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Originally published as MBC in Press, 10.1091/mbc.E06-05-0475 on August 9, 2006

Vol. 17, Issue 10, 4584-4591, October 2006

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Characterization of DNA Damage in Yeast Apoptosis Induced by Hydrogen Peroxide, Acetic Acid, and Hyperosmotic Shock

Gabriela F. Ribeiro, Manuela Côrte-Real, and Björn Johansson

Departamento de Biologia, Centro de Biologia Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal

Submitted May 31, 2006; Revised July 28, 2006; Accepted August 1, 2006
Monitoring Editor: Thomas Fox

Saccharomyces cerevisiae has been reported to die, under certain conditions, from programmed cell death with apoptotic markers. One of the most important markers is chromosomal DNA fragmentation as indicated by terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining. We found TUNEL staining in S. cerevisiae to be a consequence of both single- and double-strand DNA breaks, whereas in situ ligation specifically stained double-strand DNA breaks. Cells treated with hydrogen peroxide or acetic acid staining positively for TUNEL assay stained negatively for in situ ligation, indicating that DNA damage in both cases mainly consists of single-strand DNA breaks. Pulsed field gel electrophoresis of chromosomal DNA from cells dying from hydrogen peroxide, acetic acid, or hyperosmotic shock revealed DNA breakdown into fragments of several hundred kilobases, consistent with the higher order chromatin degradation preceding DNA laddering in apoptotic mammalian cells. DNA fragmentation was associated with death by treatment with 10 mM hydrogen peroxide but not 150 mM and was absent if cells were fixed with formaldehyde to eliminate enzyme activity before hydrogen peroxide treatment. These observations are consistent with a process that, like mammalian apoptosis, is enzyme dependent, degrades chromosomal DNA, and is activated only at low intensity of death stimuli.


This was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E06-05-0475) on August 9, 2006.

Address correspondence to: Björn Johansson (bjorn_johansson{at}bio.uminho.pt)

Abbreviations used: DSB, double-strand DNA break; ISL, in situ ligation; PBS, phosphate-buffered saline; PFGE, pulsed field gel electrophoresis; SSB, single-strand DNA break; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling.




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