Skip to main content
The Plant Cell logoLink to The Plant Cell
. 1992 Aug;4(8):915–928. doi: 10.1105/tpc.4.8.915

Secondary plasmodesmata are specific sites of localization of the tobacco mosaic virus movement protein in transgenic tobacco plants.

B Ding 1, J S Haudenshield 1, R J Hull 1, S Wolf 1, R N Beachy 1, W J Lucas 1
PMCID: PMC160184  PMID: 1392601

Abstract

Expression of the tobacco mosaic virus 30-kD movement protein (TMV MP) gene in tobacco plants increases the plasmodesmatal size exclusion limit (SEL) 10-fold between mesophyll cells in mature leaves. In the present study, we examined the structure of plasmodesmata as a function of leaf development. In young leaves of 30-kD TMV MP transgenic (line 274) and vector control (line 306) plants, almost all plasmodesmata were primary in nature. In both plant lines, secondary plasmodesmata were formed, in a basipetal pattern, as the leaves underwent expansion growth. Ultrastructural and immunolabeling studies demonstrated that in line 274 the TMV MP accumulated predominantly in secondary plasmodesmata of nonvascular tissues and was associated with a filamentous material. A developmental progression was detected in terms of the presence of TMV MP; all secondary plasmodesmata in the tip of the fourth leaf contained TMV MP in association with the filamentous material. Dye-coupling experiments demonstrated that the TMV MP-induced increase in plasmodesmatal SEL could be routinely detected in the tip of the fourth leaf, but was restricted to mesophyll and bundle sheath cells. These findings are discussed with respect to the structure and function of plasmodesmata, particularly those aspects related to virus movement.

Full Text

The Full Text of this article is available as a PDF (3.7 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Atabekov J. G., Taliansky M. E. Expression of a plant virus-coded transport function by different viral genomes. Adv Virus Res. 1990;38:201–248. doi: 10.1016/s0065-3527(08)60863-5. [DOI] [PubMed] [Google Scholar]
  2. Citovsky V., Knorr D., Schuster G., Zambryski P. The P30 movement protein of tobacco mosaic virus is a single-strand nucleic acid binding protein. Cell. 1990 Feb 23;60(4):637–647. doi: 10.1016/0092-8674(90)90667-4. [DOI] [PubMed] [Google Scholar]
  3. Citovsky V., Wong M. L., Shaw A. L., Prasad B. V., Zambryski P. Visualization and characterization of tobacco mosaic virus movement protein binding to single-stranded nucleic acids. Plant Cell. 1992 Apr;4(4):397–411. doi: 10.1105/tpc.4.4.397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Citovsky V., Zambryski P. How do plant virus nucleic acids move through intercellular connections? Bioessays. 1991 Aug;13(8):373–379. doi: 10.1002/bies.950130802. [DOI] [PubMed] [Google Scholar]
  5. Deom C. M., Oliver M. J., Beachy R. N. The 30-kilodalton gene product of tobacco mosaic virus potentiates virus movement. Science. 1987 Jul 24;237(4813):389–394. doi: 10.1126/science.237.4813.389. [DOI] [PubMed] [Google Scholar]
  6. Deom C. M., Schubert K. R., Wolf S., Holt C. A., Lucas W. J., Beachy R. N. Molecular characterization and biological function of the movement protein of tobacco mosaic virus in transgenic plants. Proc Natl Acad Sci U S A. 1990 May;87(9):3284–3288. doi: 10.1073/pnas.87.9.3284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Deom C. M., Wolf S., Holt C. A., Lucas W. J., Beachy R. N. Altered function of the tobacco mosaic virus movement protein in a hypersensitive host. Virology. 1991 Jan;180(1):251–256. doi: 10.1016/0042-6822(91)90029-b. [DOI] [PubMed] [Google Scholar]
  8. Ding B., Turgeon R., Parthasarathy M. V. Routine cryofixation of plant tissue by propane jet freezing for freeze substitution. J Electron Microsc Tech. 1991 Sep;19(1):107–117. doi: 10.1002/jemt.1060190111. [DOI] [PubMed] [Google Scholar]
  9. Madore M. A., Oross J. W., Lucas W. J. Symplastic Transport in Ipomea tricolor Source Leaves : Demonstration of Functional Symplastic Connections from Mesophyll to Minor Veins by a Novel Dye-Tracer Method. Plant Physiol. 1986 Oct;82(2):432–442. doi: 10.1104/pp.82.2.432. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Melcher U. Similarities between putative transport proteins of plant viruses. J Gen Virol. 1990 May;71(Pt 5):1009–1018. doi: 10.1099/0022-1317-71-5-1009. [DOI] [PubMed] [Google Scholar]
  11. Meshi T., Watanabe Y., Saito T., Sugimoto A., Maeda T., Okada Y. Function of the 30 kd protein of tobacco mosaic virus: involvement in cell-to-cell movement and dispensability for replication. EMBO J. 1987 Sep;6(9):2557–2563. doi: 10.1002/j.1460-2075.1987.tb02544.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Osbourn J. K., Sarkar S., Wilson T. M. Complementation of coat protein-defective TMV mutants in transgenic tobacco plants expressing TMV coat protein. Virology. 1990 Dec;179(2):921–925. doi: 10.1016/0042-6822(90)90169-r. [DOI] [PubMed] [Google Scholar]
  13. Spurr A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res. 1969 Jan;26(1):31–43. doi: 10.1016/s0022-5320(69)90033-1. [DOI] [PubMed] [Google Scholar]
  14. Weintraub M., Ragetli H. W., Leung E. Elongated virus particles in plasmodesmata. J Ultrastruct Res. 1976 Sep;56(3):351–364. doi: 10.1016/s0022-5320(76)90010-1. [DOI] [PubMed] [Google Scholar]
  15. Wolf S., Deom C. M., Beachy R. N., Lucas W. J. Movement protein of tobacco mosaic virus modifies plasmodesmatal size exclusion limit. Science. 1989 Oct 20;246(4928):377–379. doi: 10.1126/science.246.4928.377. [DOI] [PubMed] [Google Scholar]
  16. Wolf S., Deom C. M., Beachy R., Lucas W. J. Plasmodesmatal function is probed using transgenic tobacco plants that express a virus movement protein. Plant Cell. 1991 Jun;3(6):593–604. doi: 10.1105/tpc.3.6.593. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Plant Cell are provided here courtesy of Oxford University Press

RESOURCES