Complementation of M gene mutants of vesicular stomatitis virus by plasmid-derived M protein converts spherical extracellular particles into native bullet shapes

Virology

Volumn 217, Issue 1, 1996, Pages 76-87

  Lyles, Douglas S ^a   McKenzie, Margie O ^a   Kaptur, Paulina E ^a   Grant, Kenneth W ^a   Jerome, W Gray ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

M PROTEIN;

ARTICLE; CONTROLLED STUDY; ELECTRON MICROSCOPY; NONHUMAN; PLASMID; PRIORITY JOURNAL; VESICULAR STOMATITIS VIRUS; VIRUS ASSEMBLY; VIRUS MORPHOLOGY; VIRUS MUTANT; VIRUS NUCLEOCAPSID;

VACCINIA; VESICULAR STOMATITIS VIRUS;

EID: 0029913350     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1006/viro.1996.0095     Document Type: Article

References (46)

1. Atkinson, P. H., Moyer, S. A., and Summers, D. F. (1976). Assembly of vesicular stomatitis virus glycoprotein and matrix protein in HeLa cell membranes. J. Mol. Biol. 102, 613-631.
2. Barge, A., Gaudin, Y., Coulon, P., and Ruigrok, R. W. H. (1993). Vesicular stomatitis virus M protein may be inside the ribonucleocapsid coil. J. Virol. 67, 7246-7253.
3. Black, B. L., and Lyles, D. S. (1992). Vesicular stomatitis virus matrix protein inhibits host cell-directed transcription of target genes in vivo. J. Virol. 66, 4058-4064.
4. Black, B. L., Rhodes, R. B., McKenzie, M., and Lyles, D. S. (1993). The role of vesicular stomatitis virus matrix protein in inhibition of host-directed gene expression is genetically separable from its role in virus assembly. J. Virol. 67, 4814-4821.
5. Carroll, A. R., and Wagner, R. R. (1979). Role of the membrane (M) protein in endogenous inhibition of in vitro transcription by vesicular stomatitis virus. J. Virol. 29, 134-142.
6. Chong, L. D., and Rose, J. K. (1993). Membrane association of functional vesicular stomatitis virus matrix protein in vivo. J. Virol. 67, 407-414.
7. Chong, L. D., and Rose, J. K. (1994). Interactions of normal and mutant vesicular stomatitis virus matrix proteins with the plasma membrane and nucleocapsids. J. Virol. 68, 441-447.
8. Clinton, G. M., Little, S. P., Hagen, F. S., and Huang, A. S. (1978). The matrix (M) protein of vesicular stomatitis virus regulates transcription. Cell 15, 1455-1462.
9. David, A. (1973). Assembly of the vesicular stomatitis virus envelope: Incorporation of viral polypeptides into the host plasma membrane. J. Mol. Biol. 76, 135-148.
10. Flamand, A. (1970). Etude genetique du virus de la stomatite vesiculaire: Classement de mutants thermosensibles spontanes en groupes de complementation. J. Gen. Virol. 8, 187-195.
11. Fuerst, T. R., Earl, P. L., and Moss, B. N. (1987). Use of a hybrid vaccinia virus, T7 RNA polymerase system for expression of target genes. Mol. Cell. Biol. 7, 2538-2544.
12. Justice, P. A., Sun, W., Li, Y., Ye, Z., Grigera, P. R., and Wagner, R. R. (1995). Membrane vesiculation function and exocytosis of wild-type and mutant matrix proteins of vesicular stomatitis virus. J. Virol. 69, 3156-3160.
13. Kaptur, P. E., Rhodes, R. B., and Lyles, D. S. (1991). Sequences of the vesicular stomatitis virus matrix protein involved in binding to nucleocapsids. J. Virol. 65, 1057-1065.
14. Kaptur, P. E., McKenzie, M. O., Wertz, G. W., and Lyles, D. S. (1995). Assembly functions of vesicular stomatitis virus matrix protein are not disrupted by mutations at major sites of phosphorylation. Virology 206, 894-903.
15. Knipe, D. M., Baltimore, D., and Lodish, H. F. (1977a). Maturation of viral proteins in cells infected with temperature-sensitive mutants of vesicular stomatitis virus. J. Virol. 21, 1149-1158.
16. Knipe, D. M., Lodish, H. F., and Baltimore, D. (1977b). Analysis of the defects of temperature-sensitive mutants of vesicular stomatitis virus: Intracellular degradation of specific viral proteins. J. Virol. 21, 1140-1148.
17. Lefkowitz, E. J., Pattnaik, A. K., and Ball, L. A. (1990). Complementation of a vesicular stomatitis virus glycoprotein G mutant with wild-type protein expressed from either a bovine papilloma virus or a vaccinia virus vector system. Virology 178, 373-383.
18. Lefrancois, L., and Lyles, D. S. (1982). The interaction of antibody with the major surface glycoprotein of vesicular stomatitis virus. I. Analysis of neutralizing epitopes with monoclonal antibodies. Virology 121, 157-167.
19. Li, Y., Luo, L., Snyder, R. M., and Wagner, R. R. (1988a). Expression of the M gene of vesicular stomatitis virus cloned in various vaccinia virus vectors. J. Virol. 62, 776-782.
20. Li, Y., Luo, L., Snyder, R. M., and Wagner, R. R. (1988b). Site-specific mutations in vectors that express antigenic and temperature-sensitive phenotypes of the M gene of vesicular stomatitis virus. J. Virol. 62, 3729-3737.
21. Li, Y., Luo, L., and Wagner, R. R. (1989). Transcription inhibition site on the M protein of vesicular stomatitis virus located by marker rescue of mutant tsO23(III) with M-gene expression vectors. J. Virol. 63, 2841-2843.
