Takemaru Ken-Ichi, Fischer Victoria, Li Feng-Qian
Department of Pharmacological Sciences, SUNY at Stony Brook, Stony Brook, New York 11794-8651, USA.
Cell Cycle. 2009 Jan 15;8(2):210-3. doi: 10.4161/cc.8.2.7394. Epub 2009 Jan 12.
Chibby (Cby) is an evolutionarily conserved antagonist of beta-catenin, a central player of the canonical Wnt signaling pathway, which acts as a transcriptional coactivator. Cby physically interacts with the C-terminal activation domain of beta-catenin and blocks its transcriptional activation potential through competition with DNA-binding Tcf/Lef transcription factors. Our recent study revealed a second mechanism for Cby-mediated beta-catenin inhibition in which Cby cooperates with 14-3-3 adaptor proteins to facilitate nuclear export of beta-catenin, following phosphorylation of Cby by Akt kinase. Therefore, our findings unravel a novel molecular mechanism regulating the dynamic nucleo-cytoplasmic trafficking of beta-catenin and provide new insights into the cross-talk between the Wnt and Akt signaling pathways. Here, we review recent literature concerning Cby function and discuss our current understanding of the relationship between Wnt and Akt signaling.
Chibby(Cby)是β-连环蛋白的一种进化保守拮抗剂,β-连环蛋白是经典Wnt信号通路的核心分子,作为转录共激活因子发挥作用。Cby与β-连环蛋白的C端激活结构域发生物理相互作用,并通过与DNA结合Tcf/Lef转录因子竞争来阻断其转录激活潜能。我们最近的研究揭示了Cby介导的β-连环蛋白抑制的第二种机制,即Akt激酶使Cby磷酸化后,Cby与14-3-3衔接蛋白协同作用,促进β-连环蛋白的核输出。因此,我们的研究结果揭示了一种调节β-连环蛋白动态核质转运的新分子机制,并为Wnt和Akt信号通路之间的相互作用提供了新见解。在此,我们综述了有关Cby功能的近期文献,并讨论了我们目前对Wnt和Akt信号之间关系的理解。