Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions
Summary: Redox couples coordinate cellular function, but the consequences of their imbalances are unclear. This is somewhat associated with the limitations of their experimental quantification. Here we circumvent these difficulties by presenting an approach that characterizes fitness-based tolerance...
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doaj-cbf6856b3f184745901f70e1f192aeef2021-07-23T04:50:10ZengElsevieriScience2589-00422021-07-01247102697Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventionsAlvar J. Alonso-Lavin0Djordje Bajić1Juan F. Poyatos2Logic of Genomic Systems Laboratory (CNB-CSIC), Darwin 3, Campus de Cantoblanco, 28049 Madrid, SpainLogic of Genomic Systems Laboratory (CNB-CSIC), Darwin 3, Campus de Cantoblanco, 28049 Madrid, Spain; Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT, USA; Microbial Sciences Institute, Yale University, New Haven, CT, USALogic of Genomic Systems Laboratory (CNB-CSIC), Darwin 3, Campus de Cantoblanco, 28049 Madrid, Spain; Center for Genomics and Systems Biology, Department of Biology, New York University, New York, USA; Corresponding authorSummary: Redox couples coordinate cellular function, but the consequences of their imbalances are unclear. This is somewhat associated with the limitations of their experimental quantification. Here we circumvent these difficulties by presenting an approach that characterizes fitness-based tolerance profiles to redox couple imbalances using an in silico representation of metabolism. Focusing on the NADH/NAD+ redox couple in yeast, we demonstrate that reductive disequilibria generate metabolic syndromes comparable to those observed in cancer cells. The tolerance of yeast mutants to redox disequilibrium can also explain 30% of the variability in their experimentally measured chronological lifespan. Moreover, by predicting the significance of some metabolites to help stand imbalances, we correctly identify nutrients underlying mechanisms of pathology, lifespan-protecting molecules, or caloric restriction mimetics. Tolerance to redox imbalances becomes, in this way, a sound framework to recognize properties of the aging phenotype while providing a consistent biological rationale to assess anti-aging interventions.http://www.sciencedirect.com/science/article/pii/S2589004221006659Microbial metabolismSystems biologyIn silico biologyMetabolic flux analysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alvar J. Alonso-Lavin Djordje Bajić Juan F. Poyatos |
spellingShingle |
Alvar J. Alonso-Lavin Djordje Bajić Juan F. Poyatos Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions iScience Microbial metabolism Systems biology In silico biology Metabolic flux analysis |
author_facet |
Alvar J. Alonso-Lavin Djordje Bajić Juan F. Poyatos |
author_sort |
Alvar J. Alonso-Lavin |
title |
Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions |
title_short |
Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions |
title_full |
Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions |
title_fullStr |
Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions |
title_full_unstemmed |
Tolerance to NADH/NAD+ imbalance anticipates aging and anti-aging interventions |
title_sort |
tolerance to nadh/nad+ imbalance anticipates aging and anti-aging interventions |
publisher |
Elsevier |
series |
iScience |
issn |
2589-0042 |
publishDate |
2021-07-01 |
description |
Summary: Redox couples coordinate cellular function, but the consequences of their imbalances are unclear. This is somewhat associated with the limitations of their experimental quantification. Here we circumvent these difficulties by presenting an approach that characterizes fitness-based tolerance profiles to redox couple imbalances using an in silico representation of metabolism. Focusing on the NADH/NAD+ redox couple in yeast, we demonstrate that reductive disequilibria generate metabolic syndromes comparable to those observed in cancer cells. The tolerance of yeast mutants to redox disequilibrium can also explain 30% of the variability in their experimentally measured chronological lifespan. Moreover, by predicting the significance of some metabolites to help stand imbalances, we correctly identify nutrients underlying mechanisms of pathology, lifespan-protecting molecules, or caloric restriction mimetics. Tolerance to redox imbalances becomes, in this way, a sound framework to recognize properties of the aging phenotype while providing a consistent biological rationale to assess anti-aging interventions. |
topic |
Microbial metabolism Systems biology In silico biology Metabolic flux analysis |
url |
http://www.sciencedirect.com/science/article/pii/S2589004221006659 |
work_keys_str_mv |
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