Literature DB >> 20172729

The p53 orchestra: Mdm2 and Mdmx set the tone.

Mark Wade1, Yunyuan V Wang, Geoffrey M Wahl.   

Abstract

The activities of p53 cover diverse aspects of cell biology, including cell cycle control, apoptosis, metabolism, fertility, differentiation and cellular reprogramming. Although loss of p53 function engenders tumor susceptibility, hyperactivation of p53 is lethal. Therefore, p53 activity must be strictly regulated to maintain normal tissue homeostasis. Critical for the control of p53 function are its two main negative regulators: Mdm2 and Mdmx. Recent reports have provided insight into the complex mechanisms that regulate these two proteins and have revealed novel functions for each. Here, we review and evaluate models of Mdm2- and Mdmx-dependent regulation of p53 activity. Both Mdm2 and Mdmx receive input from numerous signaling pathways and interact with many proteins in addition to p53. Therefore, we also consider roles for Mdm2 and Mdmx in additional cancer-related networks, including Notch signaling and the epithelial-to-mesenchymal transition. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20172729      PMCID: PMC2910097          DOI: 10.1016/j.tcb.2010.01.009

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  129 in total

1.  Functional analysis of the roles of posttranslational modifications at the p53 C terminus in regulating p53 stability and activity.

Authors:  Lijin Feng; Tongxiang Lin; Hiroaki Uranishi; Wei Gu; Yang Xu
Journal:  Mol Cell Biol       Date:  2005-07       Impact factor: 4.272

2.  Regulation of p53-MDMX interaction by casein kinase 1 alpha.

Authors:  Lihong Chen; Changgong Li; Yu Pan; Jiandong Chen
Journal:  Mol Cell Biol       Date:  2005-08       Impact factor: 4.272

3.  Protein kinase CK1delta phosphorylates key sites in the acidic domain of murine double-minute clone 2 protein (MDM2) that regulate p53 turnover.

Authors:  Markus Winter; Diane Milne; Sylvia Dias; Roman Kulikov; Uwe Knippschild; Christine Blattner; David Meek
Journal:  Biochemistry       Date:  2004-12-28       Impact factor: 3.162

Review 4.  The canonical Notch signaling pathway: unfolding the activation mechanism.

Authors:  Raphael Kopan; Maria Xenia G Ilagan
Journal:  Cell       Date:  2009-04-17       Impact factor: 41.582

5.  The C-terminal lysines fine-tune P53 stress responses in a mouse model but are not required for stability control or transactivation.

Authors:  Kurt A Krummel; Crystal J Lee; Franck Toledo; Geoffrey M Wahl
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-08       Impact factor: 11.205

6.  Phosphorylation of Hdmx mediates its Hdm2- and ATM-dependent degradation in response to DNA damage.

Authors:  Yaron Pereg; Dganit Shkedy; Petra de Graaf; Erik Meulmeester; Marina Edelson-Averbukh; Mogjiborahman Salek; Sharon Biton; Amina F A S Teunisse; Wolf D Lehmann; Aart G Jochemsen; Yosef Shiloh
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-23       Impact factor: 11.205

7.  A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans.

Authors:  Gareth L Bond; Wenwei Hu; Elisabeth E Bond; Harlan Robins; Stuart G Lutzker; Nicoleta C Arva; Jill Bargonetti; Frank Bartel; Helge Taubert; Peter Wuerl; Kenan Onel; Linwah Yip; Shih-Jen Hwang; Louise C Strong; Guillermina Lozano; Arnold J Levine
Journal:  Cell       Date:  2004-11-24       Impact factor: 41.582

8.  Loss of HAUSP-mediated deubiquitination contributes to DNA damage-induced destabilization of Hdmx and Hdm2.

Authors:  Erik Meulmeester; Madelon M Maurice; Chris Boutell; Amina F A S Teunisse; Huib Ovaa; Tsion E Abraham; Roeland W Dirks; Aart G Jochemsen
Journal:  Mol Cell       Date:  2005-05-27       Impact factor: 17.970

9.  MdmX inhibits ARF mediated Mdm2 sumoylation.

Authors:  Mithua Ghosh; Karen Weghorst; Steven J Berberich
Journal:  Cell Cycle       Date:  2005-04-09       Impact factor: 4.534

10.  PPM1D dephosphorylates Chk1 and p53 and abrogates cell cycle checkpoints.

Authors:  Xiongbin Lu; Bonnie Nannenga; Lawrence A Donehower
Journal:  Genes Dev       Date:  2005-05-03       Impact factor: 11.361

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  226 in total

1.  MdmX is required for p53 interaction with and full induction of the Mdm2 promoter after cellular stress.

Authors:  Lynn Biderman; Masha V Poyurovsky; Yael Assia; James L Manley; Carol Prives
Journal:  Mol Cell Biol       Date:  2012-01-30       Impact factor: 4.272

Review 2.  HECT and RING finger families of E3 ubiquitin ligases at a glance.

Authors:  Meredith B Metzger; Ventzislava A Hristova; Allan M Weissman
Journal:  J Cell Sci       Date:  2012-02-01       Impact factor: 5.285

3.  Rewiring kinase specificity with a synthetic adaptor protein.

Authors:  Elissa M Hobert; Alanna Schepartz
Journal:  J Am Chem Soc       Date:  2012-02-22       Impact factor: 15.419

4.  BRIZ1 and BRIZ2 proteins form a heteromeric E3 ligase complex required for seed germination and post-germination growth in Arabidopsis thaliana.

Authors:  Mon Mandy Hsia; Judy Callis
Journal:  J Biol Chem       Date:  2010-09-01       Impact factor: 5.157

5.  5'-3'-UTR interactions regulate p53 mRNA translation and provide a target for modulating p53 induction after DNA damage.

Authors:  Jing Chen; Michael B Kastan
Journal:  Genes Dev       Date:  2010-09-13       Impact factor: 11.361

6.  Turning the RING domain protein MdmX into an active ubiquitin-protein ligase.

Authors:  Saravanakumar Iyappan; Hans-Peter Wollscheid; Alejandro Rojas-Fernandez; Andreas Marquardt; Hao-Cheng Tang; Rajesh K Singh; Martin Scheffner
Journal:  J Biol Chem       Date:  2010-08-12       Impact factor: 5.157

7.  miR-605 joins p53 network to form a p53:miR-605:Mdm2 positive feedback loop in response to stress.

Authors:  Jiening Xiao; Huixian Lin; Xiaobin Luo; Xiaoyan Luo; Zhiguo Wang
Journal:  EMBO J       Date:  2011-01-07       Impact factor: 11.598

Review 8.  p53 at a glance.

Authors:  Colleen A Brady; Laura D Attardi
Journal:  J Cell Sci       Date:  2010-08-01       Impact factor: 5.285

9.  Lithocholic acid is an endogenous inhibitor of MDM4 and MDM2.

Authors:  Simon M Vogel; Matthias R Bauer; Andreas C Joerger; Rainer Wilcken; Tobias Brandt; Dmitry B Veprintsev; Trevor J Rutherford; Alan R Fersht; Frank M Boeckler
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-03       Impact factor: 11.205

10.  Guilty as CHARGED: p53's expanding role in disease.

Authors:  Jeanine L Van Nostrand; Laura D Attardi
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

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