Abstract
The majority of viruses infecting higher plants have single-stranded, positive (or message-) sense RNA genomes. Infectious transcripts can be synthesized in vitro from full-length cDNA clones to study RNA virus biology, develop methods of disease control, and construct plant expression vectors (10,22). Tobamoviruses have a long history of experimentation and represent efficient genetic systems (2,3,4). Vectors based on the tobacco mosaic virus (TMV) genome were among the first to be developed (8) and have particular advantages for novel application(s) in the expression of foreign sequences in plants. These advantages include:
-
1.
Speed: TMV vectors carrying foreign genes move rapidly and systemically in plants (generally 7–10 days post inoculation).
-
2.
High expression levels: TMV produces more virus-encoded protein per infected cell than any other known plant virus [up to 10% of dry weight in TMV-infected tobacco plants; (1)]. Foreign proteins (18,21) and peptides (26) produced systemically in plants by TMV vectors can accumulate to 1–5% of total soluble protein. The levels of foreign proteins expressed from viral vectors are generally much higher than that obtainable from stably transformed cell lines, transgenic organisms, or plasmid DNA-based transient expression systems.
-
3.
Protein targeting: It is possible to direct the foreign protein to various subcellular locations including the endomembrane system, the cytosol, organelles, or even virion particles. Careful study and control of subcellular targeting of foreign proteins or peptides can maximize their specific activity, stability, and greatly facilitate their purification (21,27).
-
4.
Wide range of potential applications: TMV expression vectors have been used as research tools to study plant biosynthetic pathways, screen gene libraries and to express proteins toxic to plant and non-plant systems. Examples include: 1) The carotenoid biosynthetic pathway in plants has been altered by up or down-regulating enzymes responsible for the synthesis of key isoprenoid intermediates (19). The levels of intermediate products were altered up to 50 fold by expressing sequences in the plant cytoplasm in either sense or anti-sense orientation. These dramatic alterations in secondary metabolite accumulation can only be achieved by regulated induction in vegetative tissues, and are predicted to be lethal if constitutively expressed using transgenic technologies. 2) A plant gene library has been constructed in a TMV vector in order to identify expressed sequences that induce cell death in plants (C. Holt, pers. commun.). 3) Peptides or proteins such as antimicrobial peptides, animal hormones, and growth regulators that would be predicted to be toxic or accumulate poorly in microbial or transgenic expression systems have been expressed in plants from TMV vectors (27).
-
5.
Low frequency of sequence drift: Contrary to initial predictions, foreign sequences propagated in TMV-based vectors accumulate very few point mutations during multiple passages in whole plants (15).
-
6.
Broad host range: cDNA clones are available for many tobamoviruses. Functional hybrid vectors are compatible with an array of plant species.
-
7.
Plants as ideal hosts: The greatest advantages in using plant viruses as expression vectors are the characteristics of their hosts. Transfected leaves are one of the most economical sources of biomass for commercial product development and can be inexpensively scaled to meet production requirements.
-
8.
Proven utility in laboratory and field-scale production: Recombinant TMV vectors have been tested in five outdoor field trials to date. Expression characteristics, host range, persistence in the environment, and large-scale plant extraction procedures have all been evaluated (12). Multi-ton extraction of tobacco tissue grown in the field has resulted in the purification of kilogram (kg) quantities of recombinant viruses for development of vaccines and anti-microbial peptides (27).
-
9.
No biological vector: Because TMV is mechanically spread in nature (28), recombinant vectors are contained to inoculated fields (12).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Coperman, R.J., Hartman, J.R. and Watterson J.C. (1969) Phytopathology 59:1012.
Dawson, W.O., Beck D.L., Knorr D.A., and Grantham G.L. (1986) cDNA cloning of the complete genome of tobacco mosaic virus and production of infectious transcripts. Proc. Natl. Acad. Sci. (USA) 83:1832–1836.
Dawson, W.O. and Lehto, K.M. (1990) Regulation of tobamovirus gene expression. Adv. Virus Res. 38:307–342.
Dawson, W.O. (1992) Tobamovirus-Plant Interactions. Virology 186:359–367.
Deom, C.M., Lapidot M., and Beachy R.N. (1992) Plant virus movement proteins. Cell 69:221–224.
Desnick, R.J., Ioannou Y.A., and Eng C.M. (1995) α-Galactosidase A Deficiency: Fabry Disease, In: The Metabolic Bases of Inherited Diseases, C.R. Scriver, A.L. Beaudet, WS. Sly, and D. Valle (eds.) McGraw-Hill, pp. 2741–2784.
de Zoeten, G.A. and Gaard G. 1984. The presence of viral antigen in the apoplast of systemically virus-infected plants. Virus Res. 1:713–725.
Donson, J., Kearney C.M., Hilf M.E., and Dawson W.O. (1991) Systemic expression of bacterial gene by a tobacco mosaic virus-based vector. Proc. Natl. Acad. Sci. (USA) 88:7204–7208
Fitchen, J., Beachy R.N., and Hein M.B. (1995) Plant virus expressing hybrid coat protein with added murine epitope elicits autoantibody response. Vaccine 13:1051–1057.
