Comparative Proteomics Analysis Reveals Unique Early Signaling Response of Saccharomyces cerevisiae to Oxidants with Different Mechanism of Action

• Published in: International journal of molecular sciences Vol. 22; no. 1; p. 167
• Main Authors: Pandey, Prajita, Zaman, Khadiza, Prokai, Laszlo, Shulaev, Vladimir
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26.12.2020; MDPI
• Subjects: Antioxidants; Apoptosis; Biochemistry; Cell cycle; Communication; Cumene; Cumene hydroperoxide; Cytochrome; Gene expression; global untargeted proteomics; Hydrogen peroxide; MAP kinase; Menadione; Metabolism; Oxidants; Oxidative stress; Oxidizing agents; Protein synthesis; Proteins; Proteomes; Proteomics; RAN signaling; reactive oxygen species; Saccharomyces cerevisiae; Signal transduction; TOR signaling; Yeast; RAN signaling; MAPK cascade; antioxidants; reactive oxygen species; TOR signaling; oxidative stress; global untargeted proteomics
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22010167

The early signaling events involved in oxidant recognition and triggering of oxidant-specific defense mechanisms to counteract oxidative stress still remain largely elusive. Our discovery driven comparative proteomics analysis revealed unique early signaling response of the yeast on the proteome level to oxidants with a different mechanism of action as early as 3 min after treatment with four oxidants, namely H O , cumene hydroperoxide (CHP), and menadione and diamide, when protein abundances were compared using label-free quantification relying on a high-resolution mass analyzer (Orbitrap). We identified significant regulation of 196 proteins in response to H O , 569 proteins in response to CHP, 369 proteins in response to menadione and 207 proteins in response to diamide. Only 17 proteins were common across all treatments, but several more proteins were shared between two or three oxidants. Pathway analyses revealed that each oxidant triggered a unique signaling mechanism associated with cell survival and repair. Signaling pathways mostly regulated by oxidants were Ran, TOR, Rho, and eIF2. Furthermore, each oxidant regulated these pathways in a unique way indicating specificity of response to oxidants having different modes of action. We hypothesize that interplay of these signaling pathways may be important in recognizing different oxidants to trigger different downstream MAPK signaling cascades and to induce specific responses.