Evidence of recent natural selection on the Southeast Asian deletion (--(SEA)) causing α-thalassemia in South China

• Published in: BMC evolutionary biology 2013-03, Vol.13 (1), p.63-63, Article 63
• Main Authors: Qiu, Qin-Wei, Wu, Dong-Dong, Yu, Li-Hua, Yan, Ti-Zhen, Zhang, Wen, Li, Zhe-Tao, Liu, Yan-Hui, Zhang, Ya-Ping, Xu, Xiang-Min
• Format: Article
• Language: English
• Subjects: alpha-Thalassemia - genetics; Asian Continental Ancestry Group - genetics; Chromosomes, Human, Pair 16; Gene Deletion; Haplotypes; Hemoglobins - genetics; High-Throughput Nucleotide Sequencing; Humans; Malaria - genetics; Polymorphism, Single Nucleotide; Recombination, Genetic; Selection, Genetic
• ISSN: 1471-2148; 1471-2148
• DOI: 10.1186/1471-2148-13-63

The Southeast Asian deletion (--(SEA)) is the most commonly observed mutation among diverse α-thalassemia alleles in Southeast Asia and South China. It is generally argued that mutation --(SEA), like other variants causing hemoglobin disorders, is associated with protection against malaria that is endemic in these regions. However, little evidence has been provided to support this claim. We first examined the genetic imprint of recent positive selection on the --(SEA) allele and flanking sequences in the human α-globin cluster, covering a genomic region spanning ~410 kb, by genotyping 28 SNPs in a Chinese population consisting of 76 --(SEA) heterozygotes and 138 normal individuals. The pattern of linkage disequilibrium (LD) and the long-range haplotype test revealed a signature of positive selection. The network of inferred haplotypes suggested a single origin of the --(SEA) allele. Thus, our data support the hypothesis that the --(SEA) allele has been subjected to recent balancing selection, triggered by malaria.