Department of Molecular Medicine, Institute of Biotechnology, University of Texas Health Science Center at San Antonio, 15355 Lambda Drive, San Antonio, Texas 78245, USA.
EMBO Rep. 2011 Mar;12(3):216-22. doi: 10.1038/embor.2010.210. Epub 2011 Feb 4.
Regulated intramembrane proteolysis of the amyloid precursor-protein (APP) produces both a characterstic amyloid-β peptide that contributes to neuritic plaque formation and neurodegeneration in Alzheimer disease and a small APP intracellular domain (AICD) that transcriptionally activates genes implicated in Alzheimer disease pathology. Although the biochemical events leading to amyloidogenic APP processing at the cell membrane have been described in detail, comparably little is known about the mechanistic basis of AICD-dependent gene regulation in the nucleus. In this study, we show that the AICD activates transcription by targeting MED12, an RNA polymerase II transcriptional Mediator subunit that is implicated in human cognitive development. The AICD binds to MED12/Mediator in vitro and in vivo. Disruption of the AICD/MED12 interaction inhibits AICD transactivation potential and expression of AICD target genes. Mediator, in a MED12-dependent manner, occupies only AICD-bound promoter DNA, indicating that the AICD recruits Mediator to activate transcription. These results identify the MED12 interface in Mediator as a crucial transducer of AICD transactivation and a potential therapeutic target in Alzheimer disease.
淀粉样前体蛋白(APP)的调节性膜内蛋白水解产生特征性的淀粉样β肽,该肽有助于阿尔茨海默病中的神经突斑块形成和神经退行性变,以及小的 APP 细胞内结构域(AICD),该结构域转录激活与阿尔茨海默病病理学相关的基因。尽管已经详细描述了导致细胞膜上淀粉样生成 APP 加工的生化事件,但关于 AICD 依赖性核基因调控的机制基础知之甚少。在这项研究中,我们表明 AICD 通过靶向 MED12 激活转录,MED12 是 RNA 聚合酶 II 转录中介体亚基,与人类认知发育有关。AICD 在体外和体内与 MED12/Mediator 结合。破坏 AICD/MED12 相互作用会抑制 AICD 的转录激活潜力和 AICD 靶基因的表达。以 MED12 依赖性方式,中介体仅占据 AICD 结合的启动子 DNA,表明 AICD 募集中介体来激活转录。这些结果确定了中介体中的 MED12 界面是 AICD 转录激活的关键转导子,也是阿尔茨海默病的潜在治疗靶点。