Open Access Open Access  Restricted Access Subscription Access

In Silico Plum Pox Virus Silencing Via Host-retrieved miRNAs in Peach Plant


Affiliations
1 Department of Botany, Division of Science and Technology, University of Education, Lahore, Pakistan
2 Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan
3 Science and Research College of Nursing, Ummal Qura University, Makkah, Saudi Arabia
4 Department of Botany, Lahore College for Woman University, Lahore, Pakistan
 

Peach (Prunus persica) is a deciduous, edible, stone fruit producing plant, belonging to the family Rosaceae. The plant is prone to various pathogens and one of them is the plum pox virus (PPV). This is a lethal virus of peach plant causing pox disease of plum. Its attack results in 83%–100% yield loss in highly susceptible varieties of peach plant. The complete genome of PPV is 9791 base pairs with positive-sense single strand. The full-length genome of PPV encodes a large polyprotein initially, which cleaves proteolytically into ten mature proteins – coat protein, helper component proteinase, P1, P3, viral genome-linked protein, 6K1, 6K2, cylindrical inclusion protein, cylindrical inclusion protein b and NIa-pro-proteins. The objective of this study is to identify such sites in the PPV genome which can be targeted by PPV-derived miRNAs through target prediction computational tools/algorithms. A total of 214 mature miRNAs were chosen from the miRNA data­base to check their complementarity with the PPV genome. Minimum free energy, folding energy, seed pairing, target-site accessibility, pattern recognition and multiple target sites were the parameters considered for target prediction algorithms. Two out of 214 miRNAs were predicted as potential against plum pox virus by three of four tools used for target prediction. Thus, the results encourage generating transgenic, PPV-resi­stant peach plants by expression of predicted miRNAs.

Keywords

miRNAs, Peach Plant, Plum Pox Virus, Yield Loss, Target Prediction Algorithms.
User
Notifications
Font Size

