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Libue Váchová¹ and Zdena Palková²

¹ Institute of Microbiology, Academy of Sciences of the Czech Republic, 142 20 Prague-4, Czech Republic
² Department of Genetics and Microbiology, Charles University in Prague, 116 36 Prague-1, Czech Republic

Correspondence to Zdena Palková: zdenap{at}natur.cuni.cz; or to Libue Váchová: vachova{at}biomed.cas.cz

Abstract
The existence of programmed cell death (PCD) in yeast and its significance to simple unicellular organisms is still questioned. However, such doubts usually do not reflect the fact that microorganisms in nature exist predominantly within structured, multicellular communities capable of differentiation, in which a profit of individual cells is subordinated to a profit of populations. In this study, we show that some PCD features naturally appear during the development of multicellular Saccharomyces cerevisiae colonies. An ammonia signal emitted by aging colonies triggers metabolic changes that localize yeast death only in the colony center. The remaining population can exploit the released nutrients and survives. In colonies defective in Sok2p transcription factor that are unable to produce ammonia (Váchová, L., F. Devaux, H. Kucerova, M. Ricicova, C. Jacq, and Z. Palková. 2004. J. Biol. Chem. 279:37973–37981), death is spread throughout the whole population, thus decreasing the lifetime of the colony. The absence of Mca1p metacaspase or Aif1p orthologue of mammalian apoptosis-inducing factor does not prevent regulated death in yeast colonies.

Libue Váchová and Zdena Palková contributed equally to this work.

Abbreviations used in this paper: ASPase, protease cleaving after aspartate residue; BKP, bromcresol purple; DHE, dihydroethidium; GMA, glycerol medium agar; PCD, programmed cell death; PS, phosphatidylserine; ROS, reactive oxygen species; YCD, yeast cell death.

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