Little P F, Annison G, Darling S, Williamson R, Camba L, Modell B
Nature. 1980 May 15;285(5761):144-7. doi: 10.1038/285144a0.
Polymorphisms of DNA restriction sites within the human fetal globin genes have been used to identify chromosomes that carry beta-thalassaemia genes in individuals heterozygous for this disease. This has allowed an antenatal diagnosis for beta-thalassaemia to be carried out by observation of the pattern of the inherited polymorphism of a linked DNA sequence not involved in the genetic pathogenesis of the disease. In the populations we have investigated there is no constant pattern of polymorphism that segregates with the beta-thalassaemia gene. The use of linked polymorphisms should, therefore, be applicable to antenatal diagnosis both of beta-thalassaemia and of any other single-gene defect for which there is a DNA probe specific for a sequence linked to the affected locus.
人类胎儿珠蛋白基因内DNA限制性酶切位点的多态性已被用于识别携带β地中海贫血基因的染色体,这些个体为此病的杂合子。这使得通过观察与该疾病遗传发病机制无关的连锁DNA序列的遗传多态性模式来进行β地中海贫血的产前诊断成为可能。在我们所研究的人群中,不存在与β地中海贫血基因分离的恒定多态性模式。因此,连锁多态性的应用应适用于β地中海贫血以及任何其他单基因缺陷的产前诊断,对于这些疾病,存在针对与受影响基因座连锁的序列的DNA探针。