Interactions between lineage-associated transcription factors govern haematopoietic progenitor states

EMBO J. 2020 Dec 15;39(24):e104983. doi: 10.15252/embj.2020104983. Epub 2020 Oct 26.

Abstract

Recent advances in molecular profiling provide descriptive datasets of complex differentiation landscapes including the haematopoietic system, but the molecular mechanisms defining progenitor states and lineage choice remain ill-defined. Here, we employed a cellular model of murine multipotent haematopoietic progenitors (Hoxb8-FL) to knock out 39 transcription factors (TFs) followed by RNA-Seq analysis, to functionally define a regulatory network of 16,992 regulator/target gene links. Focussed analysis of the subnetworks regulated by the B-lymphoid TF Ebf1 and T-lymphoid TF Gata3 revealed a surprising role in common activation of an early myeloid programme. Moreover, Gata3-mediated repression of Pax5 emerges as a mechanism to prevent precocious B-lymphoid differentiation, while Hox-mediated activation of Meis1 suppresses myeloid differentiation. To aid interpretation of large transcriptomics datasets, we also report a new method that visualises likely transitions that a progenitor will undergo following regulatory network perturbations. Taken together, this study reveals how molecular network wiring helps to establish a multipotent progenitor state, with experimental approaches and analysis tools applicable to dissecting a broad range of both normal and perturbed cellular differentiation landscapes.

Keywords: haematopoiesis; network; progenitors; scRNA-Seq; transcription factor.

Publication types

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

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Lineage / genetics
  • Cell Lineage / physiology*
  • Epigenomics
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Hematopoiesis
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic System / metabolism*
  • Mice
  • Myeloid Ecotropic Viral Integration Site 1 Protein / metabolism
  • PAX5 Transcription Factor / genetics
  • PAX5 Transcription Factor / metabolism
  • Precursor Cells, B-Lymphoid
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • GATA3 Transcription Factor
  • Gata3 protein, mouse
  • Meis1 protein, mouse
  • Myeloid Ecotropic Viral Integration Site 1 Protein
  • PAX5 Transcription Factor
  • Pax5 protein, mouse
  • Transcription Factors

Associated data

  • GEO/GSE146128