Abstract
Physical maps of bovine papillomavirus type 1 and type 2 (BPV-1 and BPV-2) DNA were constructed from analysis of the electrophoretic mobilities of restriction endonuclease cleavage fragments from dual digests. BPV-1 DNA was sensitive to Hind III, HindIII, EcoRI, HpaI, AND BamHI, with all but HindII yielding single scissions. BPV-2 DNA was resistant to EcoRI, and HindIII had one cleavage site whereas HpaI, BamHI, and HindII yielded multiple fragments. Of four BPV-1 isolates examined, DNA from one isolate was resistant to HindIII, and another DNA isolate was resistant to BamHI. The three BPV-2 isolates examined were uniformly sensitive to the restriction endonucleases employed.
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- Barthold S. W., Koller L. D., Olson C., Studer E., Holtan A. Atypical warts in cattle. J Am Vet Med Assoc. 1974 Aug 1;165(3):276–280. [PubMed] [Google Scholar]
- Favre M., Orth G., Croissant O., Yaniv M. Human papillomavirus DNA: physical map. Proc Natl Acad Sci U S A. 1975 Dec;72(12):4810–4814. doi: 10.1073/pnas.72.12.4810. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Favre M., Orth G., Croissant O., Yaniv M. Human papillomavirus DNA: physical mapping of the cleavage sites of Bacillus amyloliquefaciens (BamI) and Haemophilus parainfluenzae (HpaII) endonucleases and evidence for partial heterogeneity. J Virol. 1977 Mar;21(3):1210–1214. doi: 10.1128/jvi.21.3.1210-1214.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Garfin D. E., Goodman H. M. Nucleotide sequences at the cleavage sites of two restriction endonucleases from Hemophilus parainfluenzae. Biochem Biophys Res Commun. 1974 Jul 10;59(1):108–116. doi: 10.1016/s0006-291x(74)80181-6. [DOI] [PubMed] [Google Scholar]
- Gissmann L., Pfister H., Zur Hausen H. Human papilloma viruses (HPV): characterization of four different isolates. Virology. 1977 Feb;76(2):569–580. doi: 10.1016/0042-6822(77)90239-2. [DOI] [PubMed] [Google Scholar]
- Jarrett W. F., McNeil P. E., Grimshaw W. T., Selman I. E., McIntyre W. I. High incidence area of cattle cancer with a possible interaction between an environmental carcinogen and a papilloma virus. Nature. 1978 Jul 20;274(5668):215–217. doi: 10.1038/274215a0. [DOI] [PubMed] [Google Scholar]
- Lancaster W. D., Olson C. Demonstration of two distinct classes of bovine papilloma virus. Virology. 1978 Sep;89(2):372–379. doi: 10.1016/0042-6822(78)90179-4. [DOI] [PubMed] [Google Scholar]
- Lancaster W. D., Theilen G. H., Olson C. Hybridization of bovine papilloma virus type 1 and type 2 DNA to DNA from virus-induced hamster tumors and naturally occurring equine tumors. Intervirology. 1979;11(4):227–233. doi: 10.1159/000149038. [DOI] [PubMed] [Google Scholar]
- Law M. F., Lancaster W. D., Howley P. M. Conserved polynucleotide sequences among the genomes of papillomaviruses. J Virol. 1979 Oct;32(1):199–207. doi: 10.1128/jvi.32.1.199-207.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loening U. E. The determination of the molecular weight of ribonucleic acid by polyacrylamide-gel electrophresis. The effects of changes in conformation. Biochem J. 1969 Jun;113(1):131–138. doi: 10.1042/bj1130131. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Parker R. C., Watson R. M., Vinograd J. Mapping of closed circular DNAs by cleavage with restriction endonucleases and calibration by agarose gel electrophoresis. Proc Natl Acad Sci U S A. 1977 Mar;74(3):851–855. doi: 10.1073/pnas.74.3.851. [DOI] [PMC free article] [PubMed] [Google Scholar]