College of Pharmacy, Seoul National University, Seoul, South Korea.
Mol Carcinog. 2011 Apr;50(4):222-34. doi: 10.1002/mc.20709.
The tumor suppressor protein p53 functions as a stress-responsive transcription factor. In response to oxidative, nitrosative, and electrophilic insults, p53 undergoes post-translational modifications, such as oxidation and covalent modification of cysteines, nitration of tyrosines, acetylation of lysines, phosphorylation of serine/threonine residues, etc. Because p53 plays a vital role in the transcriptional regulation of genes encoding proteins involved in a wide spectrum of biochemical processes including DNA repair, cell-cycle regulation, and programmed cell death, the redox-modification of p53 appears to be an important determinant of cell fate. This review highlights the redox regulation of p53 and its consequences on cellular function.
肿瘤抑制蛋白 p53 作为一种应激反应转录因子发挥作用。p53 会发生翻译后修饰,如氧化和半胱氨酸的共价修饰、酪氨酸的硝化、赖氨酸的乙酰化、丝氨酸/苏氨酸残基的磷酸化等,以应对氧化、硝化和亲电攻击。由于 p53 在转录调控中发挥着重要作用,调节参与广泛生化过程的蛋白质基因的表达,包括 DNA 修复、细胞周期调控和程序性细胞死亡,因此 p53 的氧化还原修饰似乎是决定细胞命运的重要因素。本综述重点介绍了 p53 的氧化还原调控及其对细胞功能的影响。