Inter-individual variation of several cytochrome P450 2D6 splice variants in human liver

被引:10
作者
Denson, J
Wu, YC
Yang, WJ
Zhang, J [1 ]
机构
[1] St Jude Childrens Res Hosp, Hartwell Ctr Bioinformat & Biotechnol, Memphis, TN USA
[2] St Jude Childrens Res Hosp, Dept Pharmaceut Sci, Memphis, TN USA
基金
美国国家卫生研究院;
关键词
CYP2D6; splice variants; real-time PCR; polymorphism;
D O I
10.1016/j.bbrc.2005.03.010
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
To examine the possibility that inter-individual differences in splicing partially explain the observed differences in CYP2D6 activity, we amplified its full-length cDNA in 96 human liver RNA samples and discovered five splice variants: intron 5 retention, intron 6 retention, intron 5 and intron 6 double retention, exon 3 skipping, and partial intron I retention. All of the CYP2D6 splice variants we identified are probably nonfunctional transcripts. Substantial inter-individual variation in the proportions of the CYP2D6 transcript represented by splice variants, measured by real-time PCR, suggests that the presence of these splice variants contributes to the population variation in CYP2D6 activity. Relatively high levels of intron 6 retention were not correlated with the newly discovered single nucleotide polymorphism 2988G > A in intron 6 (CMD6*41) but did correlate with the more common CYP2D6*34 allele. Our study prompts further investigations to explore the effect of these splice variants oil drug metabolism. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:498 / 504
页数:7
相关论文
共 24 条
[1]   Identification of a novel splice-site mutation in the CYP1A2 gene [J].
Allorge, D ;
Chevalier, D ;
Lo-Guidice, JM ;
Cauffiez, C ;
Suard, F ;
Baumann, P ;
Eap, CB ;
Broly, F .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 56 (03) :341-344
[2]   ESEfinder: a web resource to identify exonic splicing enhancers [J].
Cartegni, L ;
Wang, JH ;
Zhu, ZW ;
Zhang, MQ ;
Krainer, AR .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3568-3571
[3]  
DEMORAIS SMF, 1994, J BIOL CHEM, V269, P15419
[4]   Discriminative quantification of cytochrome P4502D6 and 2D7/8 pseudogene expression by TaqMan real-time reverse transcriptase polymerase chain reaction [J].
Endrizzi, K ;
Fischer, J ;
Klein, K ;
Schwab, M ;
Nüssler, A ;
Neuhaus, P ;
Eichelbaum, M ;
Zanger, UM .
ANALYTICAL BIOCHEMISTRY, 2002, 300 (02) :121-131
[5]   CHARACTERIZATION OF THE COMMON GENETIC-DEFECT IN HUMANS DEFICIENT IN DEBRISOQUINE METABOLISM [J].
GONZALEZ, FJ ;
SKODA, RC ;
KIMURA, S ;
UMENO, M ;
ZANGER, UM ;
NEBERT, DW ;
GELBOIN, HV ;
HARDWICK, JP ;
MEYER, UA .
NATURE, 1988, 331 (6155) :442-446
[6]   IDENTIFICATION OF THE PRIMARY GENE DEFECT AT THE CYTOCHROME-P450 CYP2D LOCUS [J].
GOUGH, AC ;
MILES, JS ;
SPURR, NK ;
MOSS, JE ;
GAEDIGK, A ;
EICHELBAUM, M ;
WOLF, CR .
NATURE, 1990, 347 (6295) :773-776
[7]   EVOLUTION OF A HIGHLY POLYMORPHIC HUMAN CYTOCHROME P450 GENE-CLUSTER - CYP2D6 [J].
HEIM, MH ;
MEYER, UA .
GENOMICS, 1992, 14 (01) :49-58
[8]   Alternative splicing of CYP2D mRNA in human breast tissue [J].
Huang, ZQ ;
Fasco, MJ ;
Kaminsky, LS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 343 (01) :101-108
[9]  
Huang ZQ, 1997, CANCER RES, V57, P2589
[10]   INHERITED AMPLIFICATION OF AN ACTIVE GENE IN THE CYTOCHROME-P450 CYP2D LOCUS AS A CAUSE OF ULTRARAPID METABOLISM OF DEBRISOQUINE [J].
JOHANSSON, I ;
LUNDQVIST, E ;
BERTILSSON, L ;
DAHL, ML ;
SJOQVIST, F ;
INGELMANSUNDBERG, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11825-11829