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Updated: May 5, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
The expanding universe of p53 targets
Daniel Menendez1, Alberto Inga, Michael A Resnick
1Laboratory of Molecular Genetics, National Institute of Environmental Health Science, Research Triangle Park, North Carolina 27709, USA.
Abstract:
The p53 tumour suppressor is modified through mutation or changes in expression in most cancers, leading to the altered regulation of hundreds of genes that are directly influenced by this sequence-specific transcription factor. Central to the p53 master regulatory network are the target response element (RE) sequences. The extent of p53 transactivation and transcriptional repression is influenced by many factors, including p53 levels, cofactors and the specific RE sequences, all of which contribute to the role that p53 has in the aetiology of cancer. This Review describes the identification and functionality of REs and highlights the inclusion of non-canonical REs that expand the universe of genes and regulation mechanisms in the p53 tumour suppressor network.
Insights
The p53 tumor suppressor protein regulates genes critical for cancer. This review details its response elements (REs), including non-canonical ones, expanding understanding of p53
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- The p53 tumor suppressor protein is a master regulator of the cellular response to stress.
- Mutations or altered expression of p53 are implicated in the majority of human cancers.
- p53 exerts its function by binding to specific DNA sequences known as response elements (REs).
Purpose of the Study:
- To review the identification and function of p53 target response elements (REs).
- To highlight the significance of non-canonical REs in the p53 regulatory network.
- To provide a comprehensive overview of how p53 REs contribute to cancer etiology.
Main Methods:
- Literature review of studies on p53 target REs.
- Analysis of canonical and non-canonical p53 RE sequences.
- Discussion of factors influencing p53 transactivation and repression.
Main Results:
- p53 regulates hundreds of genes through sequence-specific DNA binding.
- Canonical REs are well-characterized, but non-canonical REs expand the regulatory landscape.
- p53 levels, cofactors, and RE sequence variations modulate gene regulation.
Conclusions:
- Understanding p53 REs, including non-canonical forms, is crucial for comprehending p53's role in cancer.
- The diversity of p53 REs contributes to the complexity of p53-mediated gene regulation.
- Further research into non-canonical REs may reveal novel therapeutic targets in cancer treatment.
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