DOI QR코드

DOI QR Code

The Effect of Cucumber mosaic virus 2b Protein to Transient Expression and Transgene Silencing Mediated by Agro-infiltration

  • Choi, Min-Sue (National Institute of Agricultural Biotechnology, RDA) ;
  • Yoon, In-Sun (National Institute of Agricultural Biotechnology, RDA) ;
  • Rhee, Yong (Department of Genetic Engineering, Sungkyunkwan University) ;
  • Choi, Seung-Kook (National Institute of Agricultural Biotechnology, RDA) ;
  • Lim, Sun-Hyung (National Institute of Agricultural Biotechnology, RDA) ;
  • Won, So-Youn (National Institute of Agricultural Biotechnology, RDA) ;
  • Lee, Yeon-Hee (National Institute of Agricultural Biotechnology, RDA) ;
  • Choi, Hong-Soo (National Institute of Agricultural Science and Technology, RDA) ;
  • Lee, Suk-Chan (Department of Genetic Engineering, Sungkyunkwan University) ;
  • Kim, Kook-Hyung (Department of Agricultural Biotechnology, Seoul National University) ;
  • Lomonossoff, George (Department of Biological Chemistry, John Innes Centre) ;
  • Sohn, Seong-Han (National Institute of Agricultural Biotechnology, RDA)
  • Published : 2008.09.30

Abstract

The transient and rapid expression system of a foreign protein in planta is a very useful technique in biotechnology application. We have investigated optimum condition of Agrobacterium-infiltration technique in which expression level of foreign proteins were maximized without detrimental effects on plants using GFP and Cucumber mosaic virus 2b protein, which is known as an enhancer of gene expression and a suppressor of post-transcriptional gene silencing(PTGS). The optimum expression level of both RNA and protein of GFP with minimum leaf impairment was obtained at $OD_{600}$=0.2 of Agrobactrium inocula. The steady-state levels of GFP RNA and protein generally peaked at 3 and 7 days post-infiltration(dpi), respectively. In the presence of 2b, both the magnitude and duration of GFP expression was highly increased and we could detect GFP level until 17 dpi. On the other hands, the 2b-mediated higher accumulation of foreign proteins resulted in the repression of normal leaf growth, possibly due to the limitation of supply of energy or materials required for growth maintenance. Using this Agrobacterium-infiltration system with 2b and GFP, we tested a hypothesis for the threshold model of PTGS initiation. Four GFP transgenic lines of N. benthamiana, which shows different expression level of GFP were tested to determine the threshold level for PTGS initiation. Agrobacterium-infiltration of GFP into those GFP-transgenic plants resulted in the co-silencing of the transgenic GFP. It was found that very low concentration of Agrobacterium with GFP and GFP+2b($OD_{600}$=0.002-0.02) which could not phenotypically induce an additive GFP expression, was enough to trigger PTGS pathway in all GFP transgenic plants. This strongly indicates that each GFP-transgenic plant should be expressing the transgenic GFP at its own pre-determined level and there was no buffer zone of additive GFP-expression to the threshold. In other words, the PTGS seems to be immediately activated as a self-defensive mechanism if an internal balance of gene expression is broken.

