Eukaryotic Elongation Factor 1A Interacts with the Upstream Pseudoknot Domain in the 3′ Untranslated Region of Tobacco Mosaic Virus RNA

ABSTRACT The genomic RNA of tobacco mosaic virus (TMV), like that of other positive-strand RNA viruses, acts as a template for both translation and replication. The highly structured 3′ untranslated region (UTR) of TMV RNAs plays an important role in both processes; it is not polyadenylated but ends with a tRNA-like structure (TLS) preceded by a conserved upstream pseudoknot domain (UPD). The TLS of tobamoviral RNAs can be specifically aminoacylated and, in this state, can interact with eukaryotic elongation factor 1A (eEF1A)/GTP with high affinity. Using a UV cross-linking assay, we detected another specific binding site for eEF1A/GTP, within the UPDs of TMV and crucifer-infecting tobamovirus (crTMV), that does not require aminoacylation. A mutational analysis revealed that UPD pseudoknot conformation and some conserved primary sequence elements are required for this interaction. Its possible role in the regulation of tobamovirus gene expression and replication is discussed.

[1]  J. Hofsteenge,et al.  Recognition signal for C-mannosylation of Trp-7 in RNase 2 consists of sequence Trp-x-x-Trp. , 1998, Molecular biology of the cell.

[2]  L. Tarrago-Litvak,et al.  Elongation factor-viral genome interaction dependent on the aminoacylation of TYMV and TMV RNAs. , 1973, Nature: New biology.

[3]  Howard M. Goodman,et al.  High resolution two-dimensional electrophoresis of basic as well as acidic proteins , 1977, Cell.

[4]  K. Buck,et al.  The tobacco mosaic virus RNA polymerase complex contains a plant protein related to the RNA-binding subunit of yeast eIF-3 , 1997, Journal of virology.

[5]  C. Pleij,et al.  Three‐dimensional models of the tRNA‐like 3′ termini of some plant viral RNAs. , 1983, The EMBO journal.

[6]  P. Más,et al.  Replication of Tobacco Mosaic Virus on Endoplasmic Reticulum and Role of the Cytoskeleton and Virus Movement Protein in Intracellular Distribution of Viral RNA , 1999, The Journal of cell biology.

[7]  R. Jansen RNA–cytoskeletal associations , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[8]  D. J. Lewandowski,et al.  Full-length tobacco mosaic virus RNAs and defective RNAs have different 3' replication signals. , 2000, Virology.

[9]  C. Hemenway,et al.  Role of the 3′ tRNA-Like Structure in Tobacco Mosaic Virus Minus-Strand RNA Synthesis by the Viral RNA-Dependent RNA Polymerase In Vitro , 2000, Journal of Virology.

[10]  M. Lai Cellular factors in the transcription and replication of viral RNA genomes: a parallel to DNA-dependent RNA transcription. , 1998, Virology.

[11]  L. I. Slobin The role of eucaryotic factor Tu in protein synthesis. The measurement of the elongation factor Tu content of rabbit reticulocytes and other mammalian cells by a sensitive radioimmunoassay. , 1980, European journal of biochemistry.

[12]  J. Condeelis Elongation factor 1 alpha, translation and the cytoskeleton. , 1995, Trends in biochemical sciences.

[13]  M. Deutscher,et al.  A channeled tRNA cycle during mammalian protein synthesis. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. Lai,et al.  An internal polypyrimidine-tract-binding protein-binding site in the hepatitis C virus RNA attenuates translation, which is relieved by the 3'-untranslated sequence. , 1999, Virology.

[15]  P. Ahlquist,et al.  Formation of brome mosaic virus RNA-dependent RNA polymerase in yeast requires coexpression of viral proteins and viral RNA. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[16]  P. Ahlquist,et al.  Identification and characterization of a host protein required for efficient template selection in viral RNA replication. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[17]  R. C. Moore,et al.  Association between elongation factor-1alpha and microtubules in vivo is domain dependent and conditional. , 2000, Cell motility and the cytoskeleton.

