Korwek Zbigniew, Alster Olga
Postepy Biochem. 2014;60(2):248-62.
The genetic material is constantly subjected to DNA damage which is caused by physiological processes occuring in the cell and is exposed to exogenous DNA damaging agents. Eucariotic cells have developed a system called the DNA damage response (DDR), which is responsible for maintaining genomic inegrity. DNA damage can lead to senescence, DNA repair as well as to cell death. The key protein in the DDR pathway is p53. This protein undergoes numerous posttranslational modifications and can be involved in the activation of many genes and proteins leading to survival or cell death. In cell senescence the p53 protein leads to the induction of p21, which causes cell cycle arrest. In apoptosis p53 participates in the activation of caspases, which are responsible for the degradation of many proteins.
遗传物质不断受到DNA损伤,这种损伤由细胞内发生的生理过程引起,并暴露于外源性DNA损伤剂。真核细胞已发展出一种称为DNA损伤反应(DDR)的系统,该系统负责维持基因组的完整性。DNA损伤可导致细胞衰老、DNA修复以及细胞死亡。DDR途径中的关键蛋白是p53。该蛋白经历多种翻译后修饰,并可参与许多导致细胞存活或死亡的基因和蛋白的激活。在细胞衰老过程中,p53蛋白导致p21的诱导,从而引起细胞周期停滞。在细胞凋亡过程中,p53参与半胱天冬酶的激活,半胱天冬酶负责许多蛋白的降解。