Fodde R, Harteveld C L, Losekoot M, Giordano P C, Khan P M, Nayudu N V, Bernini L F
Department of Human Genetics, Sylvius Laboratory, University of Leiden, The Netherlands.
Ann Hum Genet. 1991 Jan;55(1):43-50. doi: 10.1111/j.1469-1809.1991.tb00397.x.
The presence of several polymorphic markers along the alpha-globin gene complex allows the identification of haplotypes associated with alpha-thalassemia determinants. These are found at very high frequencies in geographic areas where malaria is or has been endemic which suggests a positive selective role by the parasitic disease in favour of alpha(+)-thalassemia mutants. A population survey among forest tribal communities from Andhra Pradesh, India, revealed the prevalence and molecular heterogeneity of alpha(+)-thalassemia determinants presumably due to a long backdated malaria endemicity among these populations. Analysis of the tribal alpha-thalassemia haplotypes has shown a great degree of genetic heterogeneity which can be explained as the result of multiple recombination events in the presence of natural selection by malaria.
沿着α-珠蛋白基因复合体存在多个多态性标记,这使得与α-地中海贫血决定因素相关的单倍型得以识别。在疟疾流行或曾经流行的地理区域,这些单倍型的频率非常高,这表明这种寄生虫病对α(+)-地中海贫血突变体具有积极的选择作用。对印度安得拉邦森林部落社区的一项人群调查显示,α(+)-地中海贫血决定因素的患病率和分子异质性可能是由于这些人群中长期存在疟疾流行。对部落α-地中海贫血单倍型的分析表明,存在高度的遗传异质性,这可以解释为在疟疾自然选择的情况下多次重组事件的结果。