Abstract
During the transition from prometaphase to metaphase, the cross- sectional area of the central spindle of Diatoma decreases by a factor of nearly two, both at the poles and at the region of overlapping microtubules (MTs) near the spindle equator. The density of spindle MT packing stays approximately constant throughout mitosis. Optical diffraction analysis of electron micrographs shows that the packing of the MTs at the poles at all stages of mitosis is similar to that expected for a two-dimensional liquid. Analysis of the region of overlap reveals more packing regularity: during prometaphase, a square packing emerges that displays sufficient organization by late metaphase to generate five orders of diffraction; during anaphase the packing in the overlap region shifts to hexagonal; at telophase, it returns to square. From the data provided by serial section reconstructions of the central spindle, it is possible to identify the polarity of almost every spindle MT, that is, to identify one pole with which the MT is associated. Near neighbor analyses of MTs in cross sections of the overlap region show that MTs prefer antiparallel near neighbors. These near neighbors are most often found at a spacing of approximately 40 nm center-to-center, while parallel near neighbors in the zone of overlap are spaced essentially at random. These results are evidence for a specific interaction between antiparallel MTs. In some sections definite bridges between MTs can be seen. Our findings show that certain necessary conditions for a sliding filament model of anaphase spindle elongation are met.
Full Text
The Full Text of this article is available as a PDF (1.6 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allen C., Borisy G. G. Structural polarity and directional growth of microtubules of Chlamydomonas flagella. J Mol Biol. 1974 Dec 5;90(2):381–402. doi: 10.1016/0022-2836(74)90381-7. [DOI] [PubMed] [Google Scholar]
- Amos L., Klug A. Arrangement of subunits in flagellar microtubules. J Cell Sci. 1974 May;14(3):523–549. doi: 10.1242/jcs.14.3.523. [DOI] [PubMed] [Google Scholar]
- Binder L. I., Rosenbaum J. L. The in vitro assembly of flagellar outer doublet tubulin. J Cell Biol. 1978 Nov;79(2 Pt 1):500–515. doi: 10.1083/jcb.79.2.500. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cleveland D. W., Hwo S. Y., Kirschner M. W. Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin. J Mol Biol. 1977 Oct 25;116(2):207–225. doi: 10.1016/0022-2836(77)90213-3. [DOI] [PubMed] [Google Scholar]
- HUXLEY H. E. ELECTRON MICROSCOPE STUDIES ON THE STRUCTURE OF NATURAL AND SYNTHETIC PROTEIN FILAMENTS FROM STRIATED MUSCLE. J Mol Biol. 1963 Sep;7:281–308. doi: 10.1016/s0022-2836(63)80008-x. [DOI] [PubMed] [Google Scholar]
- Heath I. B., Heath M. C. Ultrastructure of mitosis in the cowpea rust fungus Uromyces phaseoli var. Vignae. J Cell Biol. 1976 Sep;70(3):592–607. doi: 10.1083/jcb.70.3.592. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heath I. B. Mitosis in the fungus Thraustotheca clavata. J Cell Biol. 1974 Jan;60(1):204–220. doi: 10.1083/jcb.60.1.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Inoué S., Ritter H., Jr Mitosis in Barbulanympha. II. Dynamics of a two-stage anaphase, nuclear morphogenesis, and cytokinesis. J Cell Biol. 1978 Jun;77(3):655–684. doi: 10.1083/jcb.77.3.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Manton I., Kowallik K., Von Stosch H. A. Observations on the fine structure and development of the spindle at mitosis and meiosis in a marine centric diatom (Lithodesmium undulatum). I. Preliminary survey of mitosis in spermatogonia. J Microsc. 1969;89(3):295–320. doi: 10.1111/j.1365-2818.1969.tb00678.x. [DOI] [PubMed] [Google Scholar]
- Margolis R. L., Wilson L., Keifer B. I. Mitotic mechanism based on intrinsic microtubule behaviour. Nature. 1978 Mar 30;272(5652):450–452. doi: 10.1038/272450a0. [DOI] [PubMed] [Google Scholar]
- Mc2ntosh J. R., Cande Z., Snyder J., Vanderslice K. Studies on the mechanism of mitosis. Ann N Y Acad Sci. 1975 Jun 30;253:407–427. doi: 10.1111/j.1749-6632.1975.tb19217.x. [DOI] [PubMed] [Google Scholar]
- McDonald K., Pickett-Heaps J. D., McIntosh J. R., Tippit D. H. On the mechanism of anaphase spindle elongation in Diatoma vulgare. J Cell Biol. 1977 Aug;74(2):377–388. doi: 10.1083/jcb.74.2.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McIntosh J. R., Landis S. C. The distribution of spindle microtubules during mitosis in cultured human cells. J Cell Biol. 1971 May 1;49(2):468–497. doi: 10.1083/jcb.49.2.468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McIntosh J. R., McDonald K. L., Edwards M. K., Ross B. M. Three-dimensional structure of the central mitotic spindle of Diatoma vulgare. J Cell Biol. 1979 Nov;83(2 Pt 1):428–442. doi: 10.1083/jcb.83.2.428. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murphy D. B., Johnson K. A., Borisy G. G. Role of tubulin-associated proteins in microtubule nucleation and elongation. J Mol Biol. 1977 Nov 25;117(1):33–52. doi: 10.1016/0022-2836(77)90021-3. [DOI] [PubMed] [Google Scholar]
- Nicklas R. B. Mitosis. Adv Cell Biol. 1971;2:225–297. doi: 10.1007/978-1-4615-9588-5_5. [DOI] [PubMed] [Google Scholar]
- Oakley B. R., Heath I. B. The arrangement of microtubules in serially sectioned spindles of the alga Cryptomonas. J Cell Sci. 1978 Jun;31:53–70. doi: 10.1242/jcs.31.1.53. [DOI] [PubMed] [Google Scholar]
- Pickett-Heaps J. D., McDonald K. L., Tippit D. H. Cell division in the pennate diatom Diatoma vulgare. Protoplasma. 1975;86(1-3):205–242. doi: 10.1007/BF01275633. [DOI] [PubMed] [Google Scholar]
- Rieder C., Bajer A. S. Heat-induced reversible hexagonal packing of spindle microtubules. J Cell Biol. 1977 Sep;74(3):717–725. doi: 10.1083/jcb.74.3.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tippit D. H., Pickett-Heaps J. D. Mitosis in the pennate diatom Surirella ovalis. J Cell Biol. 1977 Jun;73(3):705–727. doi: 10.1083/jcb.73.3.705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tippit D. H., Schulz D., Pickett-Heaps J. D. Analysis of the distribution of spindle microtubules in the diatom Fragilaria. J Cell Biol. 1978 Dec;79(3):737–763. doi: 10.1083/jcb.79.3.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tucker J. B. Initiation and differentiation of microtubule patterns in the ciliate Nassula. J Cell Sci. 1970 Nov;7(3):793–821. doi: 10.1242/jcs.7.3.793. [DOI] [PubMed] [Google Scholar]
- Warner F. D., Mitchell D. R. Structural conformation of ciliary dynein arms and the generation of sliding forces in Tetrahymena cilia. J Cell Biol. 1978 Feb;76(2):261–277. doi: 10.1083/jcb.76.2.261. [DOI] [PMC free article] [PubMed] [Google Scholar]