The Yes-associated protein 1 stabilizes p73 by preventing Itch-mediated ubiquitination of p73

被引:177
作者
Levy, D. [1 ]
Adamovich, Y. [1 ]
Reuven, N. [1 ]
Shaul, Y. [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
关键词
p73 tumor suppressor; protein stability; apoptosis; DNA damage response; Yap1;
D O I
10.1038/sj.cdd.4402063
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
Upon DNA damage signaling, p73, a member of the p53 tumor suppressor family, accumulates to support transcription of downstream apoptotic genes. p73 interacts with Yes-associated protein 1 (Yap1) through its PPPY motif, and increases p73 transactivation of apoptotic genes. The ubiquitin E3 ligase Itch, like Yap1, interacts with p73. Given the fact that both Itch and Yap1 bind p73 via the PPPY motif, we hypothesized that Yap may also function to stabilize p73 by displacing Itch binding to p73. We show that the interaction of Yap1 and p73 was necessary for p73 stabilization. Yap1 competed with Itch for binding to p73, and prevented Itch-mediated ubiquitination of p73. Treatment of cells with cisplatin leads to an increase in p73 accumulation and induction of apoptosis, but both were dramatically reduced in the presence of Yap1 siRNA. Altogether, our findings attribute a central role to Yap1 in regulating p73 accumulation and function under DNA damage signaling.
引用
收藏
页码:743 / 751
页数:9
相关论文
共 43 条
[1]  
Agami R, 1999, NATURE, V399, P809
[2]   20S proteasomal degradation of ornithine decarboxylase is regulated by NQ01 [J].
Asher, G ;
Bercovich, Z ;
Tsvetkov, P ;
Shaul, Y ;
Kahana, C .
MOLECULAR CELL, 2005, 17 (05) :645-655
[3]   A mechanism of ubiquitin-independent proteasomal degradation of the tumor suppressors p53 and p73 [J].
Asher, G ;
Tsvetkov, P ;
Kahana, C ;
Shaul, Y .
GENES & DEVELOPMENT, 2005, 19 (03) :316-321
[4]   Mdm2 binds p73α without targeting degradation [J].
Bálint, E ;
Bates, S ;
Vousden, KH .
ONCOGENE, 1999, 18 (27) :3923-3929
[5]   Akt phosphorylates the Yes-associated protein, YAP, to induce interaction with 14-3-3 and attenuation of p73-mediated apoptosis [J].
Basu, S ;
Totty, NF ;
Irwin, MS ;
Sudol, M ;
Downward, J .
MOLECULAR CELL, 2003, 11 (01) :11-23
[6]   c-Abl tyrosine kinase selectively regulates p73 nuclear matrix association [J].
Ben-Yehoyada, M ;
Ben-Dor, I ;
Shaul, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (36) :34475-34482
[7]   Ubiquitin-dependent degradation of p73 is inhibited by PML [J].
Bernassola, F ;
Salomoni, P ;
Oberst, A ;
Di Como, CJ ;
Pagano, M ;
Melino, G ;
Pandolfi, PP .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (11) :1545-1557
[8]   Stable suppression of tumorigenicity by virus-mediated RNA interference [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
CANCER CELL, 2002, 2 (03) :243-247
[9]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[10]   DNA damage-dependent acetylation of p73 dictates the selective activation of apoptotic target genes [J].
Costanzo, A ;
Merlo, P ;
Pediconi, N ;
Fulco, M ;
Sartorelli, V ;
Cole, PA ;
Fontemaggi, G ;
Fanciulli, M ;
Schiltz, L ;
Blandino, G ;
Balsano, C ;
Levrero, M .
MOLECULAR CELL, 2002, 9 (01) :175-186