Benz E J, Swerdlow P S, Forget B G
Department of Medicine, Children's Hospital Medical Center, Boston, Mass. 02115.
Blood. 1975 Jan;45(1):1-10.
Functional human globin messenger RNA was isolated from reticulocytes of two patients with homozygous beta 0-thalassemia, three patients with sickle cell beta 0-thalassemia, and one patient doubly heterozygous for beta 0-thalassemia and hemoglobin Lepore. When incubated in the Krebs type II mouse ascites tumor-cell-free system, messenger RNA from these patients actively directed the synthesis of human beta s and/or alpha- and gamma-globin chains but failed to stimulate the synthesis of any beta A-chains, even though nonthalassemic human globin mRNA preparations consistently stimulated two to four times as much beta A- or beta S-globin chain synthesis as alpha-chain synthesis when incubated in the same system under the same conditions. These results strongly suggest that functional beta A-chain-specific globin mRNA is absent in beta 0-thalassemia.
从两名纯合β⁰地中海贫血患者、三名镰状细胞β⁰地中海贫血患者以及一名β⁰地中海贫血和血红蛋白Lepore双重杂合子患者的网织红细胞中分离出功能性人珠蛋白信使核糖核酸(mRNA)。当在克雷布斯II型无小鼠腹水肿瘤细胞系统中孵育时,这些患者的信使核糖核酸积极指导人β⁰和/或α - 和γ - 珠蛋白链的合成,但未能刺激任何β⁰链的合成,尽管在相同条件下于同一系统中孵育时,非地中海贫血的人珠蛋白mRNA制剂持续刺激的β⁰或β⁰珠蛋白链合成量是α链合成量的两到四倍。这些结果强烈表明β⁰地中海贫血中不存在功能性β⁰链特异性珠蛋白mRNA。