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

Pengfei Guo, Bing Li, Wei Dong, Huabin Zhou, Li Wang, Ting Su, Christopher Carl, Yonggang Zheng, Yang Hong, Hua Deng, Duojia Pan

2024Science34 citationsDOIOpen Access PDF

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.

Topics & Concepts

Merlin (protein)RegulatorCell biologyHippo signaling pathwaySuppressorFunction (biology)Upstream and downstream (DNA)BiologyChemistrySignal transductionUpstream (networking)GeneticsGeneComputer scienceComputer networkHippo pathway signaling and YAP/TAZRNA Research and SplicingCellular Mechanics and Interactions