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

Author:

Guo Pengfei1ORCID,Li Bing1,Dong Wei2ORCID,Zhou Huabin3ORCID,Wang Li1,Su Ting1,Carl Christopher1,Zheng Yonggang1ORCID,Hong Yang2ORCID,Deng Hua1ORCID,Pan Duojia1ORCID

Affiliation:

1. Department of Physiology, Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

2. Department of Cell Biology, University of Pittsburgh, Pittsburgh, PA 15261, USA.

3. Department of Biophysics, Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

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