The role of autophagy in the regulation of yeast life span.

TitleThe role of autophagy in the regulation of yeast life span.
Publication TypeJournal Article
Year of Publication2018
AuthorsTyler JK, Johnson JE
JournalAnn N Y Acad Sci
Volume1418
Issue1
Pagination31-43
Date Published2018 04
ISSN1749-6632
KeywordsAutophagy, Endoplasmic Reticulum, Epigenesis, Genetic, Golgi Apparatus, Homeostasis, Hormesis, Humans, Lipids, Longevity, Methionine, Models, Biological, Parkinson Disease, Saccharomyces cerevisiae
Abstract

The goal of the aging field is to develop novel therapeutic interventions that extend human health span and reduce the burden of age-related disease. While organismal aging is a complex, multifactorial process, a popular theory is that cellular aging is a significant contributor to the progressive decline inherent to all multicellular organisms. To explore the molecular determinants that drive cellular aging, as well as how to retard them, researchers have utilized the highly genetically tractable budding yeast Saccharomyces cerevisiae. Indeed, every intervention known to extend both cellular and organismal health span was identified in yeast, underlining the power of this approach. Importantly, a growing body of work has implicated the process of autophagy as playing a critical role in the delay of aging. This review summarizes recent reports that have identified a role for autophagy, or autophagy factors in the extension of yeast life span. These studies demonstrate (1) that yeast remains an invaluable tool for the identification and characterization of conserved mechanisms that promote cellular longevity and are likely to be relevant to humans, and (2) that the process of autophagy has been implicated in nearly all known longevity-promoting manipulations and thus represents an ideal target for interventions aimed at improving human health span.

DOI10.1111/nyas.13549
Alternate JournalAnn N Y Acad Sci
PubMed ID29363766
PubMed Central IDPMC5934334
Grant ListR01 AG050660 / AG / NIA NIH HHS / United States
R01 CA095641 / CA / NCI NIH HHS / United States
R01 GM064475 / GM / NIGMS NIH HHS / United States
Related Faculty: 
Jessica K. Tyler, Ph.D.

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