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Physiol. Genomics (August 7, 2002). doi:10.1152/physiolgenomics.00051.2002
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Articles in PresS, published online ahead of print August 7, 2002
Physiol Genomics, 10.1152/physiolgenomics.00051.2002
Submitted on April 30, 2002
Accepted on July 5, 2002

Individual variation of gene expression and identification of co-variated genes in adipose tissue using cDNA microarrays

Stephane Boeuf1, Jaap Keijer2, Nicole L. W Franssen-Van Hal2, and Susanne Klaus1*

1 Biochemistry and Physiology of Nutrition, German Institute of Human Nutrition in Potsdam, Bergholz-Rehbruecke, Germany
2 RIKILT, Wageningen, The Netherlands

* To whom correspondence should be addressed. E-mail: klaus{at}www.dife.de.

Gene expression profiling through the application of microarrays provides comprehensive assessment of gene expression levels in a given tissue or cell population, as well as information on changes of gene expression in altered physiological or pathological situations. Microarrays are particularly suited to study interactions in the regulation of large numbers of different genes, since their expression is analyzed simultaneously. For improved understanding of the physiology of adipose tissue, and consequently obesity and diabetes, identification of co-variability in gene expression was attempted by analysis of the individual variability of gene expression in subcutaneous white and brown fat of the Siberian dwarf hamster using microarrays containing approximately 300 cDNA fragments of adipose genes. No sex dependant variability in gene expression could be found and overall individual variability was rather low with more than 80% of clones showing a coefficient of variability lower than 30%. Uncoupling protein 1 (UCP1) displayed a high variability of gene expression in brown fat, which was negatively correlated with the gene expression of complement factor B (FactB) implying a possible functional relationship.







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