Strachan Gordon D, Morgan Kathleen L, Otis Linda L, Caltagarone John, Gittis Aryn, Bowser Robert, Jordan-Sciutto Kelly L
Department of Pathology, University of Pennsylvania, 4010 Locust Street, Philadelphia, Pennsylvania 19104-6030, USA.
Biochemistry. 2004 Sep 28;43(38):12113-22. doi: 10.1021/bi0494166.
The fetal Alz-50 reactive clone 1 (FAC1) protein exhibits altered expression and subcellular localization during neuronal development and neurodegenerative diseases such as Alzheimer's disease. Using the yeast two-hybrid screen, the human orthologue of Keap1 (hKeap1) was identified as a FAC1 interacting protein. Keap1 is an important regulator of the oxidative stress response pathway through its interaction with the Nrf family of transcription factors. An interaction between full-length FAC1 and hKeap1 proteins has been demonstrated, and the FAC1 binding domain of hKeap1 has been identified as the Kelch repeats. In addition, FAC1 colocalizes with endogenous Keap1 within the cytoplasm of PT67 cells. Exogenously introduced eGFP:hKeap1 fusion protein redistributed FAC1 to colocalize with eGFP:hKeap1 in perinuclear, spherical structures. The interaction between FAC1 and hKeap1 is reduced by competition with the Nrf2 protein. However, competition by Nrf2 for hKeap1 is reduced by diethylmaleate (DEM), a known disrupter of the Nrf2:Keap1 interaction. DEM does not affect the ability of FAC1 to bind hKeap1 in our assay. These results suggest that hKeap1 regulates FAC1 in addition to its known role in control of Nrf2. Furthermore, the observed competition between FAC1 and Nrf2 for binding hKeap1 indicates that the interplay between these three proteins has important implications for neuronal response to oxidative stress.
胎儿期阿尔茨海默病相关50反应性克隆1(FAC1)蛋白在神经元发育过程以及诸如阿尔茨海默病等神经退行性疾病中表现出表达改变和亚细胞定位变化。通过酵母双杂交筛选,鉴定出Keap1的人类同源物(hKeap1)为FAC1相互作用蛋白。Keap1通过与转录因子Nrf家族相互作用,是氧化应激反应途径的重要调节因子。已证实全长FAC1和hKeap1蛋白之间存在相互作用,并且hKeap1的FAC1结合结构域已被鉴定为kelch重复序列。此外,FAC1与PT67细胞胞质内的内源性Keap1共定位。外源导入的eGFP:hKeap1融合蛋白使FAC1重新分布,与eGFP:hKeap1在核周球形结构中共定位。与Nrf2蛋白竞争会降低FAC1与hKeap1之间的相互作用。然而,二乙基马来酸酯(DEM)(一种已知的Nrf2:Keap1相互作用破坏剂)会降低Nrf2对hKeap1的竞争。在我们的实验中,DEM不影响FAC1结合hKeap1的能力。这些结果表明,hKeap1除了在控制Nrf2方面的已知作用外,还调节FAC1。此外,观察到的FAC1和Nrf2对结合hKeap1的竞争表明,这三种蛋白之间的相互作用对神经元对氧化应激的反应具有重要意义。