GENETIC-POLYMORPHISM OF INDUCTION OF CYP1A1 (EROD) ACTIVITY

被引:29
作者
CATTEAU, A
DOURIEZ, E
BEAUNE, P
POISSON, N
BONAITIPELLIE, C
LAURENT, P
机构
[1] INSERM, U155, UNITE RECH EPIDEMIOL GENET, F-75016 PARIS, FRANCE
[2] HOP INTERCOMMUNAL CRETEIL, INSERM, U139, UNITE RECH BIOPATHOL & TOXICOL PULM & RENALE, F-94010 CRETEIL, FRANCE
[3] HOP NECKER ENFANTS MALAD, CNRS, U75, UNITE RECH BIOCHIM PHARMACOL & METAB, F-75730 PARIS 15, FRANCE
来源
PHARMACOGENETICS | 1995年 / 5卷 / 02期
关键词
CYP1A1-EROD ACTIVITY; POLYMORPHISM; POPULATION AND FAMILY STUDY;
D O I
10.1097/00008571-199504000-00008
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
CYP1A1 is a cytochrome P450 which is inducible by polycyclic aromatic hydrocarbons (PAH), This induction is mediated via the Ahr locus which encodes the cytosolic Aryl hydrocarbon receptor, The induced activity of CYP1A1 can be measured in vitro by the ethoxyresorufin-O-deethylase (EROD) activity in lymphocytes after induction by benz(a)anthracene (B(a)A), Our purpose was to determine, using this assay, the genetic polymorphism of CYP1A1 induction, With this aim, a population and family study was undertaken, Using the statistical SKUMIX method, a bimodal distribution (two peaks) of the induced EROD activity among 102 unrelated individuals was obtained, We were unable to discriminate three classes of CYP1A1 induction phenotype since a trimodal distribution did not significantly improve the fit to the data (chi(1)(2) = 0.37, p > 0.9), Segregation analysis performed on 57 nuclear families gave evidence of a major gene effect together with a polygenic component, The frequency of the high induction allele is equal to 0.11 with dominance on the low induction allele, This is an accordance with two distributions, with individuals showing low and high CYP1A1 induction phenotypes in proportions of 89% and 21% respectively, However, some degree of overlap between the two distributions prevented a clear genotype classification on the basis of the phenotype measured with the EROD assay, Further analyses should not be made with a dichotomized phenotype (low and high inducers) but should use quantitative measurements.
引用
收藏
页码:110 / 119
页数:10
相关论文
共 42 条
  • [1] SENSITIVITY OF TRANSMISSION PROBABILITIES TO PATERNITY EXCLUSION IN SEGREGATION ANALYSIS
    BONAITIPELLIE, C
    POISSON, N
    BECHTEL, Y
    BECHTEL, P
    [J]. GENETIC EPIDEMIOLOGY, 1992, 9 (01) : 67 - 71
  • [2] BORRESEN AL, 1981, CLIN GENET, V19, P281
  • [3] BURKE MD, 1977, CANCER RES, V37, P460
  • [4] BUTLER MA, 1989, CANCER RES, V49, P25
  • [5] 10 NUCLEOTIDE DIFFERENCES, 5 OF WHICH CAUSE AMINO-ACID CHANGES, ARE ASSOCIATED WITH THE AH RECEPTOR LOCUS POLYMORPHISM OF C57BL/6 AND DBA/2 MICE
    CHANG, CY
    SMITH, DR
    PRASAD, VS
    SIDMAN, CL
    NEBERT, DW
    PUGA, A
    [J]. PHARMACOGENETICS, 1993, 3 (06): : 312 - 321
  • [6] RELATIONSHIP BETWEEN GENOTYPE AND FUNCTION OF THE HUMAN CYP1A1-GENE
    COSMA, G
    CROFTS, F
    TAIOLI, E
    TONIOLO, P
    GARTE, S
    [J]. JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1993, 40 (2-3): : 309 - 316
  • [7] DENISON M, 1988, P NATL ACAD SCI USA, V70, P782
  • [8] EPPIG JT, 1993, MOUSE GENOME, V8, P91
  • [9] INDUCTION OF ARYL-HYDROCARBON HYDROXYLASE-ACTIVITY AND PULMONARY-CARCINOMA
    GAHMBERG, CG
    SEKKI, A
    KOSUNEN, TU
    HOLSTI, LR
    MAKELA, O
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1979, 23 (03) : 302 - 305
  • [10] OXIDATION OF TOXIC AND CARCINOGENIC CHEMICALS BY HUMAN CYTOCHROME-P-450 ENZYMES
    GUENGERICH, FP
    SHIMADA, T
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1991, 4 (04) : 391 - 407