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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Veröffentlicht in:Human mutation 2004-01, Vol.23 (1), p.100-100
Hauptverfasser: 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
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Zusammenfassung: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.
ISSN:1059-7794
1098-1004
DOI:10.1002/humu.9210