Skip to main content
Top
Published in: Virology Journal 1/2021

Open Access 01-12-2021 | Research

Efficient translation of Eggplant mottled dwarf nucleorhabdovirus N and X genes requires both 5′ and 3′ UTRs

Authors: Ghobad Babaei, Amir Massah, Mina Koohi Habibi

Published in: Virology Journal | Issue 1/2021

Login to get access

Abstract

Background

Circularization of RNA mediated by association of translation factors and RNA elements in 5′ and 3′ UTRs is a common feature for translation control in eukaryotes. There is no information about translation in plant rhabdoviruses and little information is known in animal rhabdoviruses.

Methods

The role of 5′ and 3′ UTRs in two genes of EMDV in translation were studied using luciferase constructs and RNA structures of these sequences were analyzed by SHAPE and Inline probing.

Results

We have found that efficient translation of N and X mRNAs of nucleorhabdovirus Eggplant mottled dwarf virus (EMDV) requires elements present in both 5′ and 3′ UTRs. Luciferase reporter constructs containing precise 5′ and 3′ UTRs of the N and X genes had substantially higher translational activity compared with constructs containing only the 5′ or 3′ UTR. The 3′UTR of carmovirus Turnip crinkle virus, which contains a well-characterized cap-independent translation enhancer, was unable to complement the lack of EMDV 3′ UTR. Addition of cap analog to luciferase constructs containing the UTRs of the N gene did not restore translation, and translation of the reporter construct in the absence of the 5′ cap was higher than the capped construct. No RNA-RNA interactions between 5′ and 3′ UTRs were detected by EMSA or in-line cleavage structural assays. Deletion of 11 nucleotides from the 3′ terminus negated the synergistic activity of the 3′UTR.

