Construction and analysis of infectious transcripts from a resistance- breaking strain of tobacco vein mottling potyvirus

Archives of Virology

Volumn 141, Issue 8, 1996, Pages 1535-1552

  Nicolas, O ^a   Pirone, T P ^b   Hellmann, G M ^a  

^a Psychophysiology Lab Bowman Gray T   (United States)

^b UNIVERSITY OF KENTUCKY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NICOTIANA BENTHAMIANA; NICOTIANA TABACUM; POTYVIRUS; TABACUM; TOBACCO VEIN MOTTLING VIRUS;

EID: 0029800235     PISSN: 03048608     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01718253     Document Type: Article

References (42)

1. Atreya PL, Atreya CD, Pirone TP (1991) Amino acid substitutions in the coat protein result in loss of insect transmissibility of a plant virus. Proc Natl Acad Sci USA 88: 7 887-7 891
2. Atreya CD, Atreya PL, Thornbury DW, Pirone TP (1992) Site-directed mutations in the potyvirus HC-PRO gene affect helper component activity, virus accumulation, and symptom expression in infected tobacco plants. Virology 191: 106-111
3. Atreya PL, Lopezmoya JJ, Chu MH, Atreya CD, Pirone TP (1995) Mutational analysis of the coat protein N-terminal amino acids involved in potyvirus transmission by aphids. J Gen Virol 76: 265-270
4. Atreya CD, Pirone TP (1993) Mutational analysis of the helper component-proteinase gene of a potyvirus: effect of amino acid substitutions, deletions and gene replacement on virulence and aphid transmissibility. Proc Natl Acad Sci USA 90: 11 919-11 923
5. Atreya CD, Raccah B, Pirone TP (1990) A point mutation in the coat protein abolishes aphid transmissibility of a potyvirus. Virology 178: 161-165
6. Carrington JC, Dougherty WG (1987) Small nuclear inclusion protein encoded by a plant potyvirus genome is a protease. J Virol 61: 2 540-2 548
7. Carrington JC, Freed DD, Oh CS (1990) Expression of potyviral polyproteins in transgenic plants reveals three proteolytic activities required for complete processing. EMBO J 9: 1 347-1 353
8. Carrington JC, Freed DD, Sanders TC (1989) Autocatalytic processing of the potyvirus helper component proteinase in Escherichia coli and in vitro. J Virol 63: 4 459-4 463
9. Carrington JC, Herndon KL (1992) Characterization of the potyviral HC-Pro autoproteolytic cleavage site. Virology 187: 308-315
10. Domier LL, Franklin KM, Hunt AG, Rhoads RE, Shaw JG (1989) Infectious in vitro transcripts from cloned cDNA of a potyvirus, tobacco vein mottling virus. Proc Natl Acad Sci USA 86: 3 509-3 513
11. 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 RNA. Nucleic Acids Res 14: 5 417-5 430
12. Dougherty WG, Parks TD (1991) Post-translational processing of the tobacco etch virus 49-kDa small nuclear inclusion polyprotein: identification of an internal cleavage site and delimitation of VPg and proteinase domains. Virology 183: 449-456
13. 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: 2 775-2 783
14. Frohman MA, Dush MK, Martin GR (1988) Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc Natl Acad Sci USA 85: 8 998-9 002
15. Gallie DR, Sleat DE, Watts JW, Turner PC, Wilson TMA (1987) A comparison of eukaryotic viral 5′-leader sequences as enhancers of mRNA expression in vivo. Nucleic Acids Res 15: 8 693-8 711
16. Garcia JA, Martin MT, Cervera MT, Riechmann JL (1992) Proteolytic processing of the plum pox potyvirus polyprotein by the NIa protease at a novel cleavage site. Virology 188: 697-703
17. Gibb KS, Hellmann GM, Pirone TP (1989) Nature of resistance of a tobacco cultivar to tobacco vein mottling virus. Mol Plant Microbe Interact 2: 332-339
18. George DG, Barker WC, Hunt LT (1990) Mutation data matrix and its uses. Methods Enzymol 183: 333-351
19. Gubler U, Hoffman BJ (1983) A simple and very efficient method for generating cDNA libraries. Gene 25: 263-269