[18]  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.

[19]  J. Skuzeski,et al.  Characterization of chimeric turnip yellow mosaic virus genomes that are infectious in the absence of aminoacylation. , 1997, Virology.

[20]  K. Buck,et al.  Replication of tobacco mosaic virus RNA. , 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[21]  L. I. Slobin The Role of Eucaryotic Elongation Factor Tu in Protein Synthesis , 1980 .

[22]  C. Pleij,et al.  Similarities between the secondary structure of satellite tobacco mosaic virus and tobamovirus RNAs. , 1994, The Journal of general virology.

[23]  O. Uhlenbeck,et al.  Quantitative Assessment of EF-1α·GTP Binding to Aminoacyl-tRNAs, Aminoacyl-viral RNA, and tRNA Shows Close Correspondence to the RNA Binding Properties of EF-Tu* , 1999, The Journal of Biological Chemistry.

[24]  C. Pleij,et al.  Minimal Template Requirements for Initiation of Minus-Strand Synthesis In Vitro by the RNA-Dependent RNA Polymerase of Turnip Yellow Mosaic Virus , 1998, Journal of Virology.

[25]  K. Browning,et al.  Isolation and sequence of a cDNA encoding the cap binding protein of wheat eukaryotic protein synthesis initiation factor 4F. , 1992, Nucleic acids research.

[26]  J. Condeelis Elongation factor 1α, translation and the cytoskeleton , 1995 .

[27]  M. Lai,et al.  The 3′-Untranslated Region of Hepatitis C Virus RNA Enhances Translation from an Internal Ribosomal Entry Site , 1998, Journal of Virology.

[28]  R. Singer,et al.  Single mRNAs visualized by ultrastructural in situ hybridization are principally localized at actin filament intersections in fibroblasts , 1994, The Journal of cell biology.

[29]  G. B. Smith,et al.  Determination of the amounts of the protein synthesis initiation and elongation factors in wheat germ. , 1990, The Journal of biological chemistry.

[30]  K. Browning,et al.  Purification and properties of protein synthesis initiation and elongation factors from wheat germ. , 1986, Methods in enzymology.

[31]  L. Gold,et al.  RNA replication by Q beta replicase: a working model. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[32]  C. Pleij,et al.  The tRNA-like structure at the 3' terminus of turnip yellow mosaic virus RNA. Differences and similarities with canonical tRNA. , 1982, Nucleic acids research.

[33]  R. Joshi,et al.  Interaction of turnip yellow mosaic virus Val‐RNA with eukaryotic elongation factor EF‐1 [alpha]. Search for a function. , 1986, The EMBO journal.

[34]  Robert L. Tanguay,et al.  Isolation and Characterization of the 102-Kilodalton RNA-binding Protein That Binds to the 5′ and 3′ Translational Enhancers of Tobacco Mosaic Virus RNA* , 1996, The Journal of Biological Chemistry.

[35]  B. Pickard,et al.  Changing Patterns of Localization of the Tobacco Mosaic Virus Movement Protein and Replicase to the Endoplasmic Reticulum and Microtubules during Infection , 1998, Plant Cell.

[36]  E. Westhof,et al.  A central pseudoknotted three-way junction imposes tRNA-like mimicry and the orientation of three 5' upstream pseudoknots in the 3' terminus of tobacco mosaic virus RNA. , 1996, RNA.

[37]  V. Walbot,et al.  Functional analysis of the tobacco mosaic virus tRNA-like structure in cytoplasmic gene regulation. , 1991, Nucleic acids research.

[38]  J. Skuzeski,et al.  Aminoacylation identity switch of turnip yellow mosaic virus RNA from valine to methionine results in an infectious virus. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[39]  V. Boyko,et al.  Cellular Targets of Functional and Dysfunctional Mutants of Tobacco Mosaic Virus Movement Protein Fused to Green Fluorescent Protein , 2000, Journal of Virology.

