Skip to main content
Log in

Nucleotide sequence of the 3′ terminal region of belladonna mottle virus-Iowa (renamed Physalis mottle virus) RNA and an analysis of the relationships of tymoviral coat proteins

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

The 3′ terminal 1255nt sequence of Physalis mottle virus (PhMV) genomic RNA has been determined from a set of overlapping cDNA clones. The open reading frame (ORF) at the 3′ terminus corresponds to the amino acid sequence of the coat protein (CP) determined earlier except for the absence of the dipeptide, Lys-Leu, at position 110–111. In addition, the sequence upstream of the CP gene contains the message coding for 178 amino acid residues of the C-terminus of the putative replicase protein (RP). The sequence downstream of the CP gene contains an untranslated region whose terminal 80 nucleotides can be folded into a characteristic tRNA-like structure. A phylogenetic tree constructed after aligning separately the sequence of the CP, the replicase protein (RP) and the tRNA-like structure determined in this study with the corresponding sequences of other tymoviruses shows that PhMV wrongly named belladonna mottle virus [BDMV(I)] is a separate tymovirus and not another strain of BDMV(E) as originally envisaged. The phylogenetic tree in all the three cases is identical showing that any subset of genomic sequence of sufficient length can be used for establishing evolutionary relationships among tymoviruses.

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. Block J, Gibbs A, Mackenzie A (1987) The classification of tymoviruses by cDNA-RNA hybridization and other measures of relatedness. Arch Virol 96: 225–240

    Google Scholar 

  2. Craigen WJ, Caskey CT (1987) Translational frame shifting: where will it stop? Cell 50: 1–12

    Google Scholar 

  3. Dasgupta R, Kaesberg P (1982) Complete nucleotide sequence of the coat protein messenger RNA of brome mosaic virus and cowpea chlorotic mottle virus. Nucleic Acids Res 10: 703–713

    Google Scholar 

  4. Ding S, Keese P, Gibbs A (1989) Nucleotide sequence of the ononis yellow mosaic tymovirus genome. Virology 172: 555–563

    Google Scholar 

  5. Ding S, Keese P, Gibbs A (1990) The nucleotide sequence of the genomic RNA of Kennedya yellow mosaic tymovirus-Jervis Bay isolate: relationships with potex-and carlaviruses. J Gen Virol 71: 925–931

    Google Scholar 

  6. Ding SW, Howe J, Mackenzie A, Skotnicki M, Gibbs A (1990) Nucleotide sequence of the virion protein gene of belladonna mottle virus. Nucleic Acids Res 18: 6138

    Google Scholar 

  7. Ding S, Home J, Keese P, Mackenzie A, Meek D, Keese MO, Skotnicki M, Srifah P, Torronen M, Gibbs A (1990) The tymobox, a sequence shared by most tymoviruses: its use in molecular studies of tymoviruses. Nucleic Acids Res 18: 1181–1187

    Google Scholar 

  8. Ding S, Mackenzie A, Torronen M, Gibbs A (1990) Nucleotide sequence of the virion protein gene of cacao yellow mosaic tymovirus. Nucleic Acids Res 18: 5886

    Google Scholar 

  9. Dreher TW, Bujarski JJ, Hall TC (1984) Mutant viral RNAs synthesized in vitro show altered aminoacylation and replicase template activities. Nature 311: 171–175

    Google Scholar 

  10. Dumas P, Moras D, Florentz C, Giege R, Verlaan P, Van Belkum A, Pleij CWA (1987) 3-D graphics modelling of the tRNA-like 3′-end of turnip yellow mosaic virus RNA: structural and functional implications. J Biomol Struct Dyn 4: 707–728

    Google Scholar 

  11. Fitch WM, Margoliash E (1967) Construction of phylogenetic trees — a method based on mutation distances as estimated from cytochrome C sequences is of general applicability. Science 155: 279–284

    Google Scholar 

  12. Gething MJ, Bye J, Skehel J, Waterfield M (1980) Cloning and DNA sequencing of double stranded copies of haemagglutinin genes from H2 and H3 strains elucidates antigenic shift and drift in human influenza virus. Nature 287: 301–306

    Google Scholar 

  13. Gould AR, Symons RH (1982) Cucumber mosaic virus RNA3. Determination of the nucleotide sequence provides the amino acid sequences of protein 3A and viral coat protein. Eur J Biochem 126: 217–226

