Institute for Research in Immunology and Cancer, Université de Montréal, Montréal, Québec, Canada
Department of Pathology and Cell Biology, Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada.
Mol Cell Biol. 2018 May 29;38(12). doi: 10.1128/MCB.00070-18. Print 2018 Jun 15.
Translation is a key step in the regulation of gene expression and one of the most energy-consuming processes in the cell. In response to various stimuli, multiple signaling pathways converge on the translational machinery to regulate its function. To date, the roles of phosphoinositide 3-kinase (PI3K)/AKT and the mitogen-activated protein kinase (MAPK) pathways in the regulation of translation are among the best understood. Both pathways engage the mechanistic target of rapamycin (mTOR) to regulate a variety of components of the translational machinery. While these pathways regulate protein synthesis in homeostasis, their dysregulation results in aberrant translation leading to human diseases, including diabetes, neurological disorders, and cancer. Here we review the roles of the PI3K/AKT and MAPK pathways in the regulation of mRNA translation. We also highlight additional signaling mechanisms that have recently emerged as regulators of the translational apparatus.
翻译是基因表达调控的关键步骤,也是细胞中最耗能的过程之一。为了响应各种刺激,多种信号通路汇聚到翻译机制上,以调节其功能。迄今为止,磷酸肌醇 3-激酶(PI3K)/蛋白激酶 B(AKT)和丝裂原活化蛋白激酶(MAPK)通路在翻译调控中的作用是最被理解的。这两条通路都利用雷帕霉素(mTOR)的机械靶点来调节翻译机制的各种成分。虽然这些通路在体内平衡中调节蛋白质合成,但它们的失调导致异常翻译,从而导致人类疾病,包括糖尿病、神经紊乱和癌症。在这里,我们综述了 PI3K/AKT 和 MAPK 通路在 mRNA 翻译调控中的作用。我们还强调了最近作为翻译装置的调节剂而出现的其他信号机制。