Abstract
Engineered mutants of Theiler's murine encephalomyelitis virus (TMEV) and poliovirus having altered spacing between the oligopyrimidine and AUG moieties of a translational control element are known to generate pseudorevertants with deletions or insertions that tend to restore the wild-type structure of this element. The primary structure of the rearranged region of these pseudorevertants suggests that short direct repeats are strongly preferred as parting and anchoring sites during the jumps of the nascent strand 3' end. When the parting and anchoring sites are separated by a long RNA segment, they can be brought in close proximity by an appropriate folding of the template strand. On the basis of evidence derived from the analysis of the pseudorevertant genomes, it is proposed that a class of RNA rearrangements (some recombinations, deletions, insertions) proceed through the following steps: (i) pausing of the nascent strand caused by misincorporations (or other reasons); (ii) dissociation of the RNA polymerase together with the 3' end of the nascent strand (a kind proof-reading); and (iii) re-annealing of the nascent and template strands (precise or imprecise, but with the 3' base paired) and resumption of the synthesis.
Full text
PDF





Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Agol V. I. The 5'-untranslated region of picornaviral genomes. Adv Virus Res. 1991;40:103–180. doi: 10.1016/S0065-3527(08)60278-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beck E., Forss S., Strebel K., Cattaneo R., Feil G. Structure of the FMDV translation initiation site and of the structural proteins. Nucleic Acids Res. 1983 Nov 25;11(22):7873–7885. doi: 10.1093/nar/11.22.7873. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gmyl A. P., Pilipenko E. V., Maslova S. V., Belov G. A., Agol V. I. Functional and genetic plasticities of the poliovirus genome: quasi-infectious RNAs modified in the 5'-untranslated region yield a variety of pseudorevertants. J Virol. 1993 Oct;67(10):6309–6316. doi: 10.1128/jvi.67.10.6309-6316.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jackson R. J., Hunt S. L., Gibbs C. L., Kaminski A. Internal initiation of translation of picornavirus RNAs. Mol Biol Rep. 1994 May;19(3):147–159. doi: 10.1007/BF00986957. [DOI] [PMC free article] [PubMed] [Google Scholar]
- King A. M. Preferred sites of recombination in poliovirus RNA: an analysis of 40 intertypic cross-over sequences. Nucleic Acids Res. 1988 Dec 23;16(24):11705–11723. doi: 10.1093/nar/16.24.11705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Kuge S., Saito I., Nomoto A. Primary structure of poliovirus defective-interfering particle genomes and possible generation mechanisms of the particles. J Mol Biol. 1986 Dec 5;192(3):473–487. doi: 10.1016/0022-2836(86)90270-6. [DOI] [PubMed] [Google Scholar]
- 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]
- Pilipenko E. V., Gmyl A. P., Maslova S. V., Belov G. A., Sinyakov A. N., Huang M., Brown T. D., Agol V. I. Starting window, a distinct element in the cap-independent internal initiation of translation on picornaviral RNA. J Mol Biol. 1994 Aug 19;241(3):398–414. doi: 10.1006/jmbi.1994.1516. [DOI] [PubMed] [Google Scholar]
- Pilipenko E. V., Gmyl A. P., Maslova S. V., Khitrina E. V., Agol V. I. Attenuation of Theiler's murine encephalomyelitis virus by modifications of the oligopyrimidine/AUG tandem, a host-dependent translational cis element. J Virol. 1995 Feb;69(2):864–870. doi: 10.1128/jvi.69.2.864-870.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pilipenko E. V., Gmyl A. P., Maslova S. V., Svitkin Y. V., Sinyakov A. N., Agol V. I. Prokaryotic-like cis elements in the cap-independent internal initiation of translation on picornavirus RNA. Cell. 1992 Jan 10;68(1):119–131. doi: 10.1016/0092-8674(92)90211-t. [DOI] [PubMed] [Google Scholar]
- 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]
- Tolskaya E. A., Romanova L. I., Blinov V. M., Viktorova E. G., Sinyakov A. N., Kolesnikova M. S., Agol V. I. Studies on the recombination between RNA genomes of poliovirus: the primary structure and nonrandom distribution of crossover regions in the genomes of intertypic poliovirus recombinants. Virology. 1987 Nov;161(1):54–61. doi: 10.1016/0042-6822(87)90170-x. [DOI] [PubMed] [Google Scholar]
- Wimmer E., Hellen C. U., Cao X. Genetics of poliovirus. Annu Rev Genet. 1993;27:353–436. doi: 10.1146/annurev.ge.27.120193.002033. [DOI] [PubMed] [Google Scholar]
