The Transactivation Domains of the p53 Protein

被引:94
|
作者
Raj, Nitin [1 ]
Attardi, Laura D. [1 ,2 ]
机构
[1] Stanford Univ, Div Radiat & Canc Biol, Dept Radiat Oncol, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
来源
关键词
TRANSCRIPTIONAL ACTIVATION DOMAIN; HYDROPHOBIC AMINO-ACIDS; CREB-BINDING-PROTEIN; TUMOR-SUPPRESSOR P53; DNA-BINDING; WILD-TYPE; EMBRYONIC LETHALITY; P53-MEDIATED TRANSCRIPTION; STRUCTURAL ELEMENTS; MDM2-DEFICIENT MICE;
D O I
10.1101/cshperspect.a026047
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The p53 tumor suppressor is a transcriptional activator, with discrete domains that participate in sequence-specific DNA binding, tetramerization, and transcriptional activation. Mutagenesis and reporter studies have delineated two distinct activation domains (TADs) and specific hydrophobic residues within these TADs that are critical for their function. Knockin mice expressing p53 mutants with alterations in either or both of the two TADs have revealed that TAD1 is critical for responses to acute DNA damage, whereas both TAD1 and TAD2 participate in tumor suppression. Biochemical and structural studies have identified factors that bind either or both TADs, including general transcription factors (GTFs), chromatin modifiers, and negative regulators, helping to elaborate a model through which p53 activates transcription. Posttranslational modifications (PTMs) of the p53 TADs through phosphorylation also regulate TADactivity. Together, these studies on p53 TADs provide great insight into how p53 serves as a tumor suppressor.
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页数:18
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