Goldbach, R. and Hohn T. (1997) Plant viruses as gene vectors. Meth. Plant. Biochem. 10b: 103–120.
Gooding, G.V. and Herbert T.T. (1967) A simple technique for purification of tobacco mosaic virus in large quantities. Phytopathology 57:1285.
Grill, L.K. (1992) 1991 Tobacco field trials report and soil and plant analysis follow-up on the 1991 tobacco field trials report; Filed with the USDA-APHIS, Hyattsville, MD.
Grill, L.K. (1993) Tobacco mosaic virus as a gene expression vector. Agro. Food Industy Hi Tech. Nov/Dec. 20–23.
Hamamoto, H., Sugiyama Y., Nadagawa N., Hashida E., Matsunaga Y., Takemoto S., Watanabe Y., Okada Y. (1993) A new tobacco mosaic virus vector and its use for the systemic production of angiotensin-I-converting enzyme inhibitor in transgenic tobacco and tomato. Bio/Techology 11:930–932.
Kearney, C.M., Donson J., Jones G.E., and Dawson W.O. (1993) Low level of genetic drift in foreign sequences replicating in an RNA virus in plants. Virology 192:11–17.
Kermode, A.R. (1996) Mechanisms of intracellular protein transport and targeting in plant cells. Crit Rev. Plant Sc. 15:285–423.
Klement, Z. (1965) Method for obtaining fluid from the intercellular spaces of foliage and the fluid’s merit as substrate for phytobacterial pathogens. Phytopathology 55:1033–1034.
Kumagai, M.H., Turpen T.H., Winzettl N., Della-Cioppa G., Turpen A.M., Donson J., Hilf M.E., Grantham G.L., Dawson W.O., Chow T.P., Piatak M., Jr., and Grill L.K. (1993) Rapid, high-level expression of biologically active α-trichosanthin in transfected plants by an RNA viral vector. Proc. Natl. Acad. Sci. (USA) 90:427–430.
Kumagai, M.H., Donson J., Della-Cioppa G., Harvey D., Hanley K., and Grill L.K. (1995) Cytoplasmic inhibition of carotenoid biosynthesis with virus-derived RNA. Proc. Natl. Acad. Sci. (USA) 92:1679–1683.
Namba, K., Pattanayek R., and Stubbs G. (1989) Visualization of protein-nucleic acid interactions in a virus: refined structure of intact tobacco mosaic virus at 2.9° A resolution by X-ray fiber diffraction. J. Mol. Biol. 208:307–325.
Pogue, G.P., Turpen T.H., Hidalgo J., Cameron T.I., Murray G.J., Brady R.O., and Grill L.K. (1997) Production and purification of a highly active human α-galactosidase A using a plant virus expression system. Abstract. Amer. Soc. Virol. Meeting. Bozeman, mt; p 162.
Scholthof, H.B., Scholthof K.B.G., and Jackson A.O. (1996) Plant virus gene vectors for transient expression of foreign proteins in plants. Annu. Rev. Phytopathol. 34:299–323.
Scopes, R. K. Protein Purification: Principles and Practice. 3rd ed. Springer Verlag, NY, NY.
Siegal, A., Hari, V., and Kolacz K. (1978) The effect of tobacco mosaic virus infection on host and virus specific protein synthesis. Virology 85:494–503.
Sugiyama, Y., Hamamoto H., Takemoto S., Watanabe Y., Okada Y. (1995) Systemic production of foreign peptides on the particle surface of tobacco mosaic virus. FEBS Let. 359:247–250.
Turpen, T.H., Reinl S.J., Charoenvit Y., Hoffman S.L., Fallarme V., and Grill L.K. (1995) Malarial epitopes expressed on the surface of recombinant tobacco mosaic virus. Bio/Technology 13:53–57.
Turpen, T.H., Cameron T.I., Reinl S.J., Pogue G.P., Garger S.J., McCulloch M.J., Holtz R.B., and Grill L.K. (1997) Production of recombinant proteins in plants: Pharmaceutical applications. The Soc. Exper. Biol., Canterbury, U.K. J. Exp. Botany (Suppl.) 48:12.
Zaitlin, M. and Israel H.W. (1975) Tobacco mosaic virus (type strain). C.M.I./A.A.B. Descriptions of Plant Viruses. Wm. Culross and Son, Ltd. UK.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1998 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Pogue, G.P., Lindbo, J.A., Dawson, W.O., Turpen, T.H. (1998). Tobamovirus Transient Expression Vectors: Tools for Plant Biology and High-Level Expression of Foreign Proteins in Plants. In: Gelvin, S.B., Schilperoort, R.A. (eds) Plant Molecular Biology Manual. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5242-6_5
Download citation
DOI: https://doi.org/10.1007/978-94-011-5242-6_5
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-011-7657-6
Online ISBN: 978-94-011-5242-6
eBook Packages: Springer Book Archive