Abstract
Control genes, commonly defined as genes that are ubiquitously expressed at stable levels in different biological contexts, have been used to standardize quantitative expression studies for more than 25 yr. We analyzed a group of large mammalian microarray datasets including the NCI60 cancer cell line panel, a leukemia tumor panel, and a phorbol ester induction time course as well as human and mouse tissue panels. Twelve housekeeping genes commonly used as controls in classical expression studies (including GAPD, ACTB, B2M, TUBA, G6PD, LDHA, and HPRT) show considerable variability of expression both within and across microarray datasets. Although we can identify genes with lower variability within individual datasets by heuristic filtering, such genes invariably show different expression levels when compared across other microarray datasets. We confirm these results with an analysis of variance in a controlled mouse dataset, showing the extent of variability in gene expression across tissues. The results show the problems inherent in the classical use of control genes in estimating gene expression levels in different mammalian cell contexts, and highlight the importance of controlled study design in the construction of microarray experiments.
MeSH Terms
Animals
Gene Expression Profiling/standards,statistics & numerical data
Gene Expression Regulation/genetics
Genes, Regulator
Genetic Variation
HL-60 Cells
Humans
Jurkat Cells
Male
Mice
Mice, Inbred C57BL
RNA, Messenger/genetics
Reference Values
Transcription, Genetic
Tumor Cells, Cultured
U937 Cells
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lee Peter D
Montreal Genome Centre, McGill University Health Centre, Montreal H3G 1A4, Quebec, Canada.
Sladek Robert
Greenwood Celia M T
Hudson Thomas J
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