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PMID: 3029989 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression of the poliovirus genome from infectious cDNA is dependent upon arrangements of eukaryotic and prokaryotic sequences in recombinant plasmids.

Virology ·Vol. 157 ·No. 2 ·1987-04-00 ·Pages 560-4

Kuhn RJ, Wimmer E, Semler BL

Abstract

The introduction of a cDNA copy of poliovirus type 1 (Mahoney) into cultured primate cells results in the production of infectious virus. The level of infectious virus can be increased by incorporation of eukaryotic signals of transcription and replication. We have utilized the SV40 DNA sequence coding for the early and late promoters, the SV40 origin of replication, and the enhancer elements, along with the cDNA of poliovirus, to determine the important parameters for the level of infectious virus produced following transfection. Although plasmid replication increases the level of infectivity, the major determinant of infectivity is promoter activity.

MeSH Terms
Animals Antigens, Viral, Tumor/genetics Cell Line Chlorocebus aethiops DNA/genetics Enhancer Elements, Genetic Genes, Viral Plasmids Poliovirus/genetics,physiology Promoter Regions, Genetic Simian virus 40/genetics Transfection Virus Replication
Chemicals
Antigens, Viral, Tumor DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kuhn R J
Wimmer E
Semler B L
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1987-04-00
Pages
560-4
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Grants
NIAID NIH HHS · R01 AI022693 · United States
NIAID NIH HHS · 5RO1 AI15122-13 · United States
NIAID NIH HHS · AI 22693 · United States
NCI NIH HHS · CA 28146-06 · United States
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