J Gen Virol Faster Access
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 85 (2004), 3367-3376; DOI 10.1099/vir.0.80203-0

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 Email 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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Honkavuori, K. S.
Right arrow Articles by Kemp, G. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Honkavuori, K. S.
Right arrow Articles by Kemp, G. D.
Agricola
Right arrow Articles by Honkavuori, K. S.
Right arrow Articles by Kemp, G. D.
© 2004 Society for General Microbiology

Dual role of the adenovirus pVI C terminus as a nuclear localization signal and activator of the viral protease

K. S. Honkavuori, B. D. Pollard, M. S. Rodriguez{dagger}, R. T. Hay and G. D. Kemp

Biomolecular Sciences Building, University of St Andrews, North Haugh, St Andrews KY16 9ST, UK

Correspondence
G. D. Kemp
gdk{at}st-andrews.ac.uk

Adenain, the protease produced by adenovirus, is regulated by formation of a heterodimer with an 11 aa peptide derived from the C terminus of another adenoviral protein, pVI. Here, the role of the basic motif KRRR, which is conserved in pVI sequences from human adenovirus serotypes, was investigated. It was shown that this motif is less important than the N- or C-terminal regions in the formation of the adenain–peptide heterodimer and in the activity of the subsequent complex. This motif, however, acted as a nuclear localization signal that was capable of targeting heterologous proteins to the nucleus, resulting in a distinctive intranuclear distribution consisting of discrete foci, which is similar to that found for pVI during adenovirus infection.

{dagger}Present address: Institut Jacques Monod, CNRS, Tour 43–44, 2 Place Jussieu, 75005 Paris, France.




This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
M. Szelechowski, A. Fournier, J. Richardson, M. Eloit, and B. Klonjkowski
Functional organization of the major late transcriptional unit of canine adenovirus type 2
J. Gen. Virol., May 1, 2009; 90(5): 1215 - 1223.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
W. C. Russell
Adenoviruses: update on structure and function
J. Gen. Virol., January 1, 2009; 90(1): 1 - 20.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2004 by the Society for General Microbiology.