Comprehensive Analysis of UGT1A1 Genetic Polymorphisms in Chinese Tibetan and Han Populations

被引:4
作者
Zhang, Xiaoqing [1 ]
Meng, Xiaohong [2 ]
Wang, Yuewen [1 ]
Yan, Wei [1 ]
Yang, Jin [1 ]
机构
[1] NW Univ Xian, Natl Engn Res Ctr Miniaturized Detect Syst, Coll Life Sci, Xian 710069, Shaanxi, Peoples R China
[2] Xian High Tech Inst, Sect 504, Xian 710025, Shaanxi, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Chinese; Genetic polymorphisms; Haplotype; UGT1A1; gene; GLUCURONOSYLTRANSFERASE; 1A1; GILBERTS-SYNDROME; UDP-GLUCURONOSYLTRANSFERASES; BILIRUBIN CONCENTRATION; JAPANESE POPULATION; HAPLOTYPE STRUCTURE; MISSENSE MUTATION; SERUM BILIRUBIN; ETHNIC-GROUPS; GLUCURONIDATION;
D O I
10.1007/s10528-012-9536-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study of polymorphism of the UGT1A1 gene has not been reported in the Chinese Tibetan population, and there are no comparisons of genetic polymorphism in the gene between Chinese Han and Tibetan populations. In this study, we directly sequenced the functional regions of the UGT1A1 gene in 200 unrelated healthy Chinese volunteers, detecting 20 variations (including five novel ones). The distributions of allele and genotype frequencies differ between the two groups. UGT1A1*6 is the major reduced functional variant in the populations, and the *27 allele was detected only in the Han group. Differences in the frequencies of the UGT1A1*6/*63 genotype between the Tibetan and Han populations were statistically significant (P = 0.009). Our genetic data might provide fundamental information for the advance of personalized medicine and will facilitate genotype-phenotype studies in larger populations.
引用
收藏
页码:967 / 977
页数:11
相关论文
共 27 条
[1]  
Akaba K, 1998, BIOCHEM MOL BIOL INT, V46, P21
[2]   Haplotypes in the UGT1A1 gene and their role as genetic determinants of bilirubin concentration in healthy German volunteers [J].
Borucki, Katrin ;
Weikert, Cornelia ;
Fisher, Eva ;
Jakubiczka, Sibylle ;
Luley, Claus ;
Westphal, Sabine ;
Dierkes, Jutta .
CLINICAL BIOCHEMISTRY, 2009, 42 (16-17) :1635-1641
[3]   THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME [J].
BOSMA, PJ ;
CHOWDHURY, JR ;
BAKKER, C ;
GANTLA, S ;
DEBOER, A ;
OOSTRA, BA ;
LINDHOUT, D ;
TYTGAT, GNJ ;
JANSEN, PLM ;
ELFERINK, RPJO ;
CHOWDHURY, NR .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) :1171-1175
[4]   Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter Polymorphisms among distinct ethnic groups from Brazil [J].
Fertrin, KY ;
Gonçalves, MS ;
Saad, STO ;
Costa, FF .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 108 (02) :117-119
[5]   The structure of haplotype blocks in the human genome [J].
Gabriel, SB ;
Schaffner, SF ;
Nguyen, H ;
Moore, JM ;
Roy, J ;
Blumenstiel, B ;
Higgins, J ;
DeFelice, M ;
Lochner, A ;
Faggart, M ;
Liu-Cordero, SN ;
Rotimi, C ;
Adeyemo, A ;
Cooper, R ;
Ward, R ;
Lander, ES ;
Daly, MJ ;
Altshuler, D .
SCIENCE, 2002, 296 (5576) :2225-2229
[6]  
Guillemette C, 2000, CANCER RES, V60, P950
[7]   Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups [J].
Innocenti, F ;
Grimsley, C ;
Das, S ;
Ramírez, J ;
Cheng, C ;
Kuttab-Boulos, H ;
Ratain, MJ ;
Di Rienzo, A .
PHARMACOGENETICS, 2002, 12 (09) :725-733
[8]   UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity [J].
Iyer L. ;
Das S. ;
Janisch L. ;
Wen M. ;
Ramírez J. ;
Karrison T. ;
Fleming G.F. ;
Vokes E.E. ;
Schilsky R.L. ;
Ratain M.J. .
The Pharmacogenomics Journal, 2002, 2 (1) :43-47
[9]   Role of UGT1A1*6, UGT1A1*28 and ABCG2 c.421C>A polymorphisms in irinotecan-induced neutropenia in Asian cancer patients [J].
Jada, Srinivasa Rao ;
Lim, Robert ;
Wong, Chiung Ing ;
Shu, Xiaochen ;
Lee, Soo Chin ;
Zhou, Qingyu ;
Goh, Boon Cher ;
Chowbay, Balram .
CANCER SCIENCE, 2007, 98 (09) :1461-1467
[10]   Racial variability in haplotype frequencies of UGT1A1 and glucuronidation activity of a novel single nucleotide polymorphism 686C>T (P229L) found in an African-American [J].
Kaniwa, N ;
Kurose, K ;
Jinno, H ;
Tanaka-Kagawa, T ;
Saito, Y ;
Saeki, M ;
Sawada, J ;
Tohkin, M ;
Hasegawa, R .
DRUG METABOLISM AND DISPOSITION, 2005, 33 (03) :458-465