The DEAD-box RNA helicase, Dhh1, functions in mating by regulating Ste12 translation in Saccharomyces cerevisiae

Biochem Biophys Res Commun. 2008 Mar 14;367(3):680-6. doi: 10.1016/j.bbrc.2007.12.169. Epub 2008 Jan 7.

Abstract

The DEAD-box RNA helicase, Dhh1, is a member of a highly conserved subfamily designated RCK/p54 helicases. Dhh1 functions as mRNA decapping activator, and is localized to discrete cytoplasmic foci known as processing bodies (P-bodies). Here, we describe the essential roles of Dhh1 in the yeast mating pathway. A dhh1 deletion mutation caused a significant decrease in the protein level of Ste12, a mating-specific transcription factor, resulting in severe mating defects. We examined the accumulation of Dhh1-GFP in P-bodies during mating. Following pheromone treatment, the P-body intensity and number increased in wild-type cells, while dhh1 mutant cells failed to show P-body formation. Both the mating and P-body phenotypes of dhh1 were suppressed by overexpression of STE12 or CAF20 encoding an eIF4E inhibitor. In wild-type cells, CAF20 overexpression led to an increased level of Ste12 protein as well as highly developed P-bodies. We propose that Dhh1 and Caf20 regulate the Ste12 protein expression and the Ste12 protein level is associated with P-body formation during mating.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / physiology*
  • Gene Expression Regulation, Fungal / physiology
  • Green Fluorescent Proteins / genetics
  • Mutagenesis, Site-Directed
  • Nuclear Cap-Binding Protein Complex / biosynthesis
  • Organelles / metabolism
  • Pheromones / pharmacology
  • Protein Biosynthesis / physiology
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / physiology
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / physiology*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Saccharomyces cerevisiae Proteins / physiology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Nuclear Cap-Binding Protein Complex
  • Pheromones
  • Recombinant Fusion Proteins
  • STE12 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Green Fluorescent Proteins
  • DHH1 protein, S cerevisiae
  • DEAD-box RNA Helicases