PML, YAP, and p73 Are Components of a Proapoptotic Autoregulatory Feedback Loop

被引:207
|
作者
Lapi, Eleonora [2 ]
Di Agostino, Silvia [1 ]
Donzelli, Sara [1 ]
Gal, Hilah [3 ,4 ]
Domany, Eytan [3 ]
Rechavi, Gideon [5 ]
Pandolfi, Pier Paolo [6 ,7 ]
Givol, David [4 ]
Strano, Sabrina [1 ]
Lu, Xin [2 ]
Blandino, Giovanni [1 ]
机构
[1] Regina Elena Inst Canc Res, Translat Oncogenom Unit, I-00144 Rome, Italy
[2] Univ Oxford Branch, Ludwig Inst Canc Res, Oxford OX3 7DQ, England
[3] Weizmann Inst Sci, Dept Phys Complex Syst, IL-76100 Rehovot, Israel
[4] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[5] Chaim Sheba Med Ctr, Canc Res Ctr, IL-52621 Tel Hashomer, Israel
[6] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Canc Genet Program,Dept Med, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Canc Genet Program,Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.molcel.2008.11.019
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
p73 has been identified as a structural and functional homolog of the tumor suppressor p53. The transcriptional coactivator Yes-associated protein (YAP) has been demonstrated to interact with and to enhance p73-dependent apoptosis in response to DNA damage. Here, we show the existence of a proapoptotic autoregulatory feedback loop between p73, YAP, and the promyelocytic leukemia (PML) tumor suppressor gene. We demonstrate that PML is a direct transcriptional target of p73NAP, and we show that PML transcriptional activation by p73/YAP is under the negative control of the proto-oncogenic Akt/PKB kinase. Importantly, we find that PML and YAP physically interact through their PVPVY and WW domains, respectively, causing PML-mediated sumoylation and stabilization of YAP. Hence, we determine a mechanistic pathway in response to DNA damage that could have relevant implications for the treatment of human cancer.
引用
收藏
页码:803 / 814
页数:12
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