Department of Radiation Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Curr Genet. 2020 Apr;66(2):293-297. doi: 10.1007/s00294-019-01026-1. Epub 2019 Sep 4.
We discuss novel insight into the role and consequences of the phosphorylation of the translation initiation factor eIF2α in the context of stress responses and cell-cycle regulation. eIF2α is centrally located to regulate translation and its phosphorylation in response to different environmental challenges is one of the best characterized stress-response pathways. In addition to its role in stress management, eIF2α phosphorylation is also linked to cell-cycle progression and memory consolidation in the nervous system. The best known consequences of eIF2α phosphorylation are downregulation of global translation and stimulation of translation of some mRNAs. However, recent evidence shows that (i) eIF2α phosphorylation is not always required for the downregulation of global translation after exposure to stress and (ii) eIF2α phosphorylation does not necessarily lead to the downregulation of global translation. These results suggest that the textbook view of eIF2α phosphorylation needs to be revised and that there must be additional regulatory mechanisms at play.
我们讨论了在应激反应和细胞周期调控背景下,磷酸化翻译起始因子 eIF2α 的作用和后果的新见解。eIF2α 是调节翻译的核心,其对不同环境挑战的磷酸化反应是最具特征的应激反应途径之一。除了在应激管理中的作用外,eIF2α 磷酸化还与神经系统中的细胞周期进程和记忆巩固有关。eIF2α 磷酸化的最显著后果是下调全局翻译和刺激一些 mRNA 的翻译。然而,最近的证据表明:(i)暴露于应激后,eIF2α 磷酸化并非总是下调全局翻译所必需;(ii)eIF2α 磷酸化不一定导致全局翻译的下调。这些结果表明,需要修订教科书上关于 eIF2α 磷酸化的观点,并且必然存在其他发挥作用的调节机制。