Snf1-dependent and Snf1-independent pathways of constitutive ADH2 expression in Saccharomyces cerevisiae

Genetics. 2006 Apr;172(4):2123-38. doi: 10.1534/genetics.105.048231. Epub 2006 Jan 16.

Abstract

The transcription factor Adr1 directly activates the expression of genes encoding enzymes in numerous pathways that are upregulated after the exhaustion of glucose in the yeast Saccharomyces cerevisiae. ADH2, encoding the alcohol dehydrogenase isozyme required for ethanol oxidation, is a highly glucose-repressed, Adr1-dependent gene. Using a genetic screen we isolated >100 mutants in 12 complementation groups that exhibit ADR1-dependent constitutive ADH2 expression on glucose. Temperature-sensitive alleles are present among the new constitutive mutants, indicating that essential genes play a role in ADH2 repression. Among the genes we cloned is MOT1, encoding a repressor that inhibits TBP binding to the promoter, thus linking glucose repression with TBP access to chromatin. Two genes encoding proteins involved in vacuolar function, FAB1 and VPS35, and CDC10, encoding a nonessential septin, were also uncovered in the search, suggesting that vacuolar function and the cytoskeleton have previously unknown roles in regulating gene expression. Constitutive activation of ADH2 expression by Adr1 is SNF1-dependent in a strain with a defective MOT1 gene, whereas deletion of SNF1 did not affect constitutive ADH2 expression in the mutants affecting vacuolar or septin function. Thus, the mutant search revealed previously unknown Snf1-dependent and -independent pathways of ADH2 expression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alcohol Dehydrogenase / chemistry
  • Alcohol Dehydrogenase / genetics*
  • Alleles
  • Chromatin / metabolism
  • Gene Deletion
  • Gene Expression Regulation, Fungal*
  • Genetic Complementation Test
  • Glucose / metabolism
  • Models, Genetic
  • Mutation
  • Plasmids / metabolism
  • Protein Serine-Threonine Kinases / genetics*
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins / genetics*
  • Up-Regulation

Substances

  • Chromatin
  • Saccharomyces cerevisiae Proteins
  • ADH2 protein, S cerevisiae
  • Alcohol Dehydrogenase
  • SNF1-related protein kinases
  • Protein Serine-Threonine Kinases
  • Glucose