Antonarakis S E, Boehm C D, Serjeant G R, Theisen C E, Dover G J, Kazazian H H
Proc Natl Acad Sci U S A. 1984 Feb;81(3):853-6. doi: 10.1073/pnas.81.3.853.
In order to investigate the origin(s) of the mutation(s) leading to the beta S-globin gene in North American populations of African ancestry, we analyzed DNA polymorphisms in the beta-globin gene cluster in a large number of both beta A- and beta S-globin gene-bearing chromosomes in U.S. and Jamaican Blacks. We found 16 different haplotypes of polymorphic sites associated with 170 beta S-globin gene-bearing chromosomes. The three most common beta S haplotypes, which account for 151/170 of the beta S-globin gene-bearing chromosomes, are only rarely seen in the chromosomes bearing the beta A-globin gene in these populations (6/47). Two observations suggest multiple origins or interallelic gene conversion, or both, of the beta S mutation. First, the mutation is present in all three beta-globin gene frameworks. Second, the beta S haplotypes can be divided into four groups, each of which cannot be derived from any other by less than two crossing-over events. In summary, our observation of the beta S mutation on 16 different haplotypes in African populations can be best explained by (i) a number of simple recombination events 5' to the beta-globin gene and (ii) up to four independent mutations and/or interallelic gene conversions.
为了研究导致北美非洲裔人群中βS-珠蛋白基因发生突变的起源,我们分析了美国和牙买加黑人中大量携带βA-和βS-珠蛋白基因的染色体上β-珠蛋白基因簇中的DNA多态性。我们在与170条携带βS-珠蛋白基因的染色体相关的多态性位点中发现了16种不同的单倍型。三种最常见的βS单倍型,占携带βS-珠蛋白基因染色体的151/170,在这些人群中携带βA-珠蛋白基因的染色体中很少见(6/47)。两项观察结果表明βS突变存在多个起源或等位基因间的基因转换,或两者皆有。第一,该突变存在于所有三种β-珠蛋白基因框架中。第二,βS单倍型可分为四组,每组之间至少需要两次交叉事件才能从其他组衍生而来。总之,我们在非洲人群中观察到βS突变存在于16种不同的单倍型上,这最好用以下两点来解释:(i)在β-珠蛋白基因5'端发生了一些简单的重组事件;(ii)多达四次独立的突变和/或等位基因间的基因转换。