PTEN interacts with histone H1 and controls chromatin condensation

Cell Rep. 2014 Sep 25;8(6):2003-2014. doi: 10.1016/j.celrep.2014.08.008. Epub 2014 Sep 4.

Abstract

Chromatin organization and dynamics are integral to global gene transcription. Histone modification influences chromatin status and gene expression. PTEN plays multiple roles in tumor suppression, development, and metabolism. Here, we report on the interplay of PTEN, histone H1, and chromatin. We show that loss of PTEN leads to dissociation of histone H1 from chromatin and decondensation of chromatin. PTEN deletion also results in elevation of histone H4 acetylation at lysine 16, an epigenetic marker for chromatin activation. We found that PTEN and histone H1 physically interact through their C-terminal domains. Disruption of the PTEN C terminus promotes the chromatin association of MOF acetyltransferase and induces H4K16 acetylation. Hyperacetylation of H4K16 impairs the association of PTEN with histone H1, which constitutes regulatory feedback that may reduce chromatin stability. Our results demonstrate that PTEN controls chromatin condensation, thus influencing gene expression. We propose that PTEN regulates global gene transcription profiling through histones and chromatin remodeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Cell Line
  • Chromatin / metabolism*
  • Chromobox Protein Homolog 5
  • Chromosomal Proteins, Non-Histone / metabolism
  • Gene Expression Profiling
  • Histones / chemistry
  • Histones / genetics
  • Histones / metabolism*
  • Mice
  • PTEN Phosphohydrolase / deficiency
  • PTEN Phosphohydrolase / genetics
  • PTEN Phosphohydrolase / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Structure, Tertiary

Substances

  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • Histones
  • Chromobox Protein Homolog 5
  • PTEN Phosphohydrolase