Abstract
Three temperature-sensitive (ts) mutants of simian virus 40 (SV40) in complementation group A (tsA7, tsA28, tsA30) have been isolated and characterized in permissive and restrictive host cells. At 41 C in the AH line of African green monkey kidney cells, the mutants are deficient in an early function required to produce infectious viral deoxyribonucleic acid (DNA). Temperature-shift experiments and analysis of SV40 viral DNA replication by gel electrophoresis have provided strong evidence that the ts gene product of the three mutants is directly required to initiate each new round of viral DNA replication but is not required to complete a cycle which has already begun. The synthesis of mutant DNA molecules themselves can be initiated by a nonmutant gene product in viral complementation studies at 41 C. The cell, however, cannot substitute a host function to provide the initiator required for the replication of free viral DNA. The viral initiator is also required to establish the stable transformation of 3T3 cells.
MeSH Terms
Animals
Carbon Isotopes
Cell Line
DNA Replication
DNA, Viral/analysis,biosynthesis,pharmacology
Electrophoresis
Genes
Genetic Complementation Test
Haplorhini
Kidney
Mice
Molecular Biology
Mutation
Simian virus 40/analysis,growth & development,metabolism
Temperature
Thymidine/metabolism
Transformation, Genetic
Tritium
Viral Plaque Assay
Virus Replication
Chemicals
Carbon Isotopes
DNA, Viral
Tritium
Thymidine
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Tegtmeyer P
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20 references, click to expand
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