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
[1]   Mdm2 binds to Nbs1 at sites of DNA damage and regulates double strand break repair [J].
Alt, JR ;
Bouska, A ;
Fernandez, MR ;
Cerny, RL ;
Xiao, H ;
Eischen, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (19) :18771-18781
[2]   Stimulation of human DNA polymerase ε by MDM2 [J].
Asahara, H ;
Li, Y ;
Fuss, J ;
Haines, DS ;
Vlatkovic, N ;
Boyd, MT ;
Linn, S .
NUCLEIC ACIDS RESEARCH, 2003, 31 (09) :2451-2459
[3]   MdmX is a RING finger ubiquitin ligase capable of synergistically enhancing Mdm2 ubiquitination [J].
Badciong, JC ;
Haas, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49668-49675
[4]   TRIAD1 is negatively regulated by the MDM2 E3 ligase [J].
Bae, Seunghee ;
Jung, Jin Hyuk ;
An, In-Sook ;
Kim, Ok-Yeoun ;
Lee, Myoung Joo ;
Lee, Jae Ho ;
Park, In-Chul ;
Lee, Su-Jae ;
An, Sungkwan .
ONCOLOGY REPORTS, 2012, 28 (05) :1924-1928
[5]   Mdm2 binds p73α without targeting degradation [J].
Bálint, E ;
Bates, S ;
Vousden, KH .
ONCOGENE, 1999, 18 (27) :3923-3929
[6]   L2DTL/CDT2 and PCNA interact with p53 and regulate p53 polyubiquitination and protein stability through MDM2 and CUL4A/DDB1 complexes [J].
Banks, Damon ;
Wu, Min ;
Higa, Leigh Ann ;
Gavrilova, Nadia ;
Quan, Junmin ;
Ye, Tao ;
Kobayashi, Ryuji ;
Sun, Hong ;
Zhang, Hui .
CELL CYCLE, 2006, 5 (15) :1719-1729
[7]   REGULATION OF MDM2 EXPRESSION BY P53 - ALTERNATIVE PROMOTERS PRODUCE TRANSCRIPTS WITH NONIDENTICAL TRANSLATION POTENTIAL [J].
BARAK, Y ;
GOTTLIEB, E ;
JUVENGERSHON, T ;
OREN, M .
GENES & DEVELOPMENT, 1994, 8 (15) :1739-1749
[8]   Alternative and aberrant splicing of MDM2 mRNA in human cancer [J].
Bartel, F ;
Taubert, H ;
Harris, LC .
CANCER CELL, 2002, 2 (01) :9-15
[9]  
Biderman Lynn, 2012, Genes Cancer, V3, P264, DOI 10.1177/1947601912455331
[10]   A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans [J].
Bond, GL ;
Hu, WW ;
Bond, EE ;
Robins, H ;
Lutzker, SG ;
Arva, NC ;
Bargonetti, J ;
Bartel, F ;
Taubert, H ;
Wuerl, P ;
Onel, K ;
Yip, L ;
Hwang, SJ ;
Strong, LC ;
Lozano, G ;
Levine, AJ .
CELL, 2004, 119 (05) :591-602