Molecular studies on bromovirus capsid protein. III. Analysis of cell- to-cell movement competence of coat protein defective variants of cowpea chlorotic mottle virus

Virology

Volumn 232, Issue 2, 1997, Pages 385-395

  Rao, A L N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CAPSID PROTEIN; COAT PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CELL INTERACTION; CELL MOTION; MOSAIC VIRUS; NONHUMAN; PLANT; PRIORITY JOURNAL; VIRUS CAPSID; VIRUS INFECTION;

BROME MOSAIC VIRUS; BROMOVIRUS; BROMUS; CHENOPODIUM QUINOA; COWPEA CHLOROTIC MOTTLE VIRUS; MIRIDAE; NICOTIANA BENTHAMIANA;

EID: 0030738305     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1006/viro.1997.8579     Document Type: Article

References (52)

1. Ahlquist P. Bromoviruses. Encyclopedia of Virology. 1994;Academic Press, San Diego.
2. Allison R. F., Janda M., Ahlquist P. Infectiousin vitro. J. Virol. 62:1988;3581-3588.
3. Allison R. F., Thompson C., Ahlquist P. Regeneration of a functional RNA virus genome by recombination between deletion mutants and requirement for cowpea chlorotic mottle virus 3a and CP genes for systemic infection. Proc. Natl. Acad. Sci. USA. 87:1990;1820-1824.
4. Baulcombe D. C., Chapman S., Santa Cruz S. Jellyfish green fluorescent protein as a reporter for virus infections. Plant J. 7:1995;1045-1053.
5. Carrington J. C., Kasschau K. D., Mahajan S. K., Schaad M. Cell-to-cell and long distance transport of viruses in plants. Plant Cell. 8:1996;1669-1681.
6. Chalfie M., Tu Y., Euskirchen G., Ward W. W., Prasher D. C. Green fluorescent protein as a marker for gene expression. Science. 263:1994;802-805.
7. Cody C. W., Prasher D. C., Westler W. M., Prendergast F. G., Ward W. W. Chemical structure of the hexapeptide chromophore of theAequorea. Biochemistry. 32:1993;1212-1218.
8. Cormack B. P., Valdivia R. H., Falkow S. FACS-optimized mutants of the green fluorescent protein (GFP). Gene. 173:1996;33-38.
9. Cronin S., Verchot J., Haldeman-Cahil R., Schaad M. C., Carrington J. C. Long distance movement factor: A transport function of the potyvirus helper component proteinase. Plant J. 7:1995;549-559.
10. Dawson W. O. Tobamovirus-plant interactions. Virology. 186:1992;359-367.
11. Dawson W. O., Bubrick P., Grantham G. Modifications of the tobacco mosaic virus coat protein gene affecting replication, movement and symptomatology. Phytopathology. 78:1988;783-789.
12. De Jong W., Ahlquist P. Bromovirus host specificity and systemic infection. Semin. Virol. 2:1991;97-105.
13. De Jong W., Ahlquist P. A hybrid plant virus made by transferring the noncapsid movement protein from a rod-shaped to an icosahedral virus is competent for systemic infection. Proc. Natl. Acad. Sci. USA. 89:1992;6808-6812.
14. De Jong W., Chu A., Ahlquist P. Coding changes in the 3a cell-to-cell movement gene can extend the host range of brome mosaic virus systemic infection. Virology. 214:1995;464-474.
15. Deom C. M., Lapidot M., Beachy R. N. Plant virus movement proteins. Cell. 69:1992;221-224.
16. Dolja V. V., McBride H. J., Carrington J. C. Tagging of plant potyvirus replication and movement by insertion of β-glucuronidase into the viral polyprotein. Proc. Natl. Acad. Sci. USA. 89:1992;10208-10212.
17. Dreher T. W., Rao A. L. N., Hall T. C. Replicationin vivo. J. Mol. Biol. 206:1989;425-438.
