Molecular characterization of a satellite RNA associated with blackcurrant reversion nepovirus

Archives of Virology

Volumn 145, Issue 1, 2000, Pages 51-61

  Latvala Kilby, S ^a,b   Lemmetty, A ^b   Lehto, K ^a  

^a UNIVERSITY OF TURKU   (Finland)

^b PLANT PRODUCTION RESEARCH   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

BLACKCURRANT REVERSION NEPOVIRUS; CHICORY; CHICORY YELLOW MOTTLE NEPOVIRUS; CODON; NEPOVIRUS; OPEN READING FRAME; SATELLITE RNA; VIRUS RNA;

BREDA VIRUS; CICHORIUM INTYBUS; NEPOVIRUS; RNA VIRUSES;

EID: 0033969854     PISSN: 03048608     EISSN: None     Source Type: Journal    
DOI: 10.1007/s007050050004     Document Type: Article

References (29)

1. 1. Fitzgerald M, Shenk T (1981) The sequence 5′-AAUAAA-3′ forms part of the recognition site for polyadenylation of late SV40 mRNAs. Cell 24: 251-260
2. 2. Fritsch C, Koenig I, Murant AF, Raschke JH, Mayo MA (1984) Comparisons among satellite RNA species from five isolates of tomato black ring virus and one isolate of myrobalan latent ringspot virus. J Gen Virol 65: 289-294
3. 3. Fritsch C, Mayo M, Hemmer O (1993) Properties of the satellite RNA of nepoviruses. Biochimie 75: 561-567
4. 4. Fuchs M, Pinck M, Serghini MA, Ravelonandro M, Walter B, Pinck L (1989) The nucleotide sequence of satellite RNA in grapevine fanleaf virus strain F13. J Gen Virol 70: 955-962
5. 5. Hans F, Pinck M, Pinck L (1993) Location of the replication determinants of the satellite RNA associated with grapevine fanleaf nepovirus (strain F13). Biochimie 75: 597-603
6. 6. Hemmer O, Meyer M, Greif C, Fritsch C (1987) Comparison of the nucleotide sequences of five tomato black ring virus satellite RNAs. J Gen Virol 68: 1 823-1 833
7. 7. Hemmer O, Oncino C, Fritsch C (1993) Efficient replication of the in vitro transcripts from cloned cDNA of tomato black ring virus satellite RNA requires the 48K satellite RNA-encoded protein. Virology 194: 800-806
8. 8. Holness CL, Lomonossoff GP, Evans D, Maule AJ (1989) Identification of the initiation codons for translation of cowpea mosaic virus middle component RNA using site-directed mutagenesis of an infectious cDNA clone. Virology 172: 311-320
9. 9. Koonin EJ, Boyto VP, Dolja VV (1991) Small cysteine-rich proteins of different groups of plant RNA viruses are related to different families of nucleic acid-binding proteins. Virology 181: 395-398
10. 10. Kozak M (1986) Point mutations define a sequence flanking the AUG initiation codon that modulates translation by eucaryotic ribosomes. Cell 44: 283-292
11. 11. Kreiah S, Cooper JI, Strunk G (1993) The nucleotide sequence of a satellite RNA associated with strawberry latent ringspot virus. J Gen Virol 74: 1 163-1 165
12. 12. Latvala S, Susi P, Lemmetty A, Cox S, Jones AT, Lehto K (1997) Ribes host range and erratic distribution within plants of blackcurrant reversion associated virus provide further evidence for its role as the causal agent of reversion disease. Ann Appl Biol 131: 283-295
13. 13. Latvala S, Susi P, Kalkkinen N, Lehto K (1998) Characterization of the coat protein gene of mite-transmitted blackcurrant reversion associated nepovirus. Virus Res 53: 1-11
14. 14. Latvala-Kilby S, Lehto K (1999) The complete nucleotide sequence of RNA2 of blackcurrant reversion nepovirus. Virus Res (in press)
15. 15. Leader DP, Katan M (1988) Viral aspects of protein phosphorylation. J Gen Virol 69: 1 441-1 464
16. 16. Lemmetty A, Lehto K (1999) Successful back-inoculation confirms the role of black currant reversion associated virus as the causal agent of reversion disease. Eur J Plant Pathol 105: 297-301
17. 17. Lemmetty A, Latvala S, Jones AT, Susi P, McGavin WJ, Lehto K (1997) Purification and properties of a new virus from black currant, its affinities with nepoviruses, and its close association with black currant reversion disease. Phytopathology 87: 404-413
18. 18. Liu YY, Hellen CUT, Cooper JI, Bertioli DJ, Coates D, Bauer G (1990) The nucleotide sequence of a satellite RNA associated with Arabis mosaic nepovirus. J Gen Virol 71: 1 259-1 263
19. 19. Liu YY, Cooper JI (1993) The multiplication in plants of Arabis mosaic virus satellite RNA requires the encoded protein. J Gen Virol 74: 1 471-1 474
20. 20. 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: 24-48
21. 21. Mayo MA, Barker H, Harrison BD (1979) Polyadenylate in the RNA of five nepoviruses. J Gen Virol 43: 603-610
22. 22. Mayo MA, Barker H, Harrison BD (1982) Specificity and properties of the genome-linked proteins of nepoviruses. J Gen Virol 59: 149-162
23. 23. Mayo MA, Berns K, Fritsch C, Jackson AO, Kaper JM, Leibowitz MJ, Taylor JM (1995) Satellites. In: Murphy FA, Fauquet CM, Bishop DHJ, Ghabrial SA, Jarvis AW, Martelli GP, Mayo MA, Summers MD (eds) Virus Taxonomy. Classification and Nomenclature of Viruses. Sixth Report of the International Committee on Taxonomy of Viruses. Springer, Wien New York, pp 487-492 (Arch Virol [Suppl] 10)
24. 24. Murant AF, Mayo MA (1982) Satellites of plant viruses. Annu Rev Phytopathol 20: 49-70
25. 25. Oncino C, Hemmer O, Fritsch C (1995) Specificity in the association of tomato black ring virus satellite RNA with helper virus. Virology 213: 87-96
26. 26. Pinck L, Fuchs M, Pinck M, Ravelonandro M, Walter B (1988) A satellite RNA in grapevine fanleaf virus strain F13. J Gen Virol 69: 233-239
27. 27. Rott ME, Tremaine JH, Rochon DM (1991) Nucleotide sequence of tomato ringspot virus RNA-2. J Gen Virol 72: 1 505-1 514
28. 28. Rubino L, Tousignant ME, Steger G, Kaper JM (1990) Nucleotide sequence and structural analysis of two satellite RNAs associated with chicory yellow mottle virus. J Gen Virol 71: 1 897-1 903
29. 29. Valderde RA, Nameth ST, Jordan RL (1990) Analysis of double-stranded RNA for plant virus diagnosis. Plant Dis 74: 255-258