DeGregori James, Johnson David G
Department of Biochemistry and Molecular Genetics, University of Colorado Health Sciences Center, Aurora, CO 80045, USA.
Curr Mol Med. 2006 Nov;6(7):739-48. doi: 10.2174/1566524010606070739.
Since the discovery almost fifteen years ago that E2F transcription factors are key targets of the retinoblastoma protein (RB), studies of the E2F family have uncovered critical roles in the control of transcription, cell cycle and apoptosis. E2F proteins are encoded by at least eight genes, E2F1 through E2F8. While specific roles for individual E2Fs in mediating the effects of RB loss are emerging, it is also becoming clear that there are no simple divisions of labor among the E2F family. Instead, an individual E2F can function to activate or repress transcription, promote or impede cell cycle progression and enhance or inhibit cell death, dependent on the cellular context. While functional redundancy among E2Fs and the striking influences of cellular context on the effects of E2F loss or gain of function have prevented a simple delineation of unique functions within the E2F family, these complexities undoubtedly reflect the extensive regulation and importance of this transcription factor family.
自从大约十五年前发现E2F转录因子是视网膜母细胞瘤蛋白(RB)的关键靶点以来,对E2F家族的研究揭示了其在转录控制、细胞周期和细胞凋亡中的关键作用。E2F蛋白由至少八个基因编码,即E2F1至E2F8。虽然单个E2F在介导RB缺失效应中的特定作用正在显现,但E2F家族中也不存在简单的分工这一点也变得清晰起来。相反,单个E2F可以根据细胞环境激活或抑制转录、促进或阻碍细胞周期进程以及增强或抑制细胞死亡。虽然E2F之间的功能冗余以及细胞环境对E2F功能丧失或获得效应的显著影响阻碍了对E2F家族独特功能的简单描述,但这些复杂性无疑反映了这个转录因子家族的广泛调控及其重要性。