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dc.contributor.authorWasko, Brian
dc.date.accessioned2020-10-01T16:00:46Z
dc.date.available2020-10-01T16:00:46Z
dc.date.issued2020
dc.identifier.citationChen KL, Ven TN, Crane MM, Brunner MLC, Pun AK, Helget KL, Brower K, Chen DE, Doan H, Dillard-Telm JD, Huynh E, Feng YC, Yan Z, Golubeva A, Hsu RA, Knight R, Levin J, Mobasher V, Muir M, Omokehinde V, Screws C, Tunali E, Tran RK, Valdez L, Yang E, Kennedy SR, Herr AJ, Kaeberlein M, Wasko BM. Loss of vacuolar acidity results in iron-sulfur cluster defects and divergent homeostatic responses during aging in Saccharomyces cerevisiae. Geroscience. 2020 Apr;42(2):749-764.en_US
dc.identifier.urihttps://hdl.handle.net/10657.1/2523
dc.description.abstractThe loss of vacuolar/lysosomal acidity is an early event during aging that has been linked to mitochondrial dysfunction. However, it is unclear how loss of vacuolar acidity results in age-related dysfunction. Through unbiased genetic screens, we determine that increased iron uptake can suppress the mitochondrial respiratory deficiency phenotype of yeast vma mutants, which have lost vacuolar acidity due to genetic disruption of the vacuolar ATPase proton pump. Yeast vma mutants exhibited nuclear localization of Aft1, which turns on the iron regulon in response to iron-sulfur cluster (ISC) deficiency. This led us to find that loss of vacuolar acidity with age in wild-type yeast causes ISC defects and a DNA damage response. Using microfluidics to investigate aging at the single-cell level, we observe grossly divergent trajectories of iron homeostasis within an isogenic and environmentally homeogeneous population. One subpopulation of cells fails to mount the expected compensatory iron regulon gene expression program, and suffers progressively severe ISC deficiency with little to no activation of the iron regulon. In contract, other cells show robust iron regulon activity with limited ISC deficiency, which allows extended passage and survival through a period of genomic instability during aging. These divergent trajectories suggest that iron regulation and ISC homeostasis represent a possible target for aging interventions.en_US
dc.publisherGeroScienceen_US
dc.subjectAging; DNA damage; Geroscience; Iron-sulfur clusters; Lysosomal acidity; Vacuolar acidity; Yeast replicative lifespan.en_US
dc.titleLoss of Vacuolar Acidity Results in Iron Sulfur Cluster Defects and Divergent Homeostatic Responses During Aging in Saccharomyces Cerevisiaeen_US
dc.typeArticleen_US


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