Abstract

Studies conducted in the early 1990s showed for the first time that Saccharomyces cerevisiae can undergo cell death with hallmarks of animal apoptosis. These findings came as a surprise, since suicide machinery was unexpected in unicellular organisms. Today, apoptosis in yeast is well-documented. Apoptotic death of yeast cells has been described under various conditions and S. cerevisiae homologs of human apoptotic genes have been identified and characterized. These studies also revealed fundamental differences between yeast and animal apoptosis; in S. cerevisiae apoptosis is mainly associated with aging and stress adaptation, unlike animal apoptosis, which is essential for proper development. Further, many apoptosis regulatory genes are either missing, or highly divergent in S. cerevisiae. Therefore, in this review we will use the term apoptosis-like programed cell death (PCD) instead of apoptosis. Despite these significant differences, S. cerevisiae has been instrumental in promoting the study of heterologous apoptotic proteins, particularly from human. Work in fungi other than S. cerevisiae revealed differences in the manifestation of PCD in single cell (yeasts) and multicellular (filamentous) species. Such differences may reflect the higher complexity level of filamentous species, and hence the involvement of PCD in a wider range of processes and life styles. It is also expected that differences might be found in the apoptosis apparatus of yeast and filamentous species. In this review we focus on aspects of PCD that are unique or can be better studied in filamentous species. We will highlight the similarities and differences of the PCD machinery between yeast and filamentous species and show the value of using S. cerevisiae along with filamentous species to study apoptosis.

Highlights

  • It is possible to identify all the fungal genes that are putative homologs of known apoptotic genes or that contain a putative apoptotic domain. Searches conducted with this program www.frontiersin.org revealed that except for BIR, all other conserved apoptotic domains were absent from fungal genomes, including Bcl-2 homology (BH) domains (BH1–4), caspase recruitment domain (CARD), cellular apoptosis-susceptibility (CAS) protein, death domain (DD), death effector domain (DED), CIDE [cell death-inducing DNA fragmentation factor 45 kDa α (DFFA)-like effector], or death receptors

  • SUMMARY The realization in the early 1990s that yeast cells contain a suicide mechanism led to intense research of programed cell death (PCD) in S. cerevisiae

  • Based on these studies it is generally accepted that yeast cells contain a PCD machinery, which resembles the animal apoptosis machinery

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Summary

Introduction

Apoptotic death of yeast cells has been described under various conditions and S. cerevisiae homologs of human apoptotic genes have been identified and characterized. Work in fungi other than S. cerevisiae revealed differences in the manifestation of PCD in single cell (yeasts) and multicellular (filamentous) species. The baker’s yeast Saccharomyces cerevisiae has been developed as an eukaryotic model to study cellular and developmental processes, including programed cell death (PCD).

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