| Literature DB >> 29847803 |
Sachin Pundhir1, Felicia Kathrine Bratt Lauridsen2, Mikkel Bruhn Schuster2, Janus Schou Jakobsen2, Ying Ge2, Erwin Marten Schoof2, Nicolas Rapin1, Johannes Waage1, Marie Sigurd Hasemann2, Bo Torben Porse3.
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.Entities:
Keywords: CEBPA; PU.1; enhancer dynamics; myelopoiesis
Mesh:
Substances:
Year: 2018 PMID: 29847803 DOI: 10.1016/j.celrep.2018.05.012
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423