Waltzer L, Bienz M
MRC Laboratory of Molecular Biology, Cambridge, UK.
Nature. 1998 Oct 1;395(6701):521-5. doi: 10.1038/26785.
T-cell factor (TCF), a high-mobility-group domain protein, is the transcription factor activated by Wnt/Wingless signalling. When signalling occurs, TCF binds to its coactivator, beta-catenin/Armadillo, and stimulates the transcription of the target genes of Wnt/Wingless by binding to TCF-responsive enhancers. Inappropriate activation of TCF in the colon epithelium and other cells leads to cancer. It is therefore desirable for unstimulated cells to have a negative control mechanism to keep TCF inactive. Here we report that Drosophila CREB-binding protein (dCBP) binds to dTCF. dCBP mutants show mild Wingless overactivation phenotypes in various tissues. Consistent with this, dCBP loss-of-function suppresses the effects of armadillo mutation. Moreover, our data show that dCBP acetylates a conserved lysine in the Armadillo-binding domain of dTCF, and that this acetylation lowers the affinity of Armadillo binding to dTCF. Although CBP is a coactivator of other transcription factors, our data show that CBP represses TCF.
T细胞因子(TCF)是一种高迁移率族结构域蛋白,是由Wnt/Wingless信号通路激活的转录因子。当信号传导发生时,TCF与其共激活因子β-连环蛋白/犰狳蛋白结合,并通过与TCF反应增强子结合来刺激Wnt/Wingless靶基因的转录。结肠上皮细胞和其他细胞中TCF的不适当激活会导致癌症。因此,未受刺激的细胞需要一种负调控机制来使TCF保持无活性状态。在此我们报道,果蝇的CREB结合蛋白(dCBP)与dTCF结合。dCBP突变体在各种组织中表现出轻微的Wingless过度激活表型。与此一致的是,dCBP功能丧失抑制了犰狳蛋白突变的效应。此外,我们的数据表明,dCBP使dTCF犰狳蛋白结合结构域中的一个保守赖氨酸乙酰化,并且这种乙酰化降低了犰狳蛋白与dTCF结合的亲和力。尽管CBP是其他转录因子的共激活因子,但我们的数据表明CBP抑制TCF。