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 Brenkman, A. B.
Right arrow Articles by van der Vliet, P. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Brenkman, A. B.
Right arrow Articles by van der Vliet, P. C.

 Previous Article  |  Next Article 

Journal of Virology, August 2002, p. 8200-8207, Vol. 76, No. 16
0022-538X/02/$04.00+0     DOI: 10.1128/JVI.76.16.8200-8207.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Molecular Architecture of Adenovirus DNA Polymerase and Location of the Protein Primer

Arjan B. Brenkman, Elise C. Breure, and Peter C. van der Vliet*

University Medical Centre, Department of Physiological Chemistry and Centre for Biomedical Genetics, Utrecht, The Netherlands

Received 5 April 2002/ Accepted 13 May 2002

Adenovirus (Ad) DNA polymerase (pol) belongs to the distinct subclass of the pol{alpha} family of DNA pols that employs the precursor terminal protein (pTP) as primer. Ad pol forms a stable heterodimer with this primer, and together, they bind specifically to the core origin in order to start replication. After initiation of Ad replication, the resulting pTP-trinucleotide intermediate jumps back and pTP starts to dissociate. Compared to free Ad pol, the pTP-pol complex shows reduced polymerase and exonuclease activities, but the reason for this is not understood. Furthermore, the interaction domains between these proteins have not been defined and the contribution of each protein to origin binding is unclear. To address these questions, we used oligonucleotides with a translocation block and show here that pTP binds at the entrance of the primer binding groove of Ad pol, thereby explaining the decreased synthetic activities of the pTP-pol complex and providing insight into how pTP primes Ad replication. Employing an exonuclease-deficient mutant polymerase, we further show that the polymerase and exonuclease active sites of Ad pol are spatially distinct and that the exonuclease activity of Ad pol is located at the N-terminal part of the protein. In addition, by probing the distances between both active sites and the surface of Ad pol, we show that Ad pol binds a DNA region of 14 to 15 nucleotides. Based on these results, a model for binding of the pTP-pol complex at the origin of replication is proposed.


* Corresponding author. Mailing address: Universiteitsweg 100, P.O. Box 85060, 3508 AB Utrecht, The Netherlands. Phone: 31 302538989. Fax: 31 30 2539035. E-mail: p.c.vandervliet{at}med.uu.nl.


Journal of Virology, August 2002, p. 8200-8207, Vol. 76, No. 16
0022-538X/02/$04.00+0     DOI: 10.1128/JVI.76.16.8200-8207.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Longas, E., de Vega, M., Lazaro, J. M., Salas, M. (2006). Functional characterization of highly processive protein-primed DNA polymerases from phages Nf and GA-1, endowed with a potent strand displacement capacity. Nucleic Acids Res 34: 6051-6063 [Full Text]  
  • Mysiak, M. E., Holthuizen, P. E., van der Vliet, P. C. (2004). The adenovirus priming protein pTP contributes to the kinetics of initiation of DNA replication. Nucleic Acids Res 32: 3913-3920 [Abstract] [Full Text]  
  • van Breukelen, B., Brenkman, A. B., Holthuizen, P. E., van der Vliet, P. C. (2002). Adenovirus Type 5 DNA Binding Protein Stimulates Binding of DNA Polymerase to the Replication Origin. J. Virol. 77: 915-922 [Abstract] [Full Text]