Phylogenetic tree facilitates the understanding of gene expression data on drug metabolizing enzymes obtained by microarray analysis

被引:9
作者
Kiyosawa, N [1 ]
Watanabe, T [1 ]
Sakuma, K [1 ]
Kanbori, M [1 ]
Niino, N [1 ]
Ito, K [1 ]
Yamoto, T [1 ]
Manabe, S [1 ]
机构
[1] Sankyo Co Ltd, Med Safety Res Labs, Fukuroi, Shizuoka 4370065, Japan
关键词
microarray; drug metabolizing enzyme; phylogenetic tree; inducer;
D O I
10.1016/j.toxlet.2003.08.004
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The gene expression data of drug metabolizing enzymes (DMEs) in male F344 rat livers were examined after treatments with phenobarbital (PB), clofibrate (CPIB), 3-methylcholanthrene (3-MC) or butylated hydroxyanisole (BHA) using an Affymetrix GeneChip((R)) system. Nucleotide sequence-based phylogenetic trees combined with a heat map, that presents both quantitative and qualitative data, were created. Most DME gene probes were successfully classified into the corresponding gene families, although a few were not due to the presence of non-coding or promoter region sequences in the target gene. There were also some data discrepancies among probes of the same gene family, indicating the inappropriate design of these probes. With this method, microarray probes with confusing nomenclature and quality differences can be identified. In addition, a good correlation between the gene expression data and protein data was confirmed, indicating the usefulness of this method for the comprehensive monitoring, of DME activity in rat livers treated with xenobiotics. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:281 / 289
页数:9
相关论文
共 27 条
[1]  
*AFF INC, 2001, GEN EXPR AN TECHN MA
[2]  
*AFF INC, 2000, AFF MICR SUIT 4 0 US, P295
[3]   GENE CONVERSION IN A CYTOCHROME-P-450 GENE FAMILY [J].
ATCHISON, M ;
ADESNIK, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2300-2304
[4]   GenBank [J].
Benson, DA ;
Karsch-Mizrachi, I ;
Lipman, DJ ;
Ostell, J ;
Rapp, BA ;
Wheeler, DL .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :17-20
[5]   Identification, characterization, and crystal structure of the omega class glutathione transferases [J].
Board, PG ;
Coggan, M ;
Chelvanayagam, G ;
Easteal, S ;
Jermiin, LS ;
Schulte, GK ;
Danley, DE ;
Hoth, LR ;
Griffor, MC ;
Kamath, AV ;
Rosner, MH ;
Chrunyk, BA ;
Perregaux, DE ;
Gabel, CA ;
Geoghegan, KF ;
Pandit, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24798-24806
[6]   AH receptor-controlled transcriptional regulation and function of rat and human UDP-glucuronosyltransferase isoforms [J].
Bock, KW ;
Gschaidmeier, H ;
Heel, H ;
Lehmkoster, T ;
Munzel, PA ;
Raschko, F ;
Bock-Hennig, B .
ADVANCES IN ENZYME REGULATION, VOL 38, 1998, 38 :207-222
[7]   INDUCTION OF PHASE-I AND PHASE-II DRUG-METABOLIZING ENZYME MESSENGER-RNA, PROTEIN, AND ACTIVITY BY BHA, ETHOXYQUIN, AND OLTIPRAZ [J].
BUETLER, TM ;
GALLAGHER, EP ;
WANG, CH ;
STAHL, DL ;
HAYES, JD ;
EATON, DL .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 135 (01) :45-57
[8]   EFFECTS OF PHENOBARBITAL AND 3-METHYLCHOLANTHRENE ON SUBSTRATE-SPECIFICITY OF RAT-LIVER MICROSOMAL UDP-GLUCURONYLTRANSFERASE [J].
FROHLING, KW ;
REMMER, H ;
REXER, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 327 (01) :46-56
[9]   Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays [J].
Gerhold, D ;
Lu, MQ ;
Xu, J ;
Austin, C ;
Caskey, CT ;
Rushmore, T .
PHYSIOLOGICAL GENOMICS, 2001, 5 (04) :161-170
[10]  
HABIG WH, 1974, J BIOL CHEM, V249, P7130