TY - JOUR
T1 - XSpatial organization of hippo signaling at the plasma membrane mediated by the tumor suppressor merlin/NF2
AU - Yin, Feng
AU - Yu, Jianzhong
AU - Zheng, Yonggang
AU - Chen, Qian
AU - Zhang, Nailing
AU - Pan, Duojia
N1 - Funding Information:
We thank Dr. Rick Fehon for the gift of anti-Mer antibody, Dr. Marco Giovannini for providing FC-912 and FH-912 Schwann cells, and Dr. Vijaya Ramesh for advice on GST-NF2 purification. This study was supported in part by grants from the National Institutes of Health (EY015708) and Department of Defense (NF093145). D.P. is an investigator of the Howard Hughes Medical Institute.
PY - 2013/9/12
Y1 - 2013/9/12
N2 - 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.
AB - 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.
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U2 - 10.1016/j.cell.2013.08.025
DO - 10.1016/j.cell.2013.08.025
M3 - Article
C2 - 24012335
AN - SCOPUS:84884291548
SN - 0092-8674
VL - 154
SP - 1342
JO - Cell
JF - Cell
IS - 6
ER -