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中国南方东南亚缺失(--(SEA))引起的α-地中海贫血症的近期自然选择证据。

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

机构信息

Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, PR China.

出版信息

BMC Evol Biol. 2013 Mar 11;13:63. doi: 10.1186/1471-2148-13-63.

Abstract

BACKGROUND

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.

RESULTS

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.

CONCLUSIONS

Thus, our data support the hypothesis that the --(SEA) allele has been subjected to recent balancing selection, triggered by malaria.

摘要

背景

东南亚缺失(--(SEA))是东南亚和中国南方各种α-地中海贫血等位基因中最常见的突变。一般认为,突变--(SEA)与导致血红蛋白疾病的其他变体一样,与这些地区流行的疟疾有关。然而,几乎没有证据支持这一说法。

结果

我们首先通过对中国人群中 76 名--(SEA)杂合子和 138 名正常个体中的 28 个 SNP 进行基因分型,检查了人类α-珠蛋白簇中--(SEA)等位基因和侧翼序列上近期正选择的遗传印记,覆盖了约 410kb 的基因组区域。连锁不平衡(LD)和长程单倍型测试的模式揭示了正选择的特征。推断的单倍型网络表明--(SEA)等位基因具有单一起源。

结论

因此,我们的数据支持了这样的假设,即--(SEA)等位基因受到了疟疾引发的近期平衡选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9397/3626844/1da0f0fa490f/1471-2148-13-63-1.jpg

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