Keywords

References

  1. Abdal-Aziz, S. A., Pliego-Alfaro, F., Quesada, M. A. and Mercado, J. A. 2006. Evidence of frequent integration of non-TDNA vector backbone sequences in transgenic strawberry plant. J. Biosci. Bioeng. 6:508-510
  2. Baumberger, N. and Baulcombe, D. C. 2005. Arabidopsis ARGONAUTE1 is an RNA silencer that selectively recruits miRNAs and short interfering RNAs. Proc. Natl. Acad. Sci. USA 102:11928-11933 https://doi.org/10.1073/pnas.0505461102
  3. Bernstein, E., Caudy, A. A., Hammond, S. M. and Hannon, G. J. 2001. Role of a bidentate ribonuclease in the initiation step of RNA interference. Nature 409:363-366 https://doi.org/10.1038/35053110
  4. De Buck, S., De Wilde, C., Van Montagu, M. and Depicker A. 2000. T-DNA vector backbone sequences are frequently integrated into genome of transgenic plants obtained by Agrobacterium-mediated transformation. Mol. Breeding 6:459-468 https://doi.org/10.1023/A:1026575524345
  5. Elbashir, S. M., Lendeckel, W. and Tuschl, T. 2001. RNA interference is mediated by 21-and 22-nucleotide RNAs. Genes Dev. 15:188-200 https://doi.org/10.1101/gad.862301
  6. Fisher, R., Vaquero-Martin, C., Sack, M., Drossard, J., Emans, N. and Crmmandeur, U. 1999. Towards molecular farming in the future: transient protein expression in plants. Biotechnol. Appl. Biochem. 30:113-116
  7. Goto, K., Kobori, T., Kosaka, Y., Natsuaki, T. and Masuta, C. 2007. Characterization of silencing suppressor 2b of cucumber mosaic virus based on examination of its small RNA-binding abilities. Plant Cell Physiol. 48:1050-1060 https://doi.org/10.1093/pcp/pcm074
  8. Hamilton, A. J. and Baulcombe, D. C. 1999. A species of small antisence RNA in post-transcriptional gene silencing in plants. Science 286:950-952 https://doi.org/10.1126/science.286.5441.950
  9. Hellens, R. P., Edwards, E. A., Leyland, N. R., Bean, S. and Mullineaux, P. M. 2000. pGreen: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation. Plant Mol. Biol. 42:819-832 https://doi.org/10.1023/A:1006496308160
  10. Johansen, L. K. and Carrington, J. C. 2001. Silencing on the spot. Induction and suppression of RNA silencing in the Agrobacterium-mediated transient expression system. Plant Physiol. 126:930-938 https://doi.org/10.1104/pp.126.3.930
  11. Kapila, J., de Rycke, R., van Montagu, M. and Angenon, G. 1997. An Agrobacterium-mediated transient gene expression system for intact leaves. Plant Sci. 122:101-108 https://doi.org/10.1016/S0168-9452(96)04541-4
  12. Kim, S.-R., Lee, J., Jun, S.-H., Park, S., Kang, H.-G., Kwon, S. and An, G. 2003. Transgenic structures in T-DNA-inserted rice plants. Plant Mol. Biol. 52:761-773 https://doi.org/10.1023/A:1025093101021
  13. Kuraya, Y., Ohta, S., Fukuda, M., Hiei, Y., Murai, N., Hamada, K., Ueki, J., Imaseki, H. and Komai, T. 2004. Suppression of transfer of non-T-DNA 'vector backbone' sequences by multiple left border repeats in vectors for transformation of higher plants mediated by Agrobacterium tumefaciens. Mol. Breeding 14:309-320 https://doi.org/10.1023/B:MOLB.0000047792.77219.bb
  14. Lindbo, J. A., Silva-Rosales, L., Proebsting, W. M. and Dougherty, W. G. 1993. Induction of highly specific antiviral state in transgenic plants: Implications for regulation of gene expression and virus resistance. Plant Cell 5:1749-1759 https://doi.org/10.1105/tpc.5.12.1749
  15. Mayers, C. N., Palukaitis, P. and Carr, J. P. 2000. Subcelluar distribution analysis of the cucumber mosaic virus 2b protein. J. Gen. Viol. 81:9-226
  16. McCormac, A. C., Elliott, M. C. and Chen, D. F. 1998. A simple method for the production of highly competent cells of Agrobacterium for transformation via electroporation. Mol. Biotech. 9:155-159 https://doi.org/10.1007/BF02760816
  17. Meins, F. 2000. RNA degradation and models for post-transcriptional gene silencing. Plant Mol. Biol. 43:261-273 https://doi.org/10.1023/A:1006443731515
  18. Ratcliff, F. G., MacFarlane, S. A. and Baulcombe, D. C. 1999. Gene silencing without DNA. RNA-meditated cross-protection between viruses. Plant Cell 11:794-798
  19. Schubert, D., Lechtenberg, B., Forsbach, A., Gils, M., Bahadur, S. and Schmidt, R. 2004. Silencing in Arabidopsis T-DNA Transformants: The Predominant Role of a Gene-Specific RNA Sensing Mechanism versus Position Effects . Plant Cell 16:2561-2572 https://doi.org/10.1105/tpc.104.024547
  20. Tzfira, T., Frankman, L. R., Vaidya, M. and Citovsky, V. 2003. Site-specific integration if Agrobacterium tumefaciens T-DNA via double-stranded intermediates. Plant Physiol. 133:1011-1023 https://doi.org/10.1104/pp.103.032128
  21. Vaucheret, H., Beclin, C. and Fagard, M. 2001. Post-transcriptional gene silencing in plants. J. Cell Sci. 114:3083-3091
  22. Vionnet, O., Pinto, Y. M. and Baulcombe, D. C. 1999. Suppression of gene silencing: a general strategy used by diverse DNA and RNA viruses of plants. Proc. Natl. Acad. Sci. USA 96:14147-14152
  23. Voinnet, O. 2001. RNA silencing as a plant immune system against viruses. Trends Genet. 17:449-459 https://doi.org/10.1016/S0168-9525(01)02367-8
  24. Voinnet, O., Rivas, S., Mestre, P. and Baulcombe, D. C. 2003. An enhanced transient expression system in plants based on suppression of gene silencing by the p19 protein of tomato bushy stunt virus. Plant J. 33:949-956 https://doi.org/10.1046/j.1365-313X.2003.01676.x
  25. Zhang, X., Yuan, Y.-R., Pei, Y., Lin, S.-S., Tuschl, T., Patel, D. J. and Chua, N.-H. 2008. Cucumber mosaic virus-encoded 2b suppressor inhibits Arabidopsis Argonaute1 cleavage activity to counter plant defence. Genes Develop. 20:3255-3268

