Skip to main content
Log in

The VP3 gene of human group C rotavirus

  • Published:
Virus Genes Aims and scope Submit manuscript

Abstract

The complete nucleotide sequence of genome segment 4 from the human group C rotavirus (Bristol strain) was determined. Comparison of the nucleotide sequences of the genome termini with the consensus 5′ and 3′ terminal non-coding sequences of the human group C rotavirus genome revealed characteristic 5′ and 3′ sequence motifs. Human group C rotavirus genome segment 4 is 2, 166bp long and encodes a single open reading frame of 2,082 nucleotides (693 amino acids) starting at nucleotide 55 and terminating at nucleotide 2,136 giving a 3′ untranslated region of 30 nucleotides. Alignment with the porcine group C VP3 equivalent gene showed the human gene is one amino acid longer, and that the proteins have 84.1% amino acid sequence identity. A conserved potential nucleotide binding motif shared with the porcine VP3 sequence was identified. Analogy with the group A rotaviruses suggested that the genome segment 4 encodes the group C rotavirus guanylyltransferase.

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. EstesM.K. and CohenJ.C., Microbiol Rev53, 410–449, 1989

    Google Scholar 

  2. PrasadB.V.V. and ChiuW. in RamigR.F. (ed)Rotaviruses, Current Topics in Microbiology and Immunology, vol 185, Springer-Verlag, Berlin pp 9–29, 1994.

    Google Scholar 

  3. MitchellD.B. and BothG.W., Nucleic Acids Res.16, 624, 1988.

    Google Scholar 

  4. MitchellD.B. and BothG.W. Virology177, 324–331, 1990.

    Google Scholar 

  5. SaifL.J. and JiangB. in RamigR.F. (ed)Rotaviruses, Current Topics in Microbiology and Immunology, vol 185, Springer-Verlag, Berlin pp 339–371, 1994.

    Google Scholar 

  6. HungT., ChenG., WangC., ChouZ., ChaoT., YeW., YaoH., and MengK., Lancet 2, 1078–1079, 1983.

    Google Scholar 

  7. LambdenP.R., CookeS.J., CaulE.O., and ClarkeI.N., J. Virol66, 1817–1822, 1992.

    Google Scholar 

  8. CaulE.O., AshleyC.R., DarvilleJ.M. and BridgerJ.C., J. Med Virol30, 201–205, 1990.

    Google Scholar 

  9. CookeS.J., LambdenP.R., CaulE.O., and ClarkeI.N., Virology184, 781–785, 1991.

    Google Scholar 

  10. LambdenP.R. and ClarkeI.N. in AdolphK.W. (ed) Methods in Molecular Genetics, Molecular Virology Techniques, Part B, Vol. 7. Academic Press, Orlando FL, 1995, Chapter 23.

    Google Scholar 

  11. FieldingP.A., LambdenP.R., CaulE.O., and ClarkeI.N., Virology204, 442–446, 1994.

    Google Scholar 

  12. BremontM. Juste-LesageP., Chabanne-VautherotD., CharpilienneA., and CohenJ., Virology186, 684–692, 1992.

    Google Scholar 

  13. KozakM., J. Biol Chem266, 19867–19870, 1991.

    Google Scholar 

  14. JiangJ.M., SaifL.J., KangS.Y. and KimJ.H., J. Virol64, 3171–3178, 1990.

    Google Scholar 

  15. GriceA.S., LambdenP.R., CaulE.O., and ClarkeI.N., J. Med Virol44, 166–171, 1994.

    Google Scholar 

  16. PizarroJ.L., SandinoA.M., PizarroJ.M., FernandezJ., and SpencerE., J. Gen Virol72, 325–332, 1991.

    Google Scholar 

  17. LiuM., MattionN.M., and EstesM.K., Virology188, 77–84, 1992.

    Google Scholar 

  18. GorbalenyaA.E. and KooninE.V., Nucleic Acids Res.17, 8413–8440, 1989.

    Google Scholar 

  19. ClevelandD.R., ZarblH., and MillwardS., J. Virol60, 307–311, 1986.

    Google Scholar 

  20. SeligerL.S., ZhengK., and ShatkinA.J., J. Biol. Chem.,262, 16289–16293, 1987.

    Google Scholar 

  21. MaoZ. and JoklikW.K., Virology,185, 377–386, 1991.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Samarbaf-Zadeh, A.R., Lambden, P.R., Green, S.M. et al. The VP3 gene of human group C rotavirus. Virus Genes 13, 169–173 (1996). https://doi.org/10.1007/BF00568909

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00568909

Key Words

Navigation