A haploid-specific transcriptional response to irradiation in Saccharomyces cerevisiae

Nucleic Acids Res. 2005 Nov 30;33(20):6635-43. doi: 10.1093/nar/gki959. Print 2005.

Abstract

Eukaryotic cells respond to DNA damage by arresting the cell cycle and modulating gene expression to ensure efficient DNA repair. We used global transcriptome analysis to investigate the role of ploidy and mating-type in inducing the response to damage in various Saccharomyces cerevisiae strains. We observed a response to DNA damage specific to haploid strains that seemed to be controlled by chromatin regulatory proteins. Consistent with these microarray data, we found that mating-type factors controlled the chromatin-dependent silencing of a reporter gene. Both these analyses demonstrate the existence of an irradiation-specific response in strains (haploid or diploid) with only one mating-type factor. This response depends on the activities of Hdf1 and Sir2. Overall, our results suggest the existence of a new regulation pathway dependent on mating-type factors, chromatin structure remodeling, Sir2 and Hdf1 and independent of Mec1 kinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Nuclear / physiology
  • Chromatin / metabolism
  • Chromosomes, Bacterial
  • DNA Damage*
  • DNA Repair*
  • DNA-Binding Proteins / physiology
  • Diploidy
  • Gene Expression Regulation, Bacterial*
  • Gene Silencing
  • Genes, Bacterial
  • Haploidy*
  • Histone Deacetylases / physiology
  • Ku Autoantigen
  • Promoter Regions, Genetic
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae / radiation effects
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae / physiology
  • Sirtuin 2
  • Sirtuins / physiology
  • Transcription, Genetic / radiation effects

Substances

  • Antigens, Nuclear
  • Chromatin
  • DNA-Binding Proteins
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae
  • SIR2 protein, S cerevisiae
  • Sirtuin 2
  • Sirtuins
  • Histone Deacetylases
  • Ku Autoantigen