Charnay P, Henry L
Eur J Biochem. 1986 Sep 15;159(3):475-8. doi: 10.1111/j.1432-1033.1986.tb09910.x.
We have analysed the expression of cloned human fetal gamma-globin genes introduced into murine erythroleukemia cells by a protoplast fusion procedure. Both the wild-type a gamma-globin gene and a mutant derivative related to a phenotype of hereditary persistence of fetal hemoglobin were studied. In both cases the level of gamma-globin mRNA increased by a factor of approximately sevenfold when erythroid cell differentiation was induced by treatment with hexamethylenebisacetamide. Thus, the regulation of the expression of the cloned fetal A gamma-globin gene in murine erythroleukemia cells resembled that of cloned adult beta-globin genes.
我们通过原生质体融合程序分析了导入小鼠红白血病细胞的克隆人胎儿γ-珠蛋白基因的表达。对野生型αγ-珠蛋白基因和与胎儿血红蛋白遗传性持续存在表型相关的突变衍生物都进行了研究。在这两种情况下,当用六亚甲基双乙酰胺处理诱导红系细胞分化时,γ-珠蛋白mRNA水平增加了约7倍。因此,克隆的胎儿Aγ-珠蛋白基因在小鼠红白血病细胞中的表达调控类似于克隆的成人β-珠蛋白基因的表达调控。