Cited by

  1. Transient Co-Expression of Post-Transcriptional Gene Silencing Suppressors for Increased in Planta Expression of a Recombinant Anthrax Receptor Fusion Protein vol.12, pp.12, 2011, https://doi.org/10.3390/ijms12084975
  2. Phenotypic and Transcriptomic Analysis of Nicotiana benthamiana Expressing Cucumber mosaic virus 2b gene vol.21, pp.3, 2015, https://doi.org/10.5423/RPD.2015.21.3.186
  3. The epigenetic phenotypes in transgenic Nicotiana benthamiana for CaMV 35S-GFP are mediated by spontaneous transgene silencing vol.5, pp.3, 2011, https://doi.org/10.1007/s11816-011-0182-3
  4. Effect of Rice stripe virus NS3 on Transient Gene Expression and Transgene Co-Silencing vol.27, pp.4, 2011, https://doi.org/10.5423/PPJ.2011.27.4.310
  5. Cell-autonomous-like silencing of GFP-partitioned transgenic Nicotiana benthamiana vol.65, pp.15, 2014, https://doi.org/10.1093/jxb/eru200
  6. Regulation and function of the pepper pectin methylesterase inhibitor (CaPMEI1) gene promoter in defense and ethylene and methyl jasmonate signaling in plants vol.230, pp.6, 2009, https://doi.org/10.1007/s00425-009-1021-4
  7. Use of an anthocyanin production phenotype as a visible selection marker system in transgenic tobacco plant vol.6, pp.3, 2012, https://doi.org/10.1007/s11816-012-0215-6
  8. A strain-specific segment of the RNA-dependent RNA polymerase of grapevine fanleaf virus determines symptoms in Nicotiana species vol.94, pp.Pt_12, 2013, https://doi.org/10.1099/vir.0.057646-0