Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana 46202-5126.
Cold Spring Harb Perspect Biol. 2018 Jul 2;10(7):a032870. doi: 10.1101/cshperspect.a032870.
A central mechanism regulating translation initiation in response to environmental stress involves phosphorylation of the α subunit of eukaryotic initiation factor 2 (eIF2α). Phosphorylation of eIF2α causes inhibition of global translation, which conserves energy and facilitates reprogramming of gene expression and signaling pathways that help to restore protein homeostasis. Coincident with repression of protein synthesis, many gene transcripts involved in the stress response are not affected or are even preferentially translated in response to increased eIF2α phosphorylation by mechanisms involving upstream open reading frames (uORFs). This review highlights the mechanisms regulating eIF2α kinases, the role that uORFs play in translational control, and the impact that alteration of eIF2α phosphorylation by gene mutations or small molecule inhibitors can have on health and disease.
一种调节翻译起始以响应环境应激的中心机制涉及真核起始因子 2(eIF2α)的α亚基的磷酸化。eIF2α 的磷酸化导致全局翻译的抑制,从而节省能量并有助于重新编程基因表达和信号通路,这些通路有助于恢复蛋白质平衡。与蛋白质合成的抑制相一致,许多参与应激反应的基因转录物不受影响,甚至在 eIF2α 磷酸化增加时通过涉及上游开放阅读框(uORFs)的机制优先翻译。这篇综述强调了调节 eIF2α 激酶的机制、uORFs 在翻译控制中的作用,以及基因突变或小分子抑制剂改变 eIF2α 磷酸化对健康和疾病的影响。