Implications of circadian gene expression in kidney, liver and the effects of fasting on pharmacogenomic studies

被引:115
作者
Kita, Y
Shiozawa, N
Jin, WH
Majewski, RR
Besharse, JC
Greene, AS
Jacob, HJ
机构
[1] Med Coll Wisconsin, Human & Mol Genet Ctr, Milwaukee, WI 53228 USA
[2] Med Coll Wisconsin, Dept Physiol, Milwaukee, WI 53228 USA
[3] Med Coll Wisconsin, Bioinformat Res Ctr, Milwaukee, WI 53228 USA
[4] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53228 USA
来源
PHARMACOGENETICS | 2002年 / 12卷 / 01期
关键词
fasting; circadian; microarray; expression;
D O I
10.1097/00008571-200201000-00008
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
Pharmacogenomics offers the potential to define metabolic pathways and to provide increased knowledge of drug actions. We studied relative levels of gene expression in the rat using a microarray with 8448 rat UniGenes (1928 known genes, 6520 unknown ESTs) in the liver and kidney as a function of time of day and then of feeding regime, which are common variables in preclinical pharmacogenomic studies. We identified 597 genes, including several key metabolic pathways, whose relative expression levels are significantly affected by time of day: expression of some was further modified by feeding state. These would have sparked interest in a pharmacogenomic study. Our study demonstrates that two common variables in pharmacogenomic studies can have dramatic effects on gene expression. This study provides investigators with baseline information for both kidney and liver with respect to 'normal' changes in gene expression influenced by time of day and feeding state. It also identifies 18 new genes that should be investigated for a role in circadian rhythms in peripheral tissues. Pharmacogenetics 12:55-65 (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:55 / 65
页数:11
相关论文
共 49 条
[1]  
Alizadeh M, 2000, INVEST OPHTH VIS SCI, V41, P2357
[2]   NEGATIVE FEEDBACK DEFINING A CIRCADIAN CLOCK - AUTOREGULATION OF THE CLOCK GENE-FREQUENCY [J].
ARONSON, BD ;
JOHNSON, KA ;
LOROS, JJ ;
DUNLAP, JC .
SCIENCE, 1994, 263 (5153) :1578-1584
[3]   Resetting of circadian time peripheral tissues by glucocorticoid signaling [J].
Balsalobre, A ;
Brown, SA ;
Marcacci, L ;
Tronche, F ;
Kellendonk, C ;
Reichardt, HM ;
Schütz, G ;
Schibler, U .
SCIENCE, 2000, 289 (5488) :2344-2347
[4]   DIFFERENT HEPATOCYTES EXPRESS THE CHOLESTEROL 7-ALPHA-HYDROXYLASE GENE DURING ITS CIRCADIAN MODULATION IN-VIVO [J].
BERKOWITZ, CM ;
SHEN, CS ;
BILIR, BM ;
GUIBERT, E ;
GUMUCIO, JJ .
HEPATOLOGY, 1995, 21 (06) :1658-1667
[5]   CIRCADIAN CLOCK IN XENOPUS EYE CONTROLLING RETINAL SEROTONIN N-ACETYLTRANSFERASE [J].
BESHARSE, JC ;
IUVONE, PM .
NATURE, 1983, 305 (5930) :133-135
[6]  
CLARKE CF, 1984, J BIOL CHEM, V259, P439
[7]  
DeRisi J, 1996, NAT GENET, V14, P457
[8]   Gap junctional communication coordinates vasopressin-induced glycogenolysis in rat hepatocytes [J].
Eugenín, EA ;
González, H ;
Sáez, CG ;
Sáez, JC .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1998, 274 (06) :G1109-G1116
[9]   THE EFFECT OF DIET ON TUMOR-NECROSIS-FACTOR STIMULATION OF HEPATIC LIPOGENESIS [J].
FEINGOLD, KR ;
SOUED, M ;
SERIO, MK ;
ADI, S ;
MOSER, AH ;
GRUNFELD, C .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1990, 39 (06) :623-632
[10]   The two PAR leucine zipper proteins, TEF and DBP, display similar circadian and tissue-specific expression, but have different target promoter preferences [J].
Fonjallaz, P ;
Ossipow, V ;
Wanner, G ;
Schibler, U .
EMBO JOURNAL, 1996, 15 (02) :351-362