Boehm C D, Dowling C E, Antonarakis S E, Honig G R, Kazazian H H
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Am J Hum Genet. 1985 Jul;37(4):771-7.
In order to characterize the origin(s) of the beta C-globin gene in blacks, 25 chromosomes bearing this gene were characterized at eight polymorphic restriction sites within the beta-globin gene cluster. Twenty-two of the 25 chromosomes were identical at all sites and possessed a haplotype seen only infrequently among beta A-bearing chromosomes in black Americans. Two different haplotypes were observed among the three exceptional chromosomes. These haplotypes were identical to the most common beta C allele in the 3' end of the beta-globin gene cluster, but differed in the 5' region. Partial haplotype analysis on an additional 14 beta C alleles demonstrated complete association with the typical beta C-associated polymorphisms in the 3' region of the cluster. These data can be most easily explained by a single origin of the mutation followed by spread of the mutation to other haplotypes through meiotic recombination 5' to the beta-globin gene.
为了确定黑人中β C -珠蛋白基因的起源,在β -珠蛋白基因簇内的八个多态性限制性位点对携带该基因的25条染色体进行了特征分析。25条染色体中的22条在所有位点均相同,并且拥有一种单倍型,这种单倍型在美国黑人中携带β A的染色体中很少见。在三条异常染色体中观察到两种不同的单倍型。这些单倍型在β -珠蛋白基因簇的3'端与最常见的β C等位基因相同,但在5'区域有所不同。对另外14个β C等位基因进行的部分单倍型分析表明,它们与该基因簇3'区域中典型的β C相关多态性完全相关。这些数据最容易通过单一的突变起源来解释,随后该突变通过减数分裂重组传播到β -珠蛋白基因5'端的其他单倍型。