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红系类Krüppel样因子反式激活结构域是β-珠蛋白启动子细胞特异性诱导的关键组成部分。

The erythroid Krüppel-like factor transactivation domain is a critical component for cell-specific inducibility of a beta-globin promoter.

作者信息

Bieker J J, Southwood C M

机构信息

Brookdale Center for Molecular Biology, Mount Sinai School of Medicine, New York, New York 10029.

出版信息

Mol Cell Biol. 1995 Feb;15(2):852-60. doi: 10.1128/MCB.15.2.852.

Abstract

Erythroid Krüppel-like factor (EKLF) is an erythroid cell-specific DNA-binding protein that activates transcription from the beta-globin CACCC element, a functionally important and evolutionarily conserved component of globin as well as other erythroid cell-specific promoters and enhancers. We have attempted to elucidate the molecular role of EKLF in erythrocyte-specific transcriptional activation. First, in vivo and in vitro analyses have been used to demonstrate that the level of activation by EKLF is dependent on the orientation and number of CACCC elements, that EKLF contains separable activation and DNA-binding domains, and that the EKLF proline-rich region is a potent activator in CV-1 cells when fused to a nonrelated DNA-binding module. Second, we have established a transient assay in murine erythroleukemia cells in which reproducible levels of a reporter can be induced when linked to a locus control region enhancer-beta-globin promoter and in which induction is abolished when the promoter CAC site is mutated to a GAL site. Third, we demonstrate that the EKLF transactivation region, when fused to the GAL DNA-binding domain, can restore inducibility to this mutated construct and that this inducibility exhibits activator-, promoter-, and cell-type specificity. These results demonstrate that EKLF provides a crucial transactivation function for globin expression and further reinforce the idea that EKLF is an important regulator of CACCC element-directed transcription in erythroid cells.

摘要

红系Krüppel样因子(EKLF)是一种红系细胞特异性DNA结合蛋白,它能激活β-珠蛋白CACCC元件的转录,该元件是珠蛋白以及其他红系细胞特异性启动子和增强子在功能上重要且在进化上保守的组成部分。我们试图阐明EKLF在红细胞特异性转录激活中的分子作用。首先,体内和体外分析已用于证明EKLF的激活水平取决于CACCC元件的方向和数量,EKLF包含可分离的激活和DNA结合结构域,并且当与不相关的DNA结合模块融合时,EKLF富含脯氨酸的区域在CV-1细胞中是一种有效的激活剂。其次,我们在小鼠红白血病细胞中建立了一种瞬时分析方法,当报告基因与基因座控制区增强子-β-珠蛋白启动子连接时,可以诱导出可重复的水平,而当启动子CAC位点突变为GAL位点时,诱导作用消失。第三,我们证明,当EKLF反式激活区域与GAL DNA结合结构域融合时,可以恢复该突变构建体的诱导能力,并且这种诱导能力表现出激活剂、启动子和细胞类型特异性。这些结果表明,EKLF为珠蛋白表达提供了关键的反式激活功能,并进一步强化了EKLF是红系细胞中CACCC元件定向转录的重要调节因子这一观点。

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