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Physical characterization of a stomatitis papulosa virus genome: A cleavage map for the restriction endonucleasesHindIII andEcoRI

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Summary

The genome of stomatitis papulosa virus (aparapoxvirus) was cleaved with the restriction endonucleasesHindIII andEcoRI, each giving rise to 6 fragments respectively. Double digestion with both enzymes resulted in 8 bands, two of which contained DNA fragments in double molar concentrations as revealed by reciprocal digests of isolated DNA fragments. The genome size, estimated by summation of the molecular weights of the fragments, is approximately 86×106 daltons, some 30×106 daltons smaller than vaccinia virus (anorthopoxvirus) DNA.

The cleavage sites ofHindIII andEcoRI endonucleases were mapped on the genome by analysis of reciprocal digests of isolated DNA fragments and by cross-hybridization experiments. This yielded two mapped segments which were then oriented relative to one another by cleavage of isolated partial digestion products.

The terminal restriction fragments show rapid renaturation after alkali denaturation and subsequent neutralization, indicating that stomatitis papulosa virus DNA contains terminal cross-links analogous to those found in vaccinia virus DNA.

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References

  1. Berns, K. I., Silverman, C.: Natural occurrence of cross-linked vaccinia virus deoxyribonucleic acid. J. Virol.5, 299–304 (1970).

    Google Scholar 

  2. Denhart, D. T.: A membrane filter technique for the detection of complementary DNA. Biochem. biophys. Res. Commun.23, 641–646 (1966).

    Google Scholar 

  3. Doerfler, W., Kleinschmidt, A. K.: Denaturation pattern of the DNA of adenovirus type 2 as determined by electron microscopy. J. mol. Biol.50, 579–593 (1970).

    Google Scholar 

  4. de Filippes, F. M.: Restriction enzyme digests of rapidly renaturing fragments of vaccinia virus DNA. J. Virol.17, 227–238 (1976).

    Google Scholar 

  5. Freifelder, D.: Molecular weights of coliphages and coliphage DNA. IV. Molecular weights of DNA from bacteriophages T4, T5 and T7, and the general problem of determination of M. J. mol. Biol.45, 567–577 (1970).

    Google Scholar 

  6. Geshelin, P., Berns, K. I.: Characterization and localization of the naturally occurring cross-links in vaccinia virus DNA. J. mol. Biol.88, 785–796 (1974).

    Google Scholar 

  7. Joklik, W. K.: The purification of four strains of poxvirus. Virology18, 9–18 (1962).

    Google Scholar 

  8. Lang, D.: Molecular weights of coliphages and coliphage DNA. III. Contour length and molecular weight of DNA from bacteriophages T4, T5 and T7, and from bovine papilloma virus. J. mol. Biol.54, 557–565 (1970).

    Google Scholar 

  9. Maniatis, T., Jeffrey, A., Kleid, D. G.: Nucleotide sequences of the rightward operator of phage lambda. Proc. Nat. Acad. Sci. U.S.A.72, 1184–1188 (1975).

    Google Scholar 

  10. Mayr, A., Mahnel, H., Munz, E.: Systematisierung und Differenzierung der Pockenviren. Z. Bl. Vet. Med. B,19, 69–88 (1972).

    Google Scholar 

  11. Müller, H. K., Wittek, R., Schaffner, W., Schümperli, D., Menna, A., Wyler, R.: Comparison of five poxvirus genomes by analysis with restriction endonucleasesHindIII,BamI andEcoRI. J. gen. Virol.38, 135–147 (1978).

    Google Scholar 

  12. Munz, E.: Die Rinderpocken in der Sicht moderner virologischer Erkenntnisse. Berl. Münch. Tierärztl. Wschr.80, 201–220 (1967).

    Google Scholar 

  13. Murray, K., Murray, N. E.: Phage lambda receptor chromosomes for DNA fragments made with restriction endonuclease III ofHaemophilus influenza and restriction endonuclease I ofEscherichia coli. J. mol. Biol.98, 551–564 (1975).

    Google Scholar 

  14. Nagington, J., Newton, A. A., Horne, R. W.: The structure of orf virus. Virology23, 461–472 (1964).

    Google Scholar 

  15. Sarov, I., Becker, Y.: Studies on vaccinia virus DNA. Virology33, 369–375 (1967).

    Google Scholar 

  16. Schaffner, W., Gross, K., Telford, J., Birnstiel, M.: Molecular analysis of the histone gene cluster ofPsammechinus miliaris: II. The arrangement of the five histone-coding and spacer sequences. Cell8, 471–478 (1976).

    Google Scholar 

  17. Southern, E. M.: Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. mol. Biol.98, 503–518 (1975).

    Google Scholar 

  18. Szybalski, W., Erikson, R. L., Gentry, G. A., Gafford, L. G., Randall, C. C.: Unusual properties of fowl poxvirus DNA. Virology19, 586–589 (1963).

    Google Scholar 

  19. Thomas, M., Davis, R. W.: Studies on the cleavage of bacteriophage lambda DNA withEcoRI restriction endonuclease. J. mol. Biol.91, 315–328 (1975).

    Google Scholar 

  20. Wittek, R., Menna, A., Schümperli, D., Stoffel, S., Müller, H. K., Wyler, R.:HindIII andSstI restriction sites mapped on rabbit poxvirus and vaccinia virus. J. Virol.23, 669–678 (1977).

    Google Scholar 

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Menna, A., Wittek, R., Bachmann, P.A. et al. Physical characterization of a stomatitis papulosa virus genome: A cleavage map for the restriction endonucleasesHindIII andEcoRI. Archives of Virology 59, 145–156 (1979). https://doi.org/10.1007/BF01317904

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  • DOI: https://doi.org/10.1007/BF01317904

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