$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/14695543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fukushima-Uesaka, Hiromi</creatorcontrib><creatorcontrib>Saito, Yoshiro</creatorcontrib><creatorcontrib>Watanabe, Hidemi</creatorcontrib><creatorcontrib>Shiseki, Kisho</creatorcontrib><creatorcontrib>Saeki, Mayumi</creatorcontrib><creatorcontrib>Nakamura, Takahiro</creatorcontrib><creatorcontrib>Kurose, Kouichi</creatorcontrib><creatorcontrib>Sai, Kimie</creatorcontrib><creatorcontrib>Komamura, Kazuo</creatorcontrib><creatorcontrib>Ueno, Kazuyuki</creatorcontrib><creatorcontrib>Kamakura, Shiro</creatorcontrib><creatorcontrib>Kitakaze, Masafumi</creatorcontrib><creatorcontrib>Hanai, Sotaro</creatorcontrib><creatorcontrib>Nakajima, Toshiharu</creatorcontrib><creatorcontrib>Matsumoto, Kenji</creatorcontrib><creatorcontrib>Saito, Hirohisa</creatorcontrib><creatorcontrib>Goto, Yu-ichi</creatorcontrib><creatorcontrib>Kimura, Hideo</creatorcontrib><creatorcontrib>Katoh, Masaaki</creatorcontrib><creatorcontrib>Sugai, Kenji</creatorcontrib><creatorcontrib>Minami, Narihiro</creatorcontrib><creatorcontrib>Shirao, Kuniaki</creatorcontrib><creatorcontrib>Tamura, Tomohide</creatorcontrib><creatorcontrib>Yamamoto, Noboru</creatorcontrib><creatorcontrib>Minami, Hironobu</creatorcontrib><creatorcontrib>Ohtsu, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Teruhiko</creatorcontrib><creatorcontrib>Saijo, Nagahiro</creatorcontrib><creatorcontrib>Kitamura, Yutaka</creatorcontrib><creatorcontrib>Kamatani, Naoyuki</creatorcontrib><creatorcontrib>Ozawa, Shogo</creatorcontrib><creatorcontrib>Sawada, Jun-ichi</creatorcontrib><title>Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population</title><title>Human mutation</title><addtitle>Hum. Mutat</addtitle><description>In order to identify single nucleotide polymorphisms (SNPs) and haplotype frequencies of CYP3A4 in a Japanese population, the distal enhancer and proximal promoter regions, all exons, and the surrounding introns were sequenced from genomic DNA of 416 Japanese subjects. We found 24 SNPs, including 17 novel ones: two in the distal enhancer, four in the proximal promoter, one in the 5′‐untranslated region (UTR), seven in the introns, and three in the 3′‐UTR. The most common SNP was c.1026+12G>A (IVS10+12G>A), with a 0.249 frequency. Four non‐synonymous SNPs, c.554C>G (p.T185S, CYP3A4*16), c.830_831insA (p.E277fsX8, *6), c.878T>C (p.L293P, *18), and c.1088 C>T (p.T363M, *11) were found with frequencies of 0.014, 0.001, 0.028, and 0.002, respectively. No SNP was found in the known nuclear transcriptional factor‐binding sites in the enhancer and promoter regions. Using these 24 SNPs, 16 haplotypes were unambiguously identified, and nine haplotypes were inferred by aid of an expectation‐maximization‐based program. In addition, using data from 186 subjects enabled a close linkage to be found between CYP3A4 and CYP3A5 SNPs, especially among the SNPs at c.1026+12 in CYP3A4 and c.219‐237 (IVS3‐237, a key SNP site for CYP3A5*3), c.865+77 (IVS9+77) and c.1523 in CYP3A5. This result suggested that CYP3A4 and CYP3A5 are within the same gene block. Haplotype analysis between CYP3A4 and CYP3A5 revealed several major haplotype combinations in the CYP3A4‐CYP3A5 block. Our findings provide fundamental and useful information for genotyping CYP3A4 (and CYP3A5) in the Japanese, and probably Asian populations. © 2003 Wiley‐Liss, Inc.</description><subject>Cancer</subject><subject>Childrens health</subject><subject>CYP3A4</subject><subject>CYP3A5</subject><subject>Cytochrome</subject><subject>Cytochrome P-450 CYP3A</subject><subject>Cytochrome P-450 Enzyme System - genetics</subject><subject>Gene Frequency</subject><subject>Genetic Linkage</subject><subject>Genetic testing</subject><subject>haplotype</subject><subject>Haplotypes</subject><subject>Health sciences</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Japan</subject><subject>Japanese</subject><subject>Metabolism</subject><subject>Mutation</subject><subject>Oncology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Research