Abstract

The protein-folding chaperone Hsp90 has been proposed to buffer the phenotypic effects of mutations. The potential for Hsp90 and other putative buffers to increase robustness to mutation has had major impact on disease models, quantitative genetics, and evolutionary theory. But Hsp90 sometimes contradicts expectations for a buffer by potentiating rapid phenotypic changes that would otherwise not occur. Here, we quantify Hsp90’s ability to buffer or potentiate (i.e., diminish or enhance) the effects of genetic variation on single-cell morphological features in budding yeast. We corroborate reports that Hsp90 tends to buffer the effects of standing genetic variation in natural populations. However, we demonstrate that Hsp90 tends to have the opposite effect on genetic variation that has experienced reduced selection pressure. Specifically, Hsp90 tends to enhance, rather than diminish, the effects of spontaneous mutations and recombinations. This result implies that Hsp90 does not make phenotypes more robust to the effects of genetic perturbation. Instead, natural selection preferentially allows buffered alleles to persist and thereby creates the false impression that Hsp90 confers greater robustness.

Highlights

  • Previous work in diverse eukaryotes has demonstrated that inhibition of the protein-folding chaperone Hsp90 reveals previously hidden phenotypic effects of standing genetic variation [1,2,3,4,5,6]

  • Most biologists appreciate that natural selection filters new mutations, such that genetic variation in nature is biased

  • Studies spanning diverse species have shown that the protein Hsp90, which helps other proteins to fold properly, tends to diminish the observable effects of genetic variation

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Summary

Introduction

Previous work in diverse eukaryotes has demonstrated that inhibition of the protein-folding chaperone Hsp reveals previously hidden phenotypic effects of standing genetic variation (see “buffering” in Fig 1A) [1,2,3,4,5,6]. This result prompts an important question [7,8,9,10]: does Hsp increase an organism’s robustness to genetic perturbation? To distinguish the “robustness” hypothesis from the “selection” hypothesis, we study how Hsp

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