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多种与GATA-E盒-GATA基序结合的蛋白质调控红系Krüppel样因子(EKLF)基因。

Multiple proteins binding to a GATA-E box-GATA motif regulate the erythroid Krüppel-like factor (EKLF) gene.

作者信息

Anderson K P, Crable S C, Lingrel J B

机构信息

Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Cincinnati, Ohio 45267-0524, USA.

出版信息

J Biol Chem. 1998 Jun 5;273(23):14347-54. doi: 10.1074/jbc.273.23.14347.

Abstract

Erythroid Krüppel-like factor (EKLF) is a zinc finger transcription factor required for beta-globin gene expression and is implicated as one of the key factors necessary for the fetal to adult switch in globin gene expression. In an effort to identify factors involved in the expression of this important erythroid-specific regulatory protein, we have isolated the mouse EKLF gene and systematically analyzed the promoter region. Initially, a reporter construct with 1150 base pairs of the EKLF 5'-region was introduced into transgenic mice and shown to direct erythroid-specific expression. We continued the expression studies in erythroid cells and have identified a sequence element consisting of two GATA sites flanking an E box motif. The three sites act in concert to elevate the transcriptional activity of the EKLF promoter. Each site is essential for EKLF expression indicating that the three binding sites do not work additively, but rather function as a unit. We further show that GATA-1 binds to the two GATA sites and present evidence for binding of another factor from erythroid cell nuclear extracts to the E box motif. These results are consistent with the formation of a quaternary complex composed of an E box dimer and two GATA-1 proteins binding at a combined GATA-E box-GATA activator element in the distal EKLF promoter.

摘要

红系Krüppel样因子(EKLF)是β-珠蛋白基因表达所必需的锌指转录因子,被认为是珠蛋白基因表达从胎儿型向成人型转换所需的关键因子之一。为了确定参与这种重要的红系特异性调节蛋白表达的因子,我们分离了小鼠EKLF基因并系统地分析了其启动子区域。最初,将含有1150个碱基对的EKLF 5'-区域的报告基因构建体导入转基因小鼠,结果表明它能指导红系特异性表达。我们继续在红系细胞中进行表达研究,并鉴定出一个由两个GATA位点侧翼一个E盒基序组成的序列元件。这三个位点协同作用以提高EKLF启动子的转录活性。每个位点对于EKLF表达都是必不可少的,这表明这三个结合位点不是相加作用,而是作为一个整体起作用。我们进一步表明GATA-1与两个GATA位点结合,并提供了红系细胞核提取物中另一种因子与E盒基序结合的证据。这些结果与由一个E盒二聚体和两个在EKLF启动子远端的组合GATA-E盒-GATA激活元件处结合的GATA-1蛋白组成的四聚体复合物的形成一致。

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