Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1983 Feb;45(2):882–884. doi: 10.1128/jvi.45.2.882-884.1983

Isolation of the Ends of La Crosse Virus Small RNA as a Double-Stranded Structure

Jean L Patterson 1, Daniel Kolakofsky 1, Brian P Holloway 2, John F Obijeski 2,
PMCID: PMC256485  PMID: 6834474

Abstract

The genome of La Crosse virus, a member of the Bunyaviridae, is made up of three molecules. Circular nucleocapsid structures, in three size classes, have been isolated from La Crosse virus (Obijeski et al. J. Virol. 20:664-675, 1976). Recently, Obijeski et al. (Nucleic Acids Res. 8:2431-2438) have found that the 5′ and 3′ ends of each segment are complementary in sequence. We determined that a 5′ and 3′ end complementary structure, predicted by the rules of Tinoco et al. (Nature [London] 230:362-367), can and will anneal under certain conditions. This structure is resistant to RNase in high-salt medium and can be isolated in a reasonably high yield.

Full text

PDF
882

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bishop D. H., Calisher C. H., Casals J., Chumakov M. P., Gaidamovich S. Y., Hannoun C., Lvov D. K., Marshall I. D., Oker-Blom N., Pettersson R. F. Bunyaviridae. Intervirology. 1980;14(3-4):125–143. doi: 10.1159/000149174. [DOI] [PubMed] [Google Scholar]
  2. Bishop D. H., Gould K. G., Akashi H., Clerx-van Haaster C. M. The complete sequence and coding content of snowshoe hare bunyavirus small (S) viral RNA species. Nucleic Acids Res. 1982 Jun 25;10(12):3703–3713. doi: 10.1093/nar/10.12.3703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Donis-Keller H., Maxam A. M., Gilbert W. Mapping adenines, guanines, and pyrimidines in RNA. Nucleic Acids Res. 1977 Aug;4(8):2527–2538. doi: 10.1093/nar/4.8.2527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. England T. E., Gumport R. I., Uhlenbeck O. C. Dinucleoside pyrophosphate are substrates for T4-induced RNA ligase. Proc Natl Acad Sci U S A. 1977 Nov;74(11):4839–4842. doi: 10.1073/pnas.74.11.4839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Haaster C. C., Bishop D. H. Analyses of the 3'-terminal sequences of snowshoe hare and La Crosse Bunyaviruses. Virology. 1980 Sep;105(2):564–574. doi: 10.1016/0042-6822(80)90056-2. [DOI] [PubMed] [Google Scholar]
  6. Hefti E., Bishop D. H. The 5' nucleotide sequence of vesicular stomatitis viral RNA. J Virol. 1975 Jan;15(1):90–96. doi: 10.1128/jvi.15.1.90-96.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hewlett M. J., Pettersson R. F., Baltimore D. Circular forms of Uukuniemi virion RNA: an electron microscopic study. J Virol. 1977 Mar;21(3):1085–1093. doi: 10.1128/jvi.21.3.1085-1093.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Keene J. D., Schubert M., Lazzarini R. A. Terminal sequences of vesicular stomatitis virus RNA are both complementary and conserved. J Virol. 1979 Oct;32(1):167–174. doi: 10.1128/jvi.32.1.167-174.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kolakofsky D. Isolation and characterization of Sendai virus DI-RNAs. Cell. 1976 Aug;8(4):547–555. doi: 10.1016/0092-8674(76)90223-3. [DOI] [PubMed] [Google Scholar]
  10. Leppert M., Rittenhouse L., Perrault J., Summers D. F., Kolakofsky D. Plus and minus strand leader RNAs in negative strand virus-infected cells. Cell. 1979 Nov;18(3):735–747. doi: 10.1016/0092-8674(79)90127-2. [DOI] [PubMed] [Google Scholar]
  11. Maxam A. M., Gilbert W. A new method for sequencing DNA. Proc Natl Acad Sci U S A. 1977 Feb;74(2):560–564. doi: 10.1073/pnas.74.2.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Obijeski J. F., Bishop D. H., Palmer E. L., Murphy F. A. Segmented genome and nucleocapsid of La Crosse virus. J Virol. 1976 Dec;20(3):664–675. doi: 10.1128/jvi.20.3.664-675.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Obijeski J. F., Marchenko A. T., Bishop D. H., Cann B. W., Murphy F. A. Comparative electrophoretic analysis of the virus proteins of four rhabdoviruses. J Gen Virol. 1974 Jan;22(1):21–33. doi: 10.1099/0022-1317-22-1-21. [DOI] [PubMed] [Google Scholar]
  14. Obijeski J. F., McCauley J., Skehel J. J. Nucleotide sequences at the terminal of La Crosse virus RNAs. Nucleic Acids Res. 1980 Jun 11;8(11):2431–2438. doi: 10.1093/nar/8.11.2431. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Palmer E. L., Obijeski J. F., Webb P. A., Johnson K. M. The circular, segmented nucleocapsid of an arenavirus-Tacaribe virus. J Gen Virol. 1977 Sep;36(3):541–545. doi: 10.1099/0022-1317-36-3-541. [DOI] [PubMed] [Google Scholar]
  16. Pettersson R. F., von Bonsdorff C. H. Ribonucleoproteins of Uukuniemi virus are circular. J Virol. 1975 Feb;15(2):386–392. doi: 10.1128/jvi.15.2.386-392.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Samso A., Bouloy M., Hannoun C. Présence de ribonucléoprotéines circulaires dans le virus Lumbo (Bunyavirus) C R Acad Sci Hebd Seances Acad Sci D. 1975 Feb 10;280(6):779–782. [PubMed] [Google Scholar]
  18. Tinoco I., Jr, Uhlenbeck O. C., Levine M. D. Estimation of secondary structure in ribonucleic acids. Nature. 1971 Apr 9;230(5293):362–367. doi: 10.1038/230362a0. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES