Ghansah, A.Rockett, K.A.Clark, T. G.Wilson, M.D.Koram, K. A.Oduro, A. R.Amenga-Etego, L.Anyorigiya, T.Hodgson, A.Milligan, P.Rogers, W.O.Kwiatkowski, D.P.2013-06-262017-10-162013-06-262017-10-162012-04Ghansah, A., Rockett, K. A., Clark, T. G., Wilson, M. D., Koram, K. A., Oduro, A. R., . . . Kwiatkowski, D. P. (2012). Haplotype analyses of haemoglobin C and haemoglobin S and the dynamics of the evolutionary response to malaria in kassena-nankana district of Ghana. PLoS ONE, 7(4).19326203http://197.255.68.203/handle/123456789/4207Background: Haemoglobin S (HbS) and C (HbC) are variants of the HBB gene which both protect against malaria. It is not clear, however, how these two alleles have evolved in the West African countries where they co-exist at high frequencies. Here we use haplotypic signatures of selection to investigate the evolutionary history of the malaria-protective alleles HbS and HbC in the Kassena-Nankana District (KND) of Ghana. Methodology/Principal Findings: The haplotypic structure of HbS and HbC alleles was investigated, by genotyping 56 SNPs around the HBB locus. We found that, in the KND population, both alleles reside on extended haplotypes (approximately 1.5 Mb for HbS and 650 Kb for HbC) that are significantly less diverse than those of the ancestral HbA allele. The extended haplotypes span a recombination hotspot that is known to exist in this region of the genome Significance: Our findings show strong support for recent positive selection of both the HbS and HbC alleles and provide insights into how these two alleles have both evolved in the population of northern Ghana. © 2012 Ghansah et al.enEMTREE drug terms: hemoglobin A; hemoglobin beta chain; hemoglobin C; hemoglobin S EMTREE medical terms: allele; article; blood; case control study; ethnic group; ethnology; gene frequency; gene locus; genetic recombination; genetics; genotyping technique; Ghana; haplotype; human; malaria; methodology; molecular evolution; single nucleotide polymorphism; controlled study; evolutionary adaptation; genetic selection; genetic variability; genotype; haplotype map; heterozygosity; homozygosity; major clinical study; protein structureArticle