Global changes in chromatin accessibility and transcription following ATRX inactivation in human cancer cells

FEBS Lett. 2020 Jan;594(1):67-78. doi: 10.1002/1873-3468.13549. Epub 2019 Aug 8.

Abstract

α-Tthalassemia mental retardation X-linked (ATRX) is a chromatin remodeler frequently mutated in many cancers. Despite the binding pattern of ATRX in heterochromatin, ATRX-mediated epigenomic changes in cancer cells have not been profiled, especially for the heterochromatin regions. Here, we profiled genome-wide maps of chromatin accessibility in ATRX-intact and ATRX-null human cancer cells. We found extensive changes in chromatin accessibility in both repetitive DNA regions and non-repetitive regulatory regions following ATRX loss. These changes are highly correlated with changes in transcription, which lead to alterations in cancer-related signalling pathways, such as upregulation of the TGF-β pathway and downregulation of the cadherin family of proteins. These findings indicate that ATRX deficiency induces epigenomic changes and promotes tumorigenesis through both genome instability and shifts in transcription.

Keywords: ATRX; ATAC-seq; TGF-β; heterochromatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cadherins / genetics
  • Cadherins / metabolism
  • Carcinogenesis / genetics
  • Cell Line, Tumor
  • Chromatin / chemistry
  • Chromatin / metabolism*
  • Chromatin Assembly and Disassembly*
  • Epigenesis, Genetic
  • Gene Expression Regulation, Neoplastic*
  • Genomic Instability
  • Humans
  • Regulatory Sequences, Nucleic Acid
  • Transcriptional Activation
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism
  • X-linked Nuclear Protein / genetics
  • X-linked Nuclear Protein / metabolism*

Substances

  • Cadherins
  • Chromatin
  • Transforming Growth Factor beta
  • X-linked Nuclear Protein