MBE Advance Access originally published online on April 25, 2003
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mol. Biol. Evol. 20(6):964-968. 2003
DOI: 10.1093/molbev/msg110
© 2003 by the Society for Molecular Biology and Evolution. ISSN: 0737-4038
Evolutionary Dynamics of Oncogenes and Tumor Suppressor Genes: Higher Intensities of Purifying Selection than Other Genes
,2
* Bioinformatics Research Center, Medical College of Wisconsin, Milwaukee
Department of Ecology and Evolution, University of Chicago
Oncogenes and tumor suppressor genes (hereafter referred to as "cancer genes") result in cancer when they experience substitutions that prevent or distort their normal function. We examined evolutionary pressures acting on cancer genes and other classes of disease-related genes and compared our results to analyses of genes without known association to disease. We compared synonymous and nonsynonymous substitution rates in 3,035 human genesapproximately 10% of the genomemeasuring the intensity of purifying selection on 311 human disease genes, including 122 cancer-related genes. Although the genes examined are similar to nondisease genes in product, expression, function, and pathway affiliation, we found intriguing differences in the selective pressures experienced by cancer genes relative to other (noncancer) disease-related and nondisease-related genes. We found a statistically significant increase in the intensity of purifying selection exerted on cancer genes (the average ratio of nonsynonymous to synonymous substitutions,
, was 0.079) relative to all other disease-related genes groups (
) and nondisease-related genes (
). This difference indicates a striking increase in selection against nonsynonymous substitutions in oncogenes and tumor suppressor genes. This finding provides insight into the etiology of cancer and the differences between genes involved in cancer and those implicated in other human diseases. Specifically, we found a significant overlap between human oncogenes and tumor suppressor genes and "essential genes," human homologs of mouse lethal genes identified by knockout experiments. This insight may improve our ability to identify cancer-related genes and enhances our understanding of the nature of these genes.
Key Words: Darwinian selection purifying selection disease gene oncogene synonymous and nonsynonymous substitutions
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
Y. Zhao and R. J. Epstein Programmed Genetic Instability: A Tumor-Permissive Mechanism for Maintaining the Evolvability of Higher Species through Methylation-Dependent Mutation of DNA Repair Genes in the Male Germ Line Mol. Biol. Evol., August 1, 2008; 25(8): 1737 - 1749. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Szklarczyk, J. Heringa, S. K. Pond, and A. Nekrutenko Rapid asymmetric evolution of a dual-coding tumor suppressor INK4a/ARF locus contradicts its function PNAS, July 31, 2007; 104(31): 12807 - 12812. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Gu, Y. Gibert, T. Wirth, A. Elischer, W. Bloch, A. Meyer, O. K. Steinlein, and G. Begemann Using Gene-History and Expression Analyses to Assess the Involvement of LGI Genes in Human Disorders Mol. Biol. Evol., November 1, 2005; 22(11): 2209 - 2216. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Xing and C. Lee Colloquium Paper: Evidence of functional selection pressure for alternative splicing events that accelerate evolution of protein subsequences PNAS, September 20, 2005; 102(38): 13526 - 13531. [Abstract] [Full Text] [PDF] |
||||

