Transcriptional repression by Tup1-Ssn6

Tania M. Malavé, Sharon Y.R. Dent

Research output: Contribution to journalArticlepeer-review

118 Scopus citations

Abstract

The Tup1-Ssn6 complex from budding yeast is one of the best studied corepressors and has served as a model for the study of similar corepressor complexes in higher eukaryotes. Tup1-Ssn6 represses multiple subsets of genes when recruited to promoters by sequence-specific DNA binding repressors. Tup1-Ssn6 mediated repression involves interactions among the corepressor and hypoacetylated histones, histone deacetylases, and the RNA transcriptional machinery. Nucleosome positioning is also involved in repression of a subset of Tup1-Ssn6 regulated genes. These findings highlight the importance of chromatin modification states in Tup1-Ssn6 mediated repression. Here we review the multiple mechanisms involved in repression and discuss Tup1-Ssn6 homolog functions in higher organisms. We also present a model for how repression by Tup1-Ssn6 may be established.

Original languageEnglish (US)
Pages (from-to)437-443
Number of pages7
JournalBiochemistry and Cell Biology
Volume84
Issue number4
DOIs
StatePublished - Aug 2006

Keywords

  • -Ssn6
  • Corepressor
  • Histone deacetylases and chromatin
  • Repression
  • Transcription
  • Tup

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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