TY - JOUR
T1 - Stimulating S-adenosyl-L-methionine synthesis extends lifespan via activation of AMPK
AU - Ogawa, Takafumi
AU - Tsubakiyama, Ryohei
AU - Kanai, Muneyoshi
AU - Koyama, Tetsuya
AU - Fujii, Tsutomu
AU - Iefuji, Haruyuki
AU - Soga, Tomoyoshi
AU - Kume, Kazunori
AU - Miyakawa, Tokichi
AU - Hirata, Dai
AU - Mizunuma, Masaki
N1 - Funding Information:
We thank Drs. Hitoshi Shimoi and Atsuko Isogai for technical advice regarding the construction of the genomic library for cloning of the SSG1-1; Dr. Satoshi Harashima for communicating about the Saccharomyces cerevisiae DKD-5D-H strain background; Mr. Fuminori Ueno for performing some of the chronological lifespan experiments; and Dr. T. Keith Blackwell for critical reading of the manuscript. This work was supported by the program Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science for Scientific Research from JSPS KAKENHI Grants 24580142 and 16H04898 (to M.M.). T.O. is the recipient of the Research Fellowship of the Japan Society for the Promotion of Science for Young Scientists (DC2).
Publisher Copyright:
© 2016, National Academy of Sciences. All rights reserved.
PY - 2016/10/18
Y1 - 2016/10/18
N2 - Dietary restriction (DR), such as calorie restriction (CR) or methionine (Met) restriction, extends the lifespan of diverse model organisms. Although studies have identified several metabolites that contribute to the beneficial effects of DR, the molecular mechanism underlying the key metabolites responsible for DR regimens is not fully understood. Here we show that stimulating S-adenosyl-L-methionine (AdoMet) synthesis extended the lifespan of the budding yeast Saccharomyces cerevisiae. The AdoMet synthesis-mediated beneficial metabolic effects, which resulted from consuming both Met and ATP, mimicked CR. Indeed, stimulating AdoMet synthesis activated the universal energy-sensing regulator Snf1, which is the S. cerevisiae ortholog of AMP-activated protein kinase (AMPK), resulting in lifespan extension. Furthermore, our findings revealed that S-adenosyl-L-homocysteine contributed to longevity with a higher accumulation of AdoMet only under the severe CR (0.05% glucose) conditions. Thus, our data uncovered molecular links between Met metabolites and lifespan, suggesting a unique function of AdoMet as a reservoir of Met and ATP for cell survival.
AB - Dietary restriction (DR), such as calorie restriction (CR) or methionine (Met) restriction, extends the lifespan of diverse model organisms. Although studies have identified several metabolites that contribute to the beneficial effects of DR, the molecular mechanism underlying the key metabolites responsible for DR regimens is not fully understood. Here we show that stimulating S-adenosyl-L-methionine (AdoMet) synthesis extended the lifespan of the budding yeast Saccharomyces cerevisiae. The AdoMet synthesis-mediated beneficial metabolic effects, which resulted from consuming both Met and ATP, mimicked CR. Indeed, stimulating AdoMet synthesis activated the universal energy-sensing regulator Snf1, which is the S. cerevisiae ortholog of AMP-activated protein kinase (AMPK), resulting in lifespan extension. Furthermore, our findings revealed that S-adenosyl-L-homocysteine contributed to longevity with a higher accumulation of AdoMet only under the severe CR (0.05% glucose) conditions. Thus, our data uncovered molecular links between Met metabolites and lifespan, suggesting a unique function of AdoMet as a reservoir of Met and ATP for cell survival.
KW - AMP-activated protein kinase
KW - Calorie restriction
KW - S-adenosyl-L-homocysteine
KW - S-adenosyl-L-methionine
KW - Yeast
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U2 - 10.1073/pnas.1604047113
DO - 10.1073/pnas.1604047113
M3 - Article
C2 - 27698120
AN - SCOPUS:84991712518
SN - 0027-8424
VL - 113
SP - 11913
EP - 11918
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 42
ER -