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Updated: May 27, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
Expression of the human tumor suppressor p53 induces cell death in Pichia pastoris
Salma Abdelmoula-Souissi1, Imed Mabrouk, Ali Gargouri
1Laboratoire de Valorisation de la Biomasse et Production de Protéines chez les Eucaryotes, Centre de Biotechnologie de Sfax, University of Sfax, Sfax, Tunisia.
Abstract:
The human tumor suppressor p53 is known as guardian of genome because of its involvement in many signals related to cell life or death. In this work, we report that human p53 induces cell death in the yeast Pichia pastoris. We showed a growth inhibition effect, which increased with the p53 protein expression level in recombinant Mut(s) (methanol utilization slow) strain of Pichia. However, no effect of p53 was observed in recombinant strain of Mut(+) (methanol utilization plus) phenotype. Interestingly, human p53 induces cell death in recombinant strains Mut(s) with characteristic markers of apoptosis such as DNA fragmentation, exposure of phosphatidylserine, and reactive oxygen species generation. Taken together, our results strongly suggest that human p53 is biologically active in this heterologous context. Thus, we propose that P. pastoris could be a useful tool to better understand the biological function of human p53.
Insights
Human p53, the guardian of the genome, induces cell death in yeast. This study shows p53 triggers apoptosis in Pichia pastoris, offering a new tool for p53 research.
Area of Science:
- Molecular Biology
- Cell Biology
- Microbiology
Background:
- The human tumor suppressor p53 is a critical regulator of cell fate.
- Its role in apoptosis is well-established in mammalian systems.
Purpose of the Study:
- To investigate the biological activity of human p53 in a heterologous yeast system.
- To determine if human p53 can induce cell death in Pichia pastoris.
Main Methods:
- Expression of human p53 in recombinant Pichia pastoris strains (Mut(s) and Mut(+)).
- Assessment of growth inhibition and apoptosis markers (DNA fragmentation, phosphatidylserine exposure, ROS generation).
Main Results:
- Human p53 expression led to growth inhibition and cell death in the Mut(s) Pichia pastoris strain.
- No effect was observed in the Mut(+) strain.
- Apoptotic markers were detected in Mut(s) cells expressing p53.
Conclusions:
- Human p53 is biologically active in the heterologous yeast Pichia pastoris.
- Pichia pastoris serves as a viable model for studying human p53 function.
- This system can aid in understanding the complex roles of the guardian of the genome.
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