Hwang Sun Ok, Boswell Sarah A, Seo Jeong-Sun, Lee Sam W
Cutaneous Biology Research Center, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
J Biol Chem. 2008 May 9;283(19):13063-9. doi: 10.1074/jbc.M709656200. Epub 2008 Mar 7.
Members of the yeast p24 family, including Emp24p and Erv25p, exist as heteromeric complexes that have been proposed to cycle between the endoplasmic reticulum (ER) and Golgi compartments. The specific functions and sites of action of p24 proteins are still unknown. Here we identified a human homolog of the yeast p24 family of proteins, named ERS25 (endoplasmic reticulum stress-response protein 25), and investigated its role in stress response. ERS25 is predicted to have an ER localization signal peptide, a GOLD (Golgi dynamics) domain, which is found in several eukaryotic Golgi and lipid-trafficking proteins, a coiled-coil region, and a transmembrane domain. We demonstrate that ERS25 is localized to the ER and is induced by ER-specific stress, heat shock, and oxidative stress. The selective induction of ERS25 by brefeldin A, but not tunicamycin, implicates the involvement of ERS25 in protein trafficking between the ER and the Golgi. Small interfering RNA-mediated inhibition of ERS25 results in a significant decrease in apoptosis as well as a reduction of reactive oxygen species induced by oxidative stress. Moreover, ERS25 depletion results in a significant increase in the levels of the ER chaperone HSP70 in response to heat-shock stress through increased levels of HSF-1. We also found that inhibition of ERS25 induction in response to heat shock enhanced the binding of HSP70 to Apaf-1, which is likely to interfere in stress-mediated apoptosis. Together, the data presented here demonstrate that ERS25 may play a critical role in regulation of heat-shock response and apoptosis.
酵母p24家族成员,包括Emp24p和Erv25p,以异源复合物的形式存在,有人提出它们在内质网(ER)和高尔基体区室之间循环。p24蛋白的具体功能和作用位点仍不清楚。在这里,我们鉴定了酵母p24蛋白家族的一个人类同源物,命名为ERS25(内质网应激反应蛋白25),并研究了它在应激反应中的作用。ERS25预计有一个内质网定位信号肽、一个GOLD(高尔基体动力学)结构域(在几种真核高尔基体和脂质转运蛋白中发现)、一个卷曲螺旋区域和一个跨膜结构域。我们证明ERS25定位于内质网,并由内质网特异性应激、热休克和氧化应激诱导。布雷菲德菌素A能选择性诱导ERS25,而衣霉素则不能,这表明ERS25参与了内质网和高尔基体之间的蛋白质转运。小干扰RNA介导的ERS25抑制导致细胞凋亡显著减少,以及氧化应激诱导的活性氧减少。此外,ERS25缺失导致热休克应激时内质网伴侣HSP70水平显著升高,这是通过HSF-1水平升高实现的。我们还发现,抑制热休克反应中ERS25的诱导会增强HSP70与Apaf-1的结合,这可能会干扰应激介导的细胞凋亡。总之,本文提供的数据表明ERS25可能在热休克反应和细胞凋亡的调节中起关键作用。