20. Hellmann GM, Shaw JG, Lesnaw JA, Chu L-Y, Pirone TP, Rhoads RE (1980) Cell-free translation of tobacco vein mottling virus RNA. Virology 106: 207-216
21. Hellmann GM, Shaw JG, Rhoads RE (1988) In vitro analysis of tobacco vein mottling virus NIa cistron: evidence for a virus-encoded protease. Virology 163: 554-562
22. Jayaram C, Hill JH, Miller WA (1992) Complete nucleotide sequences of two soybean mosaic virus strains differentiated by response of soybean containing the rsv resistance gene. J Gen Virol 73: 2067-2077
23. Kavanagh T, Goulden M, Santa Cruz S, Chapman S, Barker I, Baulcombe D (1992) Molecular analysis of a resistance-breaking strain of potato virus X. Virology 189: 609-617
24. Laliberté J-F, Nicolas O, Chatel H, Lazure C, Morosoli R (1992) Release of a 22-kDa protein derived from the amino-terminal domain of the 49-kDa NIa of turnip mosaic potyvirus in Escherichia coli. Virology 190: 510-514
25. Lütcke HA, Chow KC, Mickel FS, Moss KA, Kern HF, Scheele GA (1987) Selection of AUG initiation codons differs in plants and animals. EMBO J 6: 43-48
26. Matthews REF (1991) Plant Virology, 3rd edn. Academic Press, San Diego
27. Mavankal G, Rhoads RE (1991) In vitro cleavage at or near the N-terminus of the helper component protein in the tobacco vein mottling virus polyprotein. Virology 185: 721-731
28. Miller RD (1987) TN 86. A Burley tobacco resistant to TVMV, TEV and PVY. University of Tennesee, Agriculture Experimental Station, Knoxville, TN, Bull No. 657
29. Murphy JF, Rhoads RE, Hunt AG, Shaw JG (1990)The VPg of tobacco etch virus RNA is the 49-kDa proteinaseor the N-terminal 24-kDa part of the proteinase. Virology 178: 285-288
30. Murphy JF, Rychlik W, Rhoads RE, Hunt AG, Shaw JG (1991) A tyrosine residue in the small nuclear inclusion protein of tobacco vein mottling virus links the VPg to the viral RNA. J Virol 65: 511-513
31. Padgett HS, Beachy RN (1993) Analysis of a tobacco mosaic virus strain capable of overcoming N gene-mediated resistance. Plant Cell 5: 577-586
32. Reddick BB, Miller RD, Gooding GV (1991) Resistance in N. tabacum cultivar TN 86 to naturally occurring tobacco viruses. Tobacco Sci Dec: 96-99
33. Rodríguez-Cerezo E, Gamble Klein P, Shaw JG (1991) A determinant of disease symptom severity is located in the 3′-terminal noncoding region of the RNA of a plant virus. Proc Natl Acad Sci USA 88: 9 863-9 867
34. Rodríguez-Cerezo E, Shaw JG (1991) Two newly detected nonstructural viral proteins in potyvirus-infected cells. Virology 185: 572-579
35. Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: A laboratory manual. 2nd ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY
36. 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: 2 703-2 710
37. Shukla DD, Ward CW, Brunt AA (1994) The Potyviridae. CAB International, Wallingford, Oxon, pp 74-112
38. Verchot JM, Carrington JC (1995) Debilitation of plant potyvirus infectivity by P1 proteinase-inactivating mutations and restoration by second-site modifications. J Virol 69: 1 582-1 590
39. Verchot JM, Koonin EW, Carrington JC (1991) The 35-kDa protein from the N-terminus of the potyviral polyprotein functions as a third virus-encoded proteinase. Virology 185: 527-535
40. Ward CW, McKern NM, Frenkel MJ, Shukla DD (1992) Sequence data as a major criterion for potyvirus classification. In: Barnett OW (ed) Potyvirus taxonomy. Springer, Wien New York, pp 283-297 (Arch Virol [Suppl] 5)
41. Ward CW, McKern NM, Frenkel MJ, Shukla DD (1992) Sequence data as a major criterion for potyvirus classification. In: Barnett OW (ed) Potyvirus taxonomy. Springer, Wien New York, pp 283-297 (Arch Virol [Suppl] 5)
42. 2 resistance gene in the tomato. J Virol 67: 6 432-6 438