|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 91, 49-60, Copyright © 1988 by Company of Biologists
Submitted on April 11, 1988
Accepted on May 31, 1988
1 Cell Physiology Unit, Welsh Plant Breeding Station, University College of Wales Plas Gogerddan, Aberystwyth SY23 3EB, UK
2 Dipartimento di Biologia Ainbientale, Universita di Siena Via P. A. Mattioli 4, 53100 Siena, Italy
The ellipsoidal generative cell of the pollen grain of Endymion nonscriptus usually elongates further following germination and entry into the tube, producing attenuated extensions the forward one of which may reach into the vicinity of the vegetative nucleus. This shape change is accompanied by the stretching of the microtubule cytoskeleton of the cell, identified in the present work by immunofluorescence using monoclonal antibodies to tubulin. Complementary observations of living generative cells of Iris pseudacorus showed that they undergo slow undulatory movements accompanied by variation in shape and length during passage through the tube. Such changes must presumably be accompanied by modifications of the microtubule cytoskeleton.
Colchicine at 1 mM eliminated microtubules from tubes and most generative cells of E. nonscriptus, but did not radically affect pollen-tube shape or extension growth, nor arrest the movements of the vegetative nucleus and generative cell into and through the tube. Generative cells in colchicinetreated pollen of Galanthus nivalis rounded up and failed to undergo the usual changes in shape during passage through the tube. Secondary consequences were changes in precedence in movement through the tube, and a greater dispersal along its length. On the assumption that no other cytoskeletal elements remain to be discovered, it seems likely that microfilaments rather than microtubules provide the motive force for movement in the tube, although the latter are involved in shaping the generative cell and adapting it to its passage.
Key words: pollen tube growth, angiosperm generative cells, cell shaping, microtubules, colchicine effects
Submitted on April 11, 1988
Accepted on May 31, 1988
This article has been cited by other articles:
![]() |
N. S. Poulter, S. Vatovec, and V. E. Franklin-Tong Microtubules Are a Target for Self-Incompatibility Signaling in Papaver Pollen Plant Physiology, March 1, 2008; 146(3): 1358 - 1367. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Dai, T. Chen, K. Chong, Y. Xue, S. Liu, and T. Wang Proteomics Identification of Differentially Expressed Proteins Associated with Pollen Germination and Tube Growth Reveals Characteristics of Germinated Oryza sativa Pollen Mol. Cell. Proteomics, February 1, 2007; 6(2): 207 - 230. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. D. Lazzaro, L. Cardenas, A. P. Bhatt, C. D. Justus, M. S. Phillips, T. L. Holdaway-Clarke, and P. K. Hepler Calcium gradients in conifer pollen tubes; dynamic properties differ from those seen in angiosperms J. Exp. Bot., October 1, 2005; 56(420): 2619 - 2628. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Horio and B. R. Oakley The Role of Microtubules in Rapid Hyphal Tip Growth of Aspergillus nidulans Mol. Biol. Cell, February 1, 2005; 16(2): 918 - 926. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. BALUSKA, D. VOLKMANN, and P. W. BARLOW Eukaryotic Cells and their Cell Bodies: Cell Theory Revised Ann. Bot., July 1, 2004; 94(1): 9 - 32. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Romagnoli, G. Cai, and M. Cresti In Vitro Assays Demonstrate That Pollen Tube Organelles Use Kinesin-Related Motor Proteins to Move along Microtubules PLANT CELL, January 1, 2003; 15(1): 251 - 269. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Cai, S. Romagnoli, A. Moscatelli, E. Ovidi, G. Gambellini, A. Tiezzi, and M. Cresti Identification and Characterization of a Novel Microtubule-Based Motor Associated with Membranous Organelles in Tobacco Pollen Tubes PLANT CELL, September 1, 2000; 12(9): 1719 - 1736. [Abstract] [Full Text] |
||||
![]() |
M. D. Lazzaro Microtubule organization in germinated pollen of the conifer Picea abies (Norway spruce, Pinaceae) Am. J. Botany, June 1, 1999; 86(6): 759 - 766. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Yokota and K.-i. T. a. T. Shimmen Actin-Bundling Protein Isolated from Pollen Tubes of Lily . Biochemical and Immunocytochemical Characterization Plant Physiology, April 1, 1998; 116(4): 1421 - 1429. [Abstract] [Full Text] |
||||
![]() |
D. Miller, S. Scordilis, and P. Hepler Identification and localization of three classes of myosins in pollen tubes of Lilium longiflorum and Nicotiana alata J. Cell Sci., January 7, 1995; 108(7): 2549 - 2563. [Abstract] [PDF] |
||||
![]() |
A Moscatelli, C Del Casino, L Lozzi, G Cai, M Scali, A Tiezzi, and M Cresti High molecular weight polypeptides related to dynein heavy chains in Nicotiana tabacum pollen tubes J. Cell Sci., January 3, 1995; 108(3): 1117 - 1125. [Abstract] [PDF] |
||||