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Sulfate assimilation regulates hydrogen sulfide production independent of lifespan and reactive oxygen species under methionine restriction condition in yeast

Authors
Choi, Kyung-MiKim, SorahKim, SeahyunLee, Hae MinKaya, AlaattinChun, Bok-HwanLee, Yong KwonPark, Tae-SikLee, Cheol-KooEyun, Seong-ilLee, Byung Cheon
Issue Date
30-Jun-2019
Publisher
IMPACT JOURNALS LLC
Keywords
high-throughput genetic screening; methionine restriction; hydrogen sulfide; sulfate assimilation; reactive oxygen species
Citation
AGING-US, v.11, no.12, pp.4254 - 4273
Journal Title
AGING-US
Volume
11
Number
12
Start Page
4254
End Page
4273
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/1344
DOI
10.18632/aging.102050
ISSN
1945-4589
Abstract
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.
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BioNano Technology (Department of Life Sciences)
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