Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state

Cell. 1997 Aug 22;90(4):607-14. doi: 10.1016/s0092-8674(00)80522-x.

Abstract

TFIID comprises the TATA box-binding protein and a set of highly conserved associated factors (TAF(II)s). yTAF(II)145, the core subunit of the yeast TAF(II) complex, is dispensable for transcription of most yeast genes but specifically required for progression through G1/S. Here we show that transcription of G1 and certain B-type cyclin genes is dependent upon yTAF(II)145. At high cell density or following nutrient deprivation, yeast cells cease division, enter a G0-like state, and terminate transcription of most genes. In this stationary phase, we find that the levels of yTAF(II)145, several other yTAF(II)s, and TBP are drastically reduced. Collectively, our results indicate that yTAF(II)145 and other TFIID components have a specialized role in transcriptional regulation of cell cycle progression and growth control.

Publication types

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

MeSH terms

  • CDC28 Protein Kinase, S cerevisiae / metabolism
  • Cyclin B*
  • Cyclin G
  • Cyclins / genetics*
  • DNA-Binding Proteins / physiology*
  • Fungal Proteins / genetics
  • Fungal Proteins / physiology*
  • G1 Phase
  • Gene Expression Regulation, Fungal
  • Promoter Regions, Genetic
  • RNA Polymerase II / metabolism
  • S Phase
  • Saccharomyces cerevisiae / cytology
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae Proteins*
  • TATA-Binding Protein Associated Factors*
  • Transcription Factor TFIID*
  • Transcription Factors / physiology*
  • Transcription, Genetic*

Substances

  • CLB5 protein, S cerevisiae
  • CLB6 protein, S cerevisiae
  • Cyclin B
  • Cyclin G
  • Cyclins
  • DNA-Binding Proteins
  • Fungal Proteins
  • Saccharomyces cerevisiae Proteins
  • TAF1 protein, S cerevisiae
  • TATA-Binding Protein Associated Factors
  • Transcription Factor TFIID
  • Transcription Factors
  • CDC28 Protein Kinase, S cerevisiae
  • RNA Polymerase II