AMP-Activated Protein Kinase Directly Phosphorylates and Destabilizes Hedgehog Pathway Transcription Factor GLI1 in Medulloblastoma
Author(s) -
Yen-Hsing Li,
Jia Lin Luo,
YungYi C. Mosley,
Victoria Hedrick,
Lake N. Paul,
Julia Chang,
Guangjun Zhang,
YuKuo Wang,
Max R. Banko,
Anne Brunet,
Shihuan Kuang,
JenLeih Wu,
Chun-Ju Chang,
Matthew P. Scott,
JerYen Yang
Publication year - 2015
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2015.06.054
Subject(s) - ampk , gli1 , protein kinase a , microbiology and biotechnology , hedgehog signaling pathway , amp activated protein kinase , phosphorylation , chemistry , transcription factor , hedgehog , sonic hedgehog , biology , signal transduction , biochemistry , gene
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.
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