Metabolic diversification of cells during the development of yeast colonies
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
55005623
Howard Hughes Medical Institute - United States
PubMed
19196279
DOI
10.1111/j.1462-2920.2008.01789.x
PII: EMI1789
Knihovny.cz E-resources
- MeSH
- Ammonia metabolism MeSH
- Adaptation, Physiological * MeSH
- Culture Media chemistry MeSH
- Humans MeSH
- Gene Expression Regulation, Fungal * MeSH
- Saccharomyces cerevisiae Proteins metabolism MeSH
- Saccharomyces cerevisiae growth & development metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Ammonia MeSH
- Culture Media MeSH
- Saccharomyces cerevisiae Proteins MeSH
Microorganisms in nature form organized multicellular structures (colonies, biofilms) possessing properties absent in individual cells. These are often related to the better ability of communities to survive long-lasting starvation and stress and include mechanisms of adaptation and cell specialization. Thus, yeast colonies pass through distinct developmental phases characterized by changes in pH and the production of ammonia-signalling molecules. Here, we show that Saccharomyces cerevisiae colony transition between major developmental phases (first acidic, alkali, second acidic) is accompanied by striking transcription changes, while the development within each particular phase is guided mostly at the post-transcriptional level. First- and second-acidic-phase colonies markedly differ. Second-acidic-phase colonies maintain the adaptive metabolism activated in the ammonia-producing period, supplemented by additional changes, which begin after colonies enter the second acidic phase. Cells with particular properties are not homogenously dispersed throughout the colony population, but localize to specific colony regions. Thus, cells located at the colony margin are able to export higher amounts of ammonium than central cells and to activate an adaptive metabolism. In contrast, central chronologically aged cells are unable to undergo these changes but they maintain higher levels of various stress-defence enzymes. These divergent properties of both cell types determine their consequent dissimilar fate.
References provided by Crossref.org
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