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PMID: 19067491 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Prion switching in response to environmental stress.

PLoS biology ·Vol. 6 ·No. 11 ·2008-11-25 ·Pages e294

Tyedmers J, Madariaga ML, Lindquist S

Abstract

Evolution depends on the manner in which genetic variation is translated into new phenotypes. There has been much debate about whether organisms might have specific mechanisms for "evolvability," which would generate heritable phenotypic variation with adaptive value and could act to enhance the rate of evolution. Capacitor systems, which allow the accumulation of cryptic genetic variation and release it under stressful conditions, might provide such a mechanism. In yeast, the prion [PSI(+)] exposes a large array of previously hidden genetic variation, and the phenotypes it thereby produces are advantageous roughly 25% of the time. The notion that [PSI(+)] is a mechanism for evolvability would be strengthened if the frequency of its appearance increased with stress. That is, a system that mediates even the haphazard appearance of new phenotypes, which have a reasonable chance of adaptive value would be beneficial if it were deployed at times when the organism is not well adapted to its environment. In an unbiased, high-throughput, genome-wide screen for factors that modify the frequency of [PSI(+)] induction, signal transducers and stress response genes were particularly prominent. Furthermore, prion induction increased by as much as 60-fold when cells were exposed to various stressful conditions, such as oxidative stress (H2O2) or high salt concentrations. The severity of stress and the frequency of [PSI(+)] induction were highly correlated. These findings support the hypothesis that [PSI(+)] is a mechanism to increase survival in fluctuating environments and might function as a capacitor to promote evolvability.

MeSH Terms
Adaptation, Physiological/genetics Extrachromosomal Inheritance Fungal Proteins/genetics Gene Expression Regulation, Fungal Genes, Fungal Genetic Variation Genome-Wide Association Study Peptide Termination Factors Phenotype Prions/genetics,metabolism Saccharomyces cerevisiae/genetics,physiology Saccharomyces cerevisiae Proteins/genetics,metabolism Sequence Deletion Stress, Physiological/genetics,physiology Transcriptional Activation
Chemicals
Fungal Proteins Peptide Termination Factors Prions SUP35 protein, S cerevisiae Saccharomyces cerevisiae Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tyedmers Jens
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, USA.
Madariaga Maria Lucia
Lindquist Susan
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Article Info
Journal
PLoS biology
Abbr.
PLoS Biol
ISSN
1545-7885
Published
2008-11-25
Pages
e294
Language
English
Region
United States
NLM ID
101183755
PMCID
PMC2586387
Subset
IM
Grants
NIGMS NIH HHS · R01 GM025874 · United States
NIGMS NIH HHS · R37 GM025874 · United States
Howard Hughes Medical Institute · United States
NIGMS NIH HHS · GM25874 · United States
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