    Google Scholar 

  14. Grunstein M, Hogness D (1975) Colony hybridization: a method for the isolation of cloned DNAs that contained a specific gene. Proc Natl Acad Sci USA 72: 3961–3965

    Google Scholar 

  15. Gubler U, Hoffman BJ (1983) A simple and very efficient method for generating cDNA libraries. Gene 25: 263–269

    Google Scholar 

  16. Haenni AL, Joshi S, Chapeville F (1982) tRNA-like structures in the genomes of RNA viruses. Prog Nucleic Acid Res Mol Biol 27: 85–104

    Google Scholar 

  17. Hattori M, Sakaki Y (1986) Dideoxy sequencing method using denatured plasmid templates. Anal Biochem 152: 232–238

    Google Scholar 

  18. Hopper P, Harrison SC, Sauer RT (1984) Structure of tomato bushy stunt virus coat protein sequence determination and its structural implications. J Mol Biol 177: 701–713

    Google Scholar 

  19. Hermodson MA, Abad-zapatero C, Abdel Meguid SS, Pundak S, Rossmann MG, Tremaine JH (1982) Amino acid sequence of southern bean mosaic virus coat protein and its relation to the three dimensional structure of virus. Virology 119: 133–149

    Google Scholar 

  20. Joshi RL, Ravel JM, Haenni AL (1986) Interaction of turnip yellow mosaic virus val-RNA with eukaryotic elongation factor EF-1. Search for a function. EMBO J 5: 1143–1148

    Google Scholar 

  21. Keese MEO, Keese P, Gibbs A (1989) Nucleotide sequence of the genome of eggplant mosaic tymovirus. Virology 172: 547–554

    Google Scholar 

  22. Keese P, Mackenzie A, Gibbs A (1989) Nucleotide sequence of the genome of an Australian isolate of turnip yellow mosaic tymovirus. Virology 172: 536–546

    Google Scholar 

  23. Koenig R (1976) A loop-structure in the serological classification system of tymoviruses. Virology 72: 1–5

    Google Scholar 

  24. Moline HE, Fries RE (1974) A strain of belladonna mottle virus isolated fromPhysalis heterophylla in Iowa. Phytopathology 64: 44–48

    Google Scholar 

  25. Morch MD, Boyer JC, Haenni AL (1988) Overlapping open reading frames revealed by complete nucleotide sequencing of turnip yellow mosaic virus genomic RNA. Nucleic Acids Res 16: 6157–61753

    Google Scholar 

  26. Pattana S, Keese R, Shukla D, Gibbs A (1990) The primary structure of the virion protein gene and encoded protein of erysimum latent tymovirus. J Gen Virol 71: 3085–3088

    Google Scholar 

  27. Peter R, Peter C, Dupin A, Witz J (1989) Un probleme de taxonomie des tymovirus: comparison des proteines de capside de deux Virus de la Marbrure de la Belladone. CR Acad Sci Paris 309 (S III): 599–604

    Google Scholar 

  28. Savithri HS, Erickson JW (1983) The self assembly of cowpea strain of southern bean mosaic virus. Virology 126: 328–335

    Google Scholar 

  29. Savithri HS, Munshi SK, Suryanarayana S, Divakar S, Murthy MRN (1987) Stability of belladonna mottle virus particles: the role of polyamines and calcium. J Gen Virol 68: 1533–1542

    Google Scholar 

  30. Suryanarayana S, Jacob ANK, Savithri HS (1988) Is the role of basic amino terminal arm replaced by polyamines in tymoviruses? Indian J Biochem Biophys 25: 580–584

    Google Scholar 

  31. Suryanarayana S, Rao NA, Murthy MRN, Savithri HS (1989) Primary structure of belladonna mottle virus coat protein. J Biol Chem 264: 6273–6279

    Google Scholar 

  32. Van Belkum A, Binkum J, Rietveld K, Pleij CWA, Bosch L (1987) Structural similarities among valine-accepting tRNA-like structures in tymoviral RNAs and elongator tRNAs. Biochemistry 26: 1144–1151

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jacob, A.N.K., Murthy, M.R.N. & Savithri, H.S. Nucleotide sequence of the 3′ terminal region of belladonna mottle virus-Iowa (renamed Physalis mottle virus) RNA and an analysis of the relationships of tymoviral coat proteins. Archives of Virology 123, 367–377 (1992). https://doi.org/10.1007/BF01317270

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01317270

Keywords

Navigation