Metastasis-associated protein 1/histone deacetylase 4-nucleosome remodeling and deacetylase complex regulates phosphatase and tensin homolog gene expression and function

J Biol Chem. 2012 Aug 10;287(33):27843-50. doi: 10.1074/jbc.M112.348474. Epub 2012 Jun 14.

Abstract

Metastasis-associated protein 1 (MTA1) is widely overexpressed in human cancers and is associated with malignant phenotypic changes contributing to morbidity in the associated diseases. Here we discovered for the first time that MTA1, a master chromatin modifier, transcriptionally represses the expression of phosphatase and tensin homolog (PTEN), a tumor suppressor gene, by recruiting class II histone deacetylase 4 (HDAC4) along with the transcription factor Yin-Yang 1 (YY1) onto the PTEN promoter. We also found evidence of an inverse correlation between the expression levels of MTA1 and PTEN in physiologically relevant breast cancer microarray datasets. We found that MTA1 up-regulation leads to a decreased expression of PTEN protein and stimulation of PI3K as well as phosphorylation of its signaling targets. Accordingly, selective down-regulation of MTA1 in breast cancer cells increases PTEN expression and inhibits stimulation of the PI3K/AKT signaling. Collectively, these findings provide a mechanistic role for MTA1 in transcriptional repression of PTEN, leading to modulation of the resulting signaling pathways.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Gene Expression Regulation, Enzymologic / physiology*
  • HeLa Cells
  • Histone Deacetylases / genetics
  • Histone Deacetylases / metabolism*
  • Humans
  • Mice
  • Multienzyme Complexes / genetics
  • Multienzyme Complexes / metabolism*
  • PTEN Phosphohydrolase / biosynthesis*
  • PTEN Phosphohydrolase / genetics
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Promoter Regions, Genetic / physiology
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Signal Transduction / physiology
  • Trans-Activators
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic / physiology
  • Up-Regulation / physiology
  • YY1 Transcription Factor / genetics
  • YY1 Transcription Factor / metabolism

Substances

  • MTA1 protein, human
  • Mta1 protein, mouse
  • Multienzyme Complexes
  • Repressor Proteins
  • Trans-Activators
  • Transcription Factors
  • YY1 Transcription Factor
  • YY1 protein, human
  • PTEN Phosphohydrolase
  • PTEN protein, human
  • Pten protein, mouse
  • HDAC4 protein, human
  • Hdac5 protein, mouse
  • Histone Deacetylases