This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gmyl, A. P.
Right arrow Articles by Agol, V. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gmyl, A. P.
Right arrow Articles by Agol, V. I.

 Previous Article  |  Next Article 

Journal of Virology, November 1999, p. 8958-8965, Vol. 73, No. 11
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Nonreplicative RNA Recombination in Poliovirus

Anatoly P. Gmyl,1 Evgeny V. Belousov,1,2 Svetlana V. Maslova,1 Elena V. Khitrina,1 Alexander B. Chetverin,3 and Vadim I. Agol1,2,*

Institute of Poliomyelitis and Viral Encephalitides, Russian Academy of Medical Sciences, Moscow Region 142782,1 Moscow State University, Moscow 119899,2 and Institute of Protein Research, Russian Academy of Sciences, Pushchino, Moscow Region 142292,3 Russia

Received 7 April 1999/Accepted 23 July 1999

Current models of recombination between viral RNAs are based on replicative template-switch mechanisms. The existence of nonreplicative RNA recombination in poliovirus is demonstrated in the present study by the rescue of viable viruses after cotransfections with different pairs of genomic RNA fragments with suppressed translatable and replicating capacities. Approximately 100 distinct recombinant genomes have been identified. The majority of crossovers occurred between nonhomologous segments of the partners and might have resulted from transesterification reactions, not necessarily involving an enzymatic activity. Some of the crossover loci are clustered. The origin of some of these "hot spots" could be explained by invoking structures similar to known ribozymes. A significant proportion of recombinant RNAs contained the entire 5' partner, if its 3' end was oxidized or phosphorylated prior to being mixed with the 3' partner. All of these observations are consistent with a mechanism that involves intermediary formation of the 2',3'-cyclic phosphate and 5'-hydroxyl termini. It is proposed that nonreplicative RNA recombination may contribute to evolutionarily significant RNA rearrangements.


* Corresponding author. Mailing address: Institute of Poliomyelitis, Russian Academy of Medical Sciences, Moscow Region 142782, Russia. Phone: (95) 439-90-26. Fax: (95) 439-93-21. E-mail: viago{at}ipive.genebee.msu.su.


