Related Experiment Video
Updated: Aug 24, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
To die or not to die: how does p53 decide?
Elizabeth A Slee1, Daniel J O'Connor, Xin Lu
1Imperial College School of Medicine at St Mary's, Ludwig Institute for Cancer Research, Norfolk Place, London W2 1PG, UK.
Abstract:
p53 is frequently mutated in cancer and as a result is one of the most intensely studied tumour suppressors. Analysis of the primitive forms of p53 found in Caenorhabditis elegans and Drosophila, alongside studies using transgenic mouse models, indicate that the induction of apoptosis is both the most conserved function of p53 and vital for tumour suppression. p53-mediated apoptosis occurs through a combination of mechanisms which include pathways that are both dependent and independent of alterations in gene expression. In response to genotoxic insult, these pathways probably act together, thereby amplifying the apoptotic signal. However, the picture is complicated because the p53 activity is determined by stress type and individual cellular characteristics. The numerous p53 responsive genes that have been identified also provide further means of controlling the actions of p53. The recent discoveries of proteins that interact with p53 and specifically regulate the ability of p53 to trigger apoptosis have provided further mechanistic insights into the role of p53 in inducing cell death. Understanding the molecular basis of the proapoptotic action of p53 can assist in our quest to reintroduce or reactivate p53 in human tumours.
Insights
The tumor suppressor p53
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The p53 tumor suppressor is a critical target in cancer research due to frequent mutations.
- Apoptosis induction is a conserved and vital function of p53 in tumor suppression.
- p53's role in apoptosis is complex, involving gene-dependent and independent pathways.
Purpose of the Study:
- To explore the conserved mechanisms of p53-mediated apoptosis.
- To understand how p53 activity is regulated by cellular context and stress.
- To investigate novel protein interactions influencing p53's apoptotic function.
Main Methods:
- Comparative analysis of p53 in primitive organisms (C. elegans, Drosophila).
- Studies using transgenic mouse models.
- Identification and characterization of p53-interacting proteins.
Main Results:
- Apoptosis induction by p53 is a highly conserved function across species.
- p53-mediated apoptosis involves multiple pathways, amplified by genotoxic stress.
- Cellular context and stress type modulate p53 activity.
- Interactions with specific proteins provide mechanistic insights into p53-induced apoptosis.
Conclusions:
- Understanding p53's pro-apoptotic mechanisms is key to cancer therapy.
- Reactivating or reintroducing p53 function in tumors is a therapeutic goal.
- Further research into p53 regulation and interactions can yield novel cancer treatments.
Related Concept Videos
DNA Damage Can Stall the Cell Cycle
DNA Damage can Stall the Cell Cycle
Abnormal Proliferation
Negative Regulator Molecules
Molecular Factors Affecting Cell Division
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
The Intrinsic Apoptotic Pathway

