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Updated: Jul 8, 2026

Evaluation of the Impact of Protein Aggregation on Cellular Oxidative Stress in Yeast
Published on: June 23, 2018
Redox control and oxidative stress in yeast cells
Enrique Herrero1, Joaquim Ros, Gemma Bellí
1Departament de Ciències Mèdiques Bàsiques, Universitat de Lleida, Lleida, Spain. enric.herrero@cmb.udl.cat
Reactive oxygen species alter protein function, but redox regulation by thioredoxin and glutaredoxin systems, particularly in yeast, offers crucial cellular control. These systems are vital for managing oxidative stress and maintaining cell function.
Area of Science:
- Biochemistry
- Molecular Biology
- Cell Biology
Background:
- Reactive oxygen species (ROS) can modify protein structure and function.
- Cellular defense systems like catalases, superoxide dismutases, and peroxidases manage ROS levels.
- Oxidative modification of protein sulfhydryl groups presents a dual role: impairing function or activating regulatory pathways.
Purpose of the Study:
- To investigate the role of thioredoxin and glutaredoxin systems in redox regulation within yeast cells.
- To explore the specific regulatory functions of monothiol glutaredoxins in mitochondria and nuclei.
- To understand the conserved role of these systems in metal homeostasis and gene expression control.
Main Methods:
- Analysis of redox regulation in yeast (Saccharomyces cerevisiae) using thioredoxin and glutaredoxin systems.
- Investigating the function of monothiol glutaredoxins in different cellular compartments.
- Examining the interplay between glutaredoxin and thioredoxin systems.
- Studying the role of transcription factor Yap1 and its regulation by cysteine redox state.
Main Results:
- Thioredoxin and glutaredoxin systems are crucial for redox regulation in yeast, with interplay between them.
- Monothiol glutaredoxins exhibit specific regulatory roles in mitochondria and nuclei.
- These systems are structurally conserved, indicating an important role in metal homeostasis in higher eukaryotes.
- Transcription factor Yap1's activity and nucleocytoplasmic localization are redox-dependent, influenced by Gpx3 and Ybp1.
Conclusions:
- The thioredoxin and glutaredoxin systems are key players in cellular redox homeostasis and regulation.
- Monothiol glutaredoxins possess conserved functions in eukaryotes, impacting metal homeostasis and gene expression.
- Yap1-mediated gene expression control under oxidative stress is finely tuned by protein redox state.
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