centers</subject><subject>SNP</subject><issn>1059-7794</issn><issn>1098-1004</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkU1LwzAch4MozreDX0CCB2-dSZqX5ihDN3XqDhtDEUKWpS7atbVpmfv2pkwdmEv-JM8TfuQHwClGXYwQuVw0y6YrCUY74AAjmUThlO62M5OREJJ2wKH37wihhLF4H3Qw5ZIxGh-A14Eus6Jel9bDIoW951F8RaHO57BeWFdBkxXewszlH_rNwpWrFxuGwcVWdDnU8E6XOrcBLouyyXTtivwY7KU68_bkZz8Ck5vrcW8QDZ_6t72rYeQIESjSREgiCNUyTaSZGYlJCKgp5sakGJGwkEh4YiinkptZOhNasjRhQWDI8PgIXGzeLavis7G-Vkvnjc2yEKhovEoQEnEiW_D8H_heNFUesiksBeEx4TJAZz9QM1vauSort9TVWv1-WgAuN8DKZXa9vUeqbUO1bai2DTWYPEzaIRjRxnC-tl9_hq4-FBexYGr62Ffj6ejl8R4xNYy_ARe5iXA</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Fukushima-Uesaka, Hiromi</creator><creator>Saito, Yoshiro</creator><creator>Watanabe, Hidemi</creator><creator>Shiseki, Kisho</creator><creator>Saeki, Mayumi</creator><creator>Nakamura, Takahiro</creator><creator>Kurose, Kouichi</creator><creator>Sai, Kimie</creator><creator>Komamura, Kazuo</creator><creator>Ueno, Kazuyuki</creator><creator>Kamakura, Shiro</creator><creator>Kitakaze, Masafumi</creator><creator>Hanai, Sotaro</creator><creator>Nakajima, Toshiharu</creator><creator>Matsumoto, Kenji</creator><creator>Saito, Hirohisa</creator><creator>Goto, Yu-ichi</creator><creator>Kimura, Hideo</creator><creator>Katoh, Masaaki</creator><creator>Sugai, Kenji</creator><creator>Minami, Narihiro</creator><creator>Shirao, Kuniaki</creator><creator>Tamura, Tomohide</creator><creator>Yamamoto, Noboru</creator><creator>Minami, Hironobu</creator><creator>Ohtsu, Atsushi</creator><creator>Yoshida, Teruhiko</creator><creator>Saijo, Nagahiro</creator><creator>Kitamura, Yutaka</creator><creator>Kamatani, Naoyuki</creator><creator>Ozawa, Shogo</creator><creator>Sawada, Jun-ichi</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Hindawi Limited</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200401</creationdate><title>Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population</title><author>Fukushima-Uesaka, Hiromi ; Saito, Yoshiro ; Watanabe, Hidemi ; Shiseki, Kisho ; Saeki, Mayumi ; Nakamura, Takahiro ; Kurose, Kouichi ; Sai, Kimie ; Komamura, Kazuo ; Ueno, Kazuyuki ; Kamakura, Shiro ; Kitakaze, Masafumi ; Hanai, Sotaro ; Nakajima, Toshiharu ; Matsumoto, Kenji ; Saito, Hirohisa ; Goto, Yu-ichi ; Kimura, Hideo ; Katoh, Masaaki ; Sugai, Kenji ; Minami, Narihiro ; Shirao, Kuniaki ; Tamura, Tomohide ; Yamamoto, Noboru ; Minami, Hironobu ; Ohtsu, Atsushi ; Yoshida, Teruhiko ; Saijo, Nagahiro ; Kitamura, Yutaka ; Kamatani, Naoyuki ; Ozawa, Shogo ; Sawada, Jun-ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2270-a2792724a9f89cbc912146a416ccf10222207868c46496cbfb7a95f85a9f50c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Cancer</topic><topic>Childrens health</topic><topic>CYP3A4</topic><topic>CYP3A5</topic><topic>Cytochrome</topic><topic>Cytochrome P-450 CYP3A</topic><topic>Cytochrome P-450 Enzyme System - genetics</topic><topic>Gene Frequency</topic><topic>Genetic Linkage</topic><topic>Genetic testing</topic><topic>haplotype</topic><topic>Haplotypes</topic><topic>Health sciences</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Japan</topic><topic>Japanese</topic><topic>Metabolism</topic><topic>Mutation</topic><topic>Oncology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Research centers</topic><topic>SNP</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fukushima-Uesaka, Hiromi</creatorcontrib><creatorcontrib>Saito, Yoshiro</creatorcontrib><creatorcontrib>Watanabe, Hidemi</creatorcontrib><creatorcontrib>Shiseki, Kisho</creatorcontrib><creatorcontrib>Saeki, Mayumi</creatorcontrib><creatorcontrib>Nakamura, Takahiro</creatorcontrib><creatorcontrib>Kurose, Kouichi</creatorcontrib><creatorcontrib>Sai, Kimie</creatorcontrib><creatorcontrib>Komamura, Kazuo</creatorcontrib><creatorcontrib>Ueno, Kazuyuki</creatorcontrib><creatorcontrib>Kamakura, Shiro</creatorcontrib><creatorcontrib>Kitakaze, Masafumi</creatorcontrib><creatorcontrib>Hanai, Sotaro</creatorcontrib><creatorcontrib>Nakajima, Toshiharu</creatorcontrib><creatorcontrib>Matsumoto, Kenji</creatorcontrib><creatorcontrib>Saito, Hirohisa</creatorcontrib><creatorcontrib>Goto, Yu-ichi</creatorcontrib><creatorcontrib>Kimura, Hideo</creatorcontrib><creatorcontrib>Katoh, Masaaki</creatorcontrib><creatorcontrib>Sugai, Kenji</creatorcontrib><creatorcontrib>Minami, Narihiro</creatorcontrib><creatorcontrib>Shirao, Kuniaki</creatorcontrib><creatorcontrib>Tamura, Tomohide</creatorcontrib><creatorcontrib>Yamamoto, Noboru</creatorcontrib><creatorcontrib>Minami, Hironobu</creatorcontrib><creatorcontrib>Ohtsu, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Teruhiko</creatorcontrib><creatorcontrib>Saijo, Nagahiro</creatorcontrib><creatorcontrib>Kitamura, Yutaka</creatorcontrib><creatorcontrib>Kamatani, Naoyuki</creatorcontrib><creatorcontrib>Ozawa, Shogo</creatorcontrib><creatorcontrib>Sawada, Jun-ichi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human mutation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fukushima-Uesaka, Hiromi</au><au>Saito, Yoshiro</au><au>Watanabe, Hidemi</au><au>Shiseki, Kisho</au><au>Saeki, Mayumi</au><au>Nakamura, Takahiro</au><au>Kurose, Kouichi</au><au>Sai, Kimie</au><au>Komamura, Kazuo</au><au>Ueno, Kazuyuki</au><au>Kamakura, Shiro</au><au>Kitakaze, Masafumi</au><au>Hanai, Sotaro</au><au>Nakajima, Toshiharu</au><au>Matsumoto, Kenji</au><au>Saito, Hirohisa</au><au>Goto, Yu-ichi</au><au>Kimura, Hideo</au><au>Katoh, Masaaki</au><au>Sugai, Kenji</au><au>Minami, Narihiro</au><au>Shirao, Kuniaki</au><au>Tamura, Tomohide</au><au>Yamamoto, Noboru</au><au>Minami, Hironobu</au><au>Ohtsu, Atsushi</au><au>Yoshida, Teruhiko</au><au>Saijo, Nagahiro</au><au>Kitamura, Yutaka</au><au>Kamatani, Naoyuki</au><au>Ozawa, Shogo</au><au>Sawada, Jun-ichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population</atitle><jtitle>Human mutation</jtitle><addtitle>Hum. Mutat</addtitle><date>2004-01</date><risdate>2004</risdate><volume>23</volume><issue>1</issue><spage>100</spage><epage>100</epage><pages>100-100</pages><issn>1059-7794</issn><eissn>1098-1004</eissn><abstract>In order to identify single nucleotide polymorphisms (SNPs) and haplotype frequencies of CYP3A4 in a Japanese population, the distal enhancer and proximal promoter regions, all exons, and the surrounding introns were sequenced from genomic DNA of 416 Japanese subjects. We found 24 SNPs, including 17 novel ones: two in the distal enhancer, four in the proximal promoter, one in the 5′‐untranslated region (UTR), seven in the introns, and three in the 3′‐UTR. The most common SNP was c.1026+12G>A (IVS10+12G>A), with a 0.249 frequency. Four non‐synonymous SNPs, c.554C>G (p.T185S, CYP3A4*16), c.830_831insA (p.E277fsX8, *6), c.878T>C (p.L293P, *18), and c.1088 C>T (p.T363M, *11) were found with frequencies of 0.014, 0.001, 0.028, and 0.002, respectively. No SNP was found in the known nuclear transcriptional factor‐binding sites in the enhancer and promoter regions. Using these 24 SNPs, 16 haplotypes were unambiguously identified, and nine haplotypes were inferred by aid of an expectation‐maximization‐based program. In addition, using data from 186 subjects enabled a close linkage to be found between CYP3A4 and CYP3A5 SNPs, especially among the SNPs at c.1026+12 in CYP3A4 and c.219‐237 (IVS3‐237, a key SNP site for CYP3A5*3), c.865+77 (IVS9+77) and c.1523 in CYP3A5. This result suggested that CYP3A4 and CYP3A5 are within the same gene block. Haplotype analysis between CYP3A4 and CYP3A5 revealed several major haplotype combinations in the CYP3A4‐CYP3A5 block. Our findings provide fundamental and useful information for genotyping CYP3A4 (and CYP3A5) in the Japanese, and probably Asian populations. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14695543</pmid><doi>10.1002/humu.9210</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1059-7794 |
ispartof | Human mutation, 2004-01, Vol.23 (1), p.100-100 |
issn | 1059-7794 1098-1004 |
language | eng |
recordid | cdi_proquest_miscellaneous_80073896 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Cancer Childrens health CYP3A4 CYP3A5 Cytochrome Cytochrome P-450 CYP3A Cytochrome P-450 Enzyme System - genetics Gene Frequency Genetic Linkage Genetic testing haplotype Haplotypes Health sciences Hospitals Humans Japan Japanese Metabolism Mutation Oncology Polymorphism, Single Nucleotide Research centers SNP |
title | Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population |
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