Literature DB >> 10954536

The infectivities of turnip yellow mosaic virus genomes with altered tRNA mimicry are not dependent on compensating mutations in the viral replication protein.

S A Filichkin1, K L Bransom, J B Goodwin, T W Dreher.   

Abstract

Five highly infectious turnip yellow mosaic virus (TYMV) genomes with sequence changes in their 3'-terminal regions that result in altered aminoacylation and eEF1A binding have been studied. These genomes were derived from cloned parental RNAs of low infectivity by sequential passaging in plants. Three of these genomes that are incapable of aminoacylation have been reported previously (J. B. Goodwin, J. M. Skuzeski, and T. W. Dreher, Virology 230:113-124, 1997). We now demonstrate by subcloning the 3' untranslated regions into wild-type TYMV RNA that the high infectivities and replication rates of these genomes compared to their progenitors are mostly due to a small number of mutations acquired in the 3' tRNA-like structure during passaging. Mutations in other parts of the genome, including the replication protein coding region, are not required for high infectivity but probably do play a role in optimizing viral amplification and spread in plants. Two other TYMV RNA variants of suboptimal infectivities, one that accepts methionine instead of the usual valine and one that interacts less tightly with eEF1A, were sequentially passaged to produce highly infectious genomes. The improved infectivities of these RNAs were not associated with increased replication in protoplasts, and no mutations were acquired in their 3' tRNA-like structures. Complete sequencing of one genome identified two mutations that result in amino acid changes in the movement protein gene, suggesting that improved infectivity may be a function of improved viral dissemination in plants. Our results show that the wild-type TYMV replication proteins are able to amplify genomes with 3' termini of variable sequence and tRNA mimicry. These and previous results have led to a model in which the binding of eEF1A to the 3' end to antagonize minus-strand initiation is a major role of the tRNA-like structure.

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Year:  2000        PMID: 10954536      PMCID: PMC116347          DOI: 10.1128/jvi.74.18.8368-8375.2000

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  20 in total

1.  The turnip yellow mosaic virus tRNA-like structure cannot be replaced by generic tRNA-like elements or by heterologous 3' untranslated regions known to enhance mRNA expression and stability.

Authors:  J M Skuzeski; C S Bozarth; T W Dreher
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

2.  Specific site selection in RNA resulting from a combination of nonspecific secondary structure and -CCR- boxes: initiation of minus strand synthesis by turnip yellow mosaic virus RNA-dependent RNA polymerase.

Authors:  R N Singh; T W Dreher
Journal:  RNA       Date:  1998-09       Impact factor: 4.942

3.  Quantitative assessment of EF-1alpha.GTP binding to aminoacyl-tRNAs, aminoacyl-viral RNA, and tRNA shows close correspondence to the RNA binding properties of EF-Tu.

Authors:  T W Dreher; O C Uhlenbeck; K S Browning
Journal:  J Biol Chem       Date:  1999-01-08       Impact factor: 5.157

4.  Minimal template requirements for initiation of minus-strand synthesis in vitro by the RNA-dependent RNA polymerase of turnip yellow mosaic virus.

Authors:  B A Deiman; A K Koenen; P W Verlaan; C W Pleij
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

Review 5.  Cellular factors in the transcription and replication of viral RNA genomes: a parallel to DNA-dependent RNA transcription.

Authors:  M M Lai
Journal:  Virology       Date:  1998-04-25       Impact factor: 3.616

6.  Infectious TYMV RNA from cloned cDNA: effects in vitro and in vivo of point substitutions in the initiation codons of two extensively overlapping ORFs.

Authors:  J J Weiland; T W Dreher
Journal:  Nucleic Acids Res       Date:  1989-06-26       Impact factor: 16.971

7.  Characterization of chimeric turnip yellow mosaic virus genomes that are infectious in the absence of aminoacylation.

Authors:  J B Goodwin; J M Skuzeski; T W Dreher
Journal:  Virology       Date:  1997-03-31       Impact factor: 3.616

Review 8.  The alphaviruses: gene expression, replication, and evolution.

Authors:  J H Strauss; E G Strauss
Journal:  Microbiol Rev       Date:  1994-09

9.  Identification of the cleavage site recognized by the turnip yellow mosaic virus protease.

Authors:  K L Bransom; S E Wallace; T W Dreher
Journal:  Virology       Date:  1996-03-01       Impact factor: 3.616

10.  Telomeric function of the tRNA-like structure of brome mosaic virus RNA.

Authors:  A L Rao; T W Dreher; L E Marsh; T C Hall
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

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  3 in total

1.  Multi-domain packing in the aminoacylatable 3' end of a plant viral RNA.

Authors:  John A Hammond; Robert P Rambo; Jeffrey S Kieft
Journal:  J Mol Biol       Date:  2010-04-14       Impact factor: 5.469

2.  Structural variation and functional importance of a D-loop-T-loop interaction in valine-accepting tRNA-like structures of plant viral RNAs.

Authors:  Maarten H de Smit; Alexander P Gultyaev; Mark Hilge; Hugo H J Bink; Sharief Barends; Barend Kraal; Cornelis W A Pleij
Journal:  Nucleic Acids Res       Date:  2002-10-01       Impact factor: 16.971

Review 3.  Role of tRNA-like structures in controlling plant virus replication.

Authors:  Theo W Dreher
Journal:  Virus Res       Date:  2008-07-30       Impact factor: 3.303

  3 in total

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