Obsil T, Obsilova V
Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, Prague, Czech Republic.
Oncogene. 2008 Apr 7;27(16):2263-75. doi: 10.1038/onc.2008.20.
The FOXO subgroup of forkhead transcription factors plays a central role in cell-cycle control, differentiation, metabolism control, stress response and apoptosis. Therefore, the function of these important molecules is tightly controlled by a wide range of protein-protein interactions and posttranslational modifications including phosphorylation, acetylation and ubiquitination. The mechanisms by which these processes regulate FOXO activity are mostly elusive. This review focuses on recent advances in structural studies of forkhead transcription factors and the insights they provide into the mechanism of DNA recognition. On the basis of these data, we discuss structural aspects of protein-protein interactions and posttranslational modifications that target the forkhead domain and the nuclear localization signal of FOXO proteins.
叉头转录因子的FOXO亚组在细胞周期调控、分化、代谢控制、应激反应和细胞凋亡中发挥核心作用。因此,这些重要分子的功能受到多种蛋白质-蛋白质相互作用和翻译后修饰(包括磷酸化、乙酰化和泛素化)的严格控制。这些过程调节FOXO活性的机制大多尚不清楚。本综述重点关注叉头转录因子结构研究的最新进展以及它们对DNA识别机制的见解。基于这些数据,我们讨论了针对FOXO蛋白的叉头结构域和核定位信号的蛋白质-蛋白质相互作用和翻译后修饰的结构方面。