PI4P-mediated solid-like Merlin condensates orchestrate Hippo pathway regulation

Science. 2024 Aug 9;385(6709):eadf4478. doi: 10.1126/science.adf4478. Epub 2024 Aug 9.

Abstract

Despite recent studies implicating liquid-like biomolecular condensates in diverse cellular processes, many biomolecular condensates exist in a solid-like state, and their function and regulation are less understood. We show that the tumor suppressor Merlin, an upstream regulator of the Hippo pathway, localizes to both cell junctions and medial apical cortex in Drosophila epithelia, with the latter forming solid-like condensates that activate Hippo signaling. Merlin condensation required phosphatidylinositol-4-phosphate (PI4P)-mediated plasma membrane targeting and was antagonistically controlled by Pez and cytoskeletal tension through plasma membrane PI4P regulation. The solid-like material properties of Merlin condensates are essential for physiological function and protect the condensates against external perturbations. Collectively, these findings uncover an essential role for solid-like condensates in normal physiology and reveal regulatory mechanisms for their formation and disassembly.

MeSH terms

  • Animals
  • Biomolecular Condensates* / metabolism
  • Cell Membrane / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / metabolism
  • Hippo Signaling Pathway*
  • Intercellular Junctions / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Neurofibromin 2* / genetics
  • Neurofibromin 2* / metabolism
  • Phosphatidylinositol Phosphates / metabolism
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • Drosophila Proteins
  • hpo protein, Drosophila
  • Intracellular Signaling Peptides and Proteins
  • merlin, Drosophila
  • Neurofibromin 2
  • phosphatidylinositol 4-phosphate
  • Phosphatidylinositol Phosphates
  • Protein Serine-Threonine Kinases