Activation mechanisms of the Hippo kinase signaling cascade

Sung Jun Bae, Xuelian Luo

Research output: Contribution to journalReview article

2 Citations (Scopus)

Abstract

First discovered two decades ago through genetic screens in Drosophila, the Hippo pathway has been shown to be conserved in metazoans and controls organ size and tissue homeostasis through regulating the balance between cell proliferation and apoptosis. Dysregulation of the Hippo pathway leads to aberrant tissue growth and tumorigenesis. Extensive studies in Drosophila and mammals have identified the core components of Hippo signaling, which form a central kinase cascade to ultimately control gene expression. Here, we review recent structural, biochemical, and cellular studies that have revealed intricate phosphorylation-dependent mechanisms in regulating the formation and activation of the core kinase complex in the Hippo pathway. These studies have established the dimerization-mediated activation of the Hippo kinase (mammalian Ste20-like 1 and 2 (MST1/2) in mammals), the dynamic scaffolding and allosteric roles of adaptor proteins in downstream kinase activation, and the importance of multisite linker autophosphorylation by Hippo and MST1/2 in fine-tuning the signaling strength and robustness of the Hippo pathway. We highlight the gaps in our knowledge in this field that will require further mechanistic studies.

Original languageEnglish (US)
Article numberBSR20171469
JournalBioscience Reports
Volume38
Issue number4
DOIs
StatePublished - Aug 29 2018

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Phosphotransferases
Chemical activation
Mammals
Drosophila
Tissue homeostasis
Choristoma
Phosphorylation
Organ Size
Dimerization
Cell proliferation
Gene expression
Carcinogenesis
Homeostasis
Tuning
Cell Proliferation
Tissue
Apoptosis
Gene Expression
Growth
Proteins

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Activation mechanisms of the Hippo kinase signaling cascade. / Bae, Sung Jun; Luo, Xuelian.

In: Bioscience Reports, Vol. 38, No. 4, BSR20171469, 29.08.2018.

Research output: Contribution to journalReview article

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