Corticosteroid-regulated genes in rat kidney: mining time series array data

被引:37
作者
Almon, RR
Lai, W
DuBois, DC
Jusko, WJ
机构
[1] SUNY Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Pharmaceut Sci, Buffalo, NY 14260 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2005年 / 289卷 / 05期
关键词
data mining; gene arrays; glucocorticoids; pharmacogenomics; evolutionary conservation;
D O I
10.1152/ajpendo.00196.2005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Kidney is a major target for adverse effects associated with corticosteroids. A microarray dataset was generated to examine changes in gene expression in rat kidney in response to methylprednisolone. Four control and 48 drug-treated animals were killed at 16 times after drug administration. Kidney RNA was used to query 52 individual Affymetrix chips, generating data for 15,967 different probe sets for each chip. Mining techniques applicable to time series data that identify drug-regulated changes in gene expression were applied. Four sequential filters eliminated probe sets that were not expressed in the tissue, not regulated by drug, or did not meet defined quality control standards. These filters eliminated 14,890 probe sets (94%) from further consideration. Application of judiciously chosen filters is an effective tool for data mining of time series datasets. The remaining data can then be further analyzed by clustering and mathematical modeling. Initial analysis of this filtered dataset identified a group of genes whose pattern of regulation was highly correlated with prototype corticosteroid enhanced genes. Twenty genes in this group, as well as selected genes exhibiting either downregulation or no regulation, were analyzed for 5' GRE half-sites conserved across species. In general, the results support the hypothesis that the existence of conserved DNA binding sites can serve as an important adjunct to purely analytic approaches to clustering genes into groups with common mechanisms of regulation. This dataset, as well as similar datasets on liver and muscle, are available online in a format amenable to further analysis by others.
引用
收藏
页码:E870 / E882
页数:13
相关论文
共 61 条
[1]   Gene arrays and temporal patterns of drug response: Corticosteroid effects on rat liver [J].
Richard R. Almon ;
Debra C. DuBois ;
Keri E. Pearson ;
Dietrich A Stephan ;
William J. Jusko .
Functional & Integrative Genomics, 2003, 3 (4) :171-179
[2]   Pharmacogenomic responses of rat liver to methylprednisolone: An approach to mining a rich microarray time series [J].
Almon, RR ;
Dubois, DC ;
Jin, JY ;
Jusko, WJ .
AAPS JOURNAL, 2005, 7 (01) :E156-E194
[3]   The genomic response of skeletal muscle to methylprednisolone using microarrays: tailoring data mining to the structure of the pharmacogenomic time series [J].
Almon, RR ;
DuBois, DC ;
Piel, WH ;
Jusko, WJ .
PHARMACOGENOMICS, 2004, 5 (05) :525-552
[4]   In vivo multi-tissue corticosteroid microarray time series available online at Public Expression Profile Resource (PEPR) [J].
Almon, RR ;
Chen, J ;
Snyder, G ;
DuBois, DC ;
Jusko, WJ ;
Hoffman, EP .
PHARMACOGENOMICS, 2003, 4 (06) :791-799
[5]  
ALTUS MS, 1991, J BIOL CHEM, V266, P21190
[6]  
BAXTER J, 2000, ADV INTERNAL MED, P317
[7]   DNA REGULATORY ELEMENTS FOR STEROID-HORMONES [J].
BEATO, M ;
CHALEPAKIS, G ;
SCHAUER, M ;
SLATER, EP .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1989, 32 (05) :737-748
[8]  
Bialas Michael C., 1998, Adverse Drug Reactions and Toxicological Reviews, V17, P227
[9]   Proteolipid plasmolipin:: localization in polarized cells, regulated expression and lipid raft association in CNS and PNS myelin [J].
Bosse, F ;
Hasse, B ;
Pippirs, U ;
Greiner-Petter, R ;
Müller, HW .
JOURNAL OF NEUROCHEMISTRY, 2003, 86 (02) :508-518
[10]   Cathepsin S expression is up-regulated following balloon angioplasty in the hypercholesterolemic rabbit [J].
Burns-Kurtis, CL ;
Olzinski, AR ;
Needle, S ;
Fox, JH ;
Capper, EA ;
Kelly, FM ;
McQueney, MS ;
Romanic, AM .
CARDIOVASCULAR RESEARCH, 2004, 62 (03) :610-620