Capsid protein and helper component-proteinase function as potyvirus cell-to-cell movement proteins

Virology

Volumn 237, Issue 2, 1997, Pages 283-295

  Rojas, Maria R ^a   Zerbini, F Murilo ^a   Allison, Richard F ^b   Gilbertson, Robert L ^a   Lucas, William J ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CAPSID PROTEIN; NUCLEOTIDE; PROTEINASE; VIRUS PROTEIN;

ARTICLE; BEAN; CONTROLLED STUDY; MOSAIC VIRUS; NONHUMAN; PRIORITY JOURNAL; VIRUS CELL INTERACTION;

BEAN COMMON MOSAIC NECROSIS VIRUS; ESCHERICHIA; LACTUCA; LETTUCE MOSAIC VIRUS; MIRIDAE; NIA; PHASEOLUS (ANGIOSPERM); POTYVIRUS;

EID: 0030698068     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1006/viro.1997.8777     Document Type: Article

References (51)

1. Andrews J. H., Shalla T. A. The origin, development, and conformation of amorphous inclusion body components in tobacco etch virus-infected cells. Phytopathology. 64:1974;1234-1243.
2. Atreya C. D., Pirone T. P. Mutational analysis of a helper component-proteinase gene of a potyvirus: Effects of amino acid substitutions, deletions, and gene replacement on virulence and aphid transmissibility. Proc. Natl. Acad. Sci. USA. 90:1993;11919-11923.
3. Baunoch D., Das P., Hari V. Intracellular localization of TEV capsid and inclusion proteins by immunogold labeling. J. Ultrastruct. Res. 99:1988;203-212.
4. Brantley J. D., Hunt A. G. The N-terminal protein of the polyprotein encoded by the potyvirus tobacco vein mottling virus is an RNA-binding protein. J. Gen. Virol. 74:1993;1157-1162.
5. Carrington J. C., Freed D. D., Leinicke A. J. Bipartite signal sequence mediates nuclear translocation of the plant potyviral NIa protein. Plant Cell. 3:1991;953-962.
6. Carrington J. C., Haldeman R., Dolja V., Restrepo-Hartwig M. A. Internal cleavage andtrans. J. Virol. 67:1993;6995-7000.
7. Carrington J. C., Kasschau K. D., Mahajan S. K., Schaad M. C. Cell-to-cell and long-distance transport of viruses in plants. Plant Cell. 8:1996;1669-1681.
8. Citovsky V., Zambryski P. How do plant virus nucleic acids move through intercellular connections? Bioessays. 13:1991;373-379.
9. Citovsky V., Knorr D., Schuster G., Zambryski P. The P30 movement protein of tobacco mosaic virus is a single-strand nucleic acid binding protein. Cell. 60:1990;637-647.
10. Cronin S., Verchot J., Haldeman-Cahill R., Schaad M. C., Carrington J. C. Long-distance movement factor: A transport function of the potyvirus helper component proteinase. Plant Cell. 7:1995;549-559.
11. Deom C. M., Oliver M. J., Beachy R. N. The 30-kilodalton gene product of tobacco mosaic virus potentiates virus movement. Science. 237:1987;389-394.
12. Deom C. M., Lapidot M., Beachy R. N. Plant virus movement proteins. Cell. 69:1992;221-224.
13. Ding B., Li Q., Nguyen L., Palukaitis P., Lucas W. J. Cucumber mosaic virus 3a protein potentiates cell-to-cell trafficking of CMV RNA in tobacco plants. Virology. 207:1995;345-353.
14. Dolja V. V., Boyko V. P., Agranovsky A. A., Koonin E. V. Phylogeny of capsid proteins of rod-shaped and filamentous RNA plant viruses: Two families with distinct patterns of sequence and probably structure conservation. Virology. 184:1991;79-86.
15. Dolja V. V., Haldeman R., Robertson N. L., Dougherty W. G., Carrington J. C. Distinct functions of capsid protein in assembly and movement of tobacco etch potyvirus in plants. EMBO J. 13:1994;1482-1491.
16. Dolja V. V., Haldeman-Cahill R., Montgomery A. E., VandenBosch K. A., Carrington J. C. Capsid protein determinants involved in cell-to-cell and long distance movement of tobacco etch potyvirus. Virology. 207:1995;1007-1016.
17. Dolja V. V., Herndon K., Pirone T. P., Carrington J. C. Spontaneous mutagenesis of a plant potyvirus genome after insertion of a foreign gene. J. Virol. 67:1993;5968-5975.
18. Dougherty W. G., Carrington J. C. Expression and function of potyviral gene products. Annu. Rev. Phytopathol. 26:1988;123-143.
19. Fang G. W., Allison R. F., Zambolim E. M., Maxwell D. P., Gilbertson R. L. The complete nucleotide sequence and genome organization of bean common mosaic virus (NL3 strain). Virus Res. 39:1995;13-23.
20. Fujiwara T., Geisman-Cookmeyer D., Ding B., Lommel S. A., Lucas W. J. Cell-to-cell trafficking of macromolecules through plasmodesmata potentiated by the red clover necrotic mosaic virus movement protein. Plant Cell. 5:1993;1783-1794.
21. Gilbertson R. L., Lucas W. J. How do viruses traffic on the 'vascular highway'? Trends Plant Sci. 1:1996;260-267.
