Daverkausen-Fischer Lea, Pröls Felicitas
University of Cologne, Faculty of Medicine, Institute of Anatomy II, 50931, Cologne, Germany.
Cell Death Discov. 2021 Aug 5;7(1):203. doi: 10.1038/s41420-021-00594-x.
Dual topologies of proteins at the ER membrane are known for a variety of proteins allowing the same protein to exert different functions according to the topology adopted. A dual topology of the co-chaperone ERdj4, which resides in the endoplasmic reticulum (ER), was proposed recently, a thesis that we found to align all published data and existing controversies into one whole picture. The aim of this review is to reassess all primary data available in the literature on ER-resident Hsp40 co-chaperones with respect to their topology. After careful and critical analyses of all experimental data published so far, we identified, next to ERdj4, two other co-chaperones, ERdj3 and ERdj6, that also display features of a dual topology at the ER membrane. We assume that during cellular stress subpools of some ER-resident J protein can alter their topology so that these proteins can exert different functions in order to adapt to cellular stress.
内质网(ER)膜上蛋白质的双重拓扑结构在多种蛋白质中都有发现,这使得同一蛋白质能够根据所采用的拓扑结构发挥不同的功能。最近有人提出,内质网驻留的共伴侣蛋白ERdj4具有双重拓扑结构,我们发现这一论点能将所有已发表的数据和现有争议整合为一个完整的图景。本综述的目的是重新评估文献中关于内质网驻留的Hsp40共伴侣蛋白拓扑结构的所有原始数据。在对迄今为止发表的所有实验数据进行仔细和批判性分析后,我们发现,除了ERdj4之外,另外两种共伴侣蛋白ERdj3和ERdj6在内质网膜上也表现出双重拓扑结构的特征。我们推测,在细胞应激期间,一些内质网驻留的J蛋白亚池可能会改变其拓扑结构,从而使这些蛋白质能够发挥不同的功能以适应细胞应激。