Conclusions

The results with RNA-RNA interaction suggesting that translational synergy between the UTRs may utilize alternative means. Mutation analysis in 3′UTR suggesting that the polyadenylation signal sequence contained in this location may play a critical role in translation.
Literature
1.
go back to reference Babaie Gh, Izadpanah K. Host range, distribution, isolates and transmission trials of Eggplant mottled dwarf virus. Iran J Plant Pathol. 2002;38:235–50. Babaie Gh, Izadpanah K. Host range, distribution, isolates and transmission trials of Eggplant mottled dwarf virus. Iran J Plant Pathol. 2002;38:235–50.
2.
go back to reference Babaie GH, Izadpanah K. Vector transmission of Eggplant mottled dwarf virus in Iran. J Phytopathol. 2003;151:679–82.CrossRef Babaie GH, Izadpanah K. Vector transmission of Eggplant mottled dwarf virus in Iran. J Phytopathol. 2003;151:679–82.CrossRef
3.
go back to reference Babaie Gh, Kouhi Habibi M, Massah A, Dizadji A, et al. Complete genome sequence and genome analysis of Eggplant mottled dwarf virus-Iranian Isolate. J Phytopathol. 2015;163:331–41.CrossRef Babaie Gh, Kouhi Habibi M, Massah A, Dizadji A, et al. Complete genome sequence and genome analysis of Eggplant mottled dwarf virus-Iranian Isolate. J Phytopathol. 2015;163:331–41.CrossRef
4.
go back to reference Bandyopadhyay A, Kopperud K, Anderson G, Martin K, et al. An integrated protein localization and interaction map for Potato yellow dwarf virus, type species of the genus Nucleorhabdovirus. Virology. 2010;402:61–71.PubMedCrossRef Bandyopadhyay A, Kopperud K, Anderson G, Martin K, et al. An integrated protein localization and interaction map for Potato yellow dwarf virus, type species of the genus Nucleorhabdovirus. Virology. 2010;402:61–71.PubMedCrossRef
5.
go back to reference Barr JN, Whelan SP, Wertz GW. Transcriptional control of the RNA-dependent RNA polymerase of vesicular stomatitis virus. Biochim Biophys Acta. 2002;1577:337–53.PubMedCrossRef Barr JN, Whelan SP, Wertz GW. Transcriptional control of the RNA-dependent RNA polymerase of vesicular stomatitis virus. Biochim Biophys Acta. 2002;1577:337–53.PubMedCrossRef
6.
go back to reference Barr JN, Wertz GW. Polymerase slippage at vesicular stomatitis virus gene junctions to generate poly(A) is regulated by the upstream 3′-AUAC-5′ tetranucleotide: implications for the mechanism of transcription termination. J Virol. 2001;75:6901–13.PubMedPubMedCentralCrossRef Barr JN, Wertz GW. Polymerase slippage at vesicular stomatitis virus gene junctions to generate poly(A) is regulated by the upstream 3′-AUAC-5′ tetranucleotide: implications for the mechanism of transcription termination. J Virol. 2001;75:6901–13.PubMedPubMedCentralCrossRef
7.
go back to reference Beaudoin JD, Jodoin R, Perreault JP. In-line probing of RNA G-quadruplexes. Methods. 2013;64:79–87.PubMedCrossRef Beaudoin JD, Jodoin R, Perreault JP. In-line probing of RNA G-quadruplexes. Methods. 2013;64:79–87.PubMedCrossRef
8.
go back to reference Ben-Shem A, Garreau de Loubresse N, Melnikov S, et al. The structure of the eukaryotic ribosome at 3.0 A resolution. Science. 2011;334:1524–9.PubMedCrossRef Ben-Shem A, Garreau de Loubresse N, Melnikov S, et al. The structure of the eukaryotic ribosome at 3.0 A resolution. Science. 2011;334:1524–9.PubMedCrossRef
9.
go back to reference Chattopadhyay M, Kuhlmann M, Kumar K, Simon AE. Position of the kissing-loop interaction associated with PTE-type 3′CITEs can affect enhancement of cap-independent translation. Virology. 2014;458:43–52.PubMedCrossRef Chattopadhyay M, Kuhlmann M, Kumar K, Simon AE. Position of the kissing-loop interaction associated with PTE-type 3′CITEs can affect enhancement of cap-independent translation. Virology. 2014;458:43–52.PubMedCrossRef
10.
go back to reference Connor JH, Lyles DS. Vesicular stomatitis virus infection alters the eIF4F translation initiation complex and causes dephosphorylation of the eIF4E binding protein 4E-BP1. J Virol. 2002;76:10177–87.PubMedPubMedCentralCrossRef Connor JH, Lyles DS. Vesicular stomatitis virus infection alters the eIF4F translation initiation complex and causes dephosphorylation of the eIF4E binding protein 4E-BP1. J Virol. 2002;76:10177–87.PubMedPubMedCentralCrossRef
12.
go back to reference Dietzgen RG, Calisher CH, Kurath G, Kuzmin IV, et al. Family rhabdoviridae. In: King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ, editors., et al., Virus taxonomy—ninth report of the international committee on taxonomy of viruses. Oxford: Elsevier Academic Press; 2012. p. 686–714. Dietzgen RG, Calisher CH, Kurath G, Kuzmin IV, et al. Family rhabdoviridae. In: King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ, editors., et al., Virus taxonomy—ninth report of the international committee on taxonomy of viruses. Oxford: Elsevier Academic Press; 2012. p. 686–714.
