Chang J C, Alberti A, Kan Y W
Nucleic Acids Res. 1983 Nov 25;11(22):7789-94. doi: 10.1093/nar/11.22.7789.
Digestion of DNA from a patient with homozygous beta zero thalassemia from Calabria, Italy with the restriction endonuclease Mst II produced a pattern similar to the one obtained with sickle cell trait DNA in that the Mst II site at the beta 6 position on one chromosome was abolished. We cloned the DNA from this beta-thalassemia chromosome and performed sequence analysis. The deletion of a single nucleotide (A) at the GAG codon of the beta 6 position results in a frame shift and early beta-globin chain termination. This mutation occurs on a chromosome with a haplotype similar to two other Mediterranean beta-thalassemia lesions. The Mst II enzyme is useful for prenatal diagnosis of beta thalassemia in this population.
用限制性内切酶Mst II消化来自意大利卡拉布里亚的一名纯合β0地中海贫血患者的DNA,产生的图谱与镰状细胞性状DNA的图谱相似,即一条染色体上β6位置的Mst II位点被消除。我们克隆了这条β地中海贫血染色体的DNA并进行了序列分析。β6位置的GAG密码子处单个核苷酸(A)的缺失导致移码和β珠蛋白链提前终止。这种突变发生在一条单倍型与其他两种地中海β地中海贫血病变相似的染色体上。Mst II酶可用于该人群中β地中海贫血的产前诊断。