RETRACTED: The Skp2 Promoter Integrates Signaling through the NF-κB, p53, and Akt/GSK3β Pathways to Regulate Autophagy and Apoptosis (Retracted article. See vol. 55, pg. 342, 2014)

被引:62
作者
Barre, Benjamin [1 ]
Perkins, Neil D. [1 ]
机构
[1] Univ Bristol, Sch Med Sci, Dept Cellular & Mol Med, Bristol BS8 1TD, Avon, England
关键词
CELL-CYCLE; PHOSPHORYLATION; ACTIVATION; SUBUNIT; BCL-3; STABILIZATION; DEGRADATION; INHIBITION; EXPRESSION; P27(KIP1);
D O I
10.1016/j.molcel.2010.03.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:524 / 538
页数:15
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