JVI Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
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 Google Scholar
Google Scholar
Right arrow Articles by Lyman, M. G.
Right arrow Articles by Banfield, B. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lyman, M. G.
Right arrow Articles by Banfield, B. W.
Journal of Virology, July 2006, p. 7159-7168, Vol. 80, No. 14
0022-538X/06/$08.00+0     doi:10.1128/JVI.00592-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Localization of ERK/MAP Kinase Is Regulated by the Alphaherpesvirus Tegument Protein Us2

Mathew G. Lyman,{dagger} Jessica A. Randall, Christine M. Calton,{ddagger} and Bruce W. Banfield*

Department of Microbiology and Program in Molecular Biology, University of Colorado at Denver and Health Sciences Center, Aurora, Colorado 80045

Received 23 March 2006/ Accepted 8 May 2006

Many different viruses activate the extracellular signal-regulated kinase (ERK)/mitogen-activated protein (MAP) kinase signaling pathway during infection and require ERK activation for the efficient execution of their replication programs. Despite these findings, no virus-encoded proteins have been identified that directly modulate ERK activities. In an effort to determine the function of a conserved alphaherpesvirus structural protein called Us2, we screened a yeast two-hybrid library derived from NIH 3T3 cells and identified ERK as a Us2-interacting protein. Our studies indicate that Us2 binds to ERK in virus-infected cells, mediates the incorporation of ERK into the virion, and inhibits the activation of ERK nuclear substrates. The association of Us2 with ERK leads to the sequestration of ERK at the plasma membrane and to a perinuclear vesicular compartment, thereby keeping ERK out of the nucleus. Us2 can bind to activated ERK, and the data suggest that Us2 does not inhibit ERK enzymatic activity. The treatment of cells with U0126, a specific inhibitor of ERK activation, resulted in a substantial delay in the release of virus from infected cells that was more pronounced with a virus deleted for Us2 than with parental and repaired strains, suggesting that both ERK and Us2 activities are required for efficient virus replication. This study highlights an additional complexity to the activation of ERK by viruses, namely, that localization of active ERK can be altered by virus-encoded proteins.


* Corresponding author. Mailing address: Department of Microbiology, University of Colorado at Denver and Health Sciences Center, Mail Stop 8333, P.O. Box 6511, Aurora, CO 80045. Phone: (303) 724-4206. Fax: (303) 724-4226. E-mail: bruce.banfield{at}uchsc.edu.

{dagger} Present address: Department of Molecular Biology, Princeton University, Princeton, NJ 08544.

{ddagger} Present address: Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97201.


Journal of Virology, July 2006, p. 7159-7168, Vol. 80, No. 14
0022-538X/06/$08.00+0     doi:10.1128/JVI.00592-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Mol. Cell. Biol. Microbiol. Mol. Biol. Rev.
Clin. Vaccine Immunol. ALL ASM JOURNALS

Copyright © 2006 by the American Society for Microbiology. All rights reserved.