Mechanism of hsp70i gene bookmarking

Science. 2005 Jan 21;307(5708):421-3. doi: 10.1126/science.1106478.

Abstract

In contrast to most genomic DNA in mitotic cells, the promoter regions of some genes, such as the stress-inducible hsp70i gene that codes for a heat shock protein, remain uncompacted, a phenomenon called bookmarking. Here we show that hsp70i bookmarking is mediated by a transcription factor called HSF2, which binds this promoter in mitotic cells, recruits protein phosphatase 2A, and interacts with the CAP-G subunit of the condensin enzyme to promote efficient dephosphorylation and inactivation of condensin complexes in the vicinity, thereby preventing compaction at this site. Blocking HSF2-mediated bookmarking by HSF2 RNA interference decreases hsp70i induction and survival of stressed cells in the G1 phase, which demonstrates the biological importance of gene bookmarking.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation*
  • HSP70 Heat-Shock Proteins / genetics*
  • HeLa Cells
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism*
  • Hot Temperature
  • Humans
  • Immunoprecipitation
  • Interphase
  • Mitosis*
  • Multiprotein Complexes
  • Phosphoprotein Phosphatases / metabolism
  • Phosphorylation
  • Promoter Regions, Genetic*
  • Protein Binding
  • Protein Phosphatase 2
  • Protein Subunits / metabolism
  • RNA Interference
  • RNA, Small Interfering / pharmacology
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Two-Hybrid System Techniques

Substances

  • DNA-Binding Proteins
  • HSP70 Heat-Shock Proteins
  • Heat-Shock Proteins
  • Multiprotein Complexes
  • Protein Subunits
  • RNA, Small Interfering
  • Transcription Factors
  • condensin complexes
  • HSF2 protein, human
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2
  • Adenosine Triphosphatases