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Updated: Aug 17, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
Corticosteroid-regulated genes in rat kidney: mining time series array data
Richard R Almon1, William Lai, Debra C DuBois
1Dept. of Biological Sciences, SUNY at Buffalo, Buffalo, NY 14260, USA. almon@eng.buffalo.edu
Abstract:
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.
Insights
Corticosteroids can harm kidneys. This study used gene expression data from rat kidneys treated with methylprednisolone to identify drug-regulated genes and found conserved DNA binding sites aid in understanding gene regulation.
Area of Science:
- Pharmacogenomics
- Molecular Biology
- Toxicology
Background:
- Corticosteroids, like methylprednisolone, can cause adverse kidney effects.
- Understanding gene expression changes in the kidney is crucial for assessing corticosteroid toxicity.
Purpose of the Study:
- To investigate gene expression alterations in rat kidneys following methylprednisolone administration.
- To identify drug-regulated genes and explore conserved DNA binding sites involved in corticosteroid-induced kidney changes.
Main Methods:
- Generated a microarray dataset from rat kidney RNA after methylprednisolone treatment at multiple time points.
- Applied time-series data mining techniques and sequential filters to analyze gene expression data.
- Analyzed conserved 5' GRE half-sites in regulated genes to understand regulatory mechanisms.
Main Results:
- Utilized filtering techniques to reduce a large dataset (15,967 probe sets) by 94%, focusing on relevant genes.
- Identified a group of genes with expression patterns correlated to known corticosteroid-responsive genes.
- Found evidence supporting the role of conserved DNA binding sites in grouping genes with similar regulatory mechanisms.
Conclusions:
- Filtering is effective for mining time-series gene expression data.
- Conserved DNA binding sites can complement analytical methods for gene clustering and understanding regulatory pathways.
- The generated dataset is publicly available for further research on corticosteroid effects in kidney, liver, and muscle.