[40]  A. El'skaya,et al.  Eukaryotic translation elongation factor 1 alpha: structure, expression, functions, and possible role in aminoacyl-tRNA channeling. , 1998, Progress in nucleic acid research and molecular biology.

[41]  Y. Okada,et al.  Mutational analysis of the pseudoknot region in the 3' noncoding region of tobacco mosaic virus RNA , 1990, Journal of virology.

[42]  A. Banerjee,et al.  RNA polymerase of vesicular stomatitis virus specifically associates with translation elongation factor-1 αβγ for its activity , 1998 .

[43]  V. Walbot,et al.  RNA pseudoknot domain of tobacco mosaic virus can functionally substitute for a poly(A) tail in plant and animal cells. , 1990, Genes & development.

[44]  D. Gallie A tale of two termini: a functional interaction between the termini of an mRNA is a prerequisite for efficient translation initiation. , 1998, Gene.

[45]  J. H. Strauss,et al.  Viral RNA replication. With a little help from the host. , 1999, Science.

[46]  T. Blumenthal,et al.  RNA replication: function and structure of Qbeta-replicase. , 1979, Annual review of biochemistry.

[47]  C. Pleij,et al.  RNA pseudoknots: structure, detection, and prediction. , 1989, Methods in enzymology.

[48]  R. Singer,et al.  The travels of mRNAs through all cells large and small , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[49]  L. I. Slobin Binding of eucaryotic elongation factor Tu to nucleic acids. , 1983, The Journal of biological chemistry.

[50]  S. Ueda,et al.  Isolation from Tobacco Mosaic Virus-Infected Tobacco of a Solubilized Template-Specific RNA-Dependent RNA Polymerase Containing a 126K/183K Protein Heterodimer , 1999, Journal of Virology.

[51]  J. Flanegan,et al.  Translating Ribosomes Inhibit Poliovirus Negative-Strand RNA Synthesis , 1999, Journal of Virology.

[52]  D. J. Lewandowski,et al.  Deletion of internal sequences results in tobacco mosaic virus defective RNAs that accumulate to high levels without interfering with replication of the helper virus. , 1998, Virology.

[53]  T. Dreher,et al.  Cis-preferential replication of the turnip yellow mosaic virus RNA genome. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[54]  B. Semler,et al.  Requirement of poly(rC) binding protein 2 for translation of poliovirus RNA , 1997, Journal of virology.

[55]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[56]  M. Zaitlin,et al.  Replication of tobacco mosaic virus. 3. Viral RNA metabolism in separated leaf cells. , 1971, Virology.

[57]  J. H. Strauss,et al.  With a Little Help from the Host , 1999, Science.

[58]  J. Bol,et al.  Role of the 3′-Untranslated Regions of Alfalfa Mosaic Virus RNAs in the Formation of a Transiently Expressed Replicase in Plants and in the Assembly of Virions , 2001, Journal of Virology.

[59]  C. Pleij,et al.  tRNA‐like structures , 1991 .

[60]  M. Brinton,et al.  Translation elongation factor-1 alpha interacts with the 3' stem-loop region of West Nile virus genomic RNA , 1997, Journal of virology.

[61]  J P Abrahams,et al.  Five pseudoknots are present at the 204 nucleotides long 3' noncoding region of tobacco mosaic virus RNA. , 1985, Nucleic acids research.

[62]  S. Morozov,et al.  Complete nucleotide sequence and genome organization of a tobamovirus infecting cruciferae plants , 1994, FEBS letters.

[63]  J. Nyborg,et al.  3 The Protein Biosynthesis, Elongation Cycle , 2000 .

[64]  L. Ryabova,et al.  Enhancing effect of the 3′‐untranslated region of tobacco mosaic virus RNA on protein synthesis in vitro , 1994, FEBS letters.

[65]  Frank McCormick,et al.  The GTPase superfamily: a conserved switch for diverse cell functions , 1990, Nature.

[66]  R. Quadt,et al.  Characterization of cucumber mosaic virus RNA‐dependent RNA polymerase , 1991, FEBS letters.

[67]  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.