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Distribution of Recombination Hotspots in the Human Genome--a Comparison of Computer Simulations with Real Data

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Journal PLoS One
Date 2013 Jun 19
PMID 23776462
Citations 8
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Abstract

Recombination is the main cause of genetic diversity. Thus, errors in this process can lead to chromosomal abnormalities. Recombination events are confined to narrow chromosome regions called hotspots in which characteristic DNA motifs are found. Genomic analyses have shown that both recombination hotspots and DNA motifs are distributed unevenly along human chromosomes and are much more frequent in the subtelomeric regions of chromosomes than in their central parts. Clusters of motifs roughly follow the distribution of recombination hotspots whereas single motifs show a negative correlation with the hotspot distribution. To model the phenomena related to recombination, we carried out computer Monte Carlo simulations of genome evolution. Computer simulations generated uneven distribution of hotspots with their domination in the subtelomeric regions of chromosomes. They also revealed that purifying selection eliminating defective alleles is strong enough to cause such hotspot distribution. After sufficiently long time of simulations, the structure of chromosomes reached a dynamic equilibrium, in which number and global distribution of both hotspots and defective alleles remained statistically unchanged, while their precise positions were shifted. This resembles the dynamic structure of human and chimpanzee genomes, where hotspots change their exact locations but the global distributions of recombination events are very similar.

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References
1.
Petes T . Meiotic recombination hot spots and cold spots. Nat Rev Genet. 2001; 2(5):360-9. DOI: 10.1038/35072078. View

2.
Westphal T, Reuter G . Recombinogenic effects of suppressors of position-effect variegation in Drosophila. Genetics. 2002; 160(2):609-21. PMC: 1461983. DOI: 10.1093/genetics/160.2.609. View

3.
Groenen M, Wahlberg P, Foglio M, Cheng H, Megens H, Crooijmans R . A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate. Genome Res. 2008; 19(3):510-9. PMC: 2661806. DOI: 10.1101/gr.086538.108. View

4.
Myers S, Freeman C, Auton A, Donnelly P, McVean G . A common sequence motif associated with recombination hot spots and genome instability in humans. Nat Genet. 2009; 40(9):1124-9. DOI: 10.1038/ng.213. View

5.
Frazer K, Ballinger D, Cox D, Hinds D, Stuve L, Boudreau A . A second generation human haplotype map of over 3.1 million SNPs. Nature. 2007; 449(7164):851-61. PMC: 2689609. DOI: 10.1038/nature06258. View