  • Verde, I., Abbott, A. G., Scalabrin, S., Jung, S., Shu, S., Marroni, F. and Zuccolo, A., The high-quality draft genome of peach (Prunus persica) identifies unique patterns of genetic diversity, domestication and genome evolution. Nature Genet., 2013, 45(5), 487.
  • Dunez, J. and Sutic, D., Plum pox virus. In European Handbook of Plant Disease, Blackwell, Oxford, 1988, pp. 44–46.
  • Pasquini, G. and Barba, M., The question of seed transmissibility of plum pox virus. EPPO Bull., 2006, 36(2), 287–292.
  • Cambra, M., Capote, N., Myrta, A. and Llácer, G., Plum pox virus and the estimated costs associated with sharka disease. EPPO Bull., 2006, 36(2), 202–204.
  • Kegler, H. and Hartmann, W., Present status of controlling conventional strains of plum pox virus. In Plant Virus Disease Control (eds Hadidi, A., Khetarpal, R. K. and Koganezawa, H.), APS Press, St Paul, Minnesota, USA, 1998, pp. 616–628.
  • Nemchinov, L., Crescenzi, A., Hadidi, A., Piazzolla, P. and Verderevskaya, T., Present status of the new cherry subgroup of plum pox virus (PPV-C). In Plant Virus Disease Control (eds Hadidi, A., Khetarpal, R. K. and Koganezawa, H.), APS Press, St Paul, Minnesota, USA, 1998, pp. 629–638.
  • Jacquet, C., Delecolle, B., Raccah, B., Lecoq, H., Dunez, J. and Ravelonandro, M., Use of modified plum pox virus coat protein genes developed to limit heteroencapsidation-associated risks in transgenic plants. J. General Virol., 1998, 79(6), 1509–1517.
  • Tavert-Roudet, G., Ravelonandro, M., Bachelier, J. C. and Dunez, J., Transgenic Nicotiana benthamiana plants containing the P1 gene of plum pox virus are resistant to virus challenge. Eur. J. Plant Pathol., 1998, 104(1), 103–107.
  • Barajas, D., Tenllado, F., González-Jara, P., Martínez-García, B., Atencio, F. A. and Díaz-Ruíz, J. R., Resistance to plum pox virus (PPV) in Nicotiana benthamiana plants transformed with the PPV HC-Pro silencing suppressor gene. J. Plant Pathol., 2004, 86(3), 239–248.
  • Eldem, V., Akcay, U. C., Ozhuner, E., Bakır, Y., Uranbey, S. and Unver, T., Genome-wide identification of miRNAs responsive to drought in peach (Prunus persica) by high-throughput deep sequencing. PLoS ONE, 2012, 7(12), e50298.
  • Pillai, R. S., Bhattacharyya, S. N. and Filipowicz, W., Repression of protein synthesis by miRNAs: how many mechanisms? Trends Cell Biol., 2007, 17, 118–126.
  • Ritchie, W., Flamant, S. and Rasko, J. E., miRNA: a microRNA expression profiler and classification resource designed to identify functional correlations between microRNAs and their targets. Bioinformatics, 2009, 26(2), 223–227.
  • Pani, A., Mahapatra, R. K., Behera, N. and Naik, P. K., Computational identification of sweet wormwood (Artemisia annua) microRNA and their mRNA targets. Genom., Proteom. Bioinformat., 2011, 9(6), 200–210.
  • Griffiths-Jones, S., Saini, H. K., van Dongen, S. and Enright, A. J., miRBase: tools for microRNA genomics. Nucl. Acids Res., 2007, 36, D154–D158.
  • Chaudhuri, K. and Chatterjee, R., MicroRNA detection and target prediction: integration of computational and experimental approaches. DNA Cell Biol., 2007, 26(5), 321–337.
  • Li, L., Xu, J., Yang, D., Tan, X. and Wang, H., Computational approaches for microRNA studies: a review. Mammal. Genome, 2010, 1(1–2), 1–12.
  • Witkos, M. T., Koscianska, E. and Krzyzosiak, J. W., Practical aspects of microRNA target prediction. Curr. Mol. Med., 2011, 11(2), 93–109.
  • Iqbal, M. S., Jabbar, B., Sharif, M. N., Ali, Q., Husnain, T. and Nasir, I. A., In silico MCMV silencing concludes potential hostderived miRNAs in maize. Front. Plant Sci., 2017, 8, 372.
  • Liu, H. W., Luo, L. X., Liang, C. Q., Jiang, N., Liu, P. F. and Li, J. Q., High-throughput sequencing identifies novel and conserved cucumber (Cucumis sativus L.) microRNAs in response to cucumber green mottle mosaic virus infection. PLoS ONE, 2015, 10(6), e0129002.
  • Dai, X. and Zhao, P. X., psRNATarget: a plant small RNA target analysis server. Nucleic Acids Res., 2011, 39(2), 155–159.
  • Miranda, K. C., Huynh, T., Tay, Y., Ang, Y. S., Tam, W. L., Thomson, A. M. and Rigoutsos, I., A pattern-based method for the identification of microRNA binding sites and their corresponding heteroduplexes. Cell, 2006, 126(6), 1203–1217.
  • Rehmsmeier, M., Steffen, P., Hochsmann, M. and Giegerich, R., Fast and effective prediction of microRNA/target duplexes. RNA, 2004, 10, 1507–1517.
  • Lewis, B. P., Burge, C. B. and Bartel, D. P., Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell, 2005, 120(1), 15–20.
  • Kumar, S., Stecher, G. and Tamura, K., MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol., 2016, 33(7), 1870–1874.
  • Díaz-Vivancos, P., Rubio, M. and Mesonero, V., The apoplastic antioxidant system in Prunus: response to long-term plum pox virus infection. J. Exp. Bot., 2006, 57(14), 3813–3824.
  • Hernández, J. A., Rubio, M., Olmos, E., Ros‐Barcelo, A. and Martínez‐Gómez, P., Oxidative stress induced by long‐term plum pox virus infection in peach (Prunus persica). Physiol. Plant., 2004, 122(4), 486–495.
  • Agrawal, N., Dasaradhi, P. V., Mohmmed, A., Malhotra, P., Bhatnagar, R. K. and Mukherjee, S. K., RNA interference: biology, mechanism, and applications. Microbiol. Mol. Biol. Rev., 2003, 67(4), 657–685.
  • Iqbal, M. S., Hafeez, M. N., Wattoo, J. I., Ali, A., Sharif, M. N., Rashid, B. and Nasir, I. A., Prediction of host-derived miRNAs with the potential to target PVY in potato plants. Front. Genet., 2016, 7, 159.
  • Pan, Q., Molecular characterization of the potyviral first protein (P1 protein). Electronic Thesis and Dissertation Repository, 2016, p. 4115; https://ir.lib.uwo.ca/etd/4115
  • Kasschau, K. D., Cronin, S. and Carrington, J. C., Genome amplification and long-distance movement functions associated with the central domain of tobacco etch potyvirus helper component–proteinase. Virology, 1997, 228(2), 251–262.
  • Jenner, C. E., Sanchez, F., Nettleship, S. B., Foster, G. D., Ponz, F. and Walsh, J. A., The cylindrical inclusion gene of turnip mosaic virus encodes a pathogenic determinant to the Brassica resistance gene TuRB01. Mol. Plant-Micro. Inter., 2000, 13(10), 1102–1108.
  • Jenner, C. E., Tomimura, K., Ohshima, K., Hughes, S. L. and Walsh, J. A., Mutations in Turnip mosaic virus P3 and cylindrical inclusion proteins are separately required to overcome two Brassica napus resistance genes. Virology, 2002, 300(1), 50–59.
  • Eagles, R. M., Balmori‐Melián, E., Beck, D. L., Gardner, R. C. and Forster, R. L., Characterization of NTPase, RNA‐binding and RNA‐helicase activities of the cytoplasmic inclusion protein of tamarillo mosaic potyvirus. Eur. J. Biochem., 1994, 224(2), 677–684.
  • Kekarainen, T., Savilahti, H. and Valkonen, J. P., Functional genomics on potato virus A: virus genome-wide map of sites essential for virus propagation. Genome Res., 2002, 12(4), 584–594.
  • Cui, H. and Wang, A., The plum pox virus 6K1 protein is required for viral replication and targets the viral replication complex at the early infection stage. J. Virol., 2016, 90(10), 5119–5131.
  • Huang, T. S., Wei, T., McNeil, J., Laliberté, J. F., Hong, J., Nelson, R. S. and Wang, A., Sequential recruitment of the endoplasmic reticulum and chloroplasts for plant potyvirus replication. J. Virol., 2010, 84(2), 799–809.
  • Klein, P. G., Klein, R. R., Rodriguez-Cerezo, E., Hunt, A. G. and Shaw, J. G., Mutational analysis of the tobacco vein mottling virus genome. Virology, 1994, 204(2), 759–769.
  • Dolja, V. V., Haldeman-Cahill, R., Montgomery, A. E., Vandenbosch, K. A. and Carrington, J. C., Capsid protein determinants involved in cell-to-cell and long distance movement of tobacco etch potyvirus. Virology, 1995, 206(2), 1007–1016.
  • Missiou, A., Kalantidis, K., Boutla, A., Tzortzakaki, S., Tabler, M. and Tsagris, M., Generation of transgenic potato plants highly resistant to potato virus Y (PVY) through RNA silencing. Mol. Breed., 2004, 14(2), 185–197.
  • Brigneti, G., Voinne, O., Li, W. X., Ji, L. H., Ding, S. W. and Baulcombe, D. C., Retracted: viral pathogenicity determinants are suppressors of transgene silencing in Nicotiana benthamiana. EMBO J., 1998, 17(22), 6739–6746.
  • Li, X. H., Valdez, P., Olvera, R. E. and Carrington, J. C., Functions of the tobacco etch virus RNA polymerase (NIb): subcellular transport and protein–protein interaction with VPg/proteinase (NIa). J. Virol., 1997, 71(2), 1598–1607.
  • Garcia, J. A., Riechmann, J. and Lain, S., Proteolytic activity of the plum pox potyvirus Nla-like protein in Escherichia coli. Virology, 1989, 170(2), 362–369.
  • Puustinen, P. and Mäkinen, K. M., Uridylylation of the potyvirusVPg by viral replicase NIb correlates with the nucleotide binding capacity of VPg. J. Biol. Chem., 2004, 279, 38103–38110.

