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Human Molecular Genetics Advance Access published online on August 4, 2005

Human Molecular Genetics, doi:10.1093/hmg/ddi298
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© The Author 2005. Published by Oxford University Press. All rights reserved
Received June 2, 2005
Revised August 1, 2005
Accepted August 1, 2005

Article

Functional promoter SNPs in cell cycle checkpoint genes

Hélène Bélanger 1, Patrick Beaulieu 1, Claudia Moreau 1, Damian Labuda 2, Thomas J. Hudson 3, and Daniel Sinnett 2*

1 Division of Hematology-Oncology, Research Center, Sainte-Justine Hospital, 3175 chemin de la Côte-Sainte-Catherine, Montreal, QC, H3T 1C5, Canada
2 Division of Hematology-Oncology, Research Center, Sainte-Justine Hospital, 3175 chemin de la Côte-Sainte-Catherine, Montreal, QC, H3T 1C5, Canada; Department of Pediatrics, University of Montreal (3175 Côte-Ste-Catherine, Montreal, QC, Canada, H3T 1C5)
3 McGill University and Genome Quebec Innovation Centre (740 Drive Penfield Avenue, Montreal, H3A 1A4, Canada)

* To whom correspondence should be addressed.
Daniel Sinnett, E-mail: daniel.sinnett{at}umontreal.ca


   Abstract

A substantial number of genes mutated in human cancers encode components of the cell cycle processes. Since the G1/S transition in the cell cycle is a finely regulated biological process we hypothesized that sequence variations in the promoter region of the related genes might indeed lead to abnormal expression, thus predisposing the individuals carrying these genetic variants to cancer. In this report we screened the promoter regions of 16 cell cycle checkpoint genes for DNA variants and assessed the functional impact of these promoter SNPs (pSNPs) by combining in silico analysis and in vitro functional assays. We identified 127 pSNPs including 90 with predicted impact on putative binding sites of known transcription factors. Eleven pSNPs were selected for electrophoresis mobility shift assays because of their association with predicted gains of binding sites, and 9 pSNPs showed differential allelic shifts in at least one cell lines tested. Following the subcloning of the promoter regions into a gene reporter system, we found that at least 4 promoter haplotypes associated with CCND1, E2F1, HDAC1 and RB1 significantly influenced transcriptional activity in an allele-specific manner. Although, the biological significance of these observations still remain to be demonstrated, the expected variability of expression levels in key cell cycle components might influence individual's risk of cancer.


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