School of Life Sciences, Chongqing University, Chongqing 401331, China.
Int J Mol Sci. 2021 Feb 3;22(4):1526. doi: 10.3390/ijms22041526.
The endoplasmic reticulum (ER) is a highly dynamic organelle in eukaryotic cells, which is essential for synthesis, processing, sorting of protein and lipid metabolism. However, the cells activate a defense mechanism called endoplasmic reticulum stress (ER stress) response and initiate unfolded protein response (UPR) as the unfolded proteins exceed the folding capacity of the ER due to the environmental influences or increased protein synthesis. ER stress can mediate many cellular processes, including autophagy, apoptosis and senescence. The ubiquitin-proteasome system (UPS) is involved in the degradation of more than 80% of proteins in the cells. Today, increasing numbers of studies have shown that the two important components of UPS, E3 ubiquitin ligases and deubiquitinases (DUBs), are tightly related to ER stress. In this review, we summarized the regulation of the E3 ubiquitin ligases and DUBs in ER stress.
内质网(ER)是真核细胞中一种高度动态的细胞器,对于蛋白质的合成、加工、分拣和脂质代谢至关重要。然而,当环境影响或蛋白质合成增加导致未折叠蛋白超过 ER 的折叠能力时,细胞会激活一种称为内质网应激(ER 应激)反应的防御机制,并启动未折叠蛋白反应(UPR)。ER 应激可以介导许多细胞过程,包括自噬、细胞凋亡和衰老。泛素-蛋白酶体系统(UPS)参与细胞中超过 80%的蛋白质的降解。如今,越来越多的研究表明 UPS 的两个重要组成部分,E3 泛素连接酶和去泛素化酶(DUBs),与 ER 应激密切相关。在这篇综述中,我们总结了 E3 泛素连接酶和 DUBs 在 ER 应激中的调节作用。