Burgering Boudewijn M T, Kops Geert J P L
Dept Physiological Chemistry and Centre for Biomedical Genetics, University Medical Centre Utrecht, Stratenum, The Netherlands.
Trends Biochem Sci. 2002 Jul;27(7):352-60. doi: 10.1016/s0968-0004(02)02113-8.
The FOXO family of Forkhead transcription factors, FKHR (FOXO1), FKHR-L1 (FOXO3a) and AFX (FOXO4), are regulated by the phosphoinositide-3-kinase-protein-kinase-B (PI3K-PKB/c-Akt) pathway. Direct phosphorylation by PKB results in cytoplasmic retention and inactivation, inhibiting the expression of FOXO-regulated genes, which control the cell cycle, cell death, cell metabolism and oxidative stress. This pathway appears to be well conserved throughout evolution. In the nematode Caenorhabditis elegans, it affects lifespan and controls dauer formation. Recent discoveries about FOXO regulation by PI3K-PKB signalling suggest that the PI3K-PKB-FOXO pathway might participate in similar processes in higher eukaryotes.
叉头转录因子FOXO家族,即FKHR(FOXO1)、FKHR-L1(FOXO3a)和AFX(FOXO4),受磷酸肌醇-3-激酶-蛋白激酶-B(PI3K-PKB/c-Akt)信号通路调控。蛋白激酶B的直接磷酸化导致其滞留于细胞质并失活,从而抑制FOXO调控基因的表达,这些基因控制着细胞周期、细胞死亡、细胞代谢和氧化应激。该信号通路在整个进化过程中似乎高度保守。在线虫秀丽隐杆线虫中,它影响寿命并控制滞育形成。最近关于PI3K-PKB信号对FOXO调控的发现表明,PI3K-PKB-FOXO信号通路可能在高等真核生物中参与类似过程。