Am. J. Bot.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (13)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lazzaro, M. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lazzaro, M. D.
Agricola
Right arrow Articles by Lazzaro, M. D.
(American Journal of Botany. 1999;86:759-766.)
© 1999 Botanical Society of America, Inc.

Microtubule organization in germinated pollen of the conifer Picea abies (Norway spruce, Pinaceae)1

Mark D. Lazzaro2

Department of Botany, Stockholm University, S 106 91 Stockholm, Sweden

The organization of microtubules in germinated pollen of the conifer Picea abies (Norway spruce, Pinaceae) was examined using primarily confocal microscopy. Pollination in conifers differs from angiosperms in the number of mitotic divisions between the microspore and the sperm and in the growth rate of the pollen tube. These differences may be orchestrated by the cytoskeleton, and this study finds that there are important functional differences in microtubule organization within conifer pollen compared to the angiosperm model systems. Pollen from P. abies contains two degenerated prothallial cells, a body cell, a stalk cell, and a vegetative cell. The body cell produces the sperm. In the vegetative cell, microtubules form a continuous network from within the pollen grain, out through the aperture, and down the length of the tube to the elongating tip. Within the grain, this network extends from the pollen grain wall to the body and stalk cell complex. Microtubules within the body and stalk cells form a densely packed array that enmeshes amyloplasts and the nucleus. Microtubule bundles can be traced between the body and stalk cells from the cytoplasm of the body cell to the adjoining cell wall and into the cytoplasm of the stalk cell. Body and stalk cells are connected by plasmodesmata. The organization of microtubules and the presence of plasmodesmata suggest that microtubules form a path for intercellular communication by projecting from the cytoplasm to interconnecting plasmodesmata. Microtubules in the elongating tube form a net axial array that ensheathes the vegetative nucleus. Microtubules are enriched at the elongating tip, where they form an array beneath the plasma membrane that is perpendicular to the direction of tube growth. This enriched region extends back 20 µm from the tip. There is an abrupt transition from a net perpendicular to a net axial organization at the edge of the enriched region. In medial sections, microtubules are present in the core of the elongating tip. The organization of microtubules in the tip differs from that seen in angiosperm pollen tubes.

Key Words: conifer • cytoskeleton • microtubule • Picea abies; • Pinaceae • pollen • pollen tube




This article has been cited by other articles:


Home page
J Exp BotHome page
Y. Yu, Y. Li, L. Li, J. Lin, C. Zheng, and L. Zhang
Overexpression of PwTUA1, a pollen-specific tubulin gene, increases pollen tube elongation by altering the distribution of {alpha}-tubulin and promoting vesicle transport
J. Exp. Bot., July 1, 2009; 60(9): 2737 - 2749.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
X. Sheng, Z. Hu, H. Lu, X. Wang, F. Baluska, J. Samaj, and J. Lin
Roles of the Ubiquitin/Proteasome Pathway in Pollen Tube Growth with Emphasis on MG132-Induced Alterations in Ultrastructure, Cytoskeleton, and Cell Wall Components
Plant Physiology, August 1, 2006; 141(4): 1578 - 1590.
[Abstract] [Full Text] [PDF]


Home page
Plant Physiol.Home page
X. Wang, Y. Teng, Q. Wang, X. Li, X. Sheng, M. Zheng, J. Samaj, F. Baluska, and J. Lin
Imaging of Dynamic Secretory Vesicles in Living Pollen Tubes of Picea meyeri Using Evanescent Wave Microscopy
Plant Physiology, August 1, 2006; 141(4): 1591 - 1603.
[Abstract] [Full Text] [PDF]


Home page
J Exp BotHome page
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]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the Botanical Society of America, Inc.