Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1995 Apr;69(4):2547–2556. doi: 10.1128/jvi.69.4.2547-2556.1995

Mutations in the helicase-like domain of protein 1a alter the sites of RNA-RNA recombination in brome mosaic virus.

P D Nagy 1, A Dzianott 1, P Ahlquist 1, J J Bujarski 1
PMCID: PMC188932  PMID: 7884905

Abstract

A system that uses engineered heteroduplexes to efficiently direct in vivo crossovers between brome mosaic virus (BMV) RNA1 and RNA3 (P. Nagy and J. Bujarski, Proc. Natl. Acad. Sci. USA 90:6390-6394, 1993) has been used to explore the possible involvement of BMV 1a protein, an essential RNA replication factor, in RNA recombination. Relative to wild-type 1a, several viable amino acid insertion mutations in the helicase-like domain of BMV 1a protein affected the nature and distribution of crossover sites in RNA3-RNA1 recombinants. At 24 degrees C, mutants PK19 and PK21 each increased the percentage of asymmetric crossovers, in which the RNA1 and RNA3 sites joined by recombination were not directly opposite each other on the engineered RNA3-RNA1 heteroduplex used to target recombination but rather were separated by 4 to 85 nucleotides. PK21 and another 1a mutant, PK14, also showed increases in the fraction of recombinants containing nontemplated U residues at the recombination junction. At 33 degrees C, the highest temperature that permitted infections with PK19, which is temperature sensitive for RNA replication, the mean location of RNA1-RNA3 crossovers in recombinants recovered from PK19 infections was shifted by nearly 25 bp into the energetically less stable side of the RNA1-RNA3 heteroduplex. Thus, mutations in the putative helicase domain of the 1a protein can influence BMV RNA recombination. The results are discussed in relation to models for recombination by template switching during pausing of RNA replication at a heteroduplexed region in the template.

