This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Li, C.
Right arrow Articles by Chen, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Li, C.
Right arrow Articles by Chen, J.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, November 2002, p. 7562-7571, Vol. 22, No. 21
0270-7306/02/$04.00+0     DOI: 10.1128/MCB.22.21.7562-7571.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

DNA Damage Induces MDMX Nuclear Translocation by p53-Dependent and -Independent Mechanisms

Changgong Li, Lihong Chen, and Jiandong Chen*

Molecular Oncology Program, H. Lee Moffitt Comprehensive Cancer Center and Research Institute, Tampa, Florida 33612

Received 6 May 2002/ Returned for modification 19 June 2002/ Accepted 22 July 2002

The MDM2 homolog MDMX is an important regulator of p53 activity during embryonic development. MDMX inactivation in mice results in embryonic lethality in a p53-dependent fashion. The expression level of MDMX is not induced by DNA damage, and its role in stress response is unclear. We show here that ectopically expressed MDMX is mainly localized in the cytoplasm. DNA damage promotes nuclear translocation of MDMX in cells with or without p53. Coexpression of MDM2 or p53 is sufficient to induce MDMX nuclear translocation, suggesting that activation of p53 and induction of MDM2 expression can contribute to this process. Stable transfection of MDMX into U2OS cells does not alter p53 level but results in reduced p53 DNA-binding activity and reduced MDM2 expression. The ability of ARF (alternate reading frame of INK4a) to activate p53 is also significantly inhibited by expression of MDMX. These results suggest that MDMX function may be regulated by DNA damage. Furthermore, MDMX may complement MDM2 in regulating p53 during embryonic development due to its ability to inhibit p53 in the presence of ARF.


* Corresponding author. Mailing address: H. Lee Moffitt Cancer Center, MRC3057A, 12902 Magnolia Dr., Tampa, FL 33612. Phone: (813) 903-6822. Fax: (813) 903-6817. E-mail: jchen{at}moffitt.usf.edu.


Molecular and Cellular Biology, November 2002, p. 7562-7571, Vol. 22, No. 21
0022-538X/02/$04.00+0     DOI: 10.1128/MCB.22.21.7562-7571.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Zuckerman, V., Lenos, K., Popowicz, G. M., Silberman, I., Grossman, T., Marine, J.-C., Holak, T. A., Jochemsen, A. G., Haupt, Y. (2009). c-Abl Phosphorylates Hdmx and Regulates Its Interaction with p53. J. Biol. Chem. 284: 4031-4039 [Abstract] [Full Text]  
  • Gilkes, D. M., Pan, Y., Coppola, D., Yeatman, T., Reuther, G. W., Chen, J. (2008). Regulation of MDMX Expression by Mitogenic Signaling. Mol. Cell. Biol. 28: 1999-2010 [Abstract] [Full Text]  
  • Wang, Y. V., Wade, M., Wong, E., Li, Y.-C., Rodewald, L. W., Wahl, G. M. (2007). Quantitative analyses reveal the importance of regulated Hdmx degradation for P53 activation. Proc. Natl. Acad. Sci. USA 104: 12365-12370 [Abstract] [Full Text]  
  • Hu, B., Gilkes, D. M., Farooqi, B., Sebti, S. M., Chen, J. (2006). MDMX Overexpression Prevents p53 Activation by the MDM2 Inhibitor Nutlin. J. Biol. Chem. 281: 33030-33035 [Abstract] [Full Text]  
  • Pereg, Y., Lam, S., Teunisse, A., Biton, S., Meulmeester, E., Mittelman, L., Buscemi, G., Okamoto, K., Taya, Y., Shiloh, Y., Jochemsen, A. G. (2006). Differential Roles of ATM- and Chk2-Mediated Phosphorylations of Hdmx in Response to DNA Damage.. Mol. Cell. Biol. 26: 6819-6831 [Abstract] [Full Text]  
  • Okamoto, K., Kashima, K., Pereg, Y., Ishida, M., Yamazaki, S., Nota, A., Teunisse, A., Migliorini, D., Kitabayashi, I., Marine, J.-C., Prives, C., Shiloh, Y., Jochemsen, A. G., Taya, Y. (2005). DNA Damage-Induced Phosphorylation of MdmX at Serine 367 Activates p53 by Targeting MdmX for Mdm2-Dependent Degradation. Mol. Cell. Biol. 25: 9608-9620 [Abstract] [Full Text]  
  • Chen, L., Li, C., Pan, Y., Chen, J. (2005). Regulation of p53-MDMX Interaction by Casein Kinase 1 Alpha. Mol. Cell. Biol. 25: 6509-6520 [Abstract] [Full Text]  
  • Pereg, Y., Shkedy, D., de Graaf, P., Meulmeester, E., Edelson-Averbukh, M., Salek, M., Biton, S., Teunisse, A. F. A. S., Lehmann, W. D., Jochemsen, A. G., Shiloh, Y. (2005). Phosphorylation of Hdmx mediates its Hdm2- and ATM-dependent degradation in response to DNA damage. Proc. Natl. Acad. Sci. USA 102: 5056-5061 [Abstract] [Full Text]  
  • Mancini, F., Gentiletti, F., D'Angelo, M., Giglio, S., Nanni, S., D'Angelo, C., Farsetti, A., Citro, G., Sacchi, A., Pontecorvi, A., Moretti, F. (2004). MDM4 (MDMX) Overexpression Enhances Stabilization of Stress-induced p53 and Promotes Apoptosis. J. Biol. Chem. 279: 8169-8180 [Abstract] [Full Text]  
  • de Graaf, P., Little, N. A., Ramos, Y. F. M., Meulmeester, E., Letteboer, S. J. F., Jochemsen, A. G. (2003). Hdmx Protein Stability Is Regulated by the Ubiquitin Ligase Activity of Mdm2. J. Biol. Chem. 278: 38315-38324 [Abstract] [Full Text]  
  • Pan, Y., Chen, J. (2003). MDM2 Promotes Ubiquitination and Degradation of MDMX. Mol. Cell. Biol. 23: 5113-5121 [Abstract] [Full Text]  
  • Meulmeester, E., Frenk, R., Stad, R., de Graaf, P., Marine, J.-C., Vousden, K. H., Jochemsen, A. G. (2003). Critical Role for a Central Part of Mdm2 in the Ubiquitylation of p53. Mol. Cell. Biol. 23: 4929-4938 [Abstract] [Full Text]