Journal of Virology, November 1999, p. 8958-8965, Vol. 73, No. 11
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Savolainen-Kopra, C., Samoilovich, E., Kahelin, H., Hiekka, A.-K., Hovi, T., Roivainen, M. (2009). Comparison of poliovirus recombinants: accumulation of point mutations provides further advantages. J. Gen. Virol. 90: 1859-1868 [Abstract] [Full Text]  
  • Draghici, H.-K., Varrelmann, M. (2009). Evidence that the Linker between the Methyltransferase and Helicase Domains of Potato Virus X Replicase Is Involved in Homologous RNA Recombination. J. Virol. 83: 7761-7769 [Abstract] [Full Text]  
  • Romanova, L. I., Lidsky, P. V., Kolesnikova, M. S., Fominykh, K. V., Gmyl, A. P., Sheval, E. V., Hato, S. V., van Kuppeveld, F. J. M., Agol, V. I. (2009). Antiapoptotic Activity of the Cardiovirus Leader Protein, a Viral "Security" Protein. J. Virol. 83: 7273-7284 [Abstract] [Full Text]  
  • Garcia-Ruiz, H., Ahlquist, P. (2006). Inducible Yeast System for Viral RNA Recombination Reveals Requirement for an RNA Replication Signal on Both Parental RNAs.. J. Virol. 80: 8316-8328 [Abstract] [Full Text]  
  • Wierzchoslawski, R., Bujarski, J. J. (2006). Efficient In Vitro System of Homologous Recombination in Brome Mosaic Bromovirus.. J. Virol. 80: 6182-6187 [Abstract] [Full Text]  
  • van Ooij, M. J. M., Polacek, C., Glaudemans, D. H. R. F., Kuijpers, J., van Kuppeveld, F. J. M., Andino, R., Agol, V. I., Melchers, W. J. G. (2006). Polyadenylation of genomic RNA and initiation of antigenomic RNA in a positive-strand RNA virus are controlled by the same cis-element. Nucleic Acids Res 34: 2953-2965 [Abstract] [Full Text]  
  • DeStefano, J. J., Titilope, O. (2006). Poliovirus Protein 3AB Displays Nucleic Acid Chaperone and Helix-Destabilizing Activities. J. Virol. 80: 1662-1671 [Abstract] [Full Text]  
  • Serviene, E., Jiang, Y., Cheng, C.-P., Baker, J., Nagy, P. D. (2006). Screening of the Yeast yTHC Collection Identifies Essential Host Factors Affecting Tombusvirus RNA Recombination. J. Virol. 80: 1231-1241 [Abstract] [Full Text]  
  • Simmonds, P., Welch, J. (2006). Frequency and Dynamics of Recombination within Different Species of Human Enteroviruses. J. Virol. 80: 483-493 [Abstract] [Full Text]  
  • Chetverin, A. B., Kopein, D. S., Chetverina, H. V., Demidenko, A. A., Ugarov, V. I. (2005). Viral RNA-directed RNA Polymerases Use Diverse Mechanisms to Promote Recombination between RNA Molecules. J. Biol. Chem. 280: 8748-8755 [Abstract] [Full Text]  
  • Gallei, A., Rumenapf, T., Thiel, H.-J., Becher, P. (2005). Characterization of Helper Virus-Independent Cytopathogenic Classical Swine Fever Virus Generated by an In Vivo RNA Recombination System. J. Virol. 79: 2440-2448 [Abstract] [Full Text]  
  • Appel, N., Herian, U., Bartenschlager, R. (2005). Efficient Rescue of Hepatitis C Virus RNA Replication by trans-Complementation with Nonstructural Protein 5A. J. Virol. 79: 896-909 [Abstract] [Full Text]  
  • GUDIMA, S. O., CHANG, J., TAYLOR, J. M. (2005). Reconstitution in cultured cells of replicating HDV RNA from pairs of less than full-length RNAs. RNA 11: 90-98 [Abstract] [Full Text]  
  • Gallei, A., Pankraz, A., Thiel, H.-J., Becher, P. (2004). RNA Recombination In Vivo in the Absence of Viral Replication. J. Virol. 78: 6271-6281 [Abstract] [Full Text]  
  • Hausmann, Y., Roman-Sosa, G., Thiel, H.-J., Rumenapf, T. (2004). Classical Swine Fever Virus Glycoprotein Erns Is an Endoribonuclease with an Unusual Base Specificity. J. Virol. 78: 5507-5512 [Abstract] [Full Text]  
  • Oberste, M. S., Maher, K., Pallansch, M. A. (2004). Evidence for Frequent Recombination within Species Human Enterovirus B Based on Complete Genomic Sequences of All Thirty-Seven Serotypes. J. Virol. 78: 855-867 [Abstract] [Full Text]  
  • Costa-Mattioli, M., Napoli, A. D., Ferre, V., Billaudel, S., Perez-Bercoff, R., Cristina, J. (2003). Genetic variability of hepatitis A virus. J. Gen. Virol. 84: 3191-3201 [Abstract] [Full Text]  
  • Cheng, C.-P., Nagy, P. D. (2003). Mechanism of RNA Recombination in Carmo- and Tombusviruses: Evidence for Template Switching by the RNA-Dependent RNA Polymerase In Vitro. J. Virol. 77: 12033-12047 [Abstract] [Full Text]  
  • GMYL, A. P., KORSHENKO, S. A., BELOUSOV, E. V., KHITRINA, E. V., AGOL, V. I. (2003). Nonreplicative homologous RNA recombination: Promiscuous joining of RNA pieces?. RNA 9: 1221-1231 [Abstract] [Full Text]  
  • Wierzchoslawski, R., Dzianott, A., Kunimalayan, S., Bujarski, J. J. (2003). A Transcriptionally Active Subgenomic Promoter Supports Homologous Crossovers in a Plus-Strand RNA Virus. J. Virol. 77: 6769-6776 [Abstract] [Full Text]  
  • Romani, A., Guerra, E., Trerotola, M., Alberti, S. (2003). Detection and analysis of spliced chimeric mRNAs in sequence databanks. Nucleic Acids Res 31: e17-e17 [Abstract] [Full Text]  
  • Egger, D., Bienz, K. (2002). Recombination of Poliovirus RNA Proceeds in Mixed Replication Complexes Originating from Distinct Replication Start Sites. J. Virol. 76: 10960-10971 [Abstract] [Full Text]  
  • Gauss-Muller, V., Kusov, Y. Y. (2002). Replication of a hepatitis A virus replicon detected by genetic recombination in vivo. J. Gen. Virol. 83: 2183-2192 [Abstract] [Full Text]  
  • Cuervo, N. S., Guillot, S., Romanenkova, N., Combiescu, M., Aubert-Combiescu, A., Seghier, M., Caro, V., Crainic, R., Delpeyroux, F. (2001). Genomic Features of Intertypic Recombinant Sabin Poliovirus Strains Excreted by Primary Vaccinees. J. Virol. 75: 5740-5751 [Abstract] [Full Text]