Metabolic response to MMS-mediated DNA damage in Saccharomyces cerevisiae is dependent on the glucose concentration in the medium

FEMS Yeast Res. 2009 Jun;9(4):535-51. doi: 10.1111/j.1567-1364.2009.00505.x. Epub 2009 Apr 1.

Abstract

Maintenance and adaptation of energy metabolism could play an important role in the cellular ability to respond to DNA damage. A large number of studies suggest that the sensitivity of cells to oxidants and oxidative stress depends on the activity of cellular metabolism and is dependent on the glucose concentration. In fact, yeast cells that utilize fermentative carbon sources and hence rely mainly on glycolysis for energy appear to be more sensitive to oxidative stress. Here we show that treatment of the yeast Saccharomyces cerevisiae growing on a glucose-rich medium with the DNA alkylating agent methyl methanesulphonate (MMS) triggers a rapid inhibition of respiration and enhances reactive oxygen species (ROS) production, which is accompanied by a strong suppression of glycolysis. Further, diminished activity of pyruvate kinase and glyceraldehyde-3-phosphate dehydrogenase upon MMS treatment leads to a diversion of glucose carbon to glycerol, trehalose and glycogen accumulation and an increased flux through the pentose-phosphate pathway. Such conditions finally result in a significant decline in the ATP level and energy charge. These effects are dependent on the glucose concentration in the medium. Our results clearly demonstrate that calorie restriction reduces MMS toxicity through increased respiration and reduced ROS accumulation, enhancing the survival and recovery of cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Cell Respiration / drug effects
  • DNA Damage*
  • Energy Metabolism / drug effects
  • Glucose / metabolism*
  • Glyceraldehyde-3-Phosphate Dehydrogenases / metabolism
  • Glycerol / metabolism
  • Glycogen / metabolism
  • Glycolysis / drug effects
  • Methyl Methanesulfonate / toxicity*
  • Microbial Viability
  • Pyruvate Kinase / metabolism
  • Reactive Oxygen Species / metabolism
  • Saccharomyces cerevisiae / drug effects*
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Stress, Physiological*
  • Trehalose / metabolism

Substances

  • Reactive Oxygen Species
  • Saccharomyces cerevisiae Proteins
  • Adenosine Triphosphate
  • Glycogen
  • Methyl Methanesulfonate
  • Trehalose
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Pyruvate Kinase
  • Glucose
  • Glycerol