Population Diversification in a Yeast Metabolic Program Promotes Anticipation of Environmental Shifts
Abstract
Delineating the strategies by which cells contend with combinatorial changing environments is crucial for understanding cellular regulatory organization. When presented with two carbon sources, microorganisms first consume the carbon substrate that supports the highest growth rate (e.g., glucose) and then switch to the secondary carbon source (e.g., galactose), a paradigm known as the Monod model. Sequential sugar utilization has been attributed to transcriptional repression of the secondary metabolic pathway, followed by activation of this pathway upon depletion of the preferred carbon source. In this work, we demonstrate that although Saccharomyces cerevisiae cells consume glucose before galactose, the galactose regulatory pathway is activated in a fraction of the cell population hours before glucose is fully consumed. This early activation reduces the time required for the population to transition between the two metabolic programs and provides a fitness advantage that might be crucial in competitive environments.
Additional Information
© 2015 Venturelli et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Received: July 25, 2014; accepted: December 3, 2014; published: January 27, 2015. We would like to thank Adam Rosenthal and Michael Chevalier for helpful discussions; Susan Chen and Benjamin Heineike for assistance with microscopy; João Fonseca for help with cell sorting; Lucien Bogar for assistance with flow cytometry; and Carol Gross, Sandy Johnson, and Zev Gartner for critical reading of this manuscript.Attached Files
Published - journal.pbio.1002042.pdf
Submitted - 002907.full.pdf
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Supplemental Material - journal.pbio.1002042.s002.ZIP
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Additional details
- PMCID
- PMC4307983
- Eprint ID
- 55748
- Resolver ID
- CaltechAUTHORS:20150313-113120630
- Army Research Office (ARO)
- W911NF-09-0001
- NIH
- P50 GM081879
- David and Lucile Packard Foundation
- Created
-
2015-03-13Created from EPrint's datestamp field
- Updated
-
2023-10-20Created from EPrint's last_modified field