Regulation of CBP and Tip60 coordinates histone acetylation at local and global levels during Ras-induced transformation

Carcinogenesis. 2014 Oct;35(10):2194-202. doi: 10.1093/carcin/bgu111. Epub 2014 May 22.

Abstract

Cell transformation is clearly linked to epigenetic changes. However, the role of the histone-modifying enzymes in this process is still poorly understood. In this study, we investigated the contribution of the histone acetyltransferase (HAT) enzymes to Ras-mediated transformation. Our results demonstrated that lysine acetyltransferase 5, also known as Tip60, facilitates histone acetylation of bulk chromatin in Ras-transformed cells. As a consequence, global H4 acetylation (H4K8ac and H4K12ac) increases in Ras-transformed cells, rendering a more decompacted chromatin than in parental cells. Furthermore, low levels of CREB-binding protein (CBP) lead to hypoacetylation of retinoblastoma 1 (Rb1) and cyclin-dependent kinase inhibitor 1B (Cdkn1b or p27Kip1) tumour suppressor gene promoters to facilitate Ras-mediated transformation. In agreement with these data, overexpression of Cbp counteracts Ras transforming capability in a HAT-dependent manner. Altogether our results indicate that CBP and Tip60 coordinate histone acetylation at both local and global levels to facilitate Ras-induced transformation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • CREB-Binding Protein / genetics
  • CREB-Binding Protein / metabolism*
  • Cell Transformation, Neoplastic / genetics*
  • Chromatin / metabolism
  • Chromatin / ultrastructure
  • Cyclin-Dependent Kinase Inhibitor p27 / genetics
  • Cyclin-Dependent Kinase Inhibitor p27 / metabolism
  • Genes, ras*
  • Histone Acetyltransferases / genetics
  • Histone Acetyltransferases / metabolism*
  • Histones / metabolism*
  • Lysine Acetyltransferase 5
  • Mice
  • NIH 3T3 Cells / pathology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Promoter Regions, Genetic
  • Signal Transduction
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*

Substances

  • Cdkn1b protein, mouse
  • Chromatin
  • Histones
  • Trans-Activators
  • Cyclin-Dependent Kinase Inhibitor p27
  • CREB-Binding Protein
  • Crebbp protein, mouse
  • Histone Acetyltransferases
  • Kat5 protein, mouse
  • Lysine Acetyltransferase 5
  • Phosphatidylinositol 3-Kinases