Skip to main content
Log in

Microtubule orientation in pea stem cells: a change in orientation follows the initiation of growth rate decline

  • Published:
Planta Aims and scope Submit manuscript

Abstract

The orientation of microtubules in cells of redlight-grown pea plants (Pisum sativum L.) was examined by means of immunofluorescence. Microtubules (MTs) in rapidly elongating, subepidermal cells commonly form multiple, parallel strands that run transverse to the cell's axis of elongation. By contrast, MTs in nonelongating subepidermal cells form steeply pitched helical arrays; MTs in non-elongating epidermal cells are oriented parallel to the axis of elongation. This change in orientation occurs during the time interval in which growth rate is declining. The transition is abrupt rather than gradual and occurs in both epidermal and subepidermal cells at the same time. Plants irradiated for 2 h with a growth-inhibiting fluence of blue light did not undergo the same transition, indicating that factors other than changing elongation rates must be responsible for triggering the reorganization of MT arrays.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

MT(s):

microtubule(s)

References

  • Akashi, T., Shibaoka, H. (1987) Effects of gibberellin on the arrangement and the cold stability of cortical microtubules in epidermal cells of pea internodes. Plant Cell Physiol. 28, 339–348

    Google Scholar 

  • Cyr, R.J., Bustos, M.M., Guiltinan, M.J., Fosket, D.E. (1987) Developmental modulation of tubulin protein and mRNA levels during somatic embryogenesis in cultured carrot cells. Planta 171, 365–376

    Google Scholar 

  • Kutschera, U., Bergfeld, R., Schopfer, P. (1987) Cooperation of epidermis and inner tissues in auxin-mediated growth of maize coleoptiles. Planta 170, 168–180

    Google Scholar 

  • Green, P.B. (1980) Organogenesis — a biophysical view. Annu Rev. Plant Physiol. 31, 51–82

    Google Scholar 

  • Green, P.B. (1984) Shifts in plant cell axiality: histogenetic influences on cellulose orientation in the succulent, Graptopetalum. Dev. Biol. 103, 18–27

    Google Scholar 

  • Iwata, K., Hogetsu, T. (1988) Arrangement of cortical microtubules in Avena coleoptiles and mesocotyls and Pisum epicotyls. Plant Cell Physiol. 29, 807–815

    Google Scholar 

  • Laskowski, M.J., Briggs, W.R. (1989) Regulation of pea epicotyl elongation by blue light: fluence-response relationships and growth distribution. Plant Physiol. 89, 293–298

    Google Scholar 

  • Lintilhac, P.M. (1984) Positional controls in meristem development: a caveat and an alternative. In: Positional controls in plant development, pp. 83–105, Barlow, P.W., Carr, D.J., eds. Cambridge University Press, Cambridge, UK

    Google Scholar 

  • Lloyd, C.W. (1987) The plant cytoskeleton: the impact of fluorescence microscopy. Annu. Rev. Plant Physiol. 38, 119–139

    Google Scholar 

  • Mishkind, M., Palevitz, B.A., Raikhel, N.V. (1981) Cell wall architecture: normal development and environmental modification of guard cells of the Cyperaceae and related species. Plant Cell Environ. 4, 319–328

    Google Scholar 

  • Mita, T., Shibaoka, H. (1984) Effects of S-3307, an inhibitor of gibberellin biosynthesis, on swelling of leaf sheath cells and on the arrangement of cortical microtubules in onion seedlings. Plant Cell Physiol. 25, 1531–1539

    Google Scholar 

  • Murata, T., Wada, M. (1989) Organization of cortical microtubules and microfibril deposition in response to blue-light-induced apical swelling in a tip-growing Adiantum protonema cell. Planta 178, 334–341

    Google Scholar 

  • Robinson, D.G., Quader, H. (1982) The microtubule-microfibril syndrome. In: The cytoskeleton in plant growth and development, pp. 109–126, Lloyd, C.W., ed. Academic Press, London

    Google Scholar 

  • Seagull, R.W. (1986) Changes in microtubule organization and wall microfibril orientation during in vitro cotton fiber development: an immunofluorescent study. Can. J. Bot. 64, 1373–1381

    Google Scholar 

  • Shibaoka, H. (1974) Involvement of wall microtubules in gibberellin promotion and kinetin inhibition of stem elongation. Plant Cell Physiol. 15, 255–263

    Google Scholar 

  • Spark, L.C., Darnbrough, G., Preston, R.D. (1958) Structure and mechanical properties of vegetable fibres. II. A micro-extensometer for the automatic recording of load-extension curves for single fibrous cells. J. Text. Inst. 49, T309-T316

    Google Scholar 

  • Sylvester, A.W., Williams, M.H., Green, P.B. (1989) Orientation of cortical microtubules correlates with cell shape and division direction: immunofluorescence of intact epidermis during development of Graptopetalum paraguayensis. Protoplasma, pp 91–103

  • Takeda, K., Shibaoka, H. (1981) Changes in microfibril arrangement on the inner surface of the epidermal cell walls in the epicotyl of Vigna angularis Ohwi et Ohashi during cell growth. Planta 151, 385–392

    Google Scholar 

  • Traas, J.A., Braat, P., Derksen, J.W. (1984) Changes in microtubule arrays during the differentiation of cortical root cells of Raphanus sativus. Eur J. Cell Biol. 34, 229–238

    Google Scholar 

  • Wasteneys, G.O. (1988) Microtubule organization in internodal cells of characean algae. Ph. D. thesis, Australian National University, Canberra, ACT

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Carnegie Institution of Washington Department of Plant Biology Publication No. 1062

I thank Dr. Anne W. Sylvester (University of California, Berkeley, USA) for instructing me in the use of her immunological techniques, Dr. Paul B. Green for advice and support, and Dr. winslow R. Briggs for advice, support, and careful review of the manuscript.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Laskowski, M.J. Microtubule orientation in pea stem cells: a change in orientation follows the initiation of growth rate decline. Planta 181, 44–52 (1990). https://doi.org/10.1007/BF00202323

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00202323

Key words

Navigation