## Abstract Fluorescein dye microinjection was used to demonstrate changes in communication between human epidermal keratinocytes grown in vitro after infection by the oncogenic virus, SV40. Whereas keratinocytes are normally fully coupled to each other, dye spread becomes progressively restricted
Analysis of stable and unstable viral forms in SV40-infected human keratinocytes
β Scribed by Piotr Naimski; Mark L. Steinberg
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 603 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
β¦ Synopsis
We analyzed the state of the genomic DNA of the papovavirus SV40 in human keratinocytes as viral-infected cells gradually acquired a transformed phenotype over time. Initially, the vast majority of the viral DNA is maintained either in a full-length supercoiled form or as truncated subgenomic fragments with little evidence of integration. However, analyses of clonal populations revealed great heterogeneity and instability of the viral DNA, and we were able to isolate one clonal subpopulation in which integrated forms of the virus appeared to predominate. Similarly, uncloned populations eventually ceased production of the "free" viral DNA after several years in culture and instead came to display tandemly repeated SV40 copies at a single host integration site. Interestingly, Bgl I1 digestion of host DNA generated restriction fragments containing the integrated SV40 DNA, which were of differing sizes in cultures at the 144th vs the 163rd serial passage suggesting modification or rearrangement of sequences at or near the integration site. Host sequences flanking the integrated viral DNA at the 163rd serial passage have been isolated on restriction fragments generated by Eco RI, Bam HI, and Hpa I1 digestion. These analyses suggest that the integrated virus is linearized near the Bgl I site and contains a large deletion in the SV40 early region at one of the viral-host junctions.
π SIMILAR VOLUMES
## Abstract Gene amplification contributes to carcinogenesis by enhancing protoβoncogene activity and causing chromosomal instability. The ease of detecting amplified tumorβvirus sequences has encouraged use of this system as a surrogate for studying the molecular events involved in endogenous gene
Simian virus 40 (SV40) is capable of inducing cellular DNA synthesis in permissive and nonpermissive cells. Utilizing flow cytometry, we analyzed the DNA content changes in two diploid human cell strains and two monkey cell lines. The osteogenesis imperfecta (OI) human skin fibroblasts were induced