1887

Abstract

SUMMARY

The conversion of superhelical (Form I) SV40 DNA to nicked molecular forms was studied by incubating SV40 [H]DNA for to 2 hr with monolayer cultures of monkey, human, or mouse cells in the presence of DEAE-dextran. The superhelical and the nicked DNA forms were then extracted from the cultures and separated by equilibrium centrifugation in caesium chloride-ethidium bromide (CsCl-EtBr) density gradients. About 66 and 42% of the Form I [H]DNA was converted to nicked DNA during 2 hr of adsorption to monkey and to human cells, respectively. Form I DNA was adsorbed less by mouse kidney cells than by monkey cells, and only about 25% of the input DNA was converted to nicked forms in 2 hr. The specific infectivities (p.f.u./counts/min.) of the SV40 DNA extracted from the cultures were about the same as those of the input DNA, despite the fact that as much as 69% of the extracted DNA represented nicked molecular forms.

Cultures of monkey cells infected with SV40 were synchronized by treatment with 1---arabinofuranosylcytosine (ara-C) from 2 to 24 hr after infection and pulse-labelled with [H]thymidine at 37 to 39 hr after infection. The pulse-labelled Form I and nicked forms of SV40 [H]DNA were extracted from the cells, purified by CsCl-EtBr equilibrium centrifugation and velocity sedimentation in sucrose gradients, and assayed for infectivity. The nicked (Form II) SV40 DNA obtained from infected cells was about half as infective as superhelical (Form I) SV40 DNA.

When SV40 [H]DNA was incubated with monkey kidney cells for 6 to 24 hr, 90 to 97% of the Form I DNA was converted to nicked molecular forms and specific infectivities were reduced by 85 to 98%, respectively.

These results suggest that minimally nicked SV40 DNA was about as infectious as superhelical (Form I) DNA in the SV40 DNA+DEAE-dextran plaque assay but that multiply nicked SV40 DNA was much less infectious.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-10-3-221
1971-03-01
2024-12-03
Loading full text...

Full text loading...

/deliver/fulltext/jgv/10/3/JV0100030221.html?itemId=/content/journal/jgv/10.1099/0022-1317-10-3-221&mimeType=html&fmt=ahah

References

  1. Aaronson S. A., Todaro O. J. 1969; Human diploid cell transformation by DNA extracted from the tumor virus SV 40. Science, New York 166:390
    [Google Scholar]
  2. Barbanti-Brodano G., Swetly P., Koprowski H. 1970; Early events in the infection of permissive cells with simian virus 40: adsorption, penetration, and uncoating. Journal of Virology 6:78
    [Google Scholar]
  3. Bauer W., Vinograd J. 1968; The interaction of closed circular DNA with intercalative dyes. I. The superhelix density of SV 40 DNA in the presence and absence of dye. Journal of Molecular Biology 33:141
    [Google Scholar]
  4. Bourgaux P., Bourgaux-ramoisy D., Dulbecco R. 1969; The replication of the ring-shaped DNA of polyoma virus. I. Identification of the replicative intermediate. Proceedings of the National Academy of Sciences of the United States of America 64:701
    [Google Scholar]
  5. Hirt B. 1967; Selective extraction of polyoma DNA from infected mouse cell cultures. Journal of Molecular Biology 26:365
    [Google Scholar]
  6. Hudson B., Upholt W. B., Devinny J., Vinograd J. 1969; The use of an ethidium analogue in the dye-buoyant density procedure for the isolation of closed circular DNA: The variation of the superhelix density of mitochondrial DNA. Proceedings of the National Academy of Sciences of the United States of America 62:813
    [Google Scholar]
  7. Kit S., Detorres R. A., Dubbs D. R., Salvi M. L. 1967; Induction of cellular deoxyribonucleic acid synthesis by simian virus 40. Journal of Virology 1:738
    [Google Scholar]
  8. Kit S., Kurimura T., Detorres R. A., Dubbs D. R. 1969; Simian virus 40 deoxyribonucleic acid replication. I. Effect of cycloheximide on the replication of SV 40 deoxyribonucleic acid in monkey kidney cells and in heterokaryons of SV 40-transformed and susceptible cells. Journal of Virology 3:25
    [Google Scholar]
  9. Kit S., Kurimura T., Salvi M. L., Dubbs D. R. 1968; Activation of infectious SV 40 DNA synthesis in transformed cells. Proceedings of the National Academy of Sciences of the United States of America 60:1239
    [Google Scholar]
  10. Kit S., Tokuno S., Nakajima K., Trkula D., Dk D. R. 1970; Temperature-sensitive simian virus 40 mutant defective in a late function. Journal of Virology 6:286
    [Google Scholar]
  11. Levine A. J., Kang H. S., Billheimer F. E. 1970; DNA replication in SV 40 infected cells. I. Analysis of replicating SV 40 DNA. Journal of Molecular Biology 50:549
    [Google Scholar]
  12. Mcewen C. R. 1967; Tables for estimating sedimentation through linear concentration gradients of sucrose solution. Analytical Biochemistry 20:114
    [Google Scholar]
  13. Sambrook J., Shatkin A. J. 1969; Polynucleotide ligase activity in cells infected with simian virus 40, polyoma virus, or vaccinia virus. Journal of Virology 4:719
    [Google Scholar]
  14. Sambrook J., Westphal H., Srinivasan P. R., Dulbecco R. 1968; The integrated state of viral DNA in SV 40-transformed cells. Proceedings of the National Academy of Sciences of the United States of America 60:1288
    [Google Scholar]
  15. Vinograd J., Lebowitz J., Radloff R., Watson R., Laipis P. 1965; The twisted circular form of polyoma viral DNA. Proceedings of the National Academy of Sciences of the United States of America 53:1104
    [Google Scholar]
/content/journal/jgv/10.1099/0022-1317-10-3-221
Loading
/content/journal/jgv/10.1099/0022-1317-10-3-221
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error