Enhancer and Transcription Factor Dynamics during Myeloid Differentiation Reveal an Early Differentiation Block in Cebpa null Progenitors

Cell Rep. 2018 May 29;23(9):2744-2757. doi: 10.1016/j.celrep.2018.05.012.

Abstract

Transcription factors PU.1 and CEBPA are required for the proper coordination of enhancer activity during granulocytic-monocytic (GM) lineage differentiation to form myeloid cells. However, precisely how these factors control the chronology of enhancer establishment during differentiation is not known. Through integrated analyses of enhancer dynamics, transcription factor binding, and proximal gene expression during successive stages of murine GM-lineage differentiation, we unravel the distinct kinetics by which PU.1 and CEBPA coordinate GM enhancer activity. We find no evidence of a pioneering function of PU.1 during late GM-lineage differentiation. Instead, we delineate a set of enhancers that gain accessibility in a CEBPA-dependent manner, suggesting a pioneering function of CEBPA. Analyses of Cebpa null bone marrow demonstrate that CEBPA controls PU.1 levels and, unexpectedly, that the loss of CEBPA results in an early differentiation block. Taken together, our data provide insights into how PU.1 and CEBPA functionally interact to drive GM-lineage differentiation.

Keywords: CEBPA; PU.1; enhancer dynamics; myelopoiesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • CCAAT-Enhancer-Binding Proteins / deficiency*
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Cell Differentiation / genetics*
  • Cell Line
  • Cell Lineage
  • Chromatin / metabolism
  • Enhancer Elements, Genetic / genetics*
  • Female
  • Gene Expression Regulation
  • Granulocytes / cytology
  • Granulocytes / metabolism
  • Mice
  • Monocytes / cytology
  • Monocytes / metabolism
  • Myeloid Cells / cytology*
  • Myeloid Cells / metabolism
  • Protein Binding
  • Proto-Oncogene Proteins / metabolism*
  • Trans-Activators / metabolism*

Substances

  • CCAAT-Enhancer-Binding Proteins
  • CEBPA protein, mouse
  • Chromatin
  • Proto-Oncogene Proteins
  • Trans-Activators
  • proto-oncogene protein Spi-1