MDM2's social network

被引:74
作者
Fahraeus, R. [1 ]
Olivares-Illana, V. [2 ]
机构
[1] Univ Paris 07, Hop St Louis, INSERM Unite 940, Equipe Labellisee Ligue Canc,Inst Genet Mol, Paris, France
[2] Univ Autonoma San Luis Potosi, Inst Fis, San Luis Potosi 78290, Mexico
关键词
MDM2; interactome; interactions; p53; MESSENGER-RNA STABILIZATION; DNA-DAMAGE; E3; LIGASE; UBIQUITIN LIGASE; REGULATES P53; TRANSCRIPTIONAL ACTIVITY; PROTEASOMAL DEGRADATION; ANDROGEN RECEPTOR; INDUCED APOPTOSIS; INHIBITING MDM2;
D O I
10.1038/onc.2013.410
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
MDM2 is considered a hub protein due to its capacity to interact with a large number of different partners of which p53 is most well described. MDM2 is an E3 ubiquitin ligase, and many, but not all, of its interactions relate directly to this activity, such as substrates, adaptors or bridges, promoters, inhibitors or complementary factors. Some interactions serve regulatory functions that in response to cellular stresses control the localisation and functions of MDM2 including protein kinases, ribosomal proteins and proteases. Moreover, interactions with nucleotides serve other functions such as mRNA to regulate protein synthesis and DNA to control transcription. To perform such a pleiotropic panorama of different functions, MDM2 is subjected to a multitude of post-translational modifications and is expressed in different isoforms. The large and diverse interactome is made possible due to the plasticity of MDM2 and in this review we have listed the MDM2 interactions until now and we will discuss how this multifaceted protein can interact with such a variety of substrates to provide a key intermediary role in different signalling pathways.
引用
收藏
页码:4365 / 4376
页数:12
相关论文
共 156 条
[71]   A TSG101/MDM2 regulatory loop modulates MDM2 degradation and MDM2/p53 feedback control [J].
Li, LM ;
Liao, J ;
Ruland, J ;
Mak, TW ;
Cohen, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :1619-1624
[72]   A dynamic role of HAUSP in the p53-Mdm2 pathway [J].
Li, MY ;
Brooks, CL ;
Kon, N ;
Gu, W .
MOLECULAR CELL, 2004, 13 (06) :879-886
[73]   Phosphorylation-dependent ubiquitylation and degradation of androgen receptor by Akt require Mdm2 E3 ligase [J].
Lin, HK ;
Wang, L ;
Hu, YC ;
Altuwaijri, S ;
Chang, CS .
EMBO JOURNAL, 2002, 21 (15) :4037-4048
[74]   HdmX stimulates Hdm2-mediated ubiquitination and degradation of p53 [J].
Linares, LK ;
Hengstermann, A ;
Ciechanover, A ;
Müller, S ;
Scheffner, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (21) :12009-12014
[75]   p21-activated Kinase 6 (PAK6) Inhibits Prostate Cancer Growth via Phosphorylation of Androgen Receptor and Tumorigenic E3 Ligase Murine Double Minute-2 (Mdm2) [J].
Liu, Tong ;
Li, Yang ;
Gu, Hui ;
Zhu, Ge ;
Li, Jiabin ;
Cao, Liu ;
Li, Feng .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (05) :3359-3369
[76]   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
[77]   The Wip1 phosphatase acts as a gatekeeper in the p53-Mdm2 autoregulatory loop [J].
Lu, Xiongbin ;
Ma, Ou ;
Nguyen, Thuy-Ai ;
Joness, Stephen N. ;
Oren, Moshe ;
Donehower, Lawrence A. .
CANCER CELL, 2007, 12 (04) :342-354
[78]   MDM2 regulates dihydrofolate reductase activity through monoubiquitination [J].
Maguire, Maria ;
Nield, Paul C. ;
Devling, Timothy ;
Jenkins, Rosalind E. ;
Park, B. Kevin ;
Polanski, Radoslaw ;
Vlatkovic, Nikolina ;
Boyd, Mark T. .
CANCER RESEARCH, 2008, 68 (09) :3232-3242
[79]   THE RIBOSOMAL L5 PROTEIN IS ASSOCIATED WITH MDM-2 AND MDM-2-P53 COMPLEXES [J].
MARECHAL, V ;
ELENBAAS, B ;
PIETTE, J ;
NICOLAS, JC ;
LEVINE, AJ .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (11) :7414-7420
[80]   STIMULATION OF E2F1/DP1 TRANSCRIPTIONAL ACTIVITY BY MDM2 ONCOPROTEIN [J].
MARTIN, K ;
TROUCHE, D ;
HAGEMEIER, C ;
SORENSEN, TS ;
LATHANGUE, NB ;
KOUZARIDES, T .
NATURE, 1995, 375 (6533) :691-694