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Autophagy extends lifespan via vacuolar acidification
Methionine restriction (MetR) is one of the rare regimes that prolongs lifespan across species barriers. Using a yeast model, we recently demonstrated that this lifespan extension is promoted by autophagy, which in turn requires vacuolar acidification. Our study is the first to place autophagy as on...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shared Science Publishers OG
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354602/ https://www.ncbi.nlm.nih.gov/pubmed/28357240 http://dx.doi.org/10.15698/mic2014.05.147 |
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author | Ruckenstuhl, Christoph Netzberger, Christine Entfellner, Iryna Carmona-Gutierrez, Didac Kickenweiz, Thomas Stekovic, Slaven Gleixner, Christina Schmid, Christian Klug, Lisa Hajnal, Ivan Sorgo, Alice G. Eisenberg, Tobias Büttner, Sabrina Marin͂o, Guillermo Koziel, Rafael Magnes, Christoph Sinner, Frank Pieber, Thomas R. Jansen-Dürr, Pidder Fröhlich, Kai-Uwe Kroemer, Guido Madeo, Frank |
author_facet | Ruckenstuhl, Christoph Netzberger, Christine Entfellner, Iryna Carmona-Gutierrez, Didac Kickenweiz, Thomas Stekovic, Slaven Gleixner, Christina Schmid, Christian Klug, Lisa Hajnal, Ivan Sorgo, Alice G. Eisenberg, Tobias Büttner, Sabrina Marin͂o, Guillermo Koziel, Rafael Magnes, Christoph Sinner, Frank Pieber, Thomas R. Jansen-Dürr, Pidder Fröhlich, Kai-Uwe Kroemer, Guido Madeo, Frank |
author_sort | Ruckenstuhl, Christoph |
collection | PubMed |
description | Methionine restriction (MetR) is one of the rare regimes that prolongs lifespan across species barriers. Using a yeast model, we recently demonstrated that this lifespan extension is promoted by autophagy, which in turn requires vacuolar acidification. Our study is the first to place autophagy as one of the major players required for MetR-mediated longevity. In addition, our work identifies vacuolar acidification as a key downstream element of autophagy induction under MetR, and possibly after rapamycin treatment. Unlike other amino acids, methionine plays pleiotropic roles in many metabolism-relevant pathways. For instance, methionine (i) is the N-terminal amino acid of every newly translated protein; (ii) acts as the central donor of methyl groups through S-adenosyl methionine (SAM) during methylation reactions of proteins, DNA or RNA; and (iii) provides the sulfhydryl groups for FeS-cluster formation and redox detoxification via transsulfuration to cysteine. Intriguingly, MetR causes lifespan extension, both in yeast and in rodents. We could show that in Saccharomyces cerevisiae, chronological lifespan (CLS) is increased in two specific methionine-auxotrophic strains (namely Δmet2 and Δmet15). |
format | Online Article Text |
id | pubmed-5354602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Shared Science Publishers OG |
record_format | MEDLINE/PubMed |
spelling | pubmed-53546022017-03-29 Autophagy extends lifespan via vacuolar acidification Ruckenstuhl, Christoph Netzberger, Christine Entfellner, Iryna Carmona-Gutierrez, Didac Kickenweiz, Thomas Stekovic, Slaven Gleixner, Christina Schmid, Christian Klug, Lisa Hajnal, Ivan Sorgo, Alice G. Eisenberg, Tobias Büttner, Sabrina Marin͂o, Guillermo Koziel, Rafael Magnes, Christoph Sinner, Frank Pieber, Thomas R. Jansen-Dürr, Pidder Fröhlich, Kai-Uwe Kroemer, Guido Madeo, Frank Microb Cell Microbiology Methionine restriction (MetR) is one of the rare regimes that prolongs lifespan across species barriers. Using a yeast model, we recently demonstrated that this lifespan extension is promoted by autophagy, which in turn requires vacuolar acidification. Our study is the first to place autophagy as one of the major players required for MetR-mediated longevity. In addition, our work identifies vacuolar acidification as a key downstream element of autophagy induction under MetR, and possibly after rapamycin treatment. Unlike other amino acids, methionine plays pleiotropic roles in many metabolism-relevant pathways. For instance, methionine (i) is the N-terminal amino acid of every newly translated protein; (ii) acts as the central donor of methyl groups through S-adenosyl methionine (SAM) during methylation reactions of proteins, DNA or RNA; and (iii) provides the sulfhydryl groups for FeS-cluster formation and redox detoxification via transsulfuration to cysteine. Intriguingly, MetR causes lifespan extension, both in yeast and in rodents. We could show that in Saccharomyces cerevisiae, chronological lifespan (CLS) is increased in two specific methionine-auxotrophic strains (namely Δmet2 and Δmet15). Shared Science Publishers OG 2014-05-05 /pmc/articles/PMC5354602/ /pubmed/28357240 http://dx.doi.org/10.15698/mic2014.05.147 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged. |
spellingShingle | Microbiology Ruckenstuhl, Christoph Netzberger, Christine Entfellner, Iryna Carmona-Gutierrez, Didac Kickenweiz, Thomas Stekovic, Slaven Gleixner, Christina Schmid, Christian Klug, Lisa Hajnal, Ivan Sorgo, Alice G. Eisenberg, Tobias Büttner, Sabrina Marin͂o, Guillermo Koziel, Rafael Magnes, Christoph Sinner, Frank Pieber, Thomas R. Jansen-Dürr, Pidder Fröhlich, Kai-Uwe Kroemer, Guido Madeo, Frank Autophagy extends lifespan via vacuolar acidification |
title | Autophagy extends lifespan via vacuolar acidification |
title_full | Autophagy extends lifespan via vacuolar acidification |
title_fullStr | Autophagy extends lifespan via vacuolar acidification |
title_full_unstemmed | Autophagy extends lifespan via vacuolar acidification |
title_short | Autophagy extends lifespan via vacuolar acidification |
title_sort | autophagy extends lifespan via vacuolar acidification |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354602/ https://www.ncbi.nlm.nih.gov/pubmed/28357240 http://dx.doi.org/10.15698/mic2014.05.147 |
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