3'-Terminal RNA secondary structures are important for accumulation of tomato bushy stunt virus DI RNAs.

The plus-strand RNA genome of tomato bushy stunt virus (TBSV) contains a 351-nucleotide (nt)-long 3'-untranslated region. We investigated the role of the 3'-proximal 130 nt of this sequence in viral RNA accumulation within the context of a TBSV defective interfering (DI) RNA. Sequence comparisons between different tombusviruses revealed that the 3' portion of the 130-nt sequence is highly conserved and deletion analysis confirmed that this segment is required for accumulation of DI RNAs in protoplasts. Computer-aided sequence analysis and in vitro solution structure probing indicated that the conserved sequence consists of three stem-loop (SL) structures (5'-SL3-SL2-SL1-3'). The existence of SLs 1 and 3 was also supported by comparative secondary structure analysis of sequenced tombusvirus genomes. Formation of the stem regions in all three SLs was found to be very important, and modification of the terminal loop sequences of SL1 and SL2, but not SL3, decreased DI RNA accumulation in vivo. For SL3, alterations to an internal loop resulted in significantly reduced DI RNA levels. Collectively, these data indicate that all three SLs are functionally relevant and contribute substantially to DI RNA accumulation. In addition, secondary structure analysis of other tombusvirus replicons and related virus genera revealed that a TBSV satellite RNA and members of the closely related genus Aureusvirus (family Tombusviridae) share fundamental elements of this general structural arrangement. Thus, this secondary structure model appears to extend beyond tombusvirus genomes. These conserved 3'-terminal RNA elements likely function in vivo by promoting and/or regulating minus-strand synthesis.

[1]  P. D. Nagy,et al.  A novel 3'-end repair mechanism in an RNA virus. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[2]  K. White,et al.  A Primary Determinant of Cap-Independent Translation Is Located in the 3′-Proximal Region of the Tomato Bushy Stunt Virus Genome , 1999, Journal of Virology.

[3]  D. Ray,et al.  Enhancer-like properties of an RNA element that modulates Tombusvirus RNA accumulation. , 1999, Virology.

[4]  C. Song,et al.  Requirement of a 3'-terminal stem-loop in in vitro transcription by an RNA-dependent RNA polymerase. , 1995, Journal of molecular biology.

[5]  R. Andino,et al.  Poliovirus RNA Replication Requires Genome Circularization through a Protein–Protein Bridge , 2001, Molecular Cell.

[6]  K. White,et al.  Uncoupled Expression of p33 and p92 Permits Amplification of Tomato Bushy Stunt Virus RNAs , 1998, Journal of Virology.

[7]  L. Rubino,et al.  Molecular analysis of the pothos latent virus genome. , 1997, The Journal of general virology.

[8]  T. J. Morris,et al.  Nonhomologous RNA recombination in tombusviruses: generation and evolution of defective interfering RNAs by stepwise deletions , 1994, Journal of virology.

[9]  Michael Zuker,et al.  Algorithms and Thermodynamics for RNA Secondary Structure Prediction: A Practical Guide , 1999 .

[10]  A. Simon,et al.  Polymerization of nontemplate bases before transcription initiation at the 3' ends of templates by an RNA-dependent RNA polymerase: an activity involved in 3' end repair of viral RNAs. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[11]  J. Burgyán,et al.  Sequence analysis of cymbidium ringspot virus satellite and defective interfering RNAs. , 1990, The Journal of general virology.

[12]  T. Dalmay,et al.  Localization of cis-acting sequences essential for cymbidium ringspot tombusvirus defective interfering RNA replication. , 1995, Journal of General Virology.

[13]  H. Heus,et al.  A network of heterogeneous hydrogen bonds in GNRA tetraloops. , 1996, Journal of molecular biology.

[14]  J. Flanegan,et al.  5′ cloverleaf in poliovirus RNA is a cis‐acting replication element required for negative‐strand synthesis , 2001, The EMBO journal.

[15]  F. García-Arenal,et al.  New satellite RNAs, but no DI RNAs, are found in natural populations of tomato bushy stunt tombusvirus. , 1997, Virology.

[16]  G. Martelli,et al.  Molecular biology of tombusviridae. , 1994, Advances in virus research.

[17]  J. van Duin,et al.  A long-range interaction in Qbeta RNA that bridges the thousand nucleotides between the M-site and the 3' end is required for replication. , 1998, RNA: A publication of the RNA Society.

[18]  T. Panavas,et al.  Analysis of minimal promoter sequences for plus-strand synthesis by the Cucumber necrosis virus RNA-dependent RNA polymerase. , 2002, Virology.

[19]  A. Simon,et al.  In vivo restoration of biologically active 3' ends of virus-associated RNAs by nonhomologous RNA recombination and replacement of a terminal motif , 1996, Journal of virology.

