iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72 polymorphic p53

被引:219
作者
Bergamaschi, Daniele
Samuels, Yardena
Sullivan, Alexandra
Zvelebil, Marketa
Breyssens, Hilde
Bisso, Andrea
Del Sal, Giannino
Syed, Nelofer
Smith, Paul
Gasco, Milena
Crook, Tim
Lu, Xin
机构
[1] UCL, Ludwig Inst Canc Res, London W1W 7BS, England
[2] Univ Trieste, LNCIB, I-34100 Trieste, Italy
[3] Univ Trieste, Dipartimento Biochim Biofis & Chim Macromol, I-34100 Trieste, Italy
[4] Inst Canc Res, Breakthrough Toby Robins Breast Canc Res Ctr, Lab Canc Genet & Epigenet, Chester Beatty Labs, London SW3 6JB, England
[5] S Croce & Carle Hosp, Dept Med Oncol, I-12100 Cuneo, Italy
关键词
D O I
10.1038/ng1879
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
iASPP is one of the most evolutionarily conserved inhibitors of p53, whereas ASPP1 and ASPP2 are activators of p53. We show here that, in addition to the DNA-binding domain, the ASPP family members also bind to the proline-rich region of p53, which contains the most common p53 polymorphism at codon 72. Furthermore, the ASPP family members, particularly iASPP, bind to and regulate the activity of p53Pro72 more efficiently than that of p53Arg72. Hence, escape from negative regulation by iASPP is a newly identified mechanism by which p53Arg72 activates apoptosis more efficiently than p53Pro72.
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收藏
页码:1133 / 1141
页数:9
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