Mediator protein mutations that selectively abolish activated transcription

Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):67-72. doi: 10.1073/pnas.96.1.67.

Abstract

Deletion of any one of three subunits of the yeast Mediator of transcriptional regulation, Med2, Pgd1 (Hrs1), and Sin4, abolished activation by Gal4-VP16 in vitro. By contrast, other Mediator functions, stimulation of basal transcription and of TFIIH kinase activity, were unaffected. A different but overlapping Mediator subunit dependence was found for activation by Gcn4. The genetic requirements for activation in vivo were closely coincident with those in vitro. A whole genome expression profile of a Deltamed2 strain showed diminished transcription of a subset of inducible genes but only minor effects on "basal" transcription. These findings make an important connection between transcriptional activation in vitro and in vivo, and identify Mediator as a "global" transcriptional coactivator.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell-Free System
  • DNA-Binding Proteins*
  • Fungal Proteins / metabolism
  • Gene Deletion
  • Gene Expression Regulation, Fungal*
  • Models, Genetic
  • Mutation
  • Protein Kinases / metabolism
  • Saccharomyces cerevisiae Proteins*
  • Structure-Activity Relationship
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Transcription, Genetic*
  • Transcriptional Activation*
  • Yeasts / genetics

Substances

  • DNA-Binding Proteins
  • Fungal Proteins
  • Gal-VP16
  • Saccharomyces cerevisiae Proteins
  • Trans-Activators
  • Protein Kinases
  • carboxy-terminal domain kinase