Abstract Views: 210

PDF Views: 89




  • In Silico Plum Pox Virus Silencing Via Host-retrieved miRNAs in Peach Plant

Abstract Views: 210  |  PDF Views: 89

Authors

Muhammad Naveed Shahid
Department of Botany, Division of Science and Technology, University of Education, Lahore, Pakistan
Syeda Shehnaz
Department of Botany, Division of Science and Technology, University of Education, Lahore, Pakistan
Muhammad Shehzad Iqbal
Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan
Aneela Shabbeer
Department of Botany, Division of Science and Technology, University of Education, Lahore, Pakistan
Adil Jamal
Science and Research College of Nursing, Ummal Qura University, Makkah, Saudi Arabia
Sana Khalid
Department of Botany, Lahore College for Woman University, Lahore, Pakistan

Abstract


Peach (Prunus persica) is a deciduous, edible, stone fruit producing plant, belonging to the family Rosaceae. The plant is prone to various pathogens and one of them is the plum pox virus (PPV). This is a lethal virus of peach plant causing pox disease of plum. Its attack results in 83%–100% yield loss in highly susceptible varieties of peach plant. The complete genome of PPV is 9791 base pairs with positive-sense single strand. The full-length genome of PPV encodes a large polyprotein initially, which cleaves proteolytically into ten mature proteins – coat protein, helper component proteinase, P1, P3, viral genome-linked protein, 6K1, 6K2, cylindrical inclusion protein, cylindrical inclusion protein b and NIa-pro-proteins. The objective of this study is to identify such sites in the PPV genome which can be targeted by PPV-derived miRNAs through target prediction computational tools/algorithms. A total of 214 mature miRNAs were chosen from the miRNA data­base to check their complementarity with the PPV genome. Minimum free energy, folding energy, seed pairing, target-site accessibility, pattern recognition and multiple target sites were the parameters considered for target prediction algorithms. Two out of 214 miRNAs were predicted as potential against plum pox virus by three of four tools used for target prediction. Thus, the results encourage generating transgenic, PPV-resi­stant peach plants by expression of predicted miRNAs.

Keywords


miRNAs, Peach Plant, Plum Pox Virus, Yield Loss, Target Prediction Algorithms.

References





DOI: https://doi.org/10.18520/cs%2Fv121%2Fi10%2F1316-1322