Genetic polymorphism of CYP2E1, ADH2, and ALDH2 in Mexican-American

被引:26
作者
Wan, YJY [1 ]
Poland, RE
Lin, KM
机构
[1] Univ Calif Los Angeles, Harbor Med Ctr, Dept Pathol, Torrance, CA 90509 USA
[2] Univ Calif Los Angeles, Harbor Med Ctr, Dept Psychiat, Torrance, CA 90509 USA
来源
GENETIC TESTING | 1998年 / 2卷 / 01期
关键词
D O I
10.1089/gte.1998.2.79
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The major enzymes involved in the metabolism of ethanol are alcohol dehydrogenases (ADH) and aldehyde dehydrogenase (ALDH). Some of the isozymes of ADH are expressed polymorphically, Studies investigating a causal link between ADH expression and alcoholic liver disease (ALD) have so far produced conflicting results. The cytochrome P450 2E1 (CYP2E1) represents a second enzyme that can metabolize ethanol, Although normally a minor route of metabolism, its role in chronic alcoholics may be proportionately greater than in nonalcoholics because CYP2E1 is inducible by ethanol, An Rsa I restriction fragment length polymorphism (RFLP) in the 5'-flanking region of the CYP2E1 gene has been identified. Studies have shown that the mutant allele demonstrates greater transcriptional rate, protein level, and enzyme activity when compared with the wild-type allele, The association between the Rsa I site polymorphism and ALD has been reported. In this report, we examined the genotypes of ADH2(2), ALDH2(2), and CYP2E1 in a group of healthy subjects of Mexican-American descent, The ADH2(2) and ALDH2(2) frequencies are 6% and 0%, respectively, which are similar to those which have been reported for Caucasians. In contrast, the Rsa I allele frequency of the CYP2E1 gene is 16%, which is significantly higher than in Caucasians, The high RsaI allele frequency found in Mexican-Americans suggests that it might play a role in the development of ALD in this rapidly growing minority population where ALD is common.
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页码:79 / 83
页数:5
相关论文
共 40 条
[31]  
TSUTSUMI M, 1994, HEPATOLOGY, V20, pA311
[32]   HUMAN ETHANOL-INDUCIBLE P450IIE1 - COMPLETE GENE SEQUENCE, PROMOTER CHARACTERIZATION, CHROMOSOME MAPPING, AND CDNA-DIRECTED EXPRESSION [J].
UMENO, M ;
MCBRIDE, OW ;
YANG, CS ;
GELBOIN, HV ;
GONZALEZ, FJ .
BIOCHEMISTRY, 1988, 27 (25) :9006-9013
[33]   HLA-B ALLELES AND COMPLOTYPES IN MEXICAN PATIENTS WITH SERONEGATIVE SPONDYLOARTHROPATHIES [J].
VARGASALARCON, G ;
GARCIA, A ;
BAHENA, S ;
MELINALDANA, H ;
ANDRADE, F ;
IBANEZDEKASEP, G ;
ALCOCERVARELA, J ;
ALARCONSEGOVIA, D ;
GRANADOS, J .
ANNALS OF THE RHEUMATIC DISEASES, 1994, 53 (11) :755-758
[34]   DIFFERENT REGULATION AND EXPRESSION OF THE HUMAN CYP2E1 GENE DUE TO THE RSAI POLYMORPHISM IN THE 5'-FLANKING REGION [J].
WATANABE, J ;
HAYASHI, S ;
KAWAJIRI, K .
JOURNAL OF BIOCHEMISTRY, 1994, 116 (02) :321-326
[35]   ETHNIC DIFFERENCES IN ALCOHOL SENSITIVITY [J].
WOLFF, PH .
SCIENCE, 1972, 175 (4020) :449-&
[36]  
WRIGHTON SA, 1989, BIOCHEMISTRY-US, V25, P6731
[37]  
XU Y, 1988, Genomics, V2, P209, DOI 10.1016/0888-7543(88)90004-3
[38]   CYTOCHROME P450 2E1 AND 2A6 ENZYMES AS MAJOR CATALYSTS FOR METABOLIC-ACTIVATION OF N-NITROSODIALKYLAMINES AND TOBACCO-RELATED NITROSAMINES IN HUMAN LIVER-MICROSOMES [J].
YAMAZAKI, H ;
INUI, Y ;
YUN, CH ;
GUENGERICH, FP ;
SHIMADA, T .
CARCINOGENESIS, 1992, 13 (10) :1789-1794
[39]  
YOSHIDA A, 1991, PROG NUCLEIC ACID RE, V40, P255
[40]  
YOSHIDA A, 1981, J BIOL CHEM, V256, P2430