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
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
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 Faulkner, N. E.
Right arrow Articles by Markovitz, D. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Faulkner, N. E.
Right arrow Articles by Markovitz, D. M.

 Previous Article  |  Next Article 

Journal of Virology, February 2003, p. 2276-2281, Vol. 77, No. 3
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.3.2276-2281.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Protein Phosphatase 2A Enhances Activation of Human Immunodeficiency Virus Type 1 by Phorbol Myristate Acetate

Neil E. Faulkner,1 Brian R. Lane,1 Paul J. Bock,1 and David M. Markovitz1,2*

Cellular and Molecular Biology Program,1 Division of Infectious Diseases, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48109-06402

Received 30 July 2002/ Accepted 1 November 2002

The viral replication rate in patients infected with human immunodeficiency virus type 1 (HIV-1) is controlled in part by regulation of the transcription of viral genes. The rate of transcription is determined by a complex interplay between cellular and viral proteins and the promoter elements found in the long terminal repeats. Protein phosphatase 2A (PP2A) is a phosphoprotein that plays important roles in the regulation of signal transduction and cell growth. In this report, we demonstrate that overexpression of the catalytic subunit of protein phosphatase 2A (PP2Ac) increases the basal activity of the HIV-1 promoter and, especially, enhances the promoter's response to the protein kinase C (PKC) activator 12-O-tetradecanoyl phorbol-13-acetate (PMA). Additionally, ectopic PP2Ac enhances activation of HIV-1 provirus by PMA. Okadaic acid, a potent inhibitor of PP2A, markedly reduces both HIV-1 enhancer and proviral activation. Fostriecin, a PP2A inhibitor which has been used as an antineoplastic agent in clinical trials, is also able to inhibit PMA-stimulated HIV-1 proviral activation. These observations demonstrate a role for the important cellular phosphatase PP2A in HIV-1 transcription and replication and also suggest that PKC can potentiate the activity of PP2A. PP2A is a potential target for therapeutic intervention in patients infected with HIV-1.


* Corresponding author. Mailing address: Department of Internal Medicine, Division of Infectious Diseases, 5220 MSRB III, 1150 W. Medical Center Dr., Ann Arbor, MI 48109-0640. Phone: (734) 647-1786. Fax: (734) 764-0101. E-mail: dmarkov{at}umich.edu.


Journal of Virology, February 2003, p. 2276-2281, Vol. 77, No. 3
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.3.2276-2281.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Zhou, M., Huang, K., Jung, K.-J., Cho, W.-K., Klase, Z., Kashanchi, F., Pise-Masison, C. A., Brady, J. N. (2009). Bromodomain Protein Brd4 Regulates Human Immunodeficiency Virus Transcription through Phosphorylation of CDK9 at Threonine 29. J. Virol. 83: 1036-1044 [Abstract] [Full Text]  
  • Ammosova, T., Jerebtsova, M., Beullens, M., Lesage, B., Jackson, A., Kashanchi, F., Southerland, W., Gordeuk, V. R., Bollen, M., Nekhai, S. (2005). Nuclear Targeting of Protein Phosphatase-1 by HIV-1 Tat Protein. J. Biol. Chem. 280: 36364-36371 [Abstract] [Full Text]  
  • Ylisastigui, L., Kaur, R., Johnson, H., Volker, J., He, G., Hansen, U., Margolis, D. (2005). Mitogen-Activated Protein Kinases Regulate LSF Occupancy at the Human Immunodeficiency Virus Type 1 Promoter. J. Virol. 79: 5952-5962 [Abstract] [Full Text]  
  • Deutsch, E., Cohen, A., Kazimirsky, G., Dovrat, S., Rubinfeld, H., Brodie, C., Sarid, R. (2004). Role of Protein Kinase C {delta} in Reactivation of Kaposi's Sarcoma-Associated Herpesvirus. J. Virol. 78: 10187-10192 [Abstract] [Full Text]  
  • Palaniappan, N., Kim, B. S., Sekiyama, Y., Osada, H., Reynolds, K. A. (2003). Enhancement and Selective Production of Phoslactomycin B, a Protein Phosphatase IIa Inhibitor, through Identification and Engineering of the Corresponding Biosynthetic Gene Cluster. J. Biol. Chem. 278: 35552-35557 [Abstract] [Full Text]