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PMID: 2825183 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Simian virus 40 large tumor antigen requires three core replication origin domains for DNA unwinding and replication in vitro.

Dean FB, Borowiec JA, Ishimi Y, Deb S, Tegtmeyer P, Hurwitz J

Abstract

Simian virus 40 (SV40) large tumor antigen (T antigen) unwinds DNA containing the SV40 origin of replication. The origin requirement for unwinding can be satisfied by the 64-base-pair SV40 core origin that supports T-antigen-dependent DNA replication both in vivo and in vitro. The core origin contains three domains with specific DNA sequence features. These include an inverted repeat, a central T-antigen binding domain, and an adenine- and thymine-rich domain containing a DNA bending focus. The domain and spacer requirements of the core origin for DNA unwinding and replication in vitro are strikingly similar to the origin requirements for DNA replication in vivo. Thus, each of the three functional domains of the core origin contributes directly to the initiation of duplex DNA unwinding by T antigen.

MeSH Terms
DNA Helicases DNA Mutational Analysis DNA Replication DNA, Viral/genetics DNA-Binding Proteins Simian virus 40/genetics Virus Replication
Chemicals
DNA, Viral DNA-Binding Proteins DNA Helicases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dean F B
Graduate Program in Molecular Biology, Sloan Kettering Cancer Center, New York, NY 10021.
Borowiec J A
Ishimi Y
Deb S
Tegtmeyer P
Hurwitz J
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27 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1987-12-00
Pages
8267-71
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC299523
Subset
IM
Grants
NIGMS NIH HHS · 5RO1-GM34559 · United States
NCI NIH HHS · R01-CA18808 · United States
NCI NIH HHS · R01-CA38146 · United States
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