INRA, UMR 1019 Nutrition Humaine, Centre de Clermont-Ferrand-Theix, F-63122 Saint Genès Champanelle, France and Université Clermont 1, UFR Médecine, UMR 1019 Nutrition Humaine, Clermont-Ferrand, France.
Nucleic Acids Res. 2013 Sep;41(16):7683-99. doi: 10.1093/nar/gkt563. Epub 2013 Jun 26.
In response to different environmental stresses, eIF2α phosphorylation represses global translation coincident with preferential translation of ATF4, a master regulator controlling the transcription of key genes essential for adaptative functions. Here, we establish that the eIF2α/ATF4 pathway directs an autophagy gene transcriptional program in response to amino acid starvation or endoplasmic reticulum stress. The eIF2α-kinases GCN2 and PERK and the transcription factors ATF4 and CHOP are also required to increase the transcription of a set of genes implicated in the formation, elongation and function of the autophagosome. We also identify three classes of autophagy genes according to their dependence on ATF4 and CHOP and the binding of these factors to specific promoter cis elements. Furthermore, different combinations of CHOP and ATF4 bindings to target promoters allow the trigger of a differential transcriptional response according to the stress intensity. Overall, this study reveals a novel regulatory role of the eIF2α-ATF4 pathway in the fine-tuning of the autophagy gene transcription program in response to stresses.
针对不同的环境压力,eIF2α 磷酸化会抑制全局翻译,同时优先翻译 ATF4,后者是控制适应功能关键基因转录的主调控因子。在这里,我们确定 eIF2α/ATF4 途径在氨基酸饥饿或内质网应激时指导自噬基因的转录程序。eIF2α-激酶 GCN2 和 PERK 以及转录因子 ATF4 和 CHOP 也需要增加一组与自噬体形成、伸长和功能相关的基因的转录。我们还根据 ATF4 和 CHOP 的依赖性以及这些因子与特定启动子顺式元件的结合,将自噬基因分为三类。此外,CHOP 和 ATF4 结合到靶启动子的不同组合允许根据应激强度触发差异转录反应。总的来说,这项研究揭示了 eIF2α-ATF4 途径在响应应激时精细调节自噬基因转录程序的新的调节作用。