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Logo of bmcgenoBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Genomics
 
BMC Genomics. 2009; 10: 513.
Published online Nov 5, 2009. doi:  10.1186/1471-2164-10-513
PMCID: PMC2779198
Evolution of genomic sequence inhomogeneity at mid-range scales
Ashwin Prakash,#1,7 Samuel S Shepard,#1,7 Jie He,2 Benjamin Hart,3 Miao Chen,3 Surya P Amarachintha,4 Olga Mileyeva-Biebesheimer,5 Jason Bechtel,6 and Alexei Fedorovcorresponding author6,7
1Program in Cardiovascular & Metabolic Diseases Track, Biomedical Sciences, University of Toledo Health Science Campus, Toledo, OH 43614, USA
2University of Toledo, Department of Biology, Toledo, Ohio, USA
3Dept of Medical Microbiology & Immunology, Infection, Immunity & Transplantation Track, University of Toledo, Health Science Campus, Toledo, OH 43614, USA
4Department of Biological Sciences, Bowling Green State University, Bowling Green, OH - 43403, USA
5Department of Civil Engineering, University of Toledo, Toledo, Ohio, USA
6Program in Bioinformatics and Proteomics/Genomics, University of Toledo Health Science Campus, Toledo, OH 43614, USA
7Department of Medicine, University of Toledo, Health Science Campus, Toledo, Ohio, USA
corresponding authorCorresponding author.
#Contributed equally.
Ashwin Prakash: ashwin.prakash/at/utoledo.edu; Samuel S Shepard: samuel.shepard/at/utoledo.edu; Jie He: jie.he/at/utoledo.edu; Benjamin Hart: benjamin.hart/at/utoledo.edu; Miao Chen: miao.chen/at/utoledo.edu; Surya P Amarachintha: suryaa/at/bgsu.edu; Olga Mileyeva-Biebesheimer: omileyn/at/UTNet.UToledo.Edu; Jason Bechtel: jasonmbechtel/at/gmail.com; Alexei Fedorov: alexei.fedorov/at/utoledo.edu
Received March 18, 2009; Accepted November 5, 2009.
Abstract
Background
Mid-range inhomogeneity or MRI is the significant enrichment of particular nucleotides in genomic sequences extending from 30 up to several thousands of nucleotides. The best-known manifestation of MRI is CpG islands representing CG-rich regions. Recently it was demonstrated that MRI could be observed not only for G+C content but also for all other nucleotide pairings (e.g. A+G and G+T) as well as for individual bases. Various types of MRI regions are 4-20 times enriched in mammalian genomes compared to their occurrences in random models.
Results
This paper explores how different types of mutations change MRI regions. Human, chimpanzee and Macaca mulatta genomes were aligned to study the projected effects of substitutions and indels on human sequence evolution within both MRI regions and control regions of average nucleotide composition. Over 18.8 million fixed point substitutions, 3.9 million SNPs, and indels spanning 6.9 Mb were procured and evaluated in human. They include 1.8 Mb substitutions and 1.9 Mb indels within MRI regions. Ancestral and mutant (derived) alleles for substitutions have been determined. Substitutions were grouped according to their fixation within human populations: fixed substitutions (from the human-chimp-macaca alignment), major SNPs (> 80% mutant allele frequency within humans), medium SNPs (20% - 80% mutant allele frequency), minor SNPs (3% - 20%), and rare SNPs (<3%). Data on short (< 3 bp) and medium-length (3 - 50 bp) insertions and deletions within MRI regions and appropriate control regions were analyzed for the effect of indels on the expansion or diminution of such regions as well as on changing nucleotide composition.
Conclusion
MRI regions have comparable levels of de novo mutations to the control genomic sequences with average base composition. De novo substitutions rapidly erode MRI regions, bringing their nucleotide composition toward genome-average levels. However, those substitutions that favor the maintenance of MRI properties have a higher chance to spread through the entire population. Indels have a clear tendency to maintain MRI features yet they have a smaller impact than substitutions. All in all, the observed fixation bias for mutations helps to preserve MRI regions during evolution.
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