AJP - Endo Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 289: E870-E882, 2005. First published June 28, 2005; doi:10.1152/ajpendo.00196.2005
0193-1849/05 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Tables
Right arrow All Versions of this Article:
289/5/E870    most recent
00196.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (11)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Almon, R. R.
Right arrow Articles by Jusko, W. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Almon, R. R.
Right arrow Articles by Jusko, W. J.

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

Richard R. Almon,1,2 William Lai,2 Debra C. DuBois,1,2 and William J. Jusko2

1Department of Biological Sciences and 2Department of Pharmaceutical Sciences, State University of New York at Buffalo, Buffalo, New York

Submitted 4 May 2005 ; accepted in final form 20 June 2005

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.

data mining; gene arrays; glucocorticoids; pharmacogenomics; evolutionary conservation



Address for reprint requests and other correspondence: R. Almon, 107 Hochstetter Hall, Dept. of Biological Sciences, SUNY at Buffalo, Buffalo, NY 14260 (e-mail: almon{at}eng.buffalo.edu)




This article has been cited by other articles:


Home page
Toxicol SciHome page
E. Sonneveld, A. Jonas, O. C. Meijer, A. Brouwer, and B. van der Burg
Glucocorticoid-Enhanced Expression of Dioxin Target Genes through Regulation of the Rat Aryl Hydrocarbon Receptor
Toxicol. Sci., October 1, 2007; 99(2): 455 - 469.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
R. R. Almon, D. C. DuBois, Z. Yao, E. P. Hoffman, S. Ghimbovschi, and W. J. Jusko
Microarray analysis of the temporal response of skeletal muscle to methylprednisolone: comparative analysis of two dosing regimens
Physiol Genomics, August 20, 2007; 30(3): 282 - 299.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
M. B. Yaylaoglu, B. M. Agbemafle, T. J. Oesterreicher, M. J. Finegold, C. Thaller, and S. J. Henning
Diverse patterns of cell-specific gene expression in response to glucocorticoid in the developing small intestine
Am J Physiol Gastrointest Liver Physiol, December 1, 2006; 291(6): G1041 - G1050.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2005 by the American Physiological Society.