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Volume 9


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In Silico Biology 9, 0006 (2009); ©2009, Bioinformation Systems e.V.  



Gene set enrichment analyses revealed differences in gene expression patterns between males and females

Wei Zhang1, R. Stephanie Huang1, Shiwei Duan1 and M. Eileen Dolan1,2,3*

1 Department of Medicine, The University of Chicago, Chicago, IL 60637, USA
2 Committee on Clinical Pharmacology and Pharmacogenomics, The University of Chicago, Chicago, IL 60637, USA
3 Cancer Research Center, The University of Chicago, Chicago, IL 60637, USA

* Corresponding author
   Email: edolan@medicine.bsd.uchicago.edu


Edited by E. Wingender; received July 17, 2008; revised November 06, 2008; accepted December 30, 2008; published January 03, 2009


Abstract

Men and women differ not only in their physical attributes and reproductive functions but also in many other characteristics, including the risks for some diseases as well as response to certain therapeutic treatments. Though genetically-identical for autosomal chromosomes, males and females could have gender-specific transcriptional or translational regulation, leading to differential mRNAs or protein products for some genes. To illustrate the gender-specific differences in mRNA-level expression, we compared gene expression patterns between males and females using a whole-genome microarray dataset on the unrelated HapMap lymphoblastoid cell lines derived from individuals of European (58 individuals) and African (59 individuals) ancestry. We applied the Gene Set Enrichment Analysis to identify any overrepresented predefined gene sets in either men or women. Distinct patterns of upregulation and downregulation of certain chromosomal regions and other gene sets such as targets for certain microRNAs and transcription factors were identified in males or females, suggesting their potential roles in defining the gender-specific phenotypes. Gender-specific patterns of gene expression also appeared to be different between these two populations.


Keywords: gene expression, gender difference, HapMap, lymphoblastoid cell lines, gene set enrichment