Maf1 is involved in coupling carbon metabolism to RNA polymerase III transcription

Mol Cell Biol. 2007 Nov;27(21):7693-702. doi: 10.1128/MCB.01051-07. Epub 2007 Sep 4.

Abstract

RNA polymerase III (Pol III) produces essential components of the biosynthetic machinery, and therefore its activity is tightly coupled with cell growth and metabolism. In the yeast Saccharomyces cerevisiae, Maf1 is the only known global and direct Pol III transcription repressor which mediates numerous stress signals. Here we demonstrate that transcription regulation by Maf1 is not limited to stress but is important for the switch between fermentation and respiration. Under respiratory conditions, Maf1 is activated by dephosphorylation and imported into the nucleus. The transition from a nonfermentable carbon source to that of glucose induces Maf1 phosphorylation and its relocation to the cytoplasm. The absence of Maf1-mediated control of tRNA synthesis impairs cell viability in nonfermentable carbon sources. The respiratory phenotype of maf1-Delta allowed genetic suppression studies to dissect the mechanism of Maf1 action on the Pol III transcription apparatus. Moreover, in cells grown in a nonfermentable carbon source, Maf1 regulates the levels of different tRNAs to various extents. The differences in regulation may contribute to the physiological role of Maf1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Carbon / metabolism*
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Fermentation / drug effects
  • Gene Expression Regulation, Fungal / drug effects
  • Genes, Fungal
  • Glucose / pharmacology
  • Molecular Sequence Data
  • Mutation / genetics
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Phosphorylation / drug effects
  • Protein Subunits / metabolism
  • RNA Polymerase III / chemistry
  • RNA Polymerase III / genetics*
  • RNA, Transfer / metabolism
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / enzymology*
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Subcellular Fractions / metabolism
  • Suppression, Genetic / drug effects
  • Transcription Factors / metabolism*
  • Transcription, Genetic* / drug effects
  • Up-Regulation / drug effects
  • Up-Regulation / genetics

Substances

  • MAF1 protein, S cerevisiae
  • Protein Subunits
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Carbon
  • RNA, Transfer
  • Cyclic AMP-Dependent Protein Kinases
  • RNA Polymerase III
  • Glucose