Abstract
"Spiral asters" composed of swirls of subcortical microtubules were recently described in fertilized eggs of the sea urchin Strongylocentrotus purpuratus. In our study, these structures did not occur at culture temperatures below 16 degrees C. When the culture temperature was elevated, however, "spiral asters" routinely appeared during a susceptible period before mitotic prophase when the sperm aster-diaster normally exists. A massive and protracted rotation of the cytoplasm (excluding an immobile cortex and perinuclear region) began within 1 min of exposure to elevated temperature. Fibrils of the "spiral aster" could be seen within this rotating mass even by bright- field microscopy. The identity of microtubules in these structures was confirmed by indirect immunofluorescence microscopy. A mechanistic association between "spiral aster" formation and cytoplasmic rotation was indicated by the simultaneous inhibitory effects of microtubule and dynein poisons. Inhibitors of microfilaments, however, had no effect. We infer that elevated temperature induces unique changes in the microtubules of the pre-prophase sperm aster-diaster, resulting in cytoplasmic rotation and the spiral configuration of microtubules. Comparative cytological evidence supports the idea that "spiral asters" do not normally occur in fertilized sea urchin eggs. Biogeographic evidence for S. purpuratus indicates that fertilization and development naturally occur below 15 degrees C, hence "spiral asters" in eggs of this species should be regarded as abnormalities induced in the laboratory by unnaturally elevated temperatures.
Full Text
The Full Text of this article is available as a PDF (2.5 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bestor T. H., Schatten G. Anti-tubulin immunofluorescence microscopy of microtubules present during the pronuclear movement of sea urchin fertilization. Dev Biol. 1981 Nov;88(1):80–91. doi: 10.1016/0012-1606(81)90220-7. [DOI] [PubMed] [Google Scholar]
- Blose S. H., Meltzer D. I., Feramisco J. R. 10-nm filaments are induced to collapse in living cells microinjected with monoclonal and polyclonal antibodies against tubulin. J Cell Biol. 1984 Mar;98(3):847–858. doi: 10.1083/jcb.98.3.847. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bouchard P., Penningroth S. M., Cheung A., Gagnon C., Bardin C. W. erythro-9-[3-(2-Hydroxynonyl)]adenine is an inhibitor of sperm motility that blocks dynein ATPase and protein carboxylmethylase activities. Proc Natl Acad Sci U S A. 1981 Feb;78(2):1033–1036. doi: 10.1073/pnas.78.2.1033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coffe G., Rola F. H., Soyer M. O., Pudles J. Parthenogenetic activation of sea urchin egg induces a cyclical variation of the cytoplasmic resistance to hexylene glycol-Triton X-100 treatment. Exp Cell Res. 1982 Jan;137(1):63–72. doi: 10.1016/0014-4827(82)90008-8. [DOI] [PubMed] [Google Scholar]
- Harris P. A spiral cortical fiber system in fertilized sea urchin eggs. Dev Biol. 1979 Feb;68(2):525–532. doi: 10.1016/0012-1606(79)90223-9. [DOI] [PubMed] [Google Scholar]
- Harris P., Osborn M., Weber K. A spiral array of microtubules in the fertilized sea urchin egg cortex examined by indirect immunofluorescence and electron microscopy. Exp Cell Res. 1980 Mar;126(1):227–236. doi: 10.1016/0014-4827(80)90489-9. [DOI] [PubMed] [Google Scholar]
- Harris P., Osborn M., Weber K. Distribution of tubulin-containing structures in the egg of the sea urchin Strongylocentrotus purpuratus from fertilization through first cleavage. J Cell Biol. 1980 Mar;84(3):668–679. doi: 10.1083/jcb.84.3.668. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Longo F. J. An ultrastructural analysis of mitosis and cytokinesis in the zygote of the sea urchin, Arbacