Genotyping by "cold single-strand conformation polymorphism" of the UGT1A1 promoter polymorphism in Mexican mestizos

被引:12
作者
Arámbula, E [1 ]
Vaca, G [1 ]
机构
[1] IMSS, Ctr Invest Biomed Occidente, Div Genet, Guadalajara 44281, Jalisco, Mexico
关键词
polymorphism; UGT1A1; Gilbert syndrome; SSCP; Mexican mestizos;
D O I
10.1006/bcmd.2001.0481
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since no data have previously been reported concerning both the (TA)(n) polymorphism at the promoter of the UGT1A1 gene in the Mexican population and the use of single-strand conformation polymorphism (SSCP) for the detection of such polymorphism, genotyping by SSCP in 375 G-6-PD normal (Group A) and 81 G-6-PD-deficient (Group B) mestizos belonging to 14 states was carried out. Allele frequencies for (TA)(6) and (TA)(7) repeats were 0.654 and 0.334, respectively, in Group A and 0.685 and 0.315 in Group B: in the former group, the (TA)(5) allele was also observed with a frequency of 0.012. The frequencies of the genotype (TA)(7)/(TA)(7) were 10.1% (Group A) and 8.6% (Group B). The (TA)(7)/(TA)(8) genotype was also observed in a patient with unconjugated hyperbilirubinemia. Due to the importance of its potential medical implications, the observed high frequency (10%) of the (TA)(7)/(TA)(7) genotype is stressed. Genotyping by SSCP of the (TA)(n) polymorphism is an adequate methodological option. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:86 / 90
页数:5
相关论文
共 22 条
[1]   Glucose-6-phosphate dehydrogenase mutations and haplotypes in Mexican mestizos [J].
Arámbula, E ;
Aguilar, JC ;
Vaca, G .
BLOOD CELLS MOLECULES AND DISEASES, 2000, 26 (04) :387-394
[2]   Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter:: A balanced polymorphism for regulation of bilirubin metabolism? [J].
Beutler, E ;
Gelbart, T ;
Demina, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) :8170-8174
[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]  
Chowdhury JR., 2001, The metabolic and molecular bases of inherited disease, P3063
[5]   Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome [J].
Galanello, R ;
Perseu, L ;
Melis, MA ;
Cipollina, L ;
Barella, S ;
Giagu, N ;
Turco, MP ;
Maccioni, O ;
Cao, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 99 (02) :433-436
[6]  
Guillemette C, 2000, CANCER RES, V60, P950
[7]  
Gürtler V, 1999, ELECTROPHORESIS, V20, P2841
[8]   Variability at the uridine diphosphate glucuronosyltransferase 1A1 promoter in human populations and primates [J].
Hall, D ;
Ybazeta, G ;
Destro-Bisol, G ;
Petzl-Erler, ML ;
Di Rienzo, A .
PHARMACOGENETICS, 1999, 9 (05) :591-599
[9]   COLD SSCP - A SIMPLE, RAPID AND NONRADIOACTIVE METHOD FOR OPTIMIZED SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSES [J].
HONGYO, T ;
BUZARD, GS ;
CALVERT, RJ ;
WEGHORST, CM .
NUCLEIC ACIDS RESEARCH, 1993, 21 (16) :3637-3642
[10]   UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis [J].
Iolascon, A ;
Faienza, MF ;
Moretti, A ;
Perrotta, S ;
del Giudice, EM .
BLOOD, 1998, 91 (03) :1093-1093