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PMID: 2838480 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Initiation of adenovirus DNA replication. II. Structural requirements using synthetic oligonucleotide adenovirus templates.

The Journal of biological chemistry ·Vol. 263 ·No. 20 ·1988-07-15 ·Pages 9809-17

Kenny MK, Hurwitz J

Abstract

Adenovirus (Ad) virions contain a 55-kDa terminal protein covalently linked to both 5'-ends of the linear duplex DNA genome. The origin of DNA replication is contained within the terminal 50 base pair of the inverted terminal repeats. In the accompanying paper (Kenny, M. K., Balogh, L. A., and Hurwitz, J. (1988) J. Biol. Chem. 263, 9801-9808), it was demonstrated that synthetic oligonucleotide templates which contain the Ad origin, but lack the 55-kDa terminal protein, can serve as templates for the initiation of Ad DNA replication. Partially duplex oligonucleotides that lacked up to 14 nucleotides from the 5'-end of the nontemplate (displaced) strand supported initiation as much as 20-fold more efficiently than fully duplex oligonucleotides. The removal of 18 nucleotides or more from the 5'-end of the displaced strand resulted in a sharp decrease in the ability of the DNA templates to support initiation. The poor template efficiency of certain DNAs could be explained by their inability to bind nuclear factor I. The initiation efficiency observed with other DNAs correlated with their ability to bind the preterminal protein-Ad DNA polymerase complex. At low concentrations of the Ad DNA-binding protein, protein-primed initiation was also observed on single-stranded DNAs. The single-stranded template strand of the Ad origin was at least 5-20-fold better at supporting initiation than other single-stranded DNAs. These findings suggest a model in which the 3'-end of the template strand is rendered single-stranded as a prerequisite for initiation of Ad DNA replication.

MeSH Terms
Adenosine Triphosphate/pharmacology Adenoviridae/genetics Base Sequence Binding, Competitive CCAAT-Enhancer-Binding Proteins DNA Replication DNA, Viral/genetics DNA-Binding Proteins/metabolism DNA-Directed DNA Polymerase/metabolism Deoxycytidine Monophosphate/metabolism Exonucleases/metabolism Macromolecular Substances NFI Transcription Factors Oligodeoxyribonucleotides/genetics,metabolism Protein Precursors/metabolism Templates, Genetic Transcription Factors Viral Proteins/physiology Virus Replication
Chemicals
CCAAT-Enhancer-Binding Proteins DNA, Viral DNA-Binding Proteins Macromolecular Substances NFI Transcription Factors Oligodeoxyribonucleotides Protein Precursors Transcription Factors Viral Proteins terminal protein, adenovirus Deoxycytidine Monophosphate Adenosine Triphosphate DNA-Directed DNA Polymerase Exonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kenny M K
Graduate Program in Molecular Biology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
Hurwitz J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-07-15
Pages
9809-17
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIGMS NIH HHS · GM34559 · United States
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