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Detection of DNA copy number abnormality by microarray expression analysis
Authors:Xiaofeng?Zhou  Steven?W?Cole  Shen?Hu  Email author" target="_blank">David?T?W?Wong
Institution:(1) Laboratory of Head and Neck Cancer Research, Dental Research Institute, School of Dentistry, University of California at Los Angeles, Los Angeles, Calif., USA;(2) Division of Hematology-Oncology, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, Calif., USA;(3) Division of Oral Biology & Medicine, School of Dentistry, University of California at Los Angeles, Los Angeles, Calif., USA;(4) Jonsson Comprehensive Cancer Center, University of California at Los Angeles, Los Angeles, Calif., USA;(5) Molecular Biology Institute, University of California at Los Angeles, Los Angeles, Calif., USA;(6) UCLA School of Dentistry, PO Box 951668, Los Angeles, CA 90095-1668, USA
Abstract:Gene copy-number abnormalities (CNAs) are characteristic of solid tumors and are found in association with developmental abnormalities and/or mental retardation. The ultimate impact of CNAs is exerted by the altered expression of encoded genes. We have utilized high-density oligonucleotide arrays from Affymetrix to identify DNA CNAs via their impact on mRNA expression levels. In these studies, we have used three different trisomic cell lines (trisomy 9, trisomy 18, trisomy 21) as models of CNAs and have compared mRNA expression in those trisomic cells with that observed in diploid cell lines of matched tissue origin. Our data clearly show that genes from CNA chromosome regions are substantially over-represented (P<0.000001 by chi-square analysis) in the differentially expressed subset from comparisons of all three trisomic cell lines with normal matching cells. In addition, we have been able to detect the origin of the duplication by a statistical scan for over-expressed genes. These data show that microarray detection of differential mRNA expression can be used to identify significant DNA CNAs.
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