Abstract

The transcriptional program of yeast cells undergoes dramatic changes during the shift from fermentative growth to respiratory growth. A large part of this response is mediated by the stress responsive transcription factor Msn2. During glucose exhaustion, Msn2 is activated and concentrated in the nucleus. Simultaneously, Msn2 protein levels also drop significantly under this condition. Here we show that the decrease in Msn2 concentration is due to its increased degradation. Moreover, Msn2 levels are also reduced under chronic stress or low protein kinase A (PKA) activity, both conditions that cause a predominant nuclear localization of Msn2. Similar effects were found in msn5 mutant cells that block Msn2 nuclear export. To approximate the effect of low PKA activity on Msn2, we generated a mutant form with alanine substitutions in PKA phosphorylation sites. High expression of this Msn2 mutant is detrimental for growth, suggesting that the increased degradation of nuclear Msn2 might be necessary to adapt cells to low PKA conditions after the diauxic shift or to allow growth under chronic stress conditions.

Highlights

  • In budding yeast, two redundant stress-inducible transcription factors, Msn2 and Msn4, play an important role in the response to environmental cues [1]

  • Plasmids pCUP1-PKIMSN2 and pCUP1-PKIMSN2-GFP were generated by replacing the MSN2 promoter from plasmids pYMSN2 and pYMSN2-GFP with a SacII/SalI Fragment containing the CUP1 promoter fused to the protein kinase A inhibitor (PKI) sequence

  • Msn2 Levels Are Diminished after the Diauxic Shift—Under logarithmic growth conditions yeast cells maintain a balanced level of Msn2 protein that does not change under acute stress conditions [9]

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Summary

Relevant inserts

ADH1-MSN2 ADH1-MSN2-GFP MSN2–9xmyc MSN2-GFP CUP1 Promoter-MSN2 CUP1 Promoter-MSN2-GFP CUP1 Promoter-MSN2⌬246–325 CUP1 Promoter-MSN2⌬246–325-GFP CUP1 Promoter-MSN2 S A 288,582,620,625,633 CUP1 Promoter-MSN2 S288,582,620,625,633A-GFP CUP1 Promoter-PKINES-MSN2 CUP1 Promoter-PKINES-MSN2-GFP.

TABLE II Oligonucleotides used in this study
EXPERIMENTAL PROCEDURES
RESULTS
DISCUSSION
Full Text
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