Author/Authors :
Itahana، نويسنده , , Koji and Mao، نويسنده , , Hua and Jin، نويسنده , , Aiwen and Itahana، نويسنده , , Yoko and Clegg، نويسنده , , Hilary V. and Lindstrِm، نويسنده , , Mikael S. and Bhat، نويسنده , , Krishna P. and Godfrey، نويسنده , , Virginia L. and Evan، نويسنده , , Gerard I. and Zhang، نويسنده , , Yanping، نويسنده ,
Abstract :
Summary
believed that Mdm2 suppresses p53 in two ways: transcriptional inhibition by direct binding, and degradation via its E3 ligase activity. To study these functions physiologically, we generated mice bearing a single-residue substitution (C462A) abolishing the E3 function without affecting p53 binding. Unexpectedly, homozygous mutant mice died before E7.5, and deletion of p53 rescued the lethality. Furthermore, reintroducing a switchable p53 by crossing with p53ERTAM mice surprisingly demonstrated that the mutant Mdm2C462A was rapidly degraded in a manner indistinguishable from that of the wild-type Mdm2. Hence, our data indicate that (1) the Mdm2-p53 physical interaction, without Mdm2-mediated p53 ubiquitination, cannot control p53 activity sufficiently to allow early mouse embryonic development, and (2) Mdm2ʹs E3 function is not required for Mdm2 degradation.