Costantini F, Chada K, Magram J
Science. 1986 Sep 12;233(4769):1192-4. doi: 10.1126/science.3461564.
A murine beta-thalassemia was corrected by the transfer of cloned beta-globin genes into the mouse germ line. The cloned mouse beta maj-globin gene or the cloned human beta-globin gene was introduced into mice deficient in beta-globin synthesis because of a deletion of the beta maj-globin gene. Both introduced genes produced functional beta-globin chains, leading to a reduction in one case, and elimination in another case, of the anemia and associated abnormalities of the red blood cells.
通过将克隆的β-珠蛋白基因导入小鼠生殖系,纠正了小鼠的β地中海贫血。将克隆的小鼠βmaj-珠蛋白基因或克隆的人β-珠蛋白基因导入因βmaj-珠蛋白基因缺失而缺乏β-珠蛋白合成的小鼠体内。导入的两个基因均产生功能性β-珠蛋白链,在一个案例中导致贫血减轻,在另一个案例中消除了贫血以及红细胞的相关异常。