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. 1995 Jun;69(6):3458–3464. doi: 10.1128/jvi.69.6.3458-3464.1995

The short transcript of Leishmania RNA virus is generated by RNA cleavage.

K J MacBeth 1, J L Patterson 1
PMCID: PMC189058  PMID: 7745692

Abstract

Leishmania RNA virus 1 produces a short viral RNA transcript corresponding to the 5' end of positive-sense single-stranded RNAs both in virally infected cells and in in vitro polymerase assays. We hypothesized that this short transcript was generated via cleavage of full-length positive-sense single-stranded RNA. A putative cleavage site was mapped by primer extension analysis to nucleotide 320 of the viral genome. To address the hypothesis that the short transcript is generated via cleavage at this site, two substrate RNAs that possessed viral sequence encompassing the putative cleavage site were created. When incubated with sucrose-purified viral particles, these substrate RNAs were site-specifically cleaved. The cleavage site of the in vitro-processed RNAs also mapped to viral nucleotide 320. The short-transcript-generating activity could be specifically abolished by proteinase K treatment of sucrose-purified viral particles and high concentrations of EGTA [ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid], suggesting that the activity requires a proteinaceous factor and possibly intact viral particles. The cleavage activity is directly associated with short-transcript-generating activity, since only viral particle preparations which were capable of generating the short transcript in polymerase assays were also active in the cleavage assay. Furthermore, the short-transcript-generating activity is independent of the viral polymerase's transcriptase and replicase activities. We present a working model whereby cleavage of Leishmaniavirus RNA transcripts functions in the maintenance of a low-level persistent infection.

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Selected References

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

  1. Bruenn J. A. Relationships among the positive strand and double-strand RNA viruses as viewed through their RNA-dependent RNA polymerases. Nucleic Acids Res. 1991 Jan 25;19(2):217–226. doi: 10.1093/nar/19.2.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cadd T. L., Patterson J. L. Synthesis of viruslike particles by expression of the putative capsid protein of Leishmania RNA virus in a recombinant baculovirus expression system. J Virol. 1994 Jan;68(1):358–365. doi: 10.1128/jvi.68.1.358-365.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chung I. K., Armstrong T. C., Patterson J. L. Identification of a short viral transcript in Leishmania RNA virus-infected cells. Virology. 1994 Feb;198(2):552–556. doi: 10.1006/viro.1994.1066. [DOI] [PubMed] [Google Scholar]
  4. Coderre J. A., Beverley S. M., Schimke R. T., Santi D. V. Overproduction of a bifunctional thymidylate synthetase-dihydrofolate reductase and DNA amplification in methotrexate-resistant Leishmania tropica. Proc Natl Acad Sci U S A. 1983 Apr;80(8):2132–2136. doi: 10.1073/pnas.80.8.2132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Fujimura T., Wickner R. B. Replicase of L-A virus-like particles of Saccharomyces cerevisiae. In vitro conversion of exogenous L-A and M1 single-stranded RNAs to double-stranded form. J Biol Chem. 1988 Jan 5;263(1):454–460. [PubMed] [Google Scholar]
  6. Hagler J., Shuman S. Nascent RNA cleavage by purified ternary complexes of vaccinia RNA polymerase. J Biol Chem. 1993 Jan 25;268(3):2166–2173. [PubMed] [Google Scholar]
  7. Iyer R. R. A matched set of cat vectors for rapid mutational analysis of eukaryotic promoters and enhancers. Gene. 1991 Aug 30;105(1):97–100. doi: 10.1016/0378-1119(91)90518-g. [DOI] [PubMed] [Google Scholar]
  8. Kassavetis G. A., Geiduschek E. P. RNA polymerase marching backward. Science. 1993 Feb 12;259(5097):944–945. doi: 10.1126/science.7679800. [DOI] [PubMed] [Google Scholar]
  9. Kozak M. An analysis of vertebrate mRNA sequences: intimations of translational control. J Cell Biol. 1991 Nov;115(4):887–903. doi: 10.1083/jcb.115.4.887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Patterson J. L., Holloway B., Kolakofsky D. La Crosse virions contain a primer-stimulated RNA polymerase and a methylated cap-dependent endonuclease. J Virol. 1984 Oct;52(1):215–222. doi: 10.1128/jvi.52.1.215-222.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Plotch S. J., Bouloy M., Ulmanen I., Krug R. M. A unique cap(m7GpppXm)-dependent influenza virion endonuclease cleaves capped RNAs to generate the primers that initiate viral RNA transcription. Cell. 1981 Mar;23(3):847–858. doi: 10.1016/0092-8674(81)90449-9. [DOI] [PubMed] [Google Scholar]
  12. Scheffter S., Widmer G., Patterson J. L. Complete sequence of Leishmania RNA virus 1-4 and identification of conserved sequences. Virology. 1994 Mar;199(2):479–483. doi: 10.1006/viro.1994.1149. [DOI] [PubMed] [Google Scholar]
  13. Stuart K. D., Weeks R., Guilbride L., Myler P. J. Molecular organization of Leishmania RNA virus 1. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8596–8600. doi: 10.1073/pnas.89.18.8596. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Weeks R. S., Patterson J. L., Stuart K., Widmer G. Transcribing and replicating particles in a double-stranded RNA virus from Leishmania. Mol Biochem Parasitol. 1992 Jun;52(2):207–213. doi: 10.1016/0166-6851(92)90053-m. [DOI] [PubMed] [Google Scholar]
  15. Whitehall S. K., Bardeleben C., Kassavetis G. A. Hydrolytic cleavage of nascent RNA in RNA polymerase III ternary transcription complexes. J Biol Chem. 1994 Jan 21;269(3):2299–2306. [PubMed] [Google Scholar]
  16. Wickner R. B. Double-stranded and single-stranded RNA viruses of Saccharomyces cerevisiae. Annu Rev Microbiol. 1992;46:347–375. doi: 10.1146/annurev.mi.46.100192.002023. [DOI] [PubMed] [Google Scholar]
  17. Widmer G., Keenan M. C., Patterson J. L. RNA polymerase activity is associated with viral particles isolated from Leishmania braziliensis subsp. guyanensis. J Virol. 1990 Aug;64(8):3712–3715. doi: 10.1128/jvi.64.8.3712-3715.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Widmer G., Patterson J. L. Genomic structure and RNA polymerase activity in Leishmania virus. J Virol. 1991 Aug;65(8):4211–4215. doi: 10.1128/jvi.65.8.4211-4215.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]

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