Full Text

The Full Text of this article is available as a PDF (362.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ahlquist P. Bromovirus RNA replication and transcription. Curr Opin Genet Dev. 1992 Feb;2(1):71–76. doi: 10.1016/s0959-437x(05)80325-9. [DOI] [PubMed] [Google Scholar]
  2. Ahlquist P., Dasgupta R., Kaesberg P. Nucleotide sequence of the brome mosaic virus genome and its implications for viral replication. J Mol Biol. 1984 Feb 5;172(4):369–383. doi: 10.1016/s0022-2836(84)80012-1. [DOI] [PubMed] [Google Scholar]
  3. Allison R. F., Janda M., Ahlquist P. Sequence of cowpea chlorotic mottle virus RNAs 2 and 3 and evidence of a recombination event during bromovirus evolution. Virology. 1989 Sep;172(1):321–330. doi: 10.1016/0042-6822(89)90134-7. [DOI] [PubMed] [Google Scholar]
  4. Bertholet C., Van Meir E., ten Heggeler-Bordier B., Wittek R. Vaccinia virus produces late mRNAs by discontinuous synthesis. Cell. 1987 Jul 17;50(2):153–162. doi: 10.1016/0092-8674(87)90211-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bujarski J. J., Dzianott A. M. Generation and analysis of nonhomologous RNA-RNA recombinants in brome mosaic virus: sequence complementarities at crossover sites. J Virol. 1991 Aug;65(8):4153–4159. doi: 10.1128/jvi.65.8.4153-4159.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bujarski J. J., Nagy P. D. Targeting of the site of nonhomologous genetic recombination in brome mosaic virus. Arch Virol Suppl. 1994;9:231–238. doi: 10.1007/978-3-7091-9326-6_23. [DOI] [PubMed] [Google Scholar]
  7. Cascone P. J., Carpenter C. D., Li X. H., Simon A. E. Recombination between satellite RNAs of turnip crinkle virus. EMBO J. 1990 Jun;9(6):1709–1715. doi: 10.1002/j.1460-2075.1990.tb08294.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cascone P. J., Haydar T. F., Simon A. E. Sequences and structures required for recombination between virus-associated RNAs. Science. 1993 May 7;260(5109):801–805. doi: 10.1126/science.8484119. [DOI] [PubMed] [Google Scholar]
  9. Cattaneo R. Different types of messenger RNA editing. Annu Rev Genet. 1991;25:71–88. doi: 10.1146/annurev.ge.25.120191.000443. [DOI] [PubMed] [Google Scholar]
  10. Dinant S., Janda M., Kroner P. A., Ahlquist P. Bromovirus RNA replication and transcription require compatibility between the polymerase- and helicase-like viral RNA synthesis proteins. J Virol. 1993 Dec;67(12):7181–7189. doi: 10.1128/jvi.67.12.7181-7189.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gibbs A. Molecular evolution of viruses; 'trees', 'clocks' and 'modules'. J Cell Sci Suppl. 1987;7:319–337. doi: 10.1242/jcs.1987.supplement_7.22. [DOI] [PubMed] [Google Scholar]
  12. Gorbalenya A. E., Koonin E. V. Viral proteins containing the purine NTP-binding sequence pattern. Nucleic Acids Res. 1989 Nov 11;17(21):8413–8440. doi: 10.1093/nar/17.21.8413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kao C. C., Ahlquist P. Identification of the domains required for direct interaction of the helicase-like and polymerase-like RNA replication proteins of brome mosaic virus. J Virol. 1992 Dec;66(12):7293–7302. doi: 10.1128/jvi.66.12.7293-7302.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kao C. C., Quadt R., Hershberger R. P., Ahlquist P. Brome mosaic virus RNA replication proteins 1a and 2a from a complex in vitro. J Virol. 1992 Nov;66(11):6322–6329. doi: 10.1128/jvi.66.11.6322-6329.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kirkegaard K., Baltimore D. The mechanism of RNA recombination in poliovirus. Cell. 1986 Nov 7;47(3):433–443. doi: 10.1016/0092-8674(86)90600-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Kroner P. A., Young B. M., Ahlquist P. Analysis of the role of brome mosaic virus 1a protein domains in RNA replication, using linker insertion mutagenesis. J Virol. 1990 Dec;64(12):6110–6120. doi: 10.1128/jvi.64.12.6110-6120.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kroner P., Richards D., Traynor P., Ahlquist P. Defined mutations in a small region of the brome mosaic virus 2 gene cause diverse temperature-sensitive RNA replication phenotypes. J Virol. 1989 Dec;63(12):5302–5309. doi: 10.1128/jvi.63.12.5302-5309.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lai M. M. RNA recombination in animal and plant viruses. Microbiol Rev. 1992 Mar;56(1):61–79. doi: 10.1128/mr.56.1.61-79.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Luo G. X., Luytjes W., Enami M., Palese P. The polyadenylation signal of influenza virus RNA involves a stretch of uridines followed by the RNA duplex of the panhandle structure. J Virol. 1991 Jun;65(6):2861–2867. doi: 10.1128/jvi.65.6.2861-2867.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Meyers G., Tautz N., Dubovi E. J., Thiel H. J. Viral cytopathogenicity correlated with integration of ubiquitin-coding sequences. Virology. 1991 Feb;180(2):602–616. doi: 10.1016/0042-6822(91)90074-L. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mise K., Allison R. F., Janda M., Ahlquist P. Bromovirus movement protein genes play a crucial role in host specificity. J Virol. 1993 May;67(5):2815–2823. doi: 10.1128/jvi.67.5.2815-2823.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Nagy P. D., Bujarski J. J. Genetic recombination in brome mosaic virus: effect of sequence and replication of RNA on accumulation of recombinants. J Virol. 1992 Nov;66(11):6824–6828. doi: 10.1128/jvi.66.11.6824-6828.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nagy P. D., Bujarski J. J. Targeting the site of RNA-RNA recombination in brome mosaic virus with antisense sequences. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6390–6394. doi: 10.1073/pnas.90.14.6390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Romanova L. I., Blinov V. M., Tolskaya E. A., Viktorova E. G., Kolesnikova M. S., Guseva E. A., Agol V. I. The primary structure of crossover regions of intertypic poliovirus recombinants: a model of recombination between RNA genomes. Virology. 1986 Nov;155(1):202–213. doi: 10.1016/0042-6822(86)90180-7. [DOI] [PubMed] [Google Scholar]
  25. Strauss J. H., Strauss E. G. Evolution of RNA viruses. Annu Rev Microbiol. 1988;42:657–683. doi: 10.1146/annurev.mi.42.100188.003301. [DOI] [PubMed] [Google Scholar]
  26. Thomas S. M., Lamb R. A., Paterson R. G. Two mRNAs that differ by two nontemplated nucleotides encode the amino coterminal proteins P and V of the paramyxovirus SV5. Cell. 1988 Sep 9;54(6):891–902. doi: 10.1016/S0092-8674(88)91285-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES