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. 1972 May;9(5):879–882. doi: 10.1128/jvi.9.5.879-882.1972

Release of Rubella Virus Ribonucleic Acid from Ribonucleoprotein by Polyanions

Tapani Hovi 1
PMCID: PMC356387  PMID: 5025496

Abstract

Rubella virus ribonucleoprotein was accessible to pancreatic ribonuclease, Pronase, and certain polyanions. Most of the ribonucleic acid (RNA) label was made acid-soluble by ribonuclease, whereas Pronase and the polyanions liberated 40S RNA from the ribonucleoprotein.

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Selected References

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  1. Burge B. W., Pfefferkorn E. R. Functional defects of temperature-sensitive mutants of Sindbis virus. J Mol Biol. 1968 Jul 14;35(1):193–205. doi: 10.1016/s0022-2836(68)80047-6. [DOI] [PubMed] [Google Scholar]
  2. GODAL H. C. Precipitation of human fibrinogen with heparin. Scalpel (Brux) 1960;12:56–65. [PubMed] [Google Scholar]
  3. Goldstein E. A., Pons M. W. The effect of polyvinylsulfate on the ribonucleoprotein of influenza virus. Virology. 1970 Jun;41(2):382–384. doi: 10.1016/0042-6822(70)90093-0. [DOI] [PubMed] [Google Scholar]
  4. Holmes I. H., Wark M. C., Warburton M. F. Is rubella an arbovirus? II. Ultrastructural morphology and development. Virology. 1969 Jan;37(1):15–25. doi: 10.1016/0042-6822(69)90301-8. [DOI] [PubMed] [Google Scholar]
  5. Hovi T., Vaheri A. Infectivity and some physicochemical characteristics of rubella virus ribonucleic acid. Virology. 1970 Sep;42(1):1–8. doi: 10.1016/0042-6822(70)90232-1. [DOI] [PubMed] [Google Scholar]
  6. Hovi T., Vaheri A. Rubella virus-specific ribonucleic acids in infected BHK21 cells. J Gen Virol. 1970 Jan;6(1):77–83. doi: 10.1099/0022-1317-6-1-77. [DOI] [PubMed] [Google Scholar]
  7. Käriäinen L., Söderlund H. Properties of Semliki Forest virus nucleocapsid. 1. Sensitivity to pancreatic ribonuclease. Virology. 1971 Jan;43(1):291–299. doi: 10.1016/0042-6822(71)90246-7. [DOI] [PubMed] [Google Scholar]
  8. Mettler N. E., Petrelli R. L., Casals J. Absence of antigenic cross-reactions between rubella virus and arbouviruses. Virology. 1968 Nov;36(3):503–504. doi: 10.1016/0042-6822(68)90175-x. [DOI] [PubMed] [Google Scholar]
  9. Pons M. W., Schulze I. T., Hirst G. K., Hauser R. Isolation and characterization of the ribonucleoprotein of influenza virus. Virology. 1969 Oct;39(2):250–259. doi: 10.1016/0042-6822(69)90045-2. [DOI] [PubMed] [Google Scholar]
  10. TUNIS M., REGELSON W. A comparative study of the inhibiting effects of anionic polyelectrolytes on deoxyribonucleases. Arch Biochem Biophys. 1963 Jun;101:448–455. doi: 10.1016/0003-9861(63)90502-2. [DOI] [PubMed] [Google Scholar]
  11. VAHERI A. HEPARIN AND RELATED POLYIONIC SUBSTANCES AS VIRUS INHIBITORS. Acta Pathol Microbiol Scand Suppl. 1964:SUPPL 171–17298. [PubMed] [Google Scholar]
  12. Vaheri A., Hovi T. Structural proteins and subunits of rubella virus. J Virol. 1972 Jan;9(1):10–16. doi: 10.1128/jvi.9.1.10-16.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Vaheri A., Vesikari T. Small size rubella virus antigens and soluble immune complexes: analysis by the platelet aggregation technique. Arch Gesamte Virusforsch. 1971;35(1):10–24. doi: 10.1007/BF01249748. [DOI] [PubMed] [Google Scholar]
  14. von Bonsdorff C. H., Vaheri A. Growth of rubella virus in BHK21 cells: electron microscopy of morphogenesis. J Gen Virol. 1969 Jul;5(1):47–51. doi: 10.1099/0022-1317-5-1-47. [DOI] [PubMed] [Google Scholar]

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