18. Flasinski S., Dzianott A., Pratt S., Bujarski J. Mutational analysis of the coat protein gene of brome mosaic virus: Effects on replication and movement in barley and inChenopodium hybridum. Mol. Plant-Microbe Interact. 8:1995;23-31.
19. Fujita Y., Mise K., Okuno T., Ahlquist P., Furusawa I. A single codon change in a conserved motif of a bromovirus movement protein gene confers compatibility with a new host. Virology. 223:1996;283-291.
20. Gal-On A., Kaplan I., Roossinck M. J., Palukaitis P. The kinetics of infection of zucchini squash by cucumber mosaic virus indicate a function for RNA1 in virus movement. Virology. 205:1994;280-289.
21. Heim R., Tsien R. Y. Engineering green fluorescent protein for improved brightness, longer wavelengths and fluorescence resonance energy transfer. Curr. Biol. 6:1996;178-182.
22. Heinlein M., Epel B. L., Padgett H. S., Beachy R. N. Interaction of tobamovirus movement proteins with the plant cytoskeleton. Science. 270:1995;1983-1985.
23. D. Kasteel, N. Van der Wel, J. C. Boyer, O. Van Marle, J. Wellink, R. Goldbach, J. Van Lent, 1996, Is tubular structure formation an intrinsic property of plant viral movement proteins?, Proceedings of the 3rd International Workshop on Basic and Applied Research in Plasmodesmal Biology, 50, 52, Zichron-Yakov, Israel.
24. Lapidot M., Gafny R., Ding B., Wolf S., Lucas W. J., Beachy R. N. Dysfunctional movement protein of tobacco mosaic virus that partially modifies the plasmodesmata and limits virus spread in transgenic plants. Plant J. 4:1993;959-970.
25. Lucas W. J., Gilbertson R. L. Plasmodesmata in relation to viral movement within leaf tissues. Annu. Rev. Phytopathol. 32:1994;387-412.
26. McLean B. G., Zupan J., Zambryski P. C. Tobacco mosaic virus movement protein associates with the cytoskeleton in tobacco cells. Plant Cell. 7:1995;2101-2114.
27. Mise K., Ahlquist P. Host specificity restriction by bromovirus cell-to-cell movement protein occurs after initial cell-to-cell spread of infection in nonhost plants. Virology. 206:1995;276-286.
28. Mise K., Allison R. F., Janda M., Ahlquist P. Bromovirus movement protein genes play a crucial role in host specificity. J. Virol. 67:1993;2815-2823.
29. Mori M., Zhang G. H., Kaido M., Okuno T., Furusawa I. Efficient production of human gamma interferon in tobacco protoplasts by genetically engineered brome mosaic virus RNAs. J. Gen. Virol. 74:1993;1255-1260.
30. Nelson R. S., Li G., Hodgson R. A. J., Beachy R. N., Shintaku M. Impeded phloem-dependent accumulation of the masked strain of tobacco mosaic virus. Mol. Plant-Microbe Interact. 6:1993;45-54.
31. Oparka K. J., Roberts A. G., Prior D. A. M., Chapman S., Baulcombe D. C., Santa Cruz S. Imaging the green fluorescent protein in plants - Viruses carry the torch. Protoplasma. 189:1995;133-141.
32. Padgett H. S., Epel B. L., Kahn T. W., Heinlein M., Wanatabe Y., Beachy R. N. Distribution of tobamovirus movement protein in infected cells and implications for cell-to-cell spread of infection. Plant J. 10:1996;1079-1088.
33. Petty I. T. D., Jackson A. O. Mutational analysis of barley stripe mosaic virus RNA β Virology. 179:1990;712-718.
34. Petty I. T. D., French R., Jones R. W., Jackson A. O. Identification of barley stripe mosaic virus genes involved in viral RNA replication and systemic movement. EMBO J. 9:1990;3453-3457.
35. Prasher D. C., Eckenrode V. K., Ward W. W., Prendergrast F. G., Cormicer M. J. Primary structure of theAequorea victoria. Gene. 111:1992;229-233.
