Zhang Q, Reddy P M, Yu C Y, Bastiani C, Higgs D, Stamatoyannopoulos G, Papayannopoulou T, Shen C K
Department of Genetics, University of California, Davis 95616.
Mol Cell Biol. 1993 Apr;13(4):2298-308. doi: 10.1128/mcb.13.4.2298-2308.1993.
We studied the functional interaction between human embryonic zeta 2 globin promoter and the alpha globin regulatory element (HS-40) located 40 kb upstream of the zeta 2 globin gene. It was shown by transient expression assay that HS-40 behaved as an authentic enhancer for high-level zeta 2 globin promoter activity in K562 cells, an erythroid cell line of embryonic and/or fetal origin. Although sequences located between -559 and -88 of the zeta 2 globin gene were dispensable for its expression on enhancerless plasmids, they were required for the HS-40 enhancer-mediated activity of the zeta 2 globin promoter. Site-directed mutagenesis demonstrated that this HS-40 enhancer-zeta 2 globin promoter interaction is mediated by the two GATA-1 factor binding motifs located at -230 and -104, respectively. The functional domains of HS-40 were also mapped. Bal 31 deletion mapping data suggested that one GATA-1 motif, one GT motif, and two NF-E2/AP1 motifs together formed the functional core of HS-40 in the erythroid-specific activation of the zeta 2 globin promoter. Site-directed mutagenesis further demonstrated that the enhancer function of one of the two NF-E2/AP1 motifs of HS-40 is mediated through its binding to NF-E2 but not AP1 transcription factor. Finally, we did genomic footprinting of the HS-40 enhancer region in K562 cells, adult nucleated erythroblasts, and different nonerythroid cells. All sequence motifs within the functional core of HS-40, as mapped by transient expression analysis, appeared to bind a nuclear factor(s) in living K562 cells but not in nonerythroid cells. On the other hand, only one of the apparently nonfunctional sequence motifs was bound with factors in vivo. In comparison to K562, nucleated erythroblasts from adult human bone marrow exhibited a similar but nonidentical pattern of nuclear factor binding in vivo at the HS-40 region. These data suggest that transcriptional activation of human embryonic zeta 2 globin gene and the fetal/adult alpha globin genes is mediated by erythroid cell-specific and developmental stage-specific nuclear factor-DNA complexes which form at the enhancer (HS-40) and the globin promoters.
我们研究了人类胚胎ζ2珠蛋白启动子与位于ζ2珠蛋白基因上游40 kb处的α珠蛋白调控元件(HS-40)之间的功能相互作用。瞬时表达分析表明,在K562细胞(一种胚胎和/或胎儿来源的红系细胞系)中,HS-40作为真正的增强子,可增强ζ2珠蛋白启动子的高水平活性。尽管ζ2珠蛋白基因-559至-88之间的序列对于其在无增强子质粒上的表达并非必需,但它们是HS-40增强子介导的ζ2珠蛋白启动子活性所必需的。定点诱变表明,这种HS-40增强子与ζ2珠蛋白启动子的相互作用是由分别位于-230和-104的两个GATA-1因子结合基序介导的。我们还绘制了HS-40的功能域图谱。Bal 31缺失图谱数据表明,一个GATA-1基序、一个GT基序和两个NF-E2/AP1基序共同构成了HS-40在ζ2珠蛋白启动子红系特异性激活中的功能核心。定点诱变进一步证明,HS-40的两个NF-E2/AP1基序之一的增强子功能是通过其与NF-E2而非AP1转录因子的结合来介导的。最后,我们对K562细胞、成人有核红细胞和成体非红系细胞中的HS-40增强子区域进行了基因组足迹分析。通过瞬时表达分析绘制的HS-40功能核心内的所有序列基序,在活的K562细胞中似乎都能结合一种或多种核因子,而在非红系细胞中则不能。另一方面,在体内只有一个明显无功能的序列基序能与因子结合。与K562细胞相比,成人骨髓中的有核红细胞在体内HS-40区域表现出相似但不完全相同的核因子结合模式。这些数据表明,人类胚胎ζ2珠蛋白基因和胎儿/成人α珠蛋白基因的转录激活是由在增强子(HS-40)和珠蛋白启动子处形成的红系细胞特异性和发育阶段特异性核因子-DNA复合物介导的。