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首页> 外文期刊>Journal of human genetics >Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1 and L1CAM in the Japanese population.
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Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1 and L1CAM in the Japanese population.

机译:鉴定日本人群中人N-乙酰基转移酶基因NAT1,NAT2,AANAT,ARD1和L1CAM的单核苷酸多态性(SNP)。

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By direct sequencing of regions of the human genome containing five genes belonging to the acetyltransferase family, arylamine N-acetyltransferase (NAT1), arylamine N-acetyltransferase (NAT2), arylalkylamine N-acetyltransferase (AANAT), L1 cell adhesion molecule (L1CAM), and the human homolog of Saccharomyces cerevisiae N-acetyltransferase ARD1, we identified 53 single-nucleotide polymorphisms (SNPs) and two insertion/ deletion polymorphisms in 48 healthy Japanese volunteers. NAT1 and NAT2 are so-called drug-metabolizing enzymes. In the NAT1 gene we found two SNPs and a 3-bp insertion/ deletion polymorphism that corresponded to the NAT1*3, *10, and *18A/*18B alleles reported in other populations. The frequencies of NAT1* alleles in our Japanese subjects were 52.6% for NAT1*4, 1.0% for NAT1*3, 40.6% for NAT1*10, 2.6% for NAT1*18A and 3.1% for NAT1*18B. In the NAT2 gene we found 32 SNPs and a 1-bp insertion/ deletion polymorphism; 6 SNPs within the coding region were reported previously and belonged to the slow acetylator group (NAT2*5, NAT2*6 and NAT2*7), and 2 of the 8 SNPs in the 5' flanking region were reported in the dbSNP of GenBank, but the remaining 24 SNPs and the insertion/deletion polymorphism were novel. The frequencies of NAT2* alleles in Japanese (51.3% for NAT2*4, 1.6% for *5B, 26.1% for *6A, 2.2% for *6B, 1.2% for *7A, 10.1% for *7B, 7.4% for *12A, and 1.1% for *13) were significantly different from those reported in Caucasian populations. In the AANAT gene we found 4 novel SNPs: 2 in the 5' flanking region, 1 in exon 4, and 1 in intron 3. In the two genes belonging to the N-terminal N-acetyltransferase family, we identified 9 SNPs, 7 of them novel, for ARD1, and six novel SNPs for L1CAM. Variations at these loci may contribute to an understanding of the way in which different genotypes may affect the activities of human N-acetyltransferases, especially as regards the therapeutic efficacy of certain drugs and antibiotics.
机译:通过对人类基因组区域进行直接测序,该区域包含五个属于乙酰基转移酶家族的基因,芳基胺N-乙酰基转移酶(NAT1),芳基胺N-乙酰基转移酶(NAT2),芳基烷基胺N-乙酰基转移酶(AANAT),L1细胞粘附分子(L1CAM),以及酿酒酵母N-乙酰基转移酶ARD1的人类同源物,我们在48位健康的日本志愿者中鉴定出53个单核苷酸多态性(SNP)和两个插入/缺失多态性。 NAT1和NAT2是所谓的药物代谢酶。在NAT1基因中,我们发现了两个SNP和一个3 bp插入/缺失多态性,与其他人群中报道的NAT1 * 3,* 10和* 18A / * 18B等位基因相对应。我们日本人对象中NAT1 *等位基因的频率分别为NAT1 * 4为52.6%,NAT1 * 3为1.0%,NAT1 * 10为40.6%,NAT1 * 18A为2.6%和NAT1 * 18B为3.1%。在NAT2基因中,我们发现了32个SNP和1bp的插入/缺失多态性。先前已报告了编码区内的6个SNP,它们属于慢乙酰化酶组(NAT2 * 5,NAT2 * 6和NAT2 * 7),而在5'侧翼区的8个SNP中有2个在GenBank的dbSNP中得到了报道,但其余的24个SNP和插入/删除多态性是新颖的。日语中NAT2 *等位基因的频率(NAT2 * 4的51.3%,* 5B的1.6%,* 6A的26.1%,* 6B的2.2%,* 7A的1.2%,* 7B的10.1%,* 7.4% 12A和* 13的1.1%)与白种人人群中报告的显着不同。在AANAT基因中,我们发现了4个新的SNP:5'侧翼区域中的2个,外显子4中的1个,内含子3中的1个。在属于N末端N-乙酰基转移酶家族的两个基因中,我们鉴定了9个SNP,7个其中有针对ARD1的新颖分子,以及针对L1CAM的6种新颖SNP。这些基因座的变异可能有助于人们了解不同基因型可能影响人N-乙酰基转移酶活性的方式,尤其是某些药物和抗生素的治疗功效。

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