ETO2-GLIS2 Hijacks Transcriptional Complexes to Drive Cellular Identity and Self-Renewal in Pediatric Acute Megakaryoblastic Leukemia

Cancer Cell. 2017 Mar 13;31(3):452-465. doi: 10.1016/j.ccell.2017.02.006.

Abstract

Chimeric transcription factors are a hallmark of human leukemia, but the molecular mechanisms by which they block differentiation and promote aberrant self-renewal remain unclear. Here, we demonstrate that the ETO2-GLIS2 fusion oncoprotein, which is found in aggressive acute megakaryoblastic leukemia, confers megakaryocytic identity via the GLIS2 moiety while both ETO2 and GLIS2 domains are required to drive increased self-renewal properties. ETO2-GLIS2 directly binds DNA to control transcription of associated genes by upregulation of expression and interaction with the ETS-related ERG protein at enhancer elements. Importantly, specific interference with ETO2-GLIS2 oligomerization reverses the transcriptional activation at enhancers and promotes megakaryocytic differentiation, providing a relevant interface to target in this poor-prognosis pediatric leukemia.

Keywords: AMKL; CBFA2T3; CRISPR; ChIP; ERG; GLIS; enhancer; leukemia; pediatric; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Child
  • Enhancer Elements, Genetic
  • GATA1 Transcription Factor / genetics
  • Humans
  • Leukemia, Megakaryoblastic, Acute / pathology*
  • Mice
  • Oncogene Proteins, Fusion / chemistry
  • Oncogene Proteins, Fusion / physiology*
  • Transcriptional Activation*
  • Transcriptional Regulator ERG / physiology

Substances

  • ERG protein, human
  • ETO2-GLIS2 fusion protein, human
  • GATA1 Transcription Factor
  • GATA1 protein, human
  • Oncogene Proteins, Fusion
  • Transcriptional Regulator ERG