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Transcriptional activation of human zeta 2 globin promoter by the alpha globin regulatory element (HS-40): functional role of specific nuclear factor-DNA complexes.

机译:人类Zeta 2球蛋白启动子的转录激活由α球蛋白调节元件(HS-40):特定核因子-DNA复合物的功能作用。

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摘要

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.
机译:我们研究了人类胚胎zeta 2球蛋白启动子与位于zeta 2球蛋白基因上游40 kb的alpha球蛋白调节元件(HS-40)之间的功能相互作用。通过瞬时表达测定法表明,HS-40在K562细胞(一种胚胎和/或胎儿来源的类红细胞细胞系)中充当高水平zeta 2球蛋白启动子活性的可靠增强剂。尽管位于zeta 2球蛋白基因的-559和-88之间的序列对于在无增强子质粒上的表达是可有可无的,但是它们是zeta 2球蛋白启动子的HS-40增强子介导的活性所必需的。定点诱变表明该HS-40增强子-zeta 2球蛋白启动子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。 HS-40的功能域也被映射。 Bal 31缺失作图数据表明,一个GATA-1基序,一个GT基序和两个NF-E2 / AP1基序一起形成了Zeta 2球蛋白启动子的类红细胞特异性活化中HS-40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而不是AP1转录因子的结合而介导的。最后,我们在K562细胞,成核成核成红细胞和不同非类红细胞中对HS-40增强子区域进行了基因组印迹。通过瞬时表达分析作图,HS-40功能核心内的所有序列基序似乎都结合了活K562细胞中的核因子,但未结合非红系细胞。另一方面,在体内,只有一个看似无功能的序列基序与因子结合。与K562相比,成年人类骨髓中有核的成核细胞在HS-40区域体内表现出相似但不同的核因子结合模式。这些数据表明,人类胚胎Zeta 2球蛋白基因和胎儿/成人α球蛋白基因的转录激活是由在增强子(HS-40)和细胞表面形成的类红细胞特异性细胞因子和发育阶段特异性核因子-DNA复合物介导的。球蛋白启动子。

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