13.
go back to reference Du Z, Fenn S, Tjhen R, James TL. Structure of a construct of a human poly(C)-binding protein containing the first and second KH domains reveals insights into its regulatory mechanisms. J Biol Chem. 2008;283:28757–66.PubMedPubMedCentralCrossRef Du Z, Fenn S, Tjhen R, James TL. Structure of a construct of a human poly(C)-binding protein containing the first and second KH domains reveals insights into its regulatory mechanisms. J Biol Chem. 2008;283:28757–66.PubMedPubMedCentralCrossRef
14.
go back to reference Fu ZF. Genetic comparison of the rhabdoviruses from animals and plants. Curr Top Microbiol Immunol. 2005;292:143–63. Fu ZF. Genetic comparison of the rhabdoviruses from animals and plants. Curr Top Microbiol Immunol. 2005;292:143–63.
15.
go back to reference Gao F, Reddy S, Kasprzak W, Shapiro BA, et al. The kissing-loop T-shaped structure translational enhancer of Pea enation mosaic virus can bind simultaneously to ribosomes and a 5′ proximal hairpin. J Virol. 2013;87:11987–2002.PubMedPubMedCentralCrossRef Gao F, Reddy S, Kasprzak W, Shapiro BA, et al. The kissing-loop T-shaped structure translational enhancer of Pea enation mosaic virus can bind simultaneously to ribosomes and a 5′ proximal hairpin. J Virol. 2013;87:11987–2002.PubMedPubMedCentralCrossRef
16.
go back to reference Hellen CU, Sarnow P. Internal ribosome entry sites in eukaryotic mRNA molecules. Genes Dev. 2001;15:1593–612.PubMedCrossRef Hellen CU, Sarnow P. Internal ribosome entry sites in eukaryotic mRNA molecules. Genes Dev. 2001;15:1593–612.PubMedCrossRef
17.
go back to reference Iwakawa HO, Tajima Y, Taniguchi T, Kaido M, et al. Poly(A)-binding protein facilitates translation of an uncapped/nonpolyadenylated viral RNA by binding to the 3′ untranslated region. J Virol. 2012;86:7836–49.PubMedPubMedCentralCrossRef Iwakawa HO, Tajima Y, Taniguchi T, Kaido M, et al. Poly(A)-binding protein facilitates translation of an uncapped/nonpolyadenylated viral RNA by binding to the 3′ untranslated region. J Virol. 2012;86:7836–49.PubMedPubMedCentralCrossRef
18.
go back to reference Jackson AO, Dietzgen RG, Goodin MM, Bragg JN, et al. Biology of plant rhabdoviruses. Annu Rev Phytopathol. 2005;43:623–60.PubMedCrossRef Jackson AO, Dietzgen RG, Goodin MM, Bragg JN, et al. Biology of plant rhabdoviruses. Annu Rev Phytopathol. 2005;43:623–60.PubMedCrossRef
19.
go back to reference Jackson RJ, Hellen CU, Pestova TV. The mechanism of eukaryotic translation initiation and principles of its regulation. Nat Rev Mol Cell Biol. 2010;11:113–27.PubMedPubMedCentralCrossRef Jackson RJ, Hellen CU, Pestova TV. The mechanism of eukaryotic translation initiation and principles of its regulation. Nat Rev Mol Cell Biol. 2010;11:113–27.PubMedPubMedCentralCrossRef
21.
go back to reference Kneller EL, Rakotondrafara AM, Miller WA. Cap-independent translation of plant viral RNAs. Virus Res. 2006;119:63–75.PubMedCrossRef Kneller EL, Rakotondrafara AM, Miller WA. Cap-independent translation of plant viral RNAs. Virus Res. 2006;119:63–75.PubMedCrossRef
22.
go back to reference Kong J, Ji X, Liebhaber SA. The KH-domain protein alpha CP has a direct role in mRNA stabilization independent of its cognate binding site. Mol Cell Biol. 2003;23:1125–34.PubMedPubMedCentralCrossRef Kong J, Ji X, Liebhaber SA. The KH-domain protein alpha CP has a direct role in mRNA stabilization independent of its cognate binding site. Mol Cell Biol. 2003;23:1125–34.PubMedPubMedCentralCrossRef
23.
go back to reference Le H, Tanguay RL, Balasta ML, Wei CC, et al. Translation initiation factors eIF-iso4G and eIF-4B interact with the poly(A)-binding protein and increase its RNA binding activity. J Biol Chem. 1997;272:16247–55.PubMedCrossRef Le H, Tanguay RL, Balasta ML, Wei CC, et al. Translation initiation factors eIF-iso4G and eIF-4B interact with the poly(A)-binding protein and increase its RNA binding activity. J Biol Chem. 1997;272:16247–55.PubMedCrossRef
24.
go back to reference Lee AS, Burdeinick-Kerr R, Whelan SP. A ribosome-specialized translation initiation pathway is required for cap-dependent translation of vesicular stomatitis virus mRNAs. PNAS. 2013;110:324–9.PubMedCrossRef Lee AS, Burdeinick-Kerr R, Whelan SP. A ribosome-specialized translation initiation pathway is required for cap-dependent translation of vesicular stomatitis virus mRNAs. PNAS. 2013;110:324–9.PubMedCrossRef
