Covalently closed circular DNA of avian sarcoma virus

Purification from nuclei of infected quail tumor cells and measurement by electron microscopy and gel electrophoresis

Ramareddy V. Guntaka, Oliver C. Richards, Peter R. Shank, Hsing Jien Kung, Norman Davidson, Edward Pritsch, J. Michael Bishop, Harold E. Varmus

Research output: Contribution to journalArticle

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Abstract

Avian sarcoma virus-specific DNA is synthesized three to fourfold more efficiently after infection of a Japanese quail tumor cell line (QT-6, derived from a fibrosarcoma induced with methylcholanthrene) than after infection of duck or quail embryo fibroblasts; 10 to 30 copies of viral DNA per cell are generally observed in the first 24 hours after infection at multiplicities of one to five focus-forming units per cell. During the first five hours after infection viral DNA accumulates only in the cytoplasm of QT-6 cells; thereafter viral DNA is also observed in the nucleus. Covalently closed circular forms of viral DNA (form I) accumulate exclusively in the nucleus, and they persist for at least 600 hours after infection; within 24 to 48 hours after infection, form I DNA constitutes as much as 50% of the nuclear species of viral DNA and 20 to 25% of viral DNA in whole cells. We have purified viral form I DNA about 105-fold from acutely-infected QT-6 cells by cell fractionation, sodium dodecyl sulfate/sodium chloride precipitation of cellular DNA, equilibrium density centrifugation in cesium chloride gradients containing propidium diiodide, rate zonal sedimentation in sucrose gradients, and chromatographic selection of molecules renaturing with zero-order kinetics. The length of viral form I DNA has been measured by direct observation in the electron microscope, revealing species of 6.6 × 106, 5.6 × 106 and 2 to 4 × l06 daltons. These species presumably correspond to DNA transcribed from RNA subunits of avian sarcoma virus (3.3 × 106 daltons); DNA transcribed from RNA subunits of transformation-defective deletion mutants of the virus (2.8 × 106 daltons) shown to be present in the infecting stock; and newly identified, incomplete transcripts of these RNA subunits. The size of these species and their viral specificity were confirmed by molecular hybridization after electrophoresis in agarose gels. Viral form I DNA of 5 to 7 × 106 daltons is infectious in chick embryo cells, resulting in production of avian sarcoma virus and transformation-defective virus, whereas viral form I DNA of 2 to 4 × 106 daltons is not infectious in similar tests and is presumably defective.

Original languageEnglish
Pages (from-to)337-357
Number of pages21
JournalJournal of Molecular Biology
Volume106
Issue number2
DOIs
Publication statusPublished - Sep 15 1976
Externally publishedYes

Fingerprint

Avian Sarcoma Viruses
Circular DNA
Quail
Electrophoresis
Electron Microscopy
Gels
Viral DNA
DNA
Neoplasms
Infection
RNA
Defective Viruses
Cell Fractionation
Coturnix
Methylcholanthrene
Ducks
Agar Gel Electrophoresis
Propidium
Fibrosarcoma
Chick Embryo

ASJC Scopus subject areas

  • Molecular Biology

Cite this

Covalently closed circular DNA of avian sarcoma virus : Purification from nuclei of infected quail tumor cells and measurement by electron microscopy and gel electrophoresis. / Guntaka, Ramareddy V.; Richards, Oliver C.; Shank, Peter R.; Kung, Hsing Jien; Davidson, Norman; Pritsch, Edward; Bishop, J. Michael; Varmus, Harold E.

In: Journal of Molecular Biology, Vol. 106, No. 2, 15.09.1976, p. 337-357.

Research output: Contribution to journalArticle

Guntaka, Ramareddy V. ; Richards, Oliver C. ; Shank, Peter R. ; Kung, Hsing Jien ; Davidson, Norman ; Pritsch, Edward ; Bishop, J. Michael ; Varmus, Harold E. / Covalently closed circular DNA of avian sarcoma virus : Purification from nuclei of infected quail tumor cells and measurement by electron microscopy and gel electrophoresis. In: Journal of Molecular Biology. 1976 ; Vol. 106, No. 2. pp. 337-357.
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abstract = "Avian sarcoma virus-specific DNA is synthesized three to fourfold more efficiently after infection of a Japanese quail tumor cell line (QT-6, derived from a fibrosarcoma induced with methylcholanthrene) than after infection of duck or quail embryo fibroblasts; 10 to 30 copies of viral DNA per cell are generally observed in the first 24 hours after infection at multiplicities of one to five focus-forming units per cell. During the first five hours after infection viral DNA accumulates only in the cytoplasm of QT-6 cells; thereafter viral DNA is also observed in the nucleus. Covalently closed circular forms of viral DNA (form I) accumulate exclusively in the nucleus, and they persist for at least 600 hours after infection; within 24 to 48 hours after infection, form I DNA constitutes as much as 50{\%} of the nuclear species of viral DNA and 20 to 25{\%} of viral DNA in whole cells. We have purified viral form I DNA about 105-fold from acutely-infected QT-6 cells by cell fractionation, sodium dodecyl sulfate/sodium chloride precipitation of cellular DNA, equilibrium density centrifugation in cesium chloride gradients containing propidium diiodide, rate zonal sedimentation in sucrose gradients, and chromatographic selection of molecules renaturing with zero-order kinetics. The length of viral form I DNA has been measured by direct observation in the electron microscope, revealing species of 6.6 × 106, 5.6 × 106 and 2 to 4 × l06 daltons. These species presumably correspond to DNA transcribed from RNA subunits of avian sarcoma virus (3.3 × 106 daltons); DNA transcribed from RNA subunits of transformation-defective deletion mutants of the virus (2.8 × 106 daltons) shown to be present in the infecting stock; and newly identified, incomplete transcripts of these RNA subunits. The size of these species and their viral specificity were confirmed by molecular hybridization after electrophoresis in agarose gels. Viral form I DNA of 5 to 7 × 106 daltons is infectious in chick embryo cells, resulting in production of avian sarcoma virus and transformation-defective virus, whereas viral form I DNA of 2 to 4 × 106 daltons is not infectious in similar tests and is presumably defective.",
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T2 - Purification from nuclei of infected quail tumor cells and measurement by electron microscopy and gel electrophoresis

AU - Guntaka, Ramareddy V.

AU - Richards, Oliver C.

AU - Shank, Peter R.

AU - Kung, Hsing Jien

AU - Davidson, Norman

AU - Pritsch, Edward

AU - Bishop, J. Michael

AU - Varmus, Harold E.

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