Albitar M, Katsumata M, Liebhaber S A
Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia 19104.
Mol Cell Biol. 1991 Jul;11(7):3786-94. doi: 10.1128/mcb.11.7.3786-3794.1991.
Recent studies have demonstrated that transcriptional activation of the human adult beta-globin transgene in mice by coinsertion of the beta-globin cluster locus control region (beta-LCR) results in loss of its adult restricted pattern of expression. Normal developmental control is reestablished by coinsertion of the fetal gamma-globin transgene in cis to the adult beta-globin gene. To test the generality of this interdependence of two globin genes for their proper developmental control, we generated transgenic mice in which the human adult alpha-globin genes are transcriptionally activated by the beta-LCR either alone or in cis to their corresponding embryonic zeta-globin gene. In both cases, the human globin transgenes were expressed at the appropriate developmental period. In contrast to the beta-globin gene, developmental control of the human adult alpha-globin transgenes appears to be autonomous and maintained even when activated by an adjacent locus control region.
最近的研究表明,通过共插入β-珠蛋白基因簇位点控制区(β-LCR)在小鼠中对人成人β-珠蛋白转基因进行转录激活,会导致其成人受限表达模式的丧失。通过将胎儿γ-珠蛋白转基因与成人β-珠蛋白基因顺式共插入,可重新建立正常的发育控制。为了测试两个珠蛋白基因这种相互依赖对其正常发育控制的普遍性,我们构建了转基因小鼠,其中人成人α-珠蛋白基因单独或与其相应的胚胎ζ-珠蛋白基因顺式被β-LCR转录激活。在这两种情况下,人珠蛋白转基因都在适当的发育时期表达。与β-珠蛋白基因不同,人成人α-珠蛋白转基因的发育控制似乎是自主的,即使由相邻的位点控制区激活也能维持。