Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, M13 9PT, UK.
Present address: Biosciences, College of Life and Environmental Sciences, Geoffrey Pope Building, University of Exeter, Stocker Road, Exeter, EX4 4QD, UK.
Genome Biol. 2017 Oct 27;18(1):201. doi: 10.1186/s13059-017-1338-4.
Translation factors eIF4E and eIF4G form eIF4F, which interacts with the messenger RNA (mRNA) 5' cap to promote ribosome recruitment and translation initiation. Variations in the association of eIF4F with individual mRNAs likely contribute to differences in translation initiation frequencies between mRNAs. As translation initiation is globally reprogrammed by environmental stresses, we were interested in determining whether eIF4F interactions with individual mRNAs are reprogrammed and how this may contribute to global environmental stress responses.
Using a tagged-factor protein capture and RNA-sequencing (RNA-seq) approach, we have assessed how mRNA associations with eIF4E, eIF4G1 and eIF4G2 change globally in response to three defined stresses that each cause a rapid attenuation of protein synthesis: oxidative stress induced by hydrogen peroxide and nutrient stresses caused by amino acid or glucose withdrawal. We find that acute stress leads to dynamic and unexpected changes in eIF4F-mRNA interactions that are shared among each factor and across the stresses imposed. eIF4F-mRNA interactions stabilised by stress are predominantly associated with translational repression, while more actively initiating mRNAs become relatively depleted for eIF4F. Simultaneously, other mRNAs are insulated from these stress-induced changes in eIF4F association.
Dynamic eIF4F-mRNA interaction changes are part of a coordinated early translational control response shared across environmental stresses. Our data are compatible with a model where multiple mRNA closed-loop complexes form with differing stability. Hence, unexpectedly, in the absence of other stabilising factors, rapid translation initiation on mRNAs correlates with less stable eIF4F interactions.
翻译因子 eIF4E 和 eIF4G 形成 eIF4F,与信使 RNA(mRNA)5' 帽结合,促进核糖体募集和翻译起始。eIF4F 与单个 mRNA 的结合变化可能导致 mRNA 翻译起始频率的差异。由于环境应激会全局重编程翻译起始,我们感兴趣的是确定 eIF4F 与单个 mRNA 的相互作用是否被重新编程,以及这如何有助于全局环境应激反应。
我们使用标记因子蛋白捕获和 RNA 测序(RNA-seq)方法,评估了在三种定义明确的应激下,eIF4E、eIF4G1 和 eIF4G2 与 mRNA 的整体关联如何响应而改变,这三种应激都会导致蛋白质合成迅速衰减:由过氧化氢引起的氧化应激和由氨基酸或葡萄糖耗尽引起的营养应激。我们发现,急性应激会导致 eIF4F-mRNA 相互作用发生动态且意外的变化,这些变化在每个因子和所施加的应激中都是共享的。应激稳定的 eIF4F-mRNA 相互作用主要与翻译抑制有关,而更活跃起始的 mRNA 则相对耗尽 eIF4F。同时,其他 mRNA 则不受这些应激诱导的 eIF4F 结合变化的影响。
动态的 eIF4F-mRNA 相互作用变化是环境应激共享的协调早期翻译控制反应的一部分。我们的数据与一个模型一致,该模型中形成了具有不同稳定性的多个 mRNA 闭环复合物。因此,出人意料的是,在没有其他稳定因子的情况下,mRNA 上的快速翻译起始与 eIF4F 相互作用的不稳定性相关。