|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 92, 541-550, Copyright © 1989 by Company of Biologists
Submitted on September 5, 1988
Accepted on January 4, 1989
1 INRA BP 94, 84140 Montfavet, France; I.V.T., Wageningen, The Netherlands
2 INRA BP 94, 84140 Montfavet, France
Address for reprints
Because two division planes form at right angles, male meiosis in higher plants provides striking examples of both division control and spatial programming.
To investigate these processes we have stained microtubules and actin filaments during male meiosis in the eggplant. Our results indicate the following.
(1) That microtubules and their nucleation sites are involved in the establishment of polarity; this is supported by our observation that the drug CIPC affects spindle polarity.
(2) That actin microfilaments are involved in spindle formation and integrity, but not in the establishment of polarity: cytochalasin B and D affect the organization of the spindle microtubules, but not their polarized distribution.
(3) That microtubules radiating from the daughter nuclei at the cell poles during interkinesis probably establish the future division plane by concentrating actin in that plane (cf. the proposed role of asters in positioning the contractile ring in animal cells).
(4) That this concentration of F-actin in the division plane may be involved in preparing the cytoplasm for cytokinesis and in memorizing the division plane (much as the preprophase band observed in polarized tissues does).
(5) That phragmoplast formation is a two-step process. No phragmoplast forms after metaphase I, but a four-way phragmoplast forms after metaphase II, indicating that mitosis and cytokinesis are not obligatorily coupled.
These studies demonstrate that actin and microtubules are jointly involved in the spatial coordination of the division process.
Key words: cytoskeleton, eggplant, F-actin, microtubules, meiosis
Submitted on September 5, 1988
Accepted on January 4, 1989
This article has been cited by other articles:
![]() |
C. Briere, A.-C. Bordel, H. Barthou, A. Jauneau, A. Steinmetz, G. Alibert, and M. Petitprez Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts? Plant Cell Physiol., October 15, 2003; 44(10): 1055 - 1063. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ressayre, C. Raquin, A. Mignot, B. Godelle, and P.-H. Gouyon Correlated variation in microtubule distribution, callose deposition during male post-meiotic cytokinesis, and pollen aperture number across Nicotiana species (Solanaceae) Am. J. Botany, March 1, 2002; 89(3): 393 - 400. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-L. Magnard, M. Yang, Y.-C. S. Chen, M. Leary, and S. McCormick The Arabidopsis Gene Tardy Asynchronous Meiosis Is Required for the Normal Pace and Synchrony of Cell Division during Male Meiosis Plant Physiology, November 1, 2001; 127(3): 1157 - 1166. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Silverman-Gavrila and A Forer Evidence that actin and myosin are involved in the poleward flux of tubulin in metaphase kinetochore microtubules of crane-fly spermatocytes J. Cell Sci., January 2, 2000; 113(4): 597 - 609. [Abstract] [PDF] |
||||
![]() |
R. C. Brown and B. E. Lemmon Control of division plane in normal and griseofulvin-treated microsporocytes of Magnolia J. Cell Sci., December 1, 1992; 103(4): 1031 - 1038. [Abstract] [PDF] |
||||