Department of Pharmacology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Pharmacology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Trends Cell Biol. 2020 Aug;30(8):640-652. doi: 10.1016/j.tcb.2020.05.002. Epub 2020 Jun 5.
The E2F family of transcriptional regulators sits at the center of cell cycle gene expression and plays vital roles in normal and cancer cell cycles. Whereas control of E2Fs by the retinoblastoma family of proteins is well established, much less is known about their regulation by ubiquitin pathways. Recent studies placed the Skp1-Cul1-F-box-protein (SCF) family of E3 ubiquitin ligases with the F-box protein Cyclin F at the center of E2F regulation, demonstrating temporal proteolysis of both activator and atypical repressor E2Fs. Importantly, these E2F members, in particular activator E2F1 and repressors E2F7 and E2F8, form a feedback circuit at the crossroads of cell cycle and cell death. Moreover, Cyclin F functions in a reciprocal circuit with the cell cycle E3 ligase anaphase-promoting complex/cyclosome (APC/C), which also controls E2F7 and E2F8. This review focuses on the complex contours of feedback within this circuit, highlighting the deep crosstalk between E2F, SCF-Cyclin F, and APC/C in regulating the oscillator underlying human cell cycles.
E2F 转录调控因子家族位于细胞周期基因表达的中心,在正常和癌细胞周期中发挥着至关重要的作用。虽然视网膜母细胞瘤家族蛋白对 E2F 的控制已经得到很好的证实,但它们被泛素途径调节的机制知之甚少。最近的研究将 Skp1-Cul1-F-box 蛋白(SCF)E3 泛素连接酶家族与 F-box 蛋白 Cyclin F 置于 E2F 调控的中心,证明了激活子和非典型抑制剂 E2F 的时空调解。重要的是,这些 E2F 成员,特别是激活子 E2F1 和抑制剂 E2F7 和 E2F8,在细胞周期和细胞死亡的十字路口形成了一个反馈回路。此外,Cyclin F 在细胞周期 E3 连接酶后期促进复合物/周期蛋白(APC/C)中与细胞周期 E3 连接酶形成一个反馈回路,该复合物也控制着 E2F7 和 E2F8。这篇综述重点介绍了该回路中反馈的复杂轮廓,强调了 E2F、SCF-Cyclin F 和 APC/C 在调节人类细胞周期振荡器中的深度串扰。