Interaction in vitro between the proteinase of Tomato ringspot virus (genus Nepovirus) and the eukaryotic translation initiation factor iso4E from Arabidopsis thaliana.

Eukaryotic initiation factor eIF(iso)4E binds to the cap structure of mRNAs leading to assembly of the translation complex. This factor also interacts with the potyvirus VPg and this interaction has been correlated with virus infectivity. In this study, we show an interaction between eIF(iso)4E and the proteinase (Pro) of a nepovirus (Tomato ringspot virus; ToRSV) in vitro. The ToRSV VPg did not interact with eIF(iso)4E although its presence on the VPg-Pro precursor increased the binding affinity of Pro for the initiation factor. A major determinant of the interaction was mapped to the first 93 residues of Pro. Formation of the complex was inhibited by addition of m(7)GTP (a cap analogue), suggesting that Pro-containing molecules compete with cellular mRNAs for eIF(iso)4E binding. The possible implications of this interaction for translation and/or replication of the virus genome are discussed.

[1]  D. Gallie Cap-Independent Translation Conferred by the 5′ Leader of Tobacco Etch Virus Is Eukaryotic Initiation Factor 4G Dependent , 2001, Journal of Virology.

[2]  R. Olsthoorn,et al.  Translation of a nonpolyadenylated viral RNA is enhanced by binding of viral coat protein or polyadenylation of the RNA , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. Sanfaçon,et al.  Expression and partial purification of recombinant tomato ringspot nepovirus 3C-like proteinase: comparison of the activity of the mature proteinase and the VPg-proteinase precursor , 2001, Virus Research.

[4]  R. Jackson,et al.  Activity of the Hepatitis A Virus IRES Requires Association between the Cap-Binding Translation Initiation Factor (eIF4E) and eIF4G , 2001, Journal of Virology.

[5]  Esther M. Lafuente,et al.  IRES interaction with translation initiation factors: functional characterization of novel RNA contacts with eIF3, eIF4B, and eIF4GII. , 2001, RNA.

[6]  K. Kean,et al.  Detailed Analysis of the Requirements of Hepatitis A Virus Internal Ribosome Entry Segment for the Eukaryotic Initiation Factor Complex eIF4F , 2001, Journal of Virology.

[7]  S. Paulous,et al.  Eukaryotic Initiation Factor 4G-Poly(A) Binding Protein Interaction Is Required for Poly(A) Tail-Mediated Stimulation of Picornavirus Internal Ribosome Entry Segment-Driven Translation but Not for X-Mediated Stimulation of Hepatitis C Virus Translation , 2001, Molecular and Cellular Biology.

[8]  Esther M. Lafuente,et al.  Functional interactions in internal translation initiation directed by viral and cellular IRES elements. , 2001, The Journal of general virology.

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

[10]  A. Wang,et al.  Proteolytic processing at a novel cleavage site in the N-terminal region of the tomato ringspot nepovirus RNA-1-encoded polyprotein in vitro. , 2000, The Journal of general virology.

[11]  J. Laliberté,et al.  Complex Formation between Potyvirus VPg and Translation Eukaryotic Initiation Factor 4E Correlates with Virus Infectivity , 2000, Journal of Virology.

[12]  P. Sarnow,et al.  Regulation of host cell translation by viruses and effects on cell function. , 2000, Current opinion in microbiology.

[13]  J. Carrington,et al.  Strain-specific interaction of the tobacco etch virus NIa protein with the translation initiation factor eIF4E in the yeast two-hybrid system. , 2000, Virology.

[14]  P. Vende,et al.  Efficient Translation of Rotavirus mRNA Requires Simultaneous Interaction of NSP3 with the Eukaryotic Translation Initiation Factor eIF4G and the mRNA 3′ End , 2000, Journal of Virology.

[15]  M. Katze,et al.  Translational Control of Viral Gene Expression in Eukaryotes , 2000, Microbiology and Molecular Biology Reviews.

[16]  R. Andino,et al.  Interactions of Viral Protein 3CD and Poly(rC) Binding Protein with the 5′ Untranslated Region of the Poliovirus Genome , 2000, Journal of Virology.

[17]  J. Grosclaude,et al.  Identification of the RNA-Binding, Dimerization, and eIF4GI-Binding Domains of Rotavirus Nonstructural Protein NSP3 , 1999, Journal of Virology.

[18]  H. Sanfaçon,et al.  Proteolytic processing of tomato ringspot nepovirus 3C-like protease precursors: definition of the domains for the VPg, protease and putative RNA-dependent RNA polymerase. , 1999, The Journal of general virology.

[19]  Jean Cohen,et al.  Rotavirus RNA‐binding protein NSP3 interacts with eIF4GI and evicts the poly(A) binding protein from eIF4F , 1998, The EMBO journal.

[20]  A. Gingras,et al.  The mRNA 5' cap-binding protein eIF4E and control of cell growth. , 1998, Current opinion in cell biology.

[21]  B. Cullen,et al.  Utilization of a mammalian cell-based RNA binding assay to characterize the RNA binding properties of picornavirus 3C proteinases. , 1998, RNA.

[22]  C. Camilleri,et al.  The Arabidopsis thaliana cDNAs coding for eIF4E and eIF(iso)4E are not functionally equivalent for yeast complementation and are differentially expressed during plant development. , 1998, The Plant journal : for cell and molecular biology.

[23]  J. Carrington,et al.  RNA binding activity of NIa proteinase of tobacco etch potyvirus. , 1997, Virology.

[24]  Y. Kusov,et al.  Interaction of hepatitis A virus (HAV) precursor proteins 3AB and 3ABC with the 5' and 3' termini of the HAV RNA. , 1997, Virus research.

[25]  J. Laliberté,et al.  Interaction of the viral protein genome linked of turnip mosaic potyvirus with the translational eukaryotic initiation factor (iso) 4E of Arabidopsis thaliana using the yeast two-hybrid system. , 1997, Virology.

[26]  Y. Kusov,et al.  In vitro RNA binding of the hepatitis A virus proteinase 3C (HAV 3Cpro) to secondary structure elements within the 5' terminus of the HAV genome. , 1997, RNA.

[27]  A. Porter,et al.  Sequence and Structural Determinants of the Interaction between the 5′-Noncoding Region of Picornavirus RNA and Rhinovirus Protease 3C (*) , 1995, The Journal of Biological Chemistry.

[28]  H. Sanfaçon,et al.  Tomato ringspot nepovirus protease: characterization and cleavage site specificity. , 1995, The Journal of general virology.

[29]  C. Fritsch,et al.  A possible consensus sequence for VPg of viruses in the family Comoviridae , 1994, FEBS letters.

[30]  E. Wimmer,et al.  Interaction of poliovirus polypeptide 3CDpro with the 5' and 3' termini of the poliovirus genome. Identification of viral and cellular cofactors needed for efficient binding. , 1994, The Journal of biological chemistry.

[31]  P. Ahlquist,et al.  Brome mosaic virus RNA replication proteins 1a and 2a from a complex in vitro , 1992, Journal of virology.

[32]  D. Rochon,et al.  Nucleotide sequence of tomato ringspot virus RNA1. , 1991, The Journal of general virology.

[33]  A. Sachs 10 Physical and Functional Interactions between the mRNA Cap Structure and the Poly(A) Tail , 2000 .

[34]  J. Riechmann,et al.  Highlights and prospects of potyvirus molecular biology. , 1992, The Journal of general virology.