Department of Cell Biology and Molecular Medicine, Rutgers New Jersey Medical School, Newark, NJ, USA.
Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.
Nat Commun. 2024 Jul 25;15(1):6279. doi: 10.1038/s41467-024-50393-y.
The molecular mechanisms by which FoxO transcription factors mediate diametrically opposite cellular responses, namely death and survival, remain unknown. Here we show that Mst1 phosphorylates FoxO1 Ser209/Ser215/Ser218/Thr228/Ser232/Ser243, thereby inhibiting FoxO1-mediated transcription of proapoptotic genes. On the other hand, Mst1 increases FoxO1-C/EBP-β interaction and activates C/EBP-β by phosphorylating it at Thr299, thereby promoting transcription of prosurvival genes. Myocardial ischemia/reperfusion injury is larger in cardiac-specific FoxO1 knockout mice than in control mice. However, the concurrent presence of a C/EBP-β T299E phospho-mimetic mutation reduces infarct size in cardiac-specific FoxO1 knockout mice. The C/EBP-β phospho-mimetic mutant exhibits greater binding to the promoter of prosurvival genes than wild type C/EBP-β. In conclusion, phosphorylation of FoxO1 by Mst1 inhibits binding of FoxO1 to pro-apoptotic gene promoters but enhances its binding to C/EBP-β, phosphorylation of C/EBP-β, and transcription of prosurvival genes, which stimulate protective mechanisms in the heart.
FoxO 转录因子介导的分子机制,使其能在细胞中产生截然相反的反应,即死亡和存活,目前仍不清楚。本文中,我们发现 Mst1 可使 FoxO1 的 Ser209/Ser215/Ser218/Thr228/Ser232/Ser243 发生磷酸化,从而抑制 FoxO1 对促凋亡基因的转录。另一方面,Mst1 增加 FoxO1-C/EBP-β 的相互作用,并通过磷酸化 Thr299 激活 C/EBP-β,从而促进生存相关基因的转录。与对照组相比,心脏特异性 FoxO1 敲除小鼠的心肌缺血再灌注损伤更大。然而,同时存在 C/EBP-β T299E 磷酸模拟突变会减少心脏特异性 FoxO1 敲除小鼠的梗死面积。磷酸化模拟突变的 C/EBP-β 与生存相关基因启动子的结合能力大于野生型 C/EBP-β。综上所述,Mst1 对 FoxO1 的磷酸化抑制了 FoxO1 与促凋亡基因启动子的结合,但增强了其与 C/EBP-β 的结合、C/EBP-β 的磷酸化和生存相关基因的转录,从而刺激心脏中的保护机制。