25.
go back to reference Liu H, Naismith JH. An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesis protocol. BMC Biotechnol. 2008;8:91.PubMedPubMedCentralCrossRef Liu H, Naismith JH. An efficient one-step site-directed deletion, insertion, single and multiple-site plasmid mutagenesis protocol. BMC Biotechnol. 2008;8:91.PubMedPubMedCentralCrossRef
27.
go back to reference May J, Johnson P, Saleen H, Simon AE. A sequence-independent, unstructured IRES is responsible for internal expression of the coat protein of Turnip crinkle virus. J Virol. 2017;91:e02421-e2516.PubMedPubMedCentralCrossRef May J, Johnson P, Saleen H, Simon AE. A sequence-independent, unstructured IRES is responsible for internal expression of the coat protein of Turnip crinkle virus. J Virol. 2017;91:e02421-e2516.PubMedPubMedCentralCrossRef
28.
go back to reference McCormack JC, Yuan X, Yingling YG, Kasprzak W, et al. Structural domains within the 3′ untranslated region of Turnip crinkle virus. J Virol. 2008;82:8706–20.PubMedPubMedCentralCrossRef McCormack JC, Yuan X, Yingling YG, Kasprzak W, et al. Structural domains within the 3′ untranslated region of Turnip crinkle virus. J Virol. 2008;82:8706–20.PubMedPubMedCentralCrossRef
29.
30.
go back to reference Mire CE, Whitt MA. The protease-sensitive loop of the vesicular stomatitis virus matrix protein is involved in virus assembly and protein translation. Virology. 2011;416:16–25.PubMedCrossRef Mire CE, Whitt MA. The protease-sensitive loop of the vesicular stomatitis virus matrix protein is involved in virus assembly and protein translation. Virology. 2011;416:16–25.PubMedCrossRef
31.
go back to reference Neidermyer WJ Jr, Whelan SPJ. Global analysis of polysome-associated mRNA in vesicular stomatitis virus infected cells. PLoS Pathogen. 2019;15(6):e1007875.CrossRef Neidermyer WJ Jr, Whelan SPJ. Global analysis of polysome-associated mRNA in vesicular stomatitis virus infected cells. PLoS Pathogen. 2019;15(6):e1007875.CrossRef
32.
33.
go back to reference Nuss DL, Koch G. Differential inhibition of vesicular stomatitis virus polypeptide synthesis by hypertonic initiation block. J Virol. 1975;17:283–6.PubMedCrossRef Nuss DL, Koch G. Differential inhibition of vesicular stomatitis virus polypeptide synthesis by hypertonic initiation block. J Virol. 1975;17:283–6.PubMedCrossRef
34.
go back to reference Otto GA, Lukavsky PJ, Lancaster AM, Sarnow P, Puglisi JD. Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction. RNA. 2002;8:913–23.PubMedPubMedCentralCrossRef Otto GA, Lukavsky PJ, Lancaster AM, Sarnow P, Puglisi JD. Ribosomal proteins mediate the hepatitis C virus IRES-HeLa 40S interaction. RNA. 2002;8:913–23.PubMedPubMedCentralCrossRef
35.
go back to reference Palusa S, Ndaluka C, Bowen RA, Wilusz CJ, et al. The 3′ untranslated region of the rabies virus glycoprotein mRNA specifically interacts with cellular PCBP2 protein and promotes transcript stability. PLoS ONE. 2012;7:e33561.PubMedPubMedCentralCrossRef Palusa S, Ndaluka C, Bowen RA, Wilusz CJ, et al. The 3′ untranslated region of the rabies virus glycoprotein mRNA specifically interacts with cellular PCBP2 protein and promotes transcript stability. PLoS ONE. 2012;7:e33561.PubMedPubMedCentralCrossRef
36.
go back to reference Pestova TV, Kolupaeva VG, Lomakin IB, Pilipenko EV, et al. Molecular mechanisms of translation initiation in eukaryotes. Proc Natl Acad Sci USA. 2001;98:7029–36.PubMedPubMedCentralCrossRef Pestova TV, Kolupaeva VG, Lomakin IB, Pilipenko EV, et al. Molecular mechanisms of translation initiation in eukaryotes. Proc Natl Acad Sci USA. 2001;98:7029–36.PubMedPubMedCentralCrossRef
37.
go back to reference Richter JD, Sonenberg N. Regulation of cap-dependent translation by eIF4E inhibitory proteins. Nature. 2005;433:477–80.PubMedCrossRef Richter JD, Sonenberg N. Regulation of cap-dependent translation by eIF4E inhibitory proteins. Nature. 2005;433:477–80.PubMedCrossRef
38.
go back to reference Sachs AB, Sarnow P, Hentze MW. Starting at the beginning, middle, and end: translation initiation in eukaryotes. Cell. 1997;89:831–8.PubMedCrossRef Sachs AB, Sarnow P, Hentze MW. Starting at the beginning, middle, and end: translation initiation in eukaryotes. Cell. 1997;89:831–8.PubMedCrossRef
39.
40.
