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
Ludwig Institute for Cancer Research, University College London, 91 Riding House Street, London W1W 7BS, UK.
Nat Genet. 2006 Oct;38(10):1133-41. doi: 10.1038/ng1879. Epub 2006 Sep 10.
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.
iASPP是p53最具进化保守性的抑制剂之一,而ASPP1和ASPP2是p53的激活剂。我们在此表明,除了DNA结合结构域,ASPP家族成员还与p53富含脯氨酸的区域结合,该区域包含密码子72处最常见的p53多态性。此外,ASPP家族成员,尤其是iASPP,比p53Arg72更有效地结合并调节p53Pro72的活性。因此,逃避iASPP的负调控是一种新发现的机制,通过该机制,p53Arg72比p53Pro72更有效地激活细胞凋亡。