Dormancy-to-death transition in yeast spores occurs due to gradual loss of gene-expressing ability

Journal Article (2020)
Author(s)

T.T.H. Maire (Kavli institute of nanoscience Delft, TU Delft - OLD BN/Hyun Youk Lab)

T. Allertz

Max A. Betjes (Kavli institute of nanoscience Delft)

Hyun Youk (Kavli institute of nanoscience Delft, University of Massachusetts Medical School, TU Delft - OLD BN/Hyun Youk Lab, CIFAR)

Research Group
OLD BN/Hyun Youk Lab
Copyright
© 2020 T.T.H. Maire, T. Allertz, M.A. Betjes, H.O. Youk
DOI related publication
https://doi.org/10.15252/msb.20199245
More Info
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Publication Year
2020
Language
English
Copyright
© 2020 T.T.H. Maire, T. Allertz, M.A. Betjes, H.O. Youk
Research Group
OLD BN/Hyun Youk Lab
Issue number
11
Volume number
16
Pages (from-to)
e9245
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Abstract

Dormancy is colloquially considered as extending lifespan by being still. Starved yeasts form dormant spores that wake-up (germinate) when nutrients reappear but cannot germinate (die) after some time. What sets their lifespans and how they age are open questions because what processes occur-and by how much-within each dormant spore remains unclear. With single-cell-level measurements, we discovered how dormant yeast spores age and die: spores have a quantifiable gene-expressing ability during dormancy that decreases over days to months until it vanishes, causing death. Specifically, each spore has a different probability of germinating that decreases because its ability to-without nutrients-express genes decreases, as revealed by a synthetic circuit that forces GFP expression during dormancy. Decreasing amounts of molecules required for gene expression-including RNA polymerases-decreases gene-expressing ability which then decreases chances of germinating. Spores gradually lose these molecules because they are produced too slowly compared with their degradations, causing gene-expressing ability to eventually vanish and, thus, death. Our work provides a systems-level view of dormancy-to-death transition.