Dillon N, Grosveld F
National Institute for Medical Research, Mill Hill, London, UK.
Nature. 1991 Mar 21;350(6315):252-4. doi: 10.1038/350252a0.
Erythropoiesis during human development is characterized by switches in expression of beta-like globin genes during the transition from the embryonic through fetal to adult stages. Activation and high-level expression of the genes is directed by the locus control region (LCR), located 5' to the epsilon gene. The location of the LCR and its role in directing high-level expression of the globin genes has led to the suggestion that competition from the beta gene for interaction with the LCR has a major role in silencing the fetal gamma genes during adult life. We have now constructed lines of transgenic mice containing the human A gamma globin gene linked to the LCR. We observe high-level expression of the transgene in the embryonic stages but silencing of the gene in adult animals. We conclude that the gamma gene is not deregulated by the presence of the LCR and that competition from the beta gene is not required for silencing of the gamma genes in adult life. The silencing is therefore likely to be mediated by stage-specific factors binding to sequences immediately flanking the genes.
人类发育过程中的红细胞生成的特点是,在从胚胎期到胎儿期再到成年期的转变过程中,类β珠蛋白基因的表达发生切换。这些基因的激活和高水平表达由位于ε基因5'端的基因座控制区(LCR)指导。LCR的位置及其在指导珠蛋白基因高水平表达中的作用表明,β基因与LCR相互作用的竞争在成年期沉默胎儿γ基因中起主要作用。我们现在构建了含有与LCR相连的人类Aγ珠蛋白基因的转基因小鼠品系。我们观察到转基因在胚胎期高水平表达,但在成年动物中该基因沉默。我们得出结论,γ基因不会因LCR的存在而失调,并且成年期γ基因的沉默不需要β基因的竞争。因此,这种沉默可能是由与基因紧邻序列结合的阶段特异性因子介导的。