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Render Timestamp:
3/28/2025, 6:30:46 AM EDT
3/28/2025, 10:30:46 AM UTC
Commit: 461ca8d8fe5b1efd4c01fc87e5b5eb592e2d154a
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Hippo Signaling

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SCF βTrCP YAP/TAZDegradation AMOT Hippo Signaling RTK RTK Crb YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ AMOT Crb AMOT AMOT PTPN14 PTPN14 FRMD6 FRMD6 Destruction Complex aPKC α-Catenin α-Catenin 14-3-3 14-3-3 14-3-3 Ajuba/ LIM YAP/TAZ ON-State (YAP/TAZ Inactive) OFF-State (YAP/TAZ Active) Cytoplasm Nucleus Cytoplasm Nucleus Target Gene Transcription YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ LATS1/2 MST1/2 YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ YAP/TAZ TEADs ERBB4 EGR-1 MOB1 SAV1 MAPK AMPK TAO1-3 MAPK4Ks Rho Rho TBX5 SMADs RUNX TEADs ERBB4 PRP4K EGR-1 TBX5 SMADs RUNX GPCRSignaling Growth Factor Signaling ECM GPCRSignaling Integrins ECM/Mechanical Signaling Integrins ZO-2 Adherens Junction Tight Junction ZO-2 Hippo Kinase Core LATS1/2 MST1/2 MOB1 SAV1 Hippo Kinase Core Ajuba/ LIM Adherens Junction Tight Junction NF2 NF2 YES1 ABL NF2 NF2 Ras PI3K PDK1 MARK4 RASSF STRIPAK SLMAP STRIPAK SLMAP KIBRA KIBRA SRC SAV1 NF2 PAR CK1 12/13 q/11 i/o Actin Cytoskeleton S YAP/TAZSequestration YAP/TAZSequestration Actin Cytoskeleton rev. 02/20/20 No Contact Inhibition Contact Inhibition

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Hippo signaling is an evolutionarily conserved pathway that controls organ size by regulating cell proliferation, apoptosis, and stem cell self renewal. In addition, dysregulation of the Hippo pathway contributes to cancer development. Core to the Hippo pathway is a kinase cascade, wherein Mst1/2 (ortholog of Drosophila Hippo) kinases and SAV1 form a complex to phosphorylate and activate LATS1/2. LATS1/2 kinases in turn phosphorylate and inhibit the transcription co-activators YAP and TAZ, two major downstream effectors of the Hippo pathway. When dephosphorylated, YAP/TAZ translocate into the nucleus and interact with TEAD1-4 and other transcription factors to induce expression of genes that promote cell proliferation and inhibit apoptosis. The Hippo pathway is involved in cell contact inhibition, and its activity is regulated at multiple levels: Mst1/2 and LATS1/2 are regulated by upstream molecules such as Merlin, KIBRA, RASSFs, and Ajuba; 14-3-3, α-catenin, AMOT, and ZO-2 retain YAP/TAZ in the cytoplasm, adherens junctions, or tight junctions by binding; Mst1/2 and YAP/TAZ phosphorylation and activity are modulated by phosphatases; Lats1/2 and YAP/TAZ stability are regulated by protein ubiquitination; and LATS1/2 activity is also regulated by the cytoskeleton. Despite extensive study of the Hippo pathway in the past decade, the exact nature of extracellular signals and membrane receptors regulating the Hippo pathway remains elusive.

Selected Reviews:

We would like to thank Prof. Kun-Liang Guan, University of California, San Diego, CA for contributing to this diagram.

created November 2010

revised September 2016