Transcriptional activation of the F1F0 ATP synthase α-subunit initiator element by USF2 is mediated by p300

被引:20
作者
Breen, GAM [1 ]
Jordan, EM [1 ]
机构
[1] Univ Texas, Dept Mol & Cell Biol, Richardson, TX 75083 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 1999年 / 1428卷 / 2-3期
关键词
p300; upstream stimulatory factor; transcription factor; coactivator; initiator element; F1F0 ATP synthase alpha-subunit;
D O I
10.1016/S0304-4165(99)00061-6
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
We have been studying the transcriptional regulation of the mammalian F1F0 ATP synthase a-subunit gene (ATPA), a TATA-less initiator-containing gene. We have previously determined that the transcription factor, upstream stimulatory factor 2 (USF2), can activate the A TPA gene through an initiator element in the core promoter. Here, we demonstrate that the coactivator p300 interacts functionally with USF2 proteins to potentiate the activation of the ATPA initiator element by USF2. The physiological relevance of this interaction was shown in vivo by expression of the adenovirus E1A oncoprotein. Wild-type E1A, but not EIA mutants that lacked p300-binding sites, inhibited the USF2-dependent transactivation of the ATPA initiator element. Furthermore, overexpression of p300 could reverse the inhibitory effect of E1A. Collectively, our results indicate that the USF2-dependent transcriptional activation of the ATPA initiator element is mediated by p300. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:169 / 176
页数:8
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