Stress-activated Genomic Expression Changes Serve a Preparative Role for Impending Stress in Yeast

David B. Berry, Audrey P. Gasch

Molecular Biology of the Cell · 2008 · 336 citations · 41 references

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TL;DR

Yeast cells mount a common environmental stress response (ESR) that, according to prior work, shows poor correlation between stress‑induced gene expression and genes required for survival, raising questions about the functional role of such expression changes. The authors examined how mild stress preexposure increases resistance to subsequent severe stress in yeast. They found that stress‑induced gene expression is not required for immediate survival but primes cells for future stress, with acquired resistance depending on protein synthesis and the transcription factors Msn2p/Msn4p, which act in a condition‑specific rather than generic ESR manner.

Abstract

Yeast cells respond to stress by mediating condition-specific gene expression changes and by mounting a common response to many stresses, called the environmental stress response (ESR). Giaever et al. previously revealed poor correlation between genes whose expression changes in response to acute stress and genes required to survive that stress, raising question about the role of stress-activated gene expression. Here we show that gene expression changes triggered by a single dose of stress are not required to survive that stimulus but rather serve a protective role against future stress. We characterized the increased resistance to severe stress in yeast preexposed to mild stress. This acquired stress resistance is dependent on protein synthesis during mild-stress treatment and requires the "general-stress" transcription factors Msn2p and/or Msn4p that regulate induction of many ESR genes. However, neither protein synthesis nor Msn2/4p is required for basal tolerance of a single dose of stress, despite the substantial expression changes triggered by each condition. Using microarrays, we show that Msn2p and Msn4p play nonredundant and condition-specific roles in gene-expression regulation, arguing against a generic general-stress function. This work highlights the importance of condition-specific responses in acquired stress resistance and provides new insights into the role of the ESR.

References

41