Author/Authors :
Higashitsuji، نويسنده , , Hiroaki and Higashitsuji، نويسنده , , Hisako and Itoh، نويسنده , , Katsuhiko and Sakurai، نويسنده , , Toshiharu and Nagao، نويسنده , , Toshikazu and Sumitomo، نويسنده , , Haruhiko and Masuda، نويسنده , , Tomoko and Dawson، نويسنده , , Simon and Shimada، نويسنده , , Yutaka and Mayer، نويسنده , , R. John and Fujita، نويسنده , , Jun، نويسنده ,
Abstract :
Summary
in is an ankyrin repeat oncoprotein commonly overexpressed in hepatocellular carcinomas. Gankyrin interacts with the S6 proteasomal ATPase and accelerates the degradation of the tumor suppressor Rb. We show here that gankyrin has an antiapoptotic activity in cells exposed to DNA damaging agents. Downregulation of gankyrin induces apoptosis in cells with wild-type p53. In vitro and in vivo experiments revealed that gankyrin binds to Mdm2, facilitating p53-Mdm2 binding, and increases ubiquitylation and degradation of p53. Gankyrin also enhances Mdm2 autoubiquitylation in the absence of p53. Downregulation of gankyrin reduced amounts of Mdm2 and p53 associated with the 26S proteasome. Thus, gankyrin is a cofactor that increases the activities of Mdm2 on p53 and probably targets polyubiquitylated p53 into the 26S proteasome.