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Molecular and Cellular Biology, May 2005, p. 4075-4091, Vol. 25, No. 10
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.10.4075-4091.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Dynamical Remodeling of the Transcriptome during Short-Term Anaerobiosis in Saccharomyces cerevisiae: Differential Response and Role of Msn2 and/or Msn4 and Other Factors in Galactose and Glucose Media{dagger}

Liang-Chuan Lai,1 Alexander L. Kosorukoff,2 Patricia V. Burke,1 and Kurt E. Kwast1*

Department of Molecular & Integrative Physiology,1 Department of Computer Science, University of Illinois, Urbana, Illinois2

Received 16 September 2004/ Returned for modification 19 October 2004/ Accepted 23 February 2005

In contrast to previous steady-state analyses of the O2-responsive transcriptome, here we examined the dynamics of the response to short-term anaerobiosis (2 generations) in both catabolite-repressed (glucose) and derepressed (galactose) cells, assessed the specific role that Msn2 and Msn4 play in mediating the response, and identified gene networks using a novel clustering approach. Upon shifting cells to anaerobic conditions in galactose medium, there was an acute (~10 min) yet transient (<45 min) induction of Msn2- and/or Msn4-regulated genes associated with the remodeling of reserve energy and catabolic pathways during the switch from mixed respiro-fermentative to strictly fermentative growth. Concomitantly, MCB- and SCB-regulated networks associated with the G1/S transition of the cell cycle were transiently down-regulated along with rRNA processing genes containing PAC and RRPE motifs. Remarkably, none of these gene networks were differentially expressed when cells were shifted in glucose, suggesting that a metabolically derived signal arising from the abrupt cessation of respiration, rather than O2 deprivation per se, elicits this "stress response." By ~0.2 generation of anaerobiosis in both media, more chronic, heme-dependent effects were observed, including the down-regulation of Hap1-regulated networks, derepression of Rox1-regulated networks, and activation of Upc2-regulated ones. Changes in these networks result in the functional remodeling of the cell wall, sterol and sphingolipid metabolism, and dissimilatory pathways required for long-term anaerobiosis. Overall, this study reveals that the acute withdrawal of oxygen can invoke a metabolic state-dependent "stress response" but that acclimatization to oxygen deprivation is a relatively slow process involving complex changes primarily in heme-regulated gene networks.

* Corresponding author. Mailing address: Department of Molecular & Integrative Physiology, University of Illinois, Urbana, Illinois 61801. Phone: 217-244-3122. Fax: 217-333-1133. E-mail: kwast{at}uiuc.edu.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.

Molecular and Cellular Biology, May 2005, p. 4075-4091, Vol. 25, No. 10
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.10.4075-4091.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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