1968
DOI: 10.1073/pnas.60.4.1239
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Activation of infectious SV40 synthesis in transformed cells.

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Cited by 50 publications
(26 citation statements)
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“…Furthermore, the association persisted through zonal and equilibrium sedimentation in alkali gradients, where only denatured, single-stranded DNA exists; the persistence shows that cellular and viral DNA's are held together by covalent bonds. 964 These results are strengthened by the observation that cells transformed by SV40, which, as I show below, contain a complete viral genome, do not yield infectious viral DNA on extraction (13).…”
Section: Stable and Abortive Transformation By Dna Virusesmentioning
confidence: 94%
“…Furthermore, the association persisted through zonal and equilibrium sedimentation in alkali gradients, where only denatured, single-stranded DNA exists; the persistence shows that cellular and viral DNA's are held together by covalent bonds. 964 These results are strengthened by the observation that cells transformed by SV40, which, as I show below, contain a complete viral genome, do not yield infectious viral DNA on extraction (13).…”
Section: Stable and Abortive Transformation By Dna Virusesmentioning
confidence: 94%
“…Heterokaryons formed by fusion of these transformed cells with uninfected permissive monkey cells support the activation of the resident viral genome leading to subsequent viral DNA replication, late protein synthesis, maturation and release of virus (17,34). The time course of appearance of infectious virus from heterokaryon cultures and productive infection of permissive monkey cells is similar (16,34).…”
Section: Introductionmentioning
confidence: 96%
“…For each sample, 5-ml aliquots were seeded in two plastic dishes (6 cm in diameter) and in a plastic flask (25 cm2 (ME, L) * Yields of infectious SV40 DNA were comparable to those quoted in Table 1. concentration of the extract. Untreated TSV-5 C12 cells do not shed SV40 virions spontaneously (24), nor can infectious viral DNA be extracted from them (4,18). No infectious SV40 DNA was ever found in cells treated with poly(iornithine) alone, with dilutions of Tris* HCI buffer in poly(L-ornithine), or with deoxyribonuclease in poly(L-ornithine), nor in the controls with any other extract.…”
Section: Assay For Activationmentioning
confidence: 99%