ETO2 coordinates cellular proliferation and differentiation during erythropoiesis

EMBO J. 2006 Jan 25;25(2):357-66. doi: 10.1038/sj.emboj.7600934. Epub 2006 Jan 12.


The passage from proliferation to terminal differentiation is critical for normal development and is often perturbed in malignancies. To define the molecular mechanisms that govern this process during erythropoiesis, we have used tagging/proteomics approaches and characterized protein complexes nucleated by TAL-1/SCL, a basic helix-loop-helix transcription factor that specifies the erythrocytic lineage. In addition to known TAL-1 partners, GATA-1, E2A, HEB, LMO2 and Ldb1, we identify the ETO2 repressor as a novel component recruited to TAL-1 complexes through interaction with E2A/HEB. Ectopic expression and siRNA knockdown experiments in hematopoietic progenitor cells show that ETO2 actively represses erythroid TAL-1 target genes and governs the expansion of erythroid progenitors. At the onset of erythroid differentiation, a change in the stoichiometry of ETO2 within the TAL-1 complex activates the expression of known erythroid-specific TAL-1 target genes and of Gfi-1b and p21(Cip), encoding two essential regulators of erythroid cell proliferation. These results suggest that the dynamics of ETO2 recruitment within nuclear complexes couple cell proliferation to cell differentiation and determine the onset of terminal erythroid maturation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism*
  • Cell Differentiation / physiology*
  • Cell Line
  • Cell Proliferation*
  • Chromatin Immunoprecipitation
  • Erythropoiesis / physiology*
  • Flow Cytometry
  • Gene Expression Regulation, Developmental*
  • Green Fluorescent Proteins
  • Hematopoietic Stem Cells / metabolism
  • Immunoblotting
  • Immunoprecipitation
  • Mice
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology*
  • Proto-Oncogene Proteins / metabolism*
  • RNA, Small Interfering / metabolism
  • Repressor Proteins
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*


  • Basic Helix-Loop-Helix Transcription Factors
  • Cbfa2t3 protein, mouse
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • Repressor Proteins
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Tal1 protein, mouse
  • Transcription Factors
  • Green Fluorescent Proteins