Bifurcation dynamics in lineage-commitment in bipotent progenitor cells

Dev Biol. 2007 May 15;305(2):695-713. doi: 10.1016/j.ydbio.2007.02.036. Epub 2007 Mar 3.


Lineage specification of multipotent progenitor cells is governed by a balance of lineage-affiliated transcription factors, such as GATA1 and PU.1, which regulate the choice between erythroid and myelomonocytic fates. But how ratios of lineage-determining transcription factors stabilize progenitor cells and resolve their indeterminacy to commit them to discrete, mutually exclusive fates remains unexplained. We used a simple model and experimental measurements to analyze the dynamics of a binary fate decision governed by a gene-circuit containing auto-stimulation and cross-inhibition, as embodied by the GATA1-PU.1 paradigm. This circuit generates stable attractors corresponding to erythroid and myelomonocytic fates, as well as an uncommitted metastable state characterized by coexpression of both regulators, explaining the phenomenon of "multilineage priming". GATA1 and PU.1 mRNA and transcriptome dynamics of differentiating progenitor cells confirm that commitment occurs in two stages, as suggested by the model: first, the progenitor state is destabilized in an almost symmetrical bifurcation event, resulting in a poised state at the boundary between the two lineage-specific attractors; second, the cell is driven to the respective, now accessible attractors. This minimal model captures fundamental features of binary cell fate decisions, uniting the concepts of stochastic (selective) and deterministic (instructive) regulation, and hence, may apply to a wider range of binary fate decision points.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Cell Differentiation / physiology*
  • Cell Line
  • Cell Lineage / physiology*
  • Erythroid Precursor Cells / cytology*
  • Erythroid Precursor Cells / metabolism
  • GATA1 Transcription Factor / physiology
  • Gene Expression Regulation, Developmental / physiology
  • Granulocyte Precursor Cells / cytology*
  • Granulocyte Precursor Cells / metabolism
  • Mice
  • Models, Biological*
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / metabolism
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins / genetics
  • Trans-Activators / biosynthesis
  • Trans-Activators / genetics


  • GATA1 Transcription Factor
  • Gata1 protein, mouse
  • Proto-Oncogene Proteins
  • Trans-Activators
  • proto-oncogene protein Spi-1