The p300/CBP acetyltransferases function as transcriptional coactivators of β-catenin in vertebrates

被引:490
作者
Hecht, A
Vleminckx, K
Stemmler, MP
van Roy, F
Kemler, R
机构
[1] Max Planck Inst Immunobiol, D-79108 Freiburg, Germany
[2] State Univ Ghent VIB, Dept Mol Biol, Mol Cell Biol Unit, B-9000 Ghent, Belgium
关键词
beta-catenin; p300; CBP acetylase; T-cell factor; transcriptional activation; Wnt signaling;
D O I
10.1093/emboj/19.8.1839
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
Wnt growth factors regulate a variety of developmental processes by altering specific gene expression patterns. In vertebrates beta-catenin acts as transcriptional activator, which is needed to overcome target gene repression by Groucho/TLE proteins, and to permit promoter activation as the final consequence of Wnt signaling. However, the molecular mechanisms of transcriptional activation by beta-catenin are only poorly understood. Here we demonstrate that the closely related acetyltransferases p300 and CBP potentiate beta-catenin-mediated activation of the siamois promoter, a known Wnt target. beta-catenin and p300 also synergize to stimulate a synthetic reporter gene construct, whereas activation of the cyclin DI promoter by beta-catenin is refractory to p300 stimulation. Axis formation and activation of the beta-catenin target genes siamois and Xnr-3 in Xenopus embryos are sensitive to the E1A oncoprotein, a known inhibitor of p300/CBP, The C-terminus of beta-catenin interacts directly with a region overlapping the CH-3 domain of p300. p300 could participate in alleviating promoter repression imposed by chromatin structure and in recruiting the basal transcription machinery to promoters of particular Wnt target genes.
引用
收藏
页码:1839 / 1850
页数:12
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