TY - JOUR
T1 - DNA Damage-induced MDMX Degradation Is Mediated by MDM2
AU - Kawai, Hidehiko
AU - Wiederschain, Dmitri
AU - Kitao, Hiroyuki
AU - Stuart, Jeremy
AU - Tsai, Kelvin K C
AU - Yuan, Zhi Min
PY - 2003/11/14
Y1 - 2003/11/14
N2 - Although genetic studies have demonstrated that MDMX is essential to maintain p53 activity at low levels in non-stressed cells, it is unknown whether MDMX regulates p53 activation by DNA damage. We show here that DNA damage-induced p53 induction is associated with rapid down-regulation of the MDMX protein. Significantly, interference with MDMX down-regulation results in the suppression of p53 activation by genotoxic stress. We also demonstrate that DNA damage-induced MDMX reduction is mediated by MDM2, which targets MDMX for proteasomal degradation by a distinct mechanism that permits preferential MDMX degradation and therefore ensures optimal p53 activation.
AB - Although genetic studies have demonstrated that MDMX is essential to maintain p53 activity at low levels in non-stressed cells, it is unknown whether MDMX regulates p53 activation by DNA damage. We show here that DNA damage-induced p53 induction is associated with rapid down-regulation of the MDMX protein. Significantly, interference with MDMX down-regulation results in the suppression of p53 activation by genotoxic stress. We also demonstrate that DNA damage-induced MDMX reduction is mediated by MDM2, which targets MDMX for proteasomal degradation by a distinct mechanism that permits preferential MDMX degradation and therefore ensures optimal p53 activation.
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U2 - 10.1074/jbc.M308295200
DO - 10.1074/jbc.M308295200
M3 - Article
C2 - 12963717
AN - SCOPUS:0242580250
SN - 0021-9258
VL - 278
SP - 45946
EP - 45953
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 46
ER -