A core erythroid transcriptional network is repressed by a master regulator of myelo-lymphoid differentiation

Proc Natl Acad Sci U S A. 2012 Mar 6;109(10):3832-7. doi: 10.1073/pnas.1121019109. Epub 2012 Feb 22.

Abstract

Two mechanisms that play important roles in cell fate decisions are control of a "core transcriptional network" and repression of alternative transcriptional programs by antagonizing transcription factors. Whether these two mechanisms operate together is not known. Here we report that GATA-1, SCL, and Klf1 form an erythroid core transcriptional network by co-occupying >300 genes. Importantly, we find that PU.1, a negative regulator of terminal erythroid differentiation, is a highly integrated component of this network. GATA-1, SCL, and Klf1 act to promote, whereas PU.1 represses expression of many of the core network genes. PU.1 also represses the genes encoding GATA-1, SCL, Klf1, and important GATA-1 cofactors. Conversely, in addition to repressing PU.1 expression, GATA-1 also binds to and represses >100 PU.1 myelo-lymphoid gene targets in erythroid progenitors. Mathematical modeling further supports that this dual mechanism of repressing both the opposing upstream activator and its downstream targets provides a synergistic, robust mechanism for lineage specification. Taken together, these results amalgamate two key developmental principles, namely, regulation of a core transcriptional network and repression of an alternative transcriptional program, thereby enhancing our understanding of the mechanisms that establish cellular identity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Differentiation
  • Chromatin Immunoprecipitation
  • Erythrocytes
  • Erythroid-Specific DNA-Binding Factors / metabolism*
  • GATA1 Transcription Factor / metabolism
  • Gene Expression Regulation
  • Kruppel-Like Transcription Factors / metabolism
  • Lymphocytes / cytology*
  • Mice
  • Models, Theoretical
  • Proto-Oncogene Proteins / metabolism
  • Stem Cells / cytology
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Trans-Activators / metabolism
  • Transcription, Genetic

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Erythroid-Specific DNA-Binding Factors
  • GATA1 Transcription Factor
  • Gata1 protein, mouse
  • Kruppel-Like Transcription Factors
  • Proto-Oncogene Proteins
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Tal1 protein, mouse
  • Trans-Activators
  • erythroid Kruppel-like factor
  • proto-oncogene protein Spi-1

Associated data

  • GEO/GSE35385