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PMID: 21187411 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Misfolded proteins impose a dosage-dependent fitness cost and trigger a cytosolic unfolded protein response in yeast.

Geiler-Samerotte KA, Dion MF, Budnik BA, Wang SM, Hartl DL, Drummond DA

Abstract

Evolving lineages face a constant intracellular threat: most new coding sequence mutations destabilize the folding of the encoded protein. Misfolded proteins form insoluble aggregates and are hypothesized to be intrinsically cytotoxic. Here, we experimentally isolate a fitness cost caused by toxicity of misfolded proteins. We exclude other costs of protein misfolding, such as loss of functional protein or attenuation of growth-limiting protein synthesis resources, by comparing growth rates of budding yeast expressing folded or misfolded variants of a gratuitous protein, YFP, at equal levels. We quantify a fitness cost that increases with misfolded protein abundance, up to as much as a 3.2% growth rate reduction when misfolded YFP represents less than 0.1% of total cellular protein. Comparable experiments on variants of the yeast gene orotidine-5'-phosphate decarboxylase (URA3) produce similar results. Quantitative proteomic measurements reveal that, within the cell, misfolded YFP induces coordinated synthesis of interacting cytosolic chaperone proteins in the absence of a wider stress response, providing evidence for an evolved modular response to misfolded proteins in the cytosol. These results underscore the distinct and evolutionarily relevant molecular threat of protein misfolding, independent of protein function. Assuming that most misfolded proteins impose similar costs, yeast cells express almost all proteins at steady-state levels sufficient to expose their encoding genes to selection against misfolding, lending credibility to the recent suggestion that such selection imposes a global constraint on molecular evolution.

MeSH Terms
Bacterial Proteins/chemistry Cytosol/chemistry,metabolism Evolution, Molecular Fungal Proteins/chemistry Hot Temperature Luminescent Proteins/chemistry Molecular Chaperones/chemistry Protein Denaturation Protein Folding Proteins/chemistry Proteomics/methods Saccharomyces cerevisiae/metabolism Saccharomyces cerevisiae Proteins/chemistry Transcription, Genetic
Chemicals
Bacterial Proteins Fungal Proteins Luminescent Proteins Molecular Chaperones Proteins Saccharomyces cerevisiae Proteins URA3 protein, S cerevisiae yellow fluorescent protein, Bacteria
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Geiler-Samerotte Kerry A
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA.
Dion Michael F
Budnik Bogdan A
Wang Stephanie M
Hartl Daniel L
Drummond D Allan
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
1091-6490
Published
2011-01-11
Epub
2010-00-27
Pages
680-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC3021021
Subset
IM
Grants
NIGMS NIH HHS · P50 GM068763 · United States
NIGMS NIH HHS · R01 GM079536 · United States
NIGMS NIH HHS · 1R01GM088344-01 · United States
NIGMS NIH HHS · R01 GM088344 · United States
NIGMS NIH HHS · P50GM068763 · United States
NIGMS NIH HHS · GM065169 · United States
NIGMS NIH HHS · R01 GM065169 · United States
NIGMS NIH HHS · GM079536 · United States
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