Linear or subgenomic SV40 DNAs were transfected into cells from a variety of species (including rodent, dog, muntjak, and monkey) and injected subcutaneously into neonate Syrian hamsters for tumorigenicity testing. The 'early-region' subgenomes were capable of transforming cells in vitro. Complete genomes or complementary subgenomes could transform nonpermissive and semipermissive cells, were infectious for permissive cells, and induced tumors from which infectious virus could be rescued. Tumors were not formed in neonate hamsters upon injection with subgenomic SV40 DNAs, even those capable of transforming cells in vitro. These results suggested that SV40 tumor formation in vivo may require a complete genome.
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http://dx.doi.org/10.1159/000149506 | DOI Listing |
Biochem Biophys Res Commun
June 2006
Department of Biochemistry and Cell Biology, National Institute of Infectious Diseases, 1-23-1, Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Sindbis virus replication is mediated by an RNA replicase translated from viral RNA genome. The replicase synthesizes progeny genomic RNA and shorter RNA (subgenomic RNA) carrying viral structural genes in association with cytoplasmic membranes. Here we examined the involvement of a membrane lipid, phosphatidylserine (PS), in Sindbis virus gene expression using Chinese hamster ovary cell mutants.
View Article and Find Full Text PDFJ Pathol
December 2001
Department of Pathology, University Hospitals of Ulm, Ulm, Germany.
Between 1955 and 1963, millions of children and adults were exposed to SV40-contaminated poliovirus vaccines. The oncogenic potential of this polyomavirus was revealed when intracerebral inoculation of SV40 into newborn hamsters resulted in the development of ependymomas and choroid plexus papillomas. Subsequently, SV40-like sequences were repeatedly detected in human ependymomas with broadly ranging incidence rates of 7-90%.
View Article and Find Full Text PDFDev Biol Stand
December 1998
Division of Molecular Virology, Baylor College of Medicine, Houston, TX 77030-3498, USA.
SV40 is capable of infecting humans, although its association with human diseases remains controversial. Recently, a subgenomic SV40 DNA sequence was detected by polymerase chain reaction (PCR) in certain types of human tumour tissue as well as in normal pituitary tissue. However, due to the limited DNA sequence information that was obtained in those experiments, SV40 could not be authenticated, and it was uncertain whether a related or hybrid virus (or endogenous DNA) accounted for the PCR-amplified DNA.
View Article and Find Full Text PDFGene
December 1996
Biochemistry Division, City College of the City University of New York, NY 10031, USA.
Long-term cultures of SV40-infected human keratinocytes contain integrated, but structurally altered copies of the viral sequences. The presence of these sequences is required for expression of properties associated with the transformed phenotype including immortalization. The integrated viral sequences in an anchorage-independent line of viral-transformed human keratinocytes have been found to be contained on two BamHI fragments of about 6.
View Article and Find Full Text PDFCancer Res
September 1995
Department of Medical Oncology, City of Hope National Medical Center, Duarte, California 91010, USA.
In the experiments, we examined the ability of a retroviral vector, pHaMASV, to encode two potential chemoprotective genes on separate transcription units. We previously described the pHaMSV vector, which includes the human MDR1 gene as a selectable marker and chemoprotective gene, plus an internal SV40 promoter for expressing a second heterologous gene along with MDR1 [M. E.
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