Spatial organization of Hippo signaling at the plasma membrane mediated by the tumor suppressor Merlin/NF2.
Although Merlin/NF2 was discovered two decades ago as a tumor suppressor underlying Neurofibromatosis type II, its precise molecular mechanism remains poorly understood. Recent studies in Drosophila revealed a potential link between Merlin and the Hippo pathway by placing Merlin genetically upstream of the kinase Hpo/Mst. In contrast to the commonly ... depicted linear model of Merlin functioning through Hpo/Mst, here we show that in both Drosophila and mammals, Merlin promotes downstream Hippo signaling without activating the intrinsic kinase activity of Hpo/Mst. Instead, Merlin directly binds and recruits the effector kinase Wts/Lats to the plasma membrane. Membrane recruitment, in turn, promotes Wts phosphorylation by the Hpo-Sav kinase complex. We further show that disruption of the actin cytoskeleton promotes Merlin-Wts interactions, which implicates Merlin in actin-mediated regulation of Hippo signaling. Our findings elucidate an important molecular function of Merlin and highlight the plasma membrane as a critical subcellular compartment for Hippo signal transduction.
Mesh Terms:
Amino Acid Sequence, Animals, Biological Evolution, Cell Membrane, Cytoskeleton, Drosophila Proteins, Drosophila melanogaster, Intracellular Signaling Peptides and Proteins, Mice, Molecular Sequence Data, Neurofibromin 2, Protein-Serine-Threonine Kinases, Sequence Alignment, Signal Transduction
Amino Acid Sequence, Animals, Biological Evolution, Cell Membrane, Cytoskeleton, Drosophila Proteins, Drosophila melanogaster, Intracellular Signaling Peptides and Proteins, Mice, Molecular Sequence Data, Neurofibromin 2, Protein-Serine-Threonine Kinases, Sequence Alignment, Signal Transduction
Cell
Date: Sep. 12, 2013
PubMed ID: 24012335
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