Milner P F, Huisman T H
Br J Haematol. 1976 Oct;34(2):207-20. doi: 10.1111/j.1365-2141.1976.tb00191.x.
The proportion of Hb G Philadelphia (alpha68-Asn leads to Lys) in heterozygotes has been found to have a well-defined bimodal distribution around means of 33% and 46% Hb G. microcytosis and hypochromia are consistently associated with the latter group, who also have a decreased ratio of alpha/beta-chain synthesis in the peripheral blood, but these characters are not linked to the Hb-Galpha gene, because a parent with microcytosis and 46% Hb Galpha may have offspring with 33% Hb G without significant microcytosis. In one family a subject with Hb G and Hb G2 but no Hb A or Hb A2 is presumably a homozygote for alphaG. This subject has microcytosis and a decreased ratio of alpha/beta chain synthesis. In another family a subject with Hbs H, G and G2 but without Hbs A or A2 is heterozygous for both Hb G and alpha thalassaemia I. These findings are compatible with the hypothesis that the alphaG mutation occurs on a chromosome with only a single alpha-chain locus and that the expression in heterozygotes as 46% or 33% Hb G is determined by the homologous chromosome in trans having either one or two normal alphaA genes respectively. The significance of this polymorphism for chromosomes carrying alpha-chain genes is discussed.
已发现杂合子中Hb G费城(α68 - 天冬酰胺导致赖氨酸)的比例在平均33%和46% Hb G周围呈现明确的双峰分布。小红细胞症和低色素血症始终与后一组相关,这组人的外周血中α/β链合成比例也降低,但这些特征与Hb - Galpha基因无关,因为患有小红细胞症且Hb Galpha为46%的父母可能会生出Hb G为33%且无明显小红细胞症的后代。在一个家族中,一名患有Hb G和Hb G2但无Hb A或Hb A2的受试者可能是αG的纯合子。该受试者有小红细胞症且α/β链合成比例降低。在另一个家族中,一名患有Hb H、G和G2但无Hb A或A2的受试者对于Hb G和α地中海贫血I均为杂合子。这些发现与以下假设相符:αG突变发生在仅具有单个α链基因座的染色体上,并且杂合子中作为46%或33% Hb G的表达分别由反式中具有一个或两个正常αA基因的同源染色体决定。讨论了这种多态性对携带α链基因的染色体的意义。