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The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae
Silent information regulator 2 (Sir2) is a conserved NAD(+)-dependent histone deacetylase crucial for regulating cellular stress response and the aging process in Saccharomyces cerevisiae. In this study, we investigated the molecular mechanism underlying how the absence of Sir2 can lead to altered s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666771/ https://www.ncbi.nlm.nih.gov/pubmed/38029141 http://dx.doi.org/10.3389/fmicb.2023.1285559 |
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author | Kim, Yeong Hyeock Ryu, Ji-In Devare, Mayur Nimbadas Jung, Juhye Kim, Jeong-Yoon |
author_facet | Kim, Yeong Hyeock Ryu, Ji-In Devare, Mayur Nimbadas Jung, Juhye Kim, Jeong-Yoon |
author_sort | Kim, Yeong Hyeock |
collection | PubMed |
description | Silent information regulator 2 (Sir2) is a conserved NAD(+)-dependent histone deacetylase crucial for regulating cellular stress response and the aging process in Saccharomyces cerevisiae. In this study, we investigated the molecular mechanism underlying how the absence of Sir2 can lead to altered stress susceptibilities in S. cerevisiae under different environmental and physiological conditions. In a glucose-complex medium, the sir2Δ strain showed increased sensitivity to H(2)O(2) compared to the wild-type strain during the post-diauxic phase. In contrast, it displayed increased resistance during the exponential growth phase. Transcriptome analysis of yeast cells in the post-diauxic phase indicated that the sir2Δ mutant expressed several oxidative defense genes at lower levels than the wild-type, potentially accounting for its increased susceptibility to H(2)O(2). Interestingly, however, the sir2Δras2Δ double mutant exhibited greater resistance to H(2)O(2) than the ras2Δ single mutant counterpart. We found that the expression regulation of the cytoplasmic catalase encoded by CTT1 was critical for the increased resistance to H(2)O(2) in the sir2Δras2Δ strain. The expression of the CTT1 gene was influenced by the combined effect of RAS2 deletion and the transcription factor Azf1, whose level was modulated by Sir2. These findings provide insights into the importance of understanding the intricate interactions among various factors contributing to cellular stress response. |
format | Online Article Text |
id | pubmed-10666771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106667712023-11-09 The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae Kim, Yeong Hyeock Ryu, Ji-In Devare, Mayur Nimbadas Jung, Juhye Kim, Jeong-Yoon Front Microbiol Microbiology Silent information regulator 2 (Sir2) is a conserved NAD(+)-dependent histone deacetylase crucial for regulating cellular stress response and the aging process in Saccharomyces cerevisiae. In this study, we investigated the molecular mechanism underlying how the absence of Sir2 can lead to altered stress susceptibilities in S. cerevisiae under different environmental and physiological conditions. In a glucose-complex medium, the sir2Δ strain showed increased sensitivity to H(2)O(2) compared to the wild-type strain during the post-diauxic phase. In contrast, it displayed increased resistance during the exponential growth phase. Transcriptome analysis of yeast cells in the post-diauxic phase indicated that the sir2Δ mutant expressed several oxidative defense genes at lower levels than the wild-type, potentially accounting for its increased susceptibility to H(2)O(2). Interestingly, however, the sir2Δras2Δ double mutant exhibited greater resistance to H(2)O(2) than the ras2Δ single mutant counterpart. We found that the expression regulation of the cytoplasmic catalase encoded by CTT1 was critical for the increased resistance to H(2)O(2) in the sir2Δras2Δ strain. The expression of the CTT1 gene was influenced by the combined effect of RAS2 deletion and the transcription factor Azf1, whose level was modulated by Sir2. These findings provide insights into the importance of understanding the intricate interactions among various factors contributing to cellular stress response. Frontiers Media S.A. 2023-11-09 /pmc/articles/PMC10666771/ /pubmed/38029141 http://dx.doi.org/10.3389/fmicb.2023.1285559 Text en Copyright © 2023 Kim, Ryu, Devare, Jung and Kim. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Kim, Yeong Hyeock Ryu, Ji-In Devare, Mayur Nimbadas Jung, Juhye Kim, Jeong-Yoon The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title | The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title_full | The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title_fullStr | The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title_full_unstemmed | The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title_short | The intricate role of Sir2 in oxidative stress response during the post-diauxic phase in Saccharomyces cerevisiae |
title_sort | intricate role of sir2 in oxidative stress response during the post-diauxic phase in saccharomyces cerevisiae |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666771/ https://www.ncbi.nlm.nih.gov/pubmed/38029141 http://dx.doi.org/10.3389/fmicb.2023.1285559 |
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