Buck Institute for Age Research, Novato, California 94945, USA.
J Neurosci. 2009 Dec 16;29(50):15703-12. doi: 10.1523/JNEUROSCI.4351-09.2009.
Multiple recent reports implicate amyloid precursor protein (APP) signaling in the pathogenesis of Alzheimer's disease, but the APP-dependent signaling network involved has not been defined. Here, we report a novel consensus sequence for interaction with the PDZ-1 and PDZ-2 domains of the APP-interacting proteins Mint1, Mint2, and Mint3 (X11alpha, X11beta, and X11gamma), and multiple novel interactors for these proteins, with the finding that transcriptional coactivators are highly represented among these interactors. Furthermore, we show that Mint3 interaction with a set of the transcriptional coactivators leads to nuclear localization and transactivation, whereas interaction of the same set with Mint1 or Mint2 prevents nuclear localization and transactivation. These results define new mediators of the signal transduction network mediated by APP.
多项近期报告表明淀粉样前体蛋白(APP)信号在阿尔茨海默病的发病机制中起作用,但涉及的 APP 依赖信号网络尚未确定。在这里,我们报告了一个与 APP 相互作用蛋白 Mint1、Mint2 和 Mint3(X11alpha、X11beta 和 X11gamma)的 PDZ-1 和 PDZ-2 结构域相互作用的新的共识序列,以及这些蛋白的多个新的相互作用蛋白,发现转录共激活因子在这些相互作用蛋白中高度表达。此外,我们表明 Mint3 与一组转录共激活因子的相互作用导致核定位和转录激活,而同一组与 Mint1 或 Mint2 的相互作用则阻止核定位和转录激活。这些结果定义了 APP 介导的信号转导网络的新介质。