[20]  E. G. Westaway,et al.  Essential Role of Cyclization Sequences in Flavivirus RNA Replication , 2001, Journal of Virology.

[21]  J. Burgyán,et al.  Interactions between tombusviruses and satellite RNAs of tomato bushy stunt virus: a defect in sat RNA B1 replication maps to ORF1 of a helper virus. , 1999, Virology.

[22]  P. D. Nagy,et al.  Partial purification and characterization of Cucumber necrosis virus and Tomato bushy stunt virus RNA-dependent RNA polymerases: similarities and differences in template usage between tombusvirus and carmovirus RNA-dependent RNA polymerases. , 2000, Virology.

[23]  T. J. Morris,et al.  Enhanced competitiveness of tomato bushy stunt virus defective interfering RNAs by segment duplication or nucleotide insertion , 1994, Journal of virology.

[24]  D. Ray,et al.  An Internally Located RNA Hairpin Enhances Replication of Tomato Bushy Stunt Virus RNAs , 2003, Journal of Virology.

[25]  T. Dalmay,et al.  Repair in vivo of altered 3' terminus of cymbidium ringspot tombusvirus RNA. , 1993, Virology.

[26]  T. J. Morris,et al.  The complete genome structure and synthesis of infectious RNA from clones of tomato bushy stunt virus. , 1990, Virology.

[27]  W. Allen Miller,et al.  The 3′-Terminal Structure Required for Replication of Barley Yellow Dwarf Virus RNA Contains an Embedded 3′ End , 2002 .

[28]  A. Simon,et al.  Analysis of sequences and predicted structures required for viral satellite RNA accumulation by in vivo genetic selection. , 1998, Nucleic acids research.

[29]  J. Burgyán,et al.  3' Terminal putative stem-loop structure required for the accumulation of cymbidium ringspot viral RNA. , 1995, Virology.

[30]  J. Sabina,et al.  Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. , 1999, Journal of molecular biology.

[31]  G. Martelli,et al.  Sequence analysis of pothos latent virus genomic RNA. , 1995, The Journal of general virology.

[32]  The RNA Replication Enhancer Element of Tombusviruses Contains Two Interchangeable Hairpins That Are Functional during Plus-Strand Synthesis , 2003, Journal of Virology.

[33]  H. Damude,et al.  Genome structure of cucumber leaf spot virus: sequence analysis suggests it belongs to a distinct species within the Tombusviridae. , 1997, Virus research.

[34]  A. Simon Replication, recombination, and symptom-modulation properties of the satellite RNAs of turnip crinkle virus. , 1999, Current topics in microbiology and immunology.

[35]  S. You,et al.  In Vitro RNA Synthesis from Exogenous Dengue Viral RNA Templates Requires Long Range Interactions between 5′- and 3′-Terminal Regions That Influence RNA Structure* , 2001, The Journal of Biological Chemistry.

[36]  B. Wu,et al.  An RNA domain within the 5' untranslated region of the tomato bushy stunt virus genome modulates viral RNA replication. , 2001, Journal of molecular biology.

[37]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[38]  J. Duin,et al.  Secondary Structure Model of the Last Two Domains of Single-stranded RNA Phage Qβ , 1995 .

[39]  T. Panavas,et al.  Internal initiation by the cucumber necrosis virus RNA-dependent RNA polymerase is facilitated by promoter-like sequences. , 2002, Virology.

[40]  K. White Formation and evolution ofTombusvirusdefective interfering RNAs , 1996 .

[41]  A. Simon,et al.  Analysis in vivo of turnip crinkle virus satellite RNA C variants with mutations in the 3'-terminal minus-strand promoter. , 1997, Virology.

[42]  K. Buck Comparison of The Replication of Positive-Stranded Rna Viruses of Plants and Animals , 1996, Advances in Virus Research.

[43]  T. Dreher FUNCTIONS OF THE 3'-UNTRANSLATED REGIONS OF POSITIVE STRAND RNA VIRAL GENOMES. , 1999, Annual review of phytopathology.

[44]  K. White,et al.  Formation and Amplification of a Novel Tombusvirus Defective RNA Which Lacks the 5′ Nontranslated Region of the Viral Genome , 1998, Journal of Virology.

[45]  Mutation analysis of cis-elements in the 3'- and 5'-untranslated regions of satellite tobacco necrosis virus strain C RNA. , 1999, Virology.

[46]  H. Scholthof,et al.  Host effects and sequences essential for accumulation of defective interfering RNAs of cucumber necrosis and tomato bushy stunt tombusviruses. , 1995, Virology.

[47]  P. Moore,et al.  Structural motifs in RNA. , 1999, Annual review of biochemistry.