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Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast
Endogenously produced hydrogen sulfide was proposed to be an underlying mechanism of lifespan extension via methionine restriction. However, hydrogen sulfide regulation and its beneficial effects via methionine restriction remain elusive. Here, we identified the genes required to increase hydrogen s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628990/ https://www.ncbi.nlm.nih.gov/pubmed/31254461 http://dx.doi.org/10.18632/aging.102050 |
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author | Choi, Kyung-Mi Kim, Sorah Kim, Seahyun Lee, Hae Min Kaya, Alaattin Chun, Bok-Hwan Lee, Yong Kwon Park, Tae-Sik Lee, Cheol-Koo Eyun, Seong-il Lee, Byung Cheon |
author_facet | Choi, Kyung-Mi Kim, Sorah Kim, Seahyun Lee, Hae Min Kaya, Alaattin Chun, Bok-Hwan Lee, Yong Kwon Park, Tae-Sik Lee, Cheol-Koo Eyun, Seong-il Lee, Byung Cheon |
author_sort | Choi, Kyung-Mi |
collection | PubMed |
description | Endogenously produced hydrogen sulfide was proposed to be an underlying mechanism of lifespan extension via methionine restriction. However, hydrogen sulfide regulation and its beneficial effects via methionine restriction remain elusive. Here, we identified the genes required to increase hydrogen sulfide production under methionine restriction condition using genome-wide high-throughput screening in yeast strains with single-gene deletions. Sulfate assimilation-related genes, such as MET1, MET3, MET5, and MET10, were found to be particularly crucial for hydrogen sulfide production. Interestingly, methionine restriction failed to increase hydrogen sulfide production in mutant strains; however, it successfully extended chronological lifespan and reduced reactive oxygen species levels. Altogether, our observations suggested that increased hydrogen sulfide production via methionine restriction is not the mechanism underlying extended yeast lifespan, even though increased hydrogen sulfide production occurred simultaneously with yeast lifespan extension under methionine restriction condition. |
format | Online Article Text |
id | pubmed-6628990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-66289902019-07-18 Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast Choi, Kyung-Mi Kim, Sorah Kim, Seahyun Lee, Hae Min Kaya, Alaattin Chun, Bok-Hwan Lee, Yong Kwon Park, Tae-Sik Lee, Cheol-Koo Eyun, Seong-il Lee, Byung Cheon Aging (Albany NY) Research Paper Endogenously produced hydrogen sulfide was proposed to be an underlying mechanism of lifespan extension via methionine restriction. However, hydrogen sulfide regulation and its beneficial effects via methionine restriction remain elusive. Here, we identified the genes required to increase hydrogen sulfide production under methionine restriction condition using genome-wide high-throughput screening in yeast strains with single-gene deletions. Sulfate assimilation-related genes, such as MET1, MET3, MET5, and MET10, were found to be particularly crucial for hydrogen sulfide production. Interestingly, methionine restriction failed to increase hydrogen sulfide production in mutant strains; however, it successfully extended chronological lifespan and reduced reactive oxygen species levels. Altogether, our observations suggested that increased hydrogen sulfide production via methionine restriction is not the mechanism underlying extended yeast lifespan, even though increased hydrogen sulfide production occurred simultaneously with yeast lifespan extension under methionine restriction condition. Impact Journals 2019-06-29 /pmc/articles/PMC6628990/ /pubmed/31254461 http://dx.doi.org/10.18632/aging.102050 Text en Copyright © 2019 Choi et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Choi, Kyung-Mi Kim, Sorah Kim, Seahyun Lee, Hae Min Kaya, Alaattin Chun, Bok-Hwan Lee, Yong Kwon Park, Tae-Sik Lee, Cheol-Koo Eyun, Seong-il Lee, Byung Cheon Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title | Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title_full | Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title_fullStr | Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title_full_unstemmed | Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title_short | Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
title_sort | sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6628990/ https://www.ncbi.nlm.nih.gov/pubmed/31254461 http://dx.doi.org/10.18632/aging.102050 |
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