Skip to main content
Log in

On the variability of the 3′ terminal sequence of the turnip mosaic virus genome

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

Summary

The sequence of the 3′-terminal 1223 nucleotides (nts) of a Japanese isolate of turnip mosaic virus (TuMV-Jap) RNA has been determined. The sequence reveals a single open reading frame (ORF) which terminates at a position 212 nts upstream of the 3′ poly(A)-tract. Determination of the N-terminal amino acids of TuMV-Jap coat protein (CP) mapped the CP cistron within this ORF and revealed a Glu-Ala dipeptide sequence as the putative cleavage site by which the CP is released from the viral polyprotein. The predicted amino acid sequence of the TuMV-Jap CP shows 97.2% identity with that of a Canadian isolate of TuMV (TuMV-Can) and 99% with a second, Chinese, isolate (TuMV-Chi). However, the 3′-terminal non-translated region (NTR) of TuMV-Jap RNA is significantly shorter (212 nts) than the 3′-NTR of TuMV-Can RNA (668 nts), but of equal length as the 3′-NTR of the TuMV-Chi isolate which also measures 212 nts. The 3′-NTRs of both the TuMV-Jap and TuMV-Chi RNAs show homology with the first 201 nucleotides of the TuMV-Can RNA 3′-NTR. A search in the EMBL nucleotide sequence database revealed that the 467 nt-long unique extension of the 3′-NTR of TuMV-Can RNA has 89.8% homology to a part of the chloroplast ribosomal protein 12 gene (rsp 12-gene). Irrespective of the origin of this extra sequence in the reported TuMV-Can sequence, which may have been introduced by a genuine RNA recombination event, it is concluded that the standard TuMV genome has a CP gene of 864 nts and an conserved 3′-NTR of approximately 212 nucleotides in length.

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. Allison R, Johnston RE, Dougherty WG (1986) The nucleotide sequence of the coding region of tobacco etch virus genomic RNA: evidence for the synthesis of a single polyprotein. Virology 154: 9–20

    Google Scholar 

  2. Brakke MK, van Pelt N (1970) Properties of infectious ribonucleic acid from wheat streak mosaic virus. Virology 42: 699–706

    Google Scholar 

  3. Carrington JC, Dougherty WG (1987) Small nuclear inclusion protein encoded by a plant potyvirus genome is a protease. J Virol 61: 2540–2548

    Google Scholar 

  4. Carrington JC, Cary SM, Parks TD, Dougherty WG (1989) A second proteinase encoded by a plant potyvirus genome. EMBO J 8: 365–370

    Google Scholar 

  5. Choi JK, Maeda T, Wakimoto S (1977) An improved method for the purification of turnip mosaic virus. Ann Phytopathol Soc Japan 43: 440–448

    Google Scholar 

  6. Choi JK, Wakimoto S (1979) Characterization of the protein components of turnip mosaic virus. Ann Phytopathol Soc Japan 45: 32–39

    Google Scholar 

  7. Domier LL, Franklin KM, Shahabuddin M, Hellmann GM, Overmeyer JH, Hiremath ST, Siaw MFE, Lomonossoff GP, Shaw JG, Rhoads RE (1986) The nucleotide sequence of tobacco vein mottling virus. Nucleic Acids Res 14: 5417–5430

    Google Scholar 

  8. Frenkel MJ, Ward CW, Shukla DD (1989) The use of 3′ non-coding nucleotide sequences in the taxonomy of potyviruses: application to watermelon mosaic virus 2 and soybean mosaic virus-N. J Gen Virol 70: 2775–2783

    Google Scholar 

  9. Henikoff S (1984) Unidirectional digestion with exonuclease III creates targeted break-points for DNA sequencing. Gene 28: 351–359

    Google Scholar 

  10. Kong L, Fang R, Chen Z, Mang K (1990) Molecular cloning and nucleotide sequence of coat protein gene of turnip mosaic virus. Nucleic Acids Res 18: 5555

    Google Scholar 

  11. Messing J (1983) New M13 vectors for cloning. Methods Enzymol 101: 20–78

    Google Scholar 

  12. Maiss E, Timpe U, Brisske A, Jelkmann W, Casper R, Himmler G, Mattanovich D, Katinger HWD (1989) The complete nucleotide sequence of plum pox virus RNA. J Gen Virol 70: 513–524

    Google Scholar 

  13. Mayo MA, Robinson DJ, Jolly CA, Hyman L (1989) Nucleotide sequence of potato leafroll luteovirus RNA. J Gen Virol 70: 1037–1051

    Google Scholar 

  14. Mayo MA, Jolly CA (1991) The 5′-terminal sequence of potato leafroll virus RNA: evidence of recombination between virus and host RNA. J Gen Virol 72: 2591–2595

    Google Scholar 

  15. Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chainterminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467

    Google Scholar 

  16. Sano Y, Kojima M (1989) Increase in cucumber mosaic virus concentration in Japanese radish plants co-infected with turnip mosaic virus. Ann Phytopathol Soc Japan 55: 296–302

    Google Scholar 

  17. Shukla DD, Ward CW (1988) Amino acid sequence homology of coat proteins as a basis for identification and classification of the potyvirus group. J Gen Virol 69: 2703–2710

    Google Scholar 

  18. Shukla DD, Ward CW (1989) Identification and classification of potyviruses on the basis of coat protein sequence data and serology. Arch Virol 106: 171–200

    Google Scholar 

  19. Tomlinson JA (1970) Turnip mosaic virus. CMI/AAB Descriptions of Plant Viruses, no 8

  20. Tremblay M, Nicolas O, Shinha RC, Lazure C, Laliberté J (1990) Sequence of the 3′-terminal region of turnip mosaic virus RNA and capsid protein gene. J Gen Virol 71: 2769–2772

    Google Scholar 

  21. Van der Vlugt RAA, Allefs S, de Haan P, Goldbach RW (1989) Nucleotide sequence of the 3′ terminal region of potato virus YN RNA. J Gen Virol 70: 229–233

    Google Scholar 

  22. Van der Vlugt RAA (1992) Is PeMV a strain of PVY? Arch Virol (in press)

  23. Van der Wilk F, Huisman MJ, Cornelissen BJC, Huttinga H, Goldbach R (1989) Nucleotide sequence and organization of potato leafroll virus genomic RNA. FEBS Lett 245: 51–56

    Google Scholar 

  24. Ward CW, Shukla DD (1991) Taxonomy of potyviruses: current problems and some solutions. Intervirology 32: 269–296

    Google Scholar 

  25. Yanisch-Perron C, Vieira J, Messing J (1985) Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13 mp 18 and pUC19 vectors. Gene 33: 103–119

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sano, Y., van der Vlugt, R., de Haan, P. et al. On the variability of the 3′ terminal sequence of the turnip mosaic virus genome. Archives of Virology 126, 231–238 (1992). https://doi.org/10.1007/BF01309697

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01309697

Keywords

Navigation