Physical and functional interaction among Irf8 enhancers during dendritic cell differentiation

Cell Rep. 2024 Apr 23;43(4):114107. doi: 10.1016/j.celrep.2024.114107. Epub 2024 Apr 12.

Abstract

The production of type 1 conventional dendritic cells (cDC1s) requires high expression of the transcription factor IRF8. Three enhancers at the Irf8 3' region function in a differentiation stage-specific manner. However, whether and how these enhancers interact physically and functionally remains unclear. Here, we show that the Irf8 3' enhancers directly interact with each other and contact the Irf8 gene body during cDC1 differentiation. The +56 kb enhancer, which functions from multipotent progenitor stages, activates the other 3' enhancers through an IRF8-dependent transcription factor program, that is, in trans. Then, the +32 kb enhancer, which operates in cDC1-committed cells, reversely acts in cis on the other 3' enhancers to maintain the high expression of Irf8. Indeed, mice with compound heterozygous deletion of the +56 and +32 kb enhancers are unable to generate cDC1s. These results illustrate how multiple enhancers cooperate to induce a lineage-determining transcription factor gene during cell differentiation.

Keywords: CP: Immunology; dendritic cell; enhancer; higher-order chromatin structure; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation*
  • Dendritic Cells* / cytology
  • Dendritic Cells* / metabolism
  • Enhancer Elements, Genetic* / genetics
  • Interferon Regulatory Factors* / genetics
  • Interferon Regulatory Factors* / metabolism
  • Mice
  • Mice, Inbred C57BL

Substances

  • Interferon Regulatory Factors
  • interferon regulatory factor-8