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脊椎动物GATA-1启动子中的一个回文调控位点需要GATA-1 DNA结合域的两个锌指才能进行高亲和力相互作用。

A palindromic regulatory site within vertebrate GATA-1 promoters requires both zinc fingers of the GATA-1 DNA-binding domain for high-affinity interaction.

作者信息

Trainor C D, Omichinski J G, Vandergon T L, Gronenborn A M, Clore G M, Felsenfeld G

机构信息

Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892, USA.

出版信息

Mol Cell Biol. 1996 May;16(5):2238-47. doi: 10.1128/MCB.16.5.2238.

Abstract

GATA-1, a transcription factor essential for the development of the erythroid lineage, contains two adjacent highly conserved zinc finger motifs. The carboxy-terminal finger is necessary and sufficient for specific binding to the consensus GATA recognition sequence: mutant proteins containing only the amino-terminal finger do not bind. Here we identify a DNA sequence (GATApal) for which the GATA-1 amino-terminal finger makes a critical contribution to the strength of binding. The site occurs in the GATA-1 gene promoters of chickens, mice, and humans but occurs very infrequently in other vertebrate genes known to be regulated by GATA proteins. GATApal is a palindromic site composed of one complete [(A/T)GATA(A/G)] and one partial (GAT) canonical motif. Deletion of the partial motif changes the site to a normal GATA site and also reduces by as much as eightfold the activity of the GATA-1 promoter in an erythroid precursor cell. We propose that GATApal is important for positive regulation of GATA-1 expression in erythroid cells.

摘要

GATA-1是一种对红细胞系发育至关重要的转录因子,它包含两个相邻的高度保守的锌指基序。羧基末端的锌指对于与共有GATA识别序列的特异性结合是必需且充分的:仅包含氨基末端锌指的突变蛋白不具有结合能力。在此,我们鉴定出一个DNA序列(GATApal),GATA-1的氨基末端锌指对其结合强度起着关键作用。该位点存在于鸡、小鼠和人类的GATA-1基因启动子中,但在已知受GATA蛋白调控的其他脊椎动物基因中很少出现。GATApal是一个回文位点,由一个完整的[(A/T)GATA(A/G)]和一个部分(GAT)的典型基序组成。部分基序的缺失会将该位点转变为正常的GATA位点,同时也会使红细胞前体细胞中GATA-1启动子的活性降低多达八倍。我们认为GATApal对于红细胞中GATA-1表达的正向调控很重要。

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