Chemomechanical regulation of EZH2 localization controls epithelial-mesenchymal transition

J Cell Sci. 2024 Nov 15;137(22):jcs262190. doi: 10.1242/jcs.262190. Epub 2024 Nov 25.

Abstract

The methyltransferase enhancer of zeste homolog 2 (EZH2) regulates gene expression, and aberrant EZH2 expression and signaling can drive fibrosis and cancer. However, it is not clear how chemical and mechanical signals are integrated to regulate EZH2 and gene expression. We show that culture of cells on stiff matrices in concert with transforming growth factor (TGF)-β1 promotes nuclear localization of EZH2 and an increase in the levels of the corresponding histone modification, H3K27me3, thereby regulating gene expression. EZH2 activity and expression are required for TGFβ1- and stiffness-induced increases in H3K27me3 levels as well as for morphological and gene expression changes associated with epithelial-mesenchymal transition (EMT). Inhibition of Rho associated kinase (ROCK) proteins or myosin II signaling attenuates TGFβ1-induced nuclear localization of EZH2 and decreases H3K27me3 levels in cells cultured on stiff substrata, suggesting that cellular contractility, in concert with a major cancer signaling regulator TGFβ1, modulates EZH2 subcellular localization. These findings provide a contractility-dependent mechanism by which matrix stiffness and TGFβ1 together mediate EZH2 signaling to promote EMT.

Keywords: Cell contractility; Histone modification; Matrix stiffness; Methyltransferase; Polycomb repressive complex; Transforming growth factor.

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Enhancer of Zeste Homolog 2 Protein* / genetics
  • Enhancer of Zeste Homolog 2 Protein* / metabolism
  • Epithelial-Mesenchymal Transition*
  • Histones / metabolism
  • Humans
  • Myosin Type II / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta1* / metabolism
  • rho-Associated Kinases / metabolism

Substances

  • Enhancer of Zeste Homolog 2 Protein
  • Transforming Growth Factor beta1
  • EZH2 protein, human
  • Histones
  • rho-Associated Kinases
  • Myosin Type II