Skip to main content
Log in

Molecular characterization of the 11th RNA segment from human group C rotavirus

  • Published:
Virus Genes Aims and scope Submit manuscript

Abstract

The complete nucleotide sequence of genome segment 11 from the noncultivatable, human group C rotavirus (Bristol strain) was determined. Comparison of the nucleotide sequence of the segment termini with the consensus 5′ and 3′ terminal noncoding sequences of the human group C rotavirus genome revealed characteristic 5′ and 3′ sequences. Human group C rotavirus genome segment 11 is 613 bp long and encodes a single open reading frame of 450 nucleotides (150 amino acids) starting at nucleotide 39 and terminating at nucleotide 489, leaving a long 3′ untranslated region of 124 nucleotides. The predicted translation product has a calculated molecular weight of 17.7 kD and contains four potential N-linked glycosylation sites. No significant homologies to other viral proteins were found in database searches. Hydropathy analysis predicted the human group C rotavirus genome segment 11 translation product has a hydrophilic carboxy terminus (amino acids 54–150) and a hydrophobic amino terminus (amino acids 1–53) that can be further subdivided into three short hydrophobic sequences—H1, H2, and H3. These features are analogous to the integral membrane glycoprotein NSP4 encoded by group A rotavirus gene 10.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Estes M.K. and Cohen J.C., Microbiol Rev53 410–449, 1989.

    Google Scholar 

  2. Pedley S., Bridger J.C., Chasey D., and McCrae M.A., J Gen Virol67 131–137, 1986.

    Google Scholar 

  3. Bridger J.C., Pedley S., and McCrae M.A., J Clin Microbiol23 760–763, 1986.

    Google Scholar 

  4. Saif L.J. in Saif L.J. and Theil K.W. (eds).Viral Diarrheas of Man and Animals. CRC Press, Boca Raton, FL, 1990, pp. 73–95.

    Google Scholar 

  5. Hung T., Chen G., Wang C., Chou Z., Chao T., Ye W., Yao H., and Meng K., Lancet2 1078–1079, 1983.

    Google Scholar 

  6. Saif L.J., Bohl E. H., Theil K. W., Cross R.F., and House J.A., J Clin Microbiol12 105–111, 1980.

    Google Scholar 

  7. Bridger J.C. inNovel Diarrhoea Viruses. CIBA Foundation Symposium, Vol. 128. Wiley, Chichester, UK. 1987, pp. 5–23.

    Google Scholar 

  8. Brown D.W.G., Campbell L., Tomkins D.S., and Hambling M.H., Lancet2 737–738, 1989.

    Google Scholar 

  9. Penaranda M.E., Cubitt W.D., Sinarachatanant P., Taylor D.N., Likanonsakal S., Saif L.J., and Glass R.I., J Infect Dist160 392–397, 1989.

    Google Scholar 

  10. Caul E.O., Ashley C.R., Darville J.M., and Bridger J.C., J Med Virol30 201–205, 1990.

    Google Scholar 

  11. Mattion N.M., Cohen J., and Estes M.K., in Kapikian A.Z. (ed).Viral Infections of the Gastrointestinal Tract. Marcel Dekker, New York, 1994, pp. 169–249.

    Google Scholar 

  12. Chen G-M., Hung T., and Mackow E.R., Virology175 605–609, 1990.

    Google Scholar 

  13. Petric M., Mayur K., Vonderfecht S., Eiden J., J Gen Virol72 2801–2804, 1991.

    Google Scholar 

  14. Lambden P.R., Cooke S.J., Caul E.O., and Clarke I.N., J Virol66 1817–1822, 1992.

    Google Scholar 

  15. Cooke S.J., Lambden P.R., Caul E.O., and Clarke I.N., Virology184 781–785, 1991.

    Google Scholar 

  16. Fielding P.A., Lambden P.R., Caul E.O., and Clarke I.N., Virology204 442–446, 1994.

    Google Scholar 

  17. Grice A.S., Lambden P.R., Caul E.O., and Clarke I.N., J. Med Virol44 166–171, 1994.

    Google Scholar 

  18. Lambden P.R. and Clarke I.N. in Adolph K.W. (ed).Methods in Molecular Genetics, Molecular Virology Techniques, Part B, Vol. 7. Academic Press, Orlando, FL, 1995, Chapter 23.

    Google Scholar 

  19. Kozak M., J Biol Chem266 19867–19870, 1991.

    Google Scholar 

  20. Hopp T.P. and Woods K.R., Proc Natl Acad Sci USA78 3824–3828, 1981.

    Google Scholar 

  21. Ballard A., McCrae M.A., and Desselberger U., J Gen Virol73 633–638, 1992.

    Google Scholar 

  22. Baybutt H.N. and McCrae M.A., Virus Res1 533–541, 1984.

    Google Scholar 

  23. Both G.W., Siegman L.J., Bellamy A.R., and Atkinson P.H., J Virol48 335–339, 1983.

    Google Scholar 

  24. Lopez S. and Arias C.F., J Gen Virol74 1223–1226, 1993.

    Google Scholar 

  25. Okada Y., Richardson M.A., Ikegami N., Nomoto A., and Furuichi Y., J Virol51 856–859, 1984.

    Google Scholar 

  26. Powell K.F.H., Gunn P.R., and Bellamy A.R., Nucleic Acids Res15 763, 1988.

    Google Scholar 

  27. Ward C.W., Azad A.A., and Dyall-Smith M.L., Virology144 328–336, 1985.

    Google Scholar 

  28. Bergmann C.C., Maass D., Poruchynsky S., Atkinson P.H., and Bellamy A.R., EMBO J8 1695–1703, 1989.

    Google Scholar 

  29. Chan W-K., Au K-S., and Estes M.K., Virology164 435–442, 1988.

    Google Scholar 

  30. Au K-S., Chan W-K., Burns J.W., and Estes M.K., J Virol63 4553–4562, 1989.

    Google Scholar 

  31. Nilsson M., von Bonsdorff C-H., and Svensson L., Arch Virol133 21–37, 1993.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Deng, Y., Fielding, P.A., Lambden, P.R. et al. Molecular characterization of the 11th RNA segment from human group C rotavirus. Virus Genes 10, 239–243 (1995). https://doi.org/10.1007/BF01701813

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01701813

Key words

Navigation