Identification and functional characterization of eight CYP3A4 protein variants

被引:195
作者
Eiselt, R
Domanski, TL
Zibat, A
Mueller, R
Presecan-Siedel, E
Hustert, E
Zanger, UM
Brockmoller, J
Klenk, HP
Meyer, UA
Khan, KK
He, YA
Halpert, JR
Wojnowski, L
机构
[1] EPIDAUROS Biotechnol AG, D-82347 Bernried, Germany
[2] Univ Texas, Med Branch, Dept Pharmacol & Toxicol, Galveston, TX 77550 USA
[3] Dr Margarete Fischer Bosch Inst Clin Pharmacol, Stuttgart, Germany
[4] Humboldt Univ, Univ Med Ctr Charite, Inst Clin Pharmacol, Berlin, Germany
[5] Univ Basel, Biozentrum, Div Pharmacol Neurobiol, CH-4003 Basel, Switzerland
来源
PHARMACOGENETICS | 2001年 / 11卷 / 05期
关键词
CYP3A; CYP3A4; protein variant; drug metabolism; steroid metabolism;
D O I
10.1097/00008571-200107000-00008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The genetic component of the inter-individual variability in CYP3A4 activity has been estimated to be between 60% and 90%, but the underlying genetic factors remain largely unknown. A study of 213 Middle and Western European DNA samples resulted in the identification of 18 new CYP3A4 variants, including eight protein variants, A total of 7.5% of the population studied was found to be heterozygous for one of these variants, in a bacterial heterologous expression system, two mutants, R130Q and P416L, did not result in detectable P450 holoprotein. One mutant, T363M, expressed at significantly lower levels than wild-type CYP3A4, G56D, V170I, D174H and M445T were not significantly different when compared with wild-type CYP3A4 in expression or steroid hydroxylase activity, L373F displayed a significantly altered testosterone metabolite profile and a four-fold increase in the K-m value for 1'-OH midazolam formation. The results suggest a limited contribution of CYP3A4 protein variants to the inter-individual variability of CYP3A4 activity in Caucasians, Some variants may, however, play a role in the atypical response to drugs or altered sensitivity to carcinogens. Pharmacogenetics 11:447-458 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:447 / 458
页数:12
相关论文
共 47 条
  • [1] AOYAMA T, 1989, J BIOL CHEM, V264, P10388
  • [2] Population distribution and effects on drug metabolism of a genetic variant in the 5′ promotor region of CYP3A4
    Ball, SE
    Scatina, JA
    Kao, J
    Ferron, GM
    Fruncillo, R
    Mayer, P
    Weinryb, I
    Guida, M
    Hopkins, PJ
    Warner, N
    Hall, J
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 66 (03) : 288 - 294
  • [3] ISOLATION AND SEQUENCE DETERMINATION OF A CDNA CLONE RELATED TO HUMAN CYTOCHROME-P-450 NIFEDIPINE OXIDASE
    BEAUNE, PH
    UMBENHAUER, DR
    BORK, RW
    LLOYD, RS
    GUENGERICH, FP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (21) : 8064 - 8068
  • [4] BORK RW, 1989, J BIOL CHEM, V264, P910
  • [5] Identification of the binding site on cytochrome P450 2B4 for cytochrome b5 and cytochrome P450 reductase
    Bridges, A
    Gruenke, L
    Chang, YT
    Vakser, IA
    Loew, G
    Waskell, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (27) : 17036 - 17049
  • [7] The R144C change in the CYP2C9*2 allele alters interaction of the cytochrome P450 with NADPH:cytochrome P450 oxidoreductase
    Crespi, CL
    Miller, VP
    [J]. PHARMACOGENETICS, 1997, 7 (03): : 203 - 210
  • [8] Recent advances in understanding the molecular basis of polymorphisms in genes encoding cytochrome P450 enzymes
    Daly, AK
    Fairbrother, KS
    Smart, J
    [J]. TOXICOLOGY LETTERS, 1998, 103 : 143 - 147
  • [9] Domanski TL, 2000, J PHARMACOL EXP THER, V293, P585
  • [10] Analysis of four residues within substrate recognition site 4 of human cytochrome p450 3A4:: Role in steroid hydroxylase activity and α-naphthoflavone stimulation
    Domanski, TL
    Liu, JP
    Harlow, GR
    Halpert, JR
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 350 (02) : 223 - 232