22. Goodwin P. B. Molecular size limit for movement in the symplast of theElodea. Planta. 157:1983;124-130.
23. 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.
24. Kasschau K. D., Cronin S., Carrington J. C. Genome amplification and long-distance movement functions associated with the central domain of tobacco etch potyvirus helper component-proteinase. Virology. 228:1997;251-262.
25. Klein P. G., Klein R. R., Rodriguez-Cerezo E., Hunt A. G., Shaw J. G. Mutational analysis of the tobacco vein mottling virus genome. Virology. 204:1994;759-769.
26. Lain S., Martin M. T., Riechmann J. L., Garcia J. A. Novel catalytic activity associated with positive strand RNA virus infection: Nucleic acid stimulated ATPase activity of plum pox potyvirus helicase like protein. J. Gen. Virol. 65:1991;1-6.
27. Lawson R. H., Hearon S. S. The association of pinwheel inclusions with plasmodesmata. Virology. 44:1971;454-456.
28. Lawson R. H., Hearon S. S., Smith F. F. Development of pinwheel inclusions associated with sweet potato russet crack virus. Virology. 46:1971;453-463.
29. Langenberg W. G. Virus protein association with cylindrical inclusions of two viruses that infect wheat. J. Gen. Virol. 67:1986;1161-1168.
30. Lucas W. J., Gilbertson R. L. Plasmodesmata in relation to viral movement within leaf tissues. Annu. Rev. Phytopathol. 32:1994;387-411.
31. Lucas W. J., Ding B., van der Schoot C. Plasmodesmata and the supracellular nature of plants. New Phytol. 125:1993;435-476.
32. Maia I. G., Bernardi F. Nucleic acid-binding properties of a bacterially expressed potato virus Y helper component-proteinase. J. Gen. Virol. 77:1996;869-877.
33. Maia I. G., Haenni A.-L., Bernardi F. Potyviral HC-Pro: a multifunctional protein. J. Gen. Virol. 77:1996;1335-1341.
34. Maule A. J. Virus movement in infected plants. Crit. Rev. Plant Sci. 9:1991;457-473.
35. Mise K., Ahlquist P. Host-specificity restriction by bromovirus cell-to-cell movement protein occurs after cell-to-cell spread of infection in nonhost plants. Virology. 206:1995;276-286.
36. Noueiry A. O., Lucas W. J., Gilbertson R. L. Two proteins of a plant DNA virus coordinate nuclear and plasmodesmal transport. Cell. 76:1994;925-932.
37. Oparka K. J., Boevink P., Santa Cruz S. Studying the movement of plant viruses using green fluorescent protein. Trends Plant Sci. 1:1996;412-418.
38. Oparka K. J., Roberts A. G., Roberts I. M., Prior D. A. M., Santa Cruz S. Viral coat protein is targeted to, but does not gate, plasmodesmata during cell-to-cell movement of potato virus X. Plant J. 10:1996;805-813.
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. Restrepo-Hartwig M. A., Freed D. D., Carrington J. C. Nuclear transport of plant potyviral proteins. Plant Cell. 2:1990;987-998.
41. Restrepo-Hartwig M. A., Carrington J. C. The tobacco etch potyvirus 6-kilodalton protein is membrane associated and involved in viral replication. J. Virol. 68:1994;2388-2397.
42. Riechmann J. L., Lain S., Garcia J. A. Highlights and prospects of potyvirus molecular biology. J. Gen. Virol. 73:1992;1-16.
43. Rodriguez-Cerezo E., Shaw J. G. Two newly detected nonstructural viral proteins in potyvirus-infected cells. Virology. 185:1991;572-579.
44. Shukla D., Ward C. W. Amino acid sequence homology of coat proteins as a basis for identification and classification of the potyvirus group. J. Gen. Virol. 69:1988;2703-2710.
45. Soumounou Y., Laliberte J. F. Nucleic acid-binding properties of the P1 protein of turnip mosaic potyvirus produced inEscherichia coli. J. Gen. Virol. 75:1994;2567-2573.
46. Tucker E. B. Translocation in the staminal hairs ofSetcreasea purpurea. Protoplasma. 113:1982;193-201.
47. Verchot J., Carrington J. C. Debilitation of plant potyvirus infectivity by P1 proteinase-inactivating mutations and restoration by second-site modifications. J. Virol. 69:1995;1582-1590.
48. Waigmann E., Zambryski P. Tobacco mosaic virus movement protein-mediated protein transport between trichome cells. Plant Cell. 7:1995;2069-2079.
49. Waigmann E., Lucas W. J., Citovsky V., Zambryski P. Direct functional assay for tobacco mosaic virus cell-to-cell movement protein and identification of a domain involved in increasing plasmodesmal permeability. Proc. Natl. Acad. Sci. USA. 91:1994;1433-1437.
50. 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;377-379.
51. Zerbini F. M., Koike S. T., Gilbertson R. L. Biological and molecular characterization of lettuce mosaic potyvirus isolates from the Salinas Valley of California. Phytopathology. 85:1995;746-752.