go back to reference Ventoso I, Sanz MA, Molina S, Berlanga JJ, et al. Translational resistance of late alphavirus mRNA to eIF2alpha phosphorylation: a strategy to overcome the antiviral effect of protein kinase PKR. Genes Dev. 2006;20:87–100.PubMedPubMedCentralCrossRef Ventoso I, Sanz MA, Molina S, Berlanga JJ, et al. Translational resistance of late alphavirus mRNA to eIF2alpha phosphorylation: a strategy to overcome the antiviral effect of protein kinase PKR. Genes Dev. 2006;20:87–100.PubMedPubMedCentralCrossRef
41.
go back to reference Wakeman CA, Winkler WC. Analysis of the RNA backbone: structural analysis of riboswitches by in-line probing and selective 2′-hydroxyl acylation and primer extension. Methods Mol Biol. 2009;540:173–91.PubMedCrossRef Wakeman CA, Winkler WC. Analysis of the RNA backbone: structural analysis of riboswitches by in-line probing and selective 2′-hydroxyl acylation and primer extension. Methods Mol Biol. 2009;540:173–91.PubMedCrossRef
42.
go back to reference Walker P, Blasdell K, Calisher C, Dietzgen R, et al. ICTV virus taxonomy profile: Rhabdoviridae. J Gen Virol. 2018;99:447–8.PubMedCrossRef Walker P, Blasdell K, Calisher C, Dietzgen R, et al. ICTV virus taxonomy profile: Rhabdoviridae. J Gen Virol. 2018;99:447–8.PubMedCrossRef
43.
go back to reference Wang L, Jeng KS, Lai MM. Poly(C)-binding protein 2 interacts with sequences required for viral replication in the hepatitis C virus (HCV) 5′ untranslated region and directs HCV RNA replication through circularizing the viral genome. J Virol. 2011;85:7954–64.PubMedPubMedCentralCrossRef Wang L, Jeng KS, Lai MM. Poly(C)-binding protein 2 interacts with sequences required for viral replication in the hepatitis C virus (HCV) 5′ untranslated region and directs HCV RNA replication through circularizing the viral genome. J Virol. 2011;85:7954–64.PubMedPubMedCentralCrossRef
44.
go back to reference Wang Z, Treder K, Miller WA. Structure of a viral cap-independent translation element that functions via high affinity binding to the eIF4E subunit of eIF4F. J Biol Chem. 2009;284:14189–202.PubMedPubMedCentralCrossRef Wang Z, Treder K, Miller WA. Structure of a viral cap-independent translation element that functions via high affinity binding to the eIF4E subunit of eIF4F. J Biol Chem. 2009;284:14189–202.PubMedPubMedCentralCrossRef
45.
go back to reference Welnowska E, Castello A, Moral P, Carrasco L. Translation of mRNAs from vesicular stomatitis virus and vaccinia virus is differentially blocked in cells with depletion of eIF4GI and/or eIF4GII. J Mol Biol. 2009;394:506–21.PubMedCrossRef Welnowska E, Castello A, Moral P, Carrasco L. Translation of mRNAs from vesicular stomatitis virus and vaccinia virus is differentially blocked in cells with depletion of eIF4GI and/or eIF4GII. J Mol Biol. 2009;394:506–21.PubMedCrossRef
46.
go back to reference Whelan SP, Barr JN, Wertz GW. Transcription and replication of nonsegmented negative-strand RNA viruses. Curr Top Microbiol Immunol. 2004;283:61–119.PubMed Whelan SP, Barr JN, Wertz GW. Transcription and replication of nonsegmented negative-strand RNA viruses. Curr Top Microbiol Immunol. 2004;283:61–119.PubMed
47.
go back to reference Whitlow ZW, Connor JH, Lyles DS. Preferential translation of VSV mRNAs is conferred by transcription from the viral genome. J Virol. 2006;80:11733–42.PubMedPubMedCentralCrossRef Whitlow ZW, Connor JH, Lyles DS. Preferential translation of VSV mRNAs is conferred by transcription from the viral genome. J Virol. 2006;80:11733–42.PubMedPubMedCentralCrossRef
48.
go back to reference Whitlow ZW, Connor JH, Lyles DS. New mRNAs are preferentially translated during vesicular stomatitis virus infection. J Virol. 2008;82:2286–94.PubMedCrossRef Whitlow ZW, Connor JH, Lyles DS. New mRNAs are preferentially translated during vesicular stomatitis virus infection. J Virol. 2008;82:2286–94.PubMedCrossRef
49.
go back to reference Wilkinson KA, Merino EJ, Weeks KM. Selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE): quantitative RNA structure analysis at single nucleotide resolution. Nat Protoc. 2006;1:1610–6.PubMedCrossRef Wilkinson KA, Merino EJ, Weeks KM. Selective 2′-hydroxyl acylation analyzed by primer extension (SHAPE): quantitative RNA structure analysis at single nucleotide resolution. Nat Protoc. 2006;1:1610–6.PubMedCrossRef
Metadata
Title
Efficient translation of Eggplant mottled dwarf nucleorhabdovirus N and X genes requires both 5′ and 3′ UTRs
Authors
Ghobad Babaei
Amir Massah
Mina Koohi Habibi
Publication date
01-12-2021
Publisher
BioMed Central
Published in
Virology Journal / Issue 1/2021
Electronic ISSN: 1743-422X
DOI
https://doi.org/10.1186/s12985-021-01601-4

Other articles of this Issue 1/2021

Virology Journal 1/2021 Go to the issue