Melis M, Demopulos G, Najfeld V, Zhang J W, Brice M, Papayannopoulou T, Stamatoyannopoulos G
Division of Medical Genetics, University of Washington, Seattle 98195.
Proc Natl Acad Sci U S A. 1987 Nov;84(22):8105-9. doi: 10.1073/pnas.84.22.8105.
Hybrids formed by fusing mouse erythroleukemia (MEL) cells with human fetal erythroid cells produce human fetal globin, but they switch to adult globin production as culture time advances. To obtain information on the chromosomal assignment of the elements that control gamma-to-beta switching, we analyzed the chromosomal composition of hybrids producing exclusively or predominantly human fetal globin and hybrids producing only adult human globin. No human chromosome was consistently present in hybrids expressing fetal globin and consistently absent in hybrids expressing adult globin. Subcloning experiments demonstrated identical chromosomal compositions in subclones displaying the fetal globin program and those that had switched to expression of the adult globin program. These data indicate that retention of only one human chromosome-i.e., chromosome 11--sufficient for expression of human fetal globin and the subsequent gamma-to-beta switch. The results suggest that the gamma-to-beta switch is controlled either cis to the beta-globin locus or by a trans-acting mechanism, the genes of which reside on human chromosome 11.
通过将小鼠红白血病(MEL)细胞与人胎儿红系细胞融合形成的杂种细胞能产生人胎儿珠蛋白,但随着培养时间的推进,它们会转而产生成人珠蛋白。为了获取有关控制γ向β转换的元件的染色体定位信息,我们分析了仅产生或主要产生人胎儿珠蛋白的杂种细胞以及仅产生成人珠蛋白的杂种细胞的染色体组成。在表达胎儿珠蛋白的杂种细胞中并非始终存在某条人类染色体,而在表达成人珠蛋白的杂种细胞中也并非始终缺失该染色体。亚克隆实验表明显示胎儿珠蛋白表达模式的亚克隆与已转换为成人珠蛋白表达模式的亚克隆具有相同的染色体组成。这些数据表明仅保留一条人类染色体——即11号染色体——就足以使人胎儿珠蛋白表达并随后发生γ向β的转换。结果提示γ向β的转换要么由β珠蛋白基因座顺式控制,要么由一种反式作用机制控制,该机制的基因位于人类11号染色体上。