Aberrant expression of nucleostemin activates p53 and induces cell cycle arrest via inhibition of MDM2

被引:143
作者
Dai, Mu-Shui [1 ]
Sun, Xiao-Xin [1 ]
Lu, Hua [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
关键词
D O I
10.1128/MCB.01662-07
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nucleolar protein nucleostemin (NS) is essential for cell proliferation and early embryogenesis. Both depletion and overexpression of NS reduce cell proliferation. However, the mechanisms underlying this regulation are still unclear. Here, we show that NS regulates p53 activity through the inhibition of MDM2. NS binds to the central acidic domain of MDM2 and inhibits MDM2-mediated p53 ubiquitylation and degradation. Consequently, ectopic overexpression of NS activates p53, induces G, cell cycle arrest, and inhibits cell proliferation. Interestingly, the knockdown of NS by small interfering RNA also activates p53 and induces G, arrest. These effects require the ribosomal proteins L5 and L11, since the depletion of NS enhanced their interactions with MDM2 and the knockdown of L5 or L11 abrogated the NS depletion-induced p53 activation and cell cycle arrest. These results suggest that a p53-dependent cell cycle checkpoint monitors changes of cellular NS levels via the impediment of MDM2 function.
引用
收藏
页码:4365 / 4376
页数:12
相关论文
共 55 条
[21]   Nucleolar protein NPM interacts with HDM2 and protects tumor suppressor protein p53 from HDM2-mediated degradation [J].
Kurki, S ;
Peltonen, K ;
Latonen, L ;
Kiviharju, TM ;
Ojala, PM ;
Meek, D ;
Laiho, M .
CANCER CELL, 2004, 5 (05) :465-475
[22]   Putting a finger on growth surveillance -: Insight into MDM2 zinc finger-ribosomal protein interactions [J].
Lindstrom, Mikael S. ;
Deisenroth, Chad ;
Zhang, Yanping .
CELL CYCLE, 2007, 6 (04) :434-437
[23]   Regulation of HDM2 activity by the ribosomal protein L11 [J].
Lohrum, MAE ;
Ludwig, RL ;
Kubbutat, MHG ;
Hanlon, M ;
Vousden, KH .
CANCER CELL, 2003, 3 (06) :577-587
[24]   Depletion of the nucleolar protein nucleostemin causes g1 cell cycle arrest via the p53 pathway [J].
Ma, Hanhui ;
Pederson, Thoru .
MOLECULAR BIOLOGY OF THE CELL, 2007, 18 (07) :2630-2635
[25]   ATM-dependent phosphorylation of Mdm2 on serine 395: role in p53 activation by DNA damage [J].
Maya, R ;
Balass, M ;
Kim, ST ;
Shkedy, D ;
Leal, JFM ;
Shifman, O ;
Moas, M ;
Buschmann, T ;
Ronai, Z ;
Shiloh, Y ;
Kastan, MB ;
Katzir, E ;
Oren, M .
GENES & DEVELOPMENT, 2001, 15 (09) :1067-1077
[26]   Critical role for a central part of Mdm2 in the ubiquitylation of p53 [J].
Meulmeester, E ;
Frenk, R ;
Stad, R ;
de Graaf, P ;
Marine, JC ;
Vousden, KH ;
Jochemsen, AG .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (14) :4929-4938
[27]   An N-terminal p14ARF peptide blocks Mdm2-dependent ubiquitination in vitro and can activate p53 in vivo [J].
Midgley, CA ;
Desterro, JMP ;
Saville, MK ;
Howard, S ;
Sparks, A ;
Hay, RT ;
Lane, DP .
ONCOGENE, 2000, 19 (19) :2312-2323
[28]   Decision making by p53: life, death and cancer [J].
Oren, M .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (04) :431-442
[29]   p19ARF links the tumour suppressor p53 to Ras [J].
Palmero, I ;
Pantoja, C ;
Serrano, M .
NATURE, 1998, 395 (6698) :125-126
[30]   S6-haploinsufficiency activates the p53 tumor suppressor [J].
Panic, Linda ;
Montagne, Jacques ;
Cokaric, Maja ;
Volarevic, Sinisa .
CELL CYCLE, 2007, 6 (01) :20-24