SSX2 is a novel DNA-binding protein that antagonizes polycomb group body formation and gene repression

Nucleic Acids Res. 2014 Oct;42(18):11433-46. doi: 10.1093/nar/gku852. Epub 2014 Sep 23.

Abstract

Polycomb group (PcG) complexes regulate cellular identity through epigenetic programming of chromatin. Here, we show that SSX2, a germline-specific protein ectopically expressed in melanoma and other types of human cancers, is a chromatin-associated protein that antagonizes BMI1 and EZH2 PcG body formation and derepresses PcG target genes. SSX2 further negatively regulates the level of the PcG-associated histone mark H3K27me3 in melanoma cells, and there is a clear inverse correlation between SSX2/3 expression and H3K27me3 in spermatogenesis. However, SSX2 does not affect the overall composition and stability of PcG complexes, and there is no direct concordance between SSX2 and BMI1/H3K27me3 presence at regulated genes. This suggests that SSX2 antagonizes PcG function through an indirect mechanism, such as modulation of chromatin structure. SSX2 binds double-stranded DNA in a sequence non-specific manner in agreement with the observed widespread association with chromatin. Our results implicate SSX2 in regulation of chromatin structure and function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Chromatin / metabolism
  • DNA / chemistry
  • DNA / metabolism
  • Enhancer of Zeste Homolog 2 Protein
  • Gene Expression Regulation, Neoplastic*
  • Histones / metabolism
  • Humans
  • Melanoma / genetics
  • Melanoma / metabolism
  • Neoplasm Proteins / metabolism*
  • Neoplasm Proteins / physiology
  • Polycomb Repressive Complex 1 / antagonists & inhibitors
  • Polycomb Repressive Complex 1 / chemistry
  • Polycomb Repressive Complex 1 / metabolism
  • Polycomb Repressive Complex 2 / antagonists & inhibitors
  • Polycomb Repressive Complex 2 / chemistry
  • Polycomb Repressive Complex 2 / metabolism
  • Polycomb-Group Proteins / antagonists & inhibitors*
  • Repressor Proteins / metabolism*
  • Repressor Proteins / physiology
  • Spermatogenesis

Substances

  • BMI1 protein, human
  • Chromatin
  • Histones
  • Neoplasm Proteins
  • Polycomb-Group Proteins
  • Repressor Proteins
  • synovial sarcoma X breakpoint proteins
  • DNA
  • EZH2 protein, human
  • Enhancer of Zeste Homolog 2 Protein
  • Polycomb Repressive Complex 2
  • Polycomb Repressive Complex 1