36. Rao A. L. N., Duggal R., Lahser F., Hall T. C. Analysis of RNA replication in plant viruses. Adolph K. W. Methods in Molecular Genetics: Molecular Virology Techniques. 1994;216-236 Academic Press, Orlando.
37. Rao A. L. N., Grantham G. L. A spontaneous mutation in the movement protein gene of brome mosaic virus modulates symptom phenotype inNicotiana benthamiana. J. Virol. 69:1995a;2689-2691.
38. Rao A. L. N., Grantham G. L. Biological significance of the seven amino-terminal basic residues of brome mosaic virus coat protein. Virology. 211:1995b;42-52.
39. Rao A. L. N., Grantham G. L. Molecular studies on bromovirus capsid protein. II. Functional analysis of the amino terminal arginine rich motif and its role in encapsidation, movement and pathology. Virology. 226:1996;294-305.
40. Ritzenthaler C., Schmit A. C., Michler P., Stussi-Garaud C., Pinck L. Grapevine fanleaf nepovirus P38 putative movement protein is located on tubulesin vivo. Mol. Plant-Microbe Interact. 8:1995;379-387.
41. Rizzuto R., Brini M., De Giorgi F., Rossi R., Heim R., Tsien R. Y., Pozzan T. Double labelling of subcellular structures with organelle-targeted GFP mutants in vivo. Curr. Biol. 6:1996;183-188.
42. Sacher R., Ahlquist P. Effects of deletions in the N-terminal basic arm of brome mosaic virus coat protein on RNA packaging and systemic infection. J. Virol. 63:1989;4545-4552.
43. Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning: A Laboratory Manual. 1992;Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
44. Schmitz I., Rao A. L. N. Molecular studies on bromovirus capsid protein. I. Characterization of cell-to-cell movement-defective RNA3 variants of brome mosaic virus. Virology. 226:1996;281-293.
45. Scholthof H. B., Morris T. J., Jackson A. O. The capsid protein gene of tomato bushy stunt virus is dispensable for systemic movement and can be replaced for localized expression of foreign genes.Mol. Plant-Microbe Interact. 6:1993;309-322.
46. Scholthof H. B., Scholthof K.-B. G., Kikkert M., Jackson A. O. Tomato bushy stunt virus spread is regulated by two nested genes that function in cell-to-cell movement and host-dependent systemic invasion. Virology. 213:1995;425-438.
47. Shintaku M. H., Zhang L., Palukaitis P. A single amino acid substitution in the coat protein of cucumber mosaic virus induces chlorosis in tobacco. Plant Cell. 4:1992;751-757.
48. Speir J. A., Munshi S., Wang G., Baker T. S., Johnson J. E. Structure of the native and swollen forms of cowpea chlorotic mottle virus determined by X-ray crystallography and cry-electron microscopy. Structure. 3:1995;63-78.
49. Traynor P., Young B. M., Ahlquist P. Deletion analysis of brome mosaic virus 2a protein: Effects on RNA replication and systemic spread. J. Virol. 65:1991;2807-2815.
50. Van Lent J., Storms M., Van der Meer F., Wellink J., Goldbach R. Tubular structures involved in movement of cowpea mosaic virus are formed in infected protoplasts. J. Gen. Virol. 72:1991;2615-2623.
51. Weiland J. J., Edwards M. C. A single nucleotide substitution in the aa gene confers oat pathogenicity barley stripe mosaic virus strait ND 18. Mol. Plant-Microbe Interact. 9:1996;62-67.
52. Wolf S., Deom C. M., Beachy R. N., Lucas W. J. Movement protein of tobacco mosaic virus modifies plasmodesmata size exclusion limit. Science. 246:1989;337-339.