The multiple mechanisms that regulate p53 activity and cell fate

被引:769
作者
Hafner, Antonina [1 ,5 ]
Bulyk, Martha L. [2 ,3 ,4 ]
Jambhekar, Ashwini [1 ]
Lahav, Galit [1 ]
机构
[1] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Div Genet, 75 Francis St, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[5] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
C-TERMINAL DOMAIN; DAMAGE-INDUCED PHOSPHORYLATION; DNA-BINDING COOPERATIVITY; GENE-EXPRESSION; TRANSCRIPTION-FACTOR; CYCLE ARREST; POSTTRANSLATIONAL MODIFICATIONS; TUMOR-SUPPRESSION; WILD-TYPE; P53-DEPENDENT TRANSCRIPTION;
D O I
10.1038/s41580-019-0110-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tumour suppressor p53 has a central role in the response to cellular stress. Activated p53 transcriptionally regulates hundreds of genes that are involved in multiple biological processes, including in DNA damage repair, cell cycle arrest, apoptosis and senescence. In the context of DNA damage, p53 is thought to be a decision-making transcription factor that selectively activates genes as part of specific gene expression programmes to determine cellular outcomes. In this Review, we discuss the multiple molecular mechanisms of p53 regulation and how they modulate the induction of apoptosis or cell cycle arrest following DNA damage. Specifically, we discuss how the interaction of p53 with DNA and chromatin affects gene expression, and how p53 post-translational modifications, its temporal expression dynamics and its interactions with chromatin regulators and transcription factors influence cell fate. These multiple layers of regulation enable p53 to execute cellular responses that are appropriate for specific cellular states and environmental conditions.
引用
收藏
页码:199 / 210
页数:12
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