Embury S H, Lebo R V, Dozy A M, Kan Y W
J Clin Invest. 1979 Jun;63(6):1307-10. doi: 10.1172/JCI109426.
The alpha-thalassemia syndromes are a group of inherited anemias, the clinical severity of which has been shown to increase with the number of alpha-globin structural genes deleted. Employing restriction endonuclease gene mapping, we defined the organization of the alpha-globin genes in cellular DNA from Chinese subjects with various alpha-thalassemia syndromes. The four alpha-globin genes of normals are at two loci located on a 23.0-kilobase pair (kb) Eco RI fragment. In deletion type hemoglobin-H disease the 5' alpha-globin locus is deleted and the single 3' alpha-globin locus is found on a 19.0-kb Eco RI fragment. In alpha-thalassemia-2 there are two alpha-globin genes on a 23.0-kb Eco RI fragment and one on a 19.0-kb fragment. In alpha-thalassemia-1 and the nondeletion type of hemoglobin-H disease the two alpha-globin genes are at two loci on one chromosome and none reside on the other chromosome.
α地中海贫血综合征是一组遗传性贫血症,其临床严重程度已显示会随着缺失的α珠蛋白结构基因数量的增加而加重。我们利用限制性内切酶基因图谱法,确定了患有各种α地中海贫血综合征的中国受试者细胞DNA中α珠蛋白基因的组织情况。正常人的四个α珠蛋白基因位于两个位点,位于一个23.0千碱基对(kb)的Eco RI片段上。在缺失型血红蛋白H病中,5'α珠蛋白位点被删除,单个3'α珠蛋白位点位于一个19.0 kb的Eco RI片段上。在α地中海贫血-2中,一个23.0 kb的Eco RI片段上有两个α珠蛋白基因,一个19.0 kb的片段上有一个。在α地中海贫血-1和非缺失型血红蛋白H病中,两个α珠蛋白基因位于一条染色体的两个位点上,另一条染色体上没有。