The Swi/Snf chromatin remodeling complex is required for ribosomal DNA and telomeric silencing in Saccharomyces cerevisiae

Mol Cell Biol. 2004 Sep;24(18):8227-35. doi: 10.1128/MCB.24.18.8227-8235.2004.

Abstract

The Swi/Snf chromatin remodeling complex has been previously demonstrated to be required for transcriptional activation and repression of a subset of genes in Saccharomyces cerevisiae. In this work we demonstrate that Swi/Snf is also required for repression of RNA polymerase II-dependent transcription in the ribosomal DNA (rDNA) locus (rDNA silencing). This repression appears to be independent of both Sir2 and Set1, two factors known to be required for rDNA silencing. In contrast to many other rDNA silencing mutants that have elevated levels of rDNA recombination, snf2Delta mutants have a significantly decreased level of rDNA recombination. Additional studies have demonstrated that Swi/Snf is also required for silencing of genes near telomeres while having no detectable effect on silencing of HML or HMR.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases
  • Base Sequence
  • Chromatin Assembly and Disassembly
  • DNA, Fungal / genetics
  • DNA, Ribosomal / genetics
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Gene Silencing
  • Genes, Fungal
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism
  • Histone-Lysine N-Methyltransferase
  • Mutagenesis
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism*
  • Promoter Regions, Genetic
  • Recombination, Genetic
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae / genetics
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae / metabolism
  • Sirtuin 2
  • Sirtuins / genetics
  • Sirtuins / metabolism
  • Telomere / genetics
  • Telomere / metabolism
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • beta-Fructofuranosidase / genetics

Substances

  • DNA, Fungal
  • DNA, Ribosomal
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Saccharomyces cerevisiae Proteins
  • Silent Information Regulator Proteins, Saccharomyces cerevisiae
  • Trans-Activators
  • Transcription Factors
  • Histone-Lysine N-Methyltransferase
  • SET1 protein, S cerevisiae
  • SUC2 protein, S cerevisiae
  • beta-Fructofuranosidase
  • SIR2 protein, S cerevisiae
  • Sirtuin 2
  • Sirtuins
  • Histone Deacetylases
  • Adenosine Triphosphatases
  • SNF2 protein, S cerevisiae