期刊
MOLECULAR CELL
卷 38, 期 4, 页码 524-538出版社
CELL PRESS
DOI: 10.1016/j.molcel.2010.03.018
关键词
-
资金
- Association of International Cancer Research [08-0430]
NF-kappa B and p53 are important regulators of the cellular response to stress. Here, we identify the Skp2 gene as being both an NF-kappa B and p53 target after DNA damage. However, Skp2 expression can be either induced or repressed in a manner requiring both the p52 NF-kappa B subunit and p53, with subsequent effects on autophagy, apoptosis, and p53 function. This process is regulated by the Akt(PKB)/ GSK3 beta pathway. When Akt is active, GSK3 beta is repressed, allowing p52 and p53 to cooperatively induce Skp2 expression. However, if Akt is inactive, GSK3 beta phosphorylates p52 at Ser 222. This modification disrupts p52 homodimer/Bcl-3 complexes and facilitates transcriptional repression by p52/c-Rel. The Skp2 promoter therefore integrates signaling through the NF-kappa B, p53, and Akt/GSK3 beta pathways to regulate cell fate in response to DNA damage.
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