Molecular studies on Bromovirus capsid protein. VI. Contributions of the N-terminal arginine-rich motif of BMV capsid protein to virion stability and RNA packaging

Virology

Volumn 270, Issue 2, 2000, Pages 377-385

  Choi, Yoon Gi ^a   Grantham, George L ^a   Rao, A L N ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CAPSID PROTEIN; VIRUS RNA;

ARTICLE; CONTROLLED STUDY; GENETIC STABILITY; MOSAIC VIRUS; NONHUMAN; PLANT LEAF; PRIORITY JOURNAL; PROTEIN RNA BINDING; REACTION ANALYSIS; SITE DIRECTED MUTAGENESIS; VIRUS ASSEMBLY;

BROME MOSAIC VIRUS; BROMOVIRUS; BROMUS; CHENOPODIUM QUINOA; MIRIDAE; RNA VIRUSES;

EID: 0343012080     PISSN: 00426822     EISSN: None     Source Type: Journal    
DOI: 10.1006/viro.2000.0312     Document Type: Article

References (25)

1. Ahlquist P. Bromoviruses. Webster R.G., Granoff A. Encyclopedia of Virology. 1994;181-185 Academic Press, San Diego.
2. Burd C. G., Dreyfuss G. Conserved structures and diversity of functions of RNA-binding proteins. Science. 265:1994;615-621.
3. Dreher T. W., Rao A. L. N., Hall T. C. Replication in vivo of mutant brome mosaic virus RNAs defective in aminoacylation. J. Mol. Biol. 206:1989;425-438.
4. Duggal R., Hall T. C. Identification of domains in brome mosaic virus RNA-1 and coat protein necessary for specific interaction and encapsidation. J. Virol. 67:1993;6406-6412.
5. Fox J. M., Johnson J. E., Young M. RNA/protein interactions in icosahedral virus assembly. Semin. Virol. 5:1994;51-60.
6. Krol M. A., Olson N. H., Tate J., Johnson J. E., Baker T. S., Ahlquist P. RNA-controlled polymorphism in the in vivo assembly of 180-subunit and 120-subunit virions from a single coat protein. Proc. Natl. Acad. Sci. USA. 96:1999;13650-13655.
7. Lazinski D., Grzatzielska E., Das A. Sequence-specific recognition of RNA hairpins by bacteriophage antiterminators requires a conserved arginine-rich motif. Cell. 59:1989;207-218.
8. Miller W. A., Dreher T. W., Hall T. C. Synthesis of brome mosaic virus subgenomic RNA in vitro by initiation on (-) sense genomic RNA. Nature. 313:1985;68-70.
9. Moosic J. P., McKean D. J., Sish D. S., Kaesberg P. Primary structure of brome mosaic virus coat protein. Virology. 129:1983;517-520.
10. Osman F., Choi Y. G., Grantham G. L., Rao A. L. N. Molecular studies on bromovirus capsid protein. V. Evidence for the specificity of brome mosaic virus encapsidation using RNA3 chimera of brome mosaic and cucumber mosaic viruses expressing heterologous coat proteins. Virology. 251:1998;438-448.
11. Rao A. L. N. Molecular basis of symptomatology. Mundahar C. L. Molecular Biology of Plant Viruses. 1999;201-210 Kluwer Academic, Boston.
12. Rao A. L. N., Dreher T. W., Marsh L. E., Hall T. C. Telomeric function of the tRNA-like structure of brome mosaic virus RNA. Proc. Natl. Acad. Sci. USA. 86:1989;5335-5339.
13. Rao, A. L. N., Duggal, R., Lahser, F., and Hall, T. C.1994. Analysis of RNA replication in plant viruses. InMethods in Molecular Genetics: Molecular Virology Techniques (K. W. Adolph, Ed.), Vol. 4, pp. 216-236. Academic Press, Orlando, FL.
14. Rao A. L. N., Grantham G. L. Biological significance of the seven amino-terminal basic residues of brome mosaic virus coat protein. Virology. 211:1995;42-52.
15. 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.
16. 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.
17. Sambrook J., Fritsch E. F., Maniatis T. Molecular cloning: A Laboratory Manual. 1989;Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
18. Schmitz I., Rao A. L. N. Molecular studies on bromovirus capsid protein: I. Characterization of cell-to-cell defective RNA3 variants of brome mosaic virus. Virology. 226:1996;281-293.
19. Sgro J., Jacrot B., Chroboczek J. Identification of regions of brome mosaic virus coat protein chemically cross-linked in situ to viral RNA. Eur. J. Biochem. 154:1986;69-76.
20. Speir J. A., Munshi S., Wang S., Baker T. J., Johnson J. E. Structures of the native and swollen forms of cowpea chlorotic mottle virus determined by X-ray crystallography and cryoelectron microscopy. Structure. 3:1995;63-78.
21. Tan R., Frankel A. D. Structural variety of arginine-rich RNA binding peptides. Proc. Natl. Acad. Sci. USA. 92:1995;5282-5286.
22. Van der Graaf M., Scheek R. M., van der Linden C. C., Hemminga M. A. Conformation of a pentacosapeptide representing the RNA-binding N-terminus of cowpea chlorotic mottle virus coat protein in the presence of oligophosphates: A two-dimensional proton nuclear magnetic resonance and distance geometry study. Biochemistry. 31:1992;9177-9182.
23. Verduin B. J. M. Degradation of cowpea chlorotic mottle virus ribonucleic acid in situ. J. Gen. Virol. 39:1978;131-147.
24. Vriend G., Verduin B. J. M., Hemminga M. A. Role of the N-terminal part of the coat protein in the assembly of cowpea chlorotic mottle virus: A 500 MHz proton nuclear magnetic resonance study and structural calculations. J. Mol. Biol. 191:1986;453-460.
25. Zhao X., Fox J. M., Olson N. H., Baker T. M., Young M. J. In vitro assembly of cowpea chlorotic mottle virus from coat protein expressed in Escherichia coli and in vitro-transcribed viral cDNAs. Virology. 207:1995;486-494.