Transcription factor antagonism regulates heterogeneity in embryonic stem cell states

Mol Cell. 2022 Dec 1;82(23):4410-4427.e12. doi: 10.1016/j.molcel.2022.10.022. Epub 2022 Nov 9.

Abstract

Gene expression heterogeneity underlies cell states and contributes to developmental robustness. While heterogeneity can arise from stochastic transcriptional processes, the extent to which it is regulated is unclear. Here, we characterize the regulatory program underlying heterogeneity in murine embryonic stem cell (mESC) states. We identify differentially active and transcribed enhancers (DATEs) across states. DATEs regulate differentially expressed genes and are distinguished by co-binding of transcription factors Klf4 and Zfp281. In contrast to other factors that interact in a positive feedback network stabilizing mESC cell-type identity, Klf4 and Zfp281 drive opposing transcriptional and chromatin programs. Abrogation of factor binding to DATEs dampens variation in gene expression, and factor loss alters kinetics of switching between states. These results show antagonism between factors at enhancers results in gene expression heterogeneity and formation of cell states, with implications for the generation of diverse cell types during development.

Keywords: Klf4; Zfp281; cell-to-cell variation; embryonic stem cell state; enhancer RNA; gene expression variation; transcription factors.

Publication types

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

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Chromatin / genetics
  • Chromatin / metabolism
  • Embryonic Stem Cells* / metabolism
  • Enhancer Elements, Genetic
  • Gene Expression Regulation
  • Mice
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism

Substances

  • Chromatin
  • Transcription Factors
  • Zfp281 protein, mouse
  • Klf4 protein, mouse