PUBLICATION

AMP-Activated Protein Kinase Directly Phosphorylates and Destabilizes Hedgehog Pathway Transcription Factor GLI1 in Medulloblastoma

Authors
Li, Y.H., Luo, J., Mosley, Y.Y., Hedrick, V.E., Paul, L.N., Chang, J., Zhang, G., Wang, Y.K., Banko, M.R., Brunet, A., Kuang, S., Wu, J.L., Chang, C.J., Scott, M.P., Yang, J.Y.
ID
ZDB-PUB-170214-146
Date
2015
Source
Cell Reports   12: 599-609 (Journal)
Registered Authors
Wu, Jen-Leih, Zhang, GuangJun
Keywords
none
MeSH Terms
  • 3T3 Cells
  • AMP-Activated Protein Kinases/metabolism*
  • Amino Acid Sequence
  • Animals
  • Cell Line, Tumor
  • HEK293 Cells
  • Humans
  • Medulloblastoma/metabolism*
  • Mice
  • Molecular Sequence Data
  • Phosphorylation
  • Protein Processing, Post-Translational*
  • Protein Stability
  • Transcription Factors/chemistry
  • Transcription Factors/metabolism*
  • Zebrafish
  • Zinc Finger Protein GLI1
PubMed
26190112 Full text @ Cell Rep.
Abstract
The Hedgehog (Hh) pathway regulates cell differentiation and proliferation during development by controlling the Gli transcription factors. Cell fate decisions and progression toward organ and tissue maturity must be coordinated, and how an energy sensor regulates the Hh pathway is not clear. AMP-activated protein kinase (AMPK) is an important sensor of energy stores and controls protein synthesis and other energy-intensive processes. AMPK is directly responsive to intracellular AMP levels, inhibiting a wide range of cell activities if ATP is low and AMP is high. Thus, AMPK can affect development by influencing protein synthesis and other processes needed for growth and differentiation. Activation of AMPK reduces GLI1 protein levels and stability, thus blocking Sonic-hedgehog-induced transcriptional activity. AMPK phosphorylates GLI1 at serines 102 and 408 and threonine 1074. Mutation of these three sites into alanine prevents phosphorylation by AMPK. This leads to increased GLI1 protein stability, transcriptional activity, and oncogenic potency.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping