Ets-1 binds cooperatively to the palindromic Ets-binding sites in the p53 promoter

被引:29
作者
Baillat, David
Laitem, Clelia
Leprivier, Gabriel
Margerin, Charline
Aumercier, Marc [1 ]
机构
[1] Univ Lille 1, Inst Pasteur Lille, Inst Biol Lille, CNRS,UMR 8161, F-59021 Lille, France
关键词
p53; promoter; Transcriptional regulation; Ets-1; Oncogene; Cooperative binding; Surface plasmon resonance; PROTEIN-PROTEIN INTERACTIONS; DOMAIN; FAMILY; GENE;
D O I
10.1016/j.bbrc.2008.11.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Due to its autoinhibition for DNA binding, the Ets-1 transcription factor must interact with partners to enhance its affinity for DNA. In a study on the stromelysin-1 promoter, we showed that Ets-1 binds cooperatively to two Ets-binding sites (EBS) organized in palindrome, thereby circumventing the need for a binding partner to Counteract autoinhibition. This leads to the formation of an Ets-1-DNA-Ets-1 ternary complex necessary for promoter activation. Here we show that Ets-1 also binds cooperatively to the EBS palindrome of the human p53 promoter, despite the presence of a degenerate EBS to which Ets-1 cannot otherwise bind. Transcriptional transactivation through this palindrome fully correlates to Ets-1 binding. Thus, the cooperative binding model that we initially proposed for the stromelysin-1 promoter may be a general mechanism of Ets-1 binding to palindromic EBS separated by 4 bp and a way to counteract binding site degeneracy. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:213 / 217
页数:5
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