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

Cell Rep

The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark; Novo Nordisk Foundation Center for Stem Cell Bology, DanStem, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark. Electronic address:

Published: May 2018

AI Article Synopsis

  • Transcription factors PU.1 and CEBPA are crucial for coordinating enhancer activity during the differentiation of granulocytic-monocytic cells into myeloid cells, but their specific roles are not fully understood.
  • The study analyzes changes in enhancer dynamics, transcription factor binding, and gene expression in mouse models to reveal how PU.1 and CEBPA regulate these processes differently, with CEBPA showing a pioneering role in enhancer accessibility.
  • Findings indicate that CEBPA influences PU.1 levels and is essential for proper differentiation, as its absence leads to an early block in the differentiation process, highlighting their collaborative roles in GM-lineage development.

Article 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.

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Source
http://dx.doi.org/10.1016/j.celrep.2018.05.012DOI Listing

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