Journal
HUMAN MUTATION
Volume 30, Issue 8, Pages 1189-1198Publisher
WILEY
DOI: 10.1002/humu.21020
Keywords
gene conversion; recombination-inducing sequence motifs; non-B DNA
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Funding
- INSERM (Institut National de la Sante et de la Recherche Medicale), France
- BIOBASE GmbH
- National Institutes of Health [NS37554, ES11347]
- Robert A. Welch Foundation
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A variety of DNA sequence motifs including inverted repeats, minisatellites, and the chi recombination hotspot, have been reported in association with gene conversion in human genes causing inherited disease. However, no methodical statistically based analysis has been performed to formalize these observations. We have performed an in silico analysis of the DNA sequence tracts involved in 27 nonoverlapping gene conversion events in 19 different genes reported in the context of inherited disease. We found that gene conversion events tend to occur within (C+G), and CpG-rich regions and that sequences with the potential to form non-B-DNA structures, and which may be involved in the generation of double-strand breaks that could, in turn, serve to promote gene conversion, occur disproportionately within maximal converted tracts and/or short flanking regions. Maximal converted tracts were also found to be enriched (P<0.01) in a truncated version of the chi-element (a TGGTGG motif), immunoglobulin heavy chain class switch repeats, translin target sites and several novel motifs including (or overlapping) the classical meiotic recombination hotspot, CCTCCCCT. Finally, gene cone versions tend to occur in genomic regions that have the potential to fold into stable hairpin conformations. These findings support the concept that recombination-inducing motifs, in association with alternative DNA conformations, can promote recombination in the human genome. Hum Mutat 30, 1189-1198, 2009. (C) 2009 Wiley-Liss, Inc.
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