22. Li, Y., Luo, L., Schubert, M., Wagner, R. R., and Kang, C. Y. (1993). Viral liposomes released from insect cells infected with recombinant baculovirus expressing the matrix protein of vesicular stomatitis virus. J. Virol. 67, 4415-4420.
23. Lyles, D. S., Puddington, L., and McCreedy, B. J. (1988). Vesicular stomatitis virus M protein in the nuclei of infected cells. J. Virol. 62, 4387-4392.
24. Lyles, D. S., Varela, V. A., and Parce, J. W. (1990). Dynamic nature of the quaternary structure of the vesicular stomatitis virus envelope glycoprotein. Biochemistry 29, 2442-2449.
25. 125I]iodonaphthyl azide labeling and specific cross-linking. Biochemistry 20, 6872-6877.
26. McCreedy, B. J., and Lyles, D. S. (1989). Distribution of M protein and nucleocapsid protein of vesicular stomatitis virus in infected cell plasma membranes. Virus Res. 14, 189-206.
27. McCreedy, B. J., McKinnon, K. P., and Lyles, D. S. (1990). Solubility of vesicular stomatitis virus M protein in the cytosol of infected cells or isolated from virions. J. Virol. 64, 902-906.
28. Morita, K., Vanderoef, R., and Lenard, J. (1987). Phenotypic reversants of temperature-sensitive M protein mutants of vesicular stomatitis virus: Sequence analysis and functional characterization. J. Virol. 61, 256-263.
29. Newcomb, W. W., and Brown, J. C. (1981). Role of the vesicular stomatitis virus matrix protein in maintaining the viral nucleocapsid in the condensed form found in native virions. J. Virol. 39, 295-299.
30. Newcomb, W. W., Tobin, G. J., McGowan, J. J., and Brown, J. C. (1982). In vitro reassembly of vesicular stomatitis virus skeletons. J. Virol. 41, 1055-1062.
31. Odenwald, W. F., Arnheiter, H., Dubois-Dalq, M., and Lazzarini, R. A. (1986). Stereo images of vesicular stomatitis virus assembly. J. Virol. 57, 922-932.
32. Ohno, S., and Ohtake, N. (1987). Immunocytochemical study of the intracellular localization of M protein of vesicular stomatitis virus. Histochem. J. 19, 297-306.
33. Ono, K., Dubois-Dalq, M., Schubert, M., and Lazzarini, R. A. (1987). A mutated membrane protein of vesicular stomatitis virus has an abnormal distribution within the infected cell and causes defective budding. J. Virol. 61, 1332-1341.
34. Pal, R., Barenholz, Y., and Wagner, R. R. (1987). Vesicular stomatitis virus membrane proteins and their interactions with lipid bilayers. Biochim. Biophys. Actz 906, 175-193.
35. Rolls, M. M., Webster, P., Balba, N. H., and Pose, J. K. (1994). Novel infectious particles generated by expression of the vesicular stomatitis virus glycoprotein from a self-replicating RNA. Cell 79, 497-506.
36. Rose, J. K., and Gallione, C. J. (1981). Nucleotide sequences of the mRNAs encoding the vesicular stomatitis virus G and M proteins determined from cDNA clones containing the complete coding regions. J. Virol. 39, 519-528.
37. Schnitzer, T. J., and Lodish, H. F. (1979). Noninfectious vesicular stomatitis virus particles deficient in the viral nucleocapsid. J. Virol. 29, 443-447.
38. Sun, W., Huang, L., and Wagner, R. R. (1994). Common distribution of antigenic determinants and complementation activity on matrix proteins of two vesicular stomatitis virus serotypes. J. Gen. Virol. 75, 937-943.
39. Thomas, D., Newcomb, W. W., Brown, J. C., Wall, J. S., Hainfeld, J. F., Trus, B. L., and Steven, A. C. (1985). Mass and molecular composition of vesicular stomatitis virus: a scanning transmission electron microscopy analysis. J. Virol. 54, 598-607.
40. Whitaker-Dowling, P., and Youngner, J. S. (1987). Viral interference-dominance of mutant viruses over wild-type virus in mixed infections. Microbiol. Rev. 51, 179-191.
41. Whitt, M. A., and Rose, J. K. (1991). Fatty acylation is not required for membrane fusion activity of glycoprotein assembly into VSV virions. Virology 185, 875-878.
42. Whitt, M. A., Chong, L., and Rose, J. K. (1989). Glycoprotein cytoplasmic domain sequences required for rescue of a vesicular stomatitis virus glycoprotein mutant. J. Virol. 63, 3569-3578.
43. Whitt, M. A., Buonocore, L., Prehaud, C., and Rose, J. K. (1991). Membrane fusion activity, oligomerization, and assembly of the rabies virus glycoprotein. Virology 185, 681-688.
44. Wilson, T., and Lenard, J. (1981). Interaction of wild-type and mutant M protein of vesicular stomatitis virus with nucleocapsids in vitro. Biochemistry 20, 1349-1354.
45. Ye, Z., Sun, W., Suryanarayana, K., Justice, P., Robinson, D., and Wagner, R. R. (1994). Membrane-binding domains and cytopathogenesis of the matrix protein of vesicular stomatitis virus. J. Virol. 68, 7386-7396.
46. Youngner, J. S., Frielle, D. W., and Whitaker-Dowling, P. (1986). Dominance of temperature-sensitive phenotypes. I. Studies of the mechanism of inhibition of the growth of wild-type vesicular stomatitis virus. Virology 155, 225-235.