Bates S, Vousden K H
ABL-Basic Research Program, NCI-FCRDC, Frederick, MD 21702-1201, USA.
Curr Opin Genet Dev. 1996 Feb;6(1):12-8. doi: 10.1016/s0959-437x(96)90004-0.
The cell cycle arrest and apoptotic functions of p53 both contribute to the role of this tumour suppressor protein in preventing replication of cells suffering DNA damage. Although the ability of p53 to function as a sequence-specific transcription factor appears to be directly and causally linked to the implementation of an arrest at the G1 stage of the cell cycle, the contribution of transcriptional activation to the apoptotic response is less clear. It seems likely that several p53 activities, both transcriptionally dependent and transcriptionally independent, can play a role in mediating cell death. The requirement for each of these functions appears to depend on the cell type, the cell environment and other genetic alterations already sustained by the cell in which p53 function is activated.
p53的细胞周期阻滞和凋亡功能均有助于这种肿瘤抑制蛋白在防止DNA受损细胞复制中发挥作用。尽管p53作为序列特异性转录因子发挥功能的能力似乎与细胞周期G1期的阻滞直接相关且存在因果联系,但转录激活对凋亡反应的贡献尚不清楚。似乎几种p53活性,包括转录依赖性和转录非依赖性活性,都可能在介导细胞死亡中发挥作用。这些功能中每一种的需求似乎取决于细胞类型、细胞环境以及p53功能被激活的细胞中已经存在的其他基因改变。