Different activities of the largest subunit of replication protein A cooperate during SV40 DNA replication

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Poonam Taneja - , Vanderbilt University (Author)
  • Irene Boche - , Vanderbilt University (Author)
  • Hella Hartmann - , Core Facility Light Microscopy, Leibniz Institute on Aging - Fritz Lipmann Institute (Author)
  • Heinz Peter Nasheuer - , University of Galway (Author)
  • Frank Grosse - , Leibniz Institute on Aging - Fritz Lipmann Institute (Author)
  • Ellen Fanning - , Vanderbilt University (Author)
  • Klaus Weisshart - , Leibniz Institute on Aging - Fritz Lipmann Institute (Author)

Abstract

Replication protein A (RPA) is a stable heterotrimeric complex consisting of p70, p32 and p14 subunits. The protein plays a crucial role in SV40 minichromosome replication. Peptides of p70 representing interaction sites for the smaller two subunits, DNA as well as the viral initiator protein large T-antigen (Tag) and the cellular DNA polymerase α-primase (Pol) all interfered with the replication process indicating the importance of the different p70 activities in this process. Inhibition by the peptide disrupting protein-protein interactions was observed only during the pre-initiation stage prior to primer synthesis, suggesting the formation of a stable initiation complex between RPA, Tag and Pol at the primer end.

Details

Original languageEnglish
Pages (from-to)3973-3978
Number of pages6
JournalFEBS letters
Volume581
Issue number21
Publication statusPublished - 21 Aug 2007
Peer-reviewedYes

External IDs

PubMed 17673209
ORCID /0000-0002-7133-7474/work/142251279

Keywords

Keywords

  • Protein-protein interaction, Replication protein A, SV40 DNA replication