p53AIP1, a potential mediator of p53-dependent apoptosis, and its regulation by Ser-46-phosphorylated p53

  • Cell. 2000 Sep 15;102(6):849-62. doi: 10.1016/s0092-8674(00)00073-8.
K Oda  1 ,  H Arakawa ,  T Tanaka ,  K Matsuda ,  C Tanikawa ,  T Mori ,  H Nishimori ,  K Tamai ,  T Tokino ,  Y Nakamura ,  Y Taya
Affiliations
  • 1. Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, University of Tokyo, Japan.
Abstract

Through direct cloning of p53 binding sequences from human genomic DNA, we have isolated a novel gene, designated p53AIP1 (p53-regulated Apoptosis-Inducing Protein 1), whose expression is inducible by wild-type p53. Ectopically expressed p53AIP1, which is localized within mitochondria, leads to apoptotic cell death through dissipation of mitochondrial A(psi)m. We have found that upon severe DNA damage, Ser-46 on p53 is phosphorylated and Apoptosis is induced. In addition, substitution of Ser-46 inhibits the ability of p53 to induce Apoptosis and selectively blocks expression of p53AIP1. Our results suggest that p53AIP1 is likely to play an important role in mediating p53-dependent Apoptosis, and phosphorylation of Ser-46 regulates the transcriptional activation of this apoptosis-inducing gene.