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Detailed analysis of the site 3 region of the human beta-globin dominant control region.

机译:人类β-珠蛋白显性控制区的位点3区域的详细分析。

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摘要

Four DNase I hypersensitive sites characterize the human beta-globin Dominant Control Region (DCR) providing position independent, high levels of erythroid specific expression to linked homologous and heterologous genes when introduced into cultured cells or in transgenic mice. We have delineated the hypersensitive site located 10.5 kbp upstream of the epsilon-globin gene by short range DNase I sensitivity mapping to a 600 bp region. Using transgenic mice and MEL cells the functional part of this region was further mapped to a 300 bp central core, which provides position independent, high level expression. It contains a number of ubiquitous and erythroid specific protein binding sites, including the previously described factors NF-E1 (GF1) and NF-E2. The latter binds to a dimer of the consensus binding sequence for jun/fos. The presence of this sequence is required for the function of the element, but single or multimerized copies of this site failed to give position independent, high levels of expression in transgenic mice or MEL cells. We therefore conclude that a combination of factor binding sites is necessary to allow site 3 to function as a strong transcriptional activator, resulting in position independent expression of the beta-globin gene.
机译:四个DNase I超敏位点表征了人类β-珠蛋白的主要控制区(DCR),当将其引入培养的细胞或转基因小鼠中时,可提供与位置无关的高水平的类胡萝卜素特异性表达,从而与连接的同源和异源基因相关。我们已经通过定位到600 bp区域的短距离DNase I敏感性描述了位于ε-珠蛋白基因上游10.5 kbp的超敏位点。使用转基因小鼠和MEL细胞,该区域的功能部分被进一步定位到300 bp的中央核心,该核心提供了位置无关的高水平表达。它包含许多普遍存在的和红系特异性蛋白结合位点,包括先前描述的因子NF-E1(GF1)和NF-E2。后者与jun / fos的共有结合序列的二聚体结合。该序列的存在对于元件的功能是必需的,但是该位点的单拷贝或多聚拷贝不能在转基因小鼠或MEL细胞中提供与位置无关的高水平表达。因此,我们得出结论,必须结合因子结合位点才能使位点3发挥强大的转录激活剂的作用,从而导致位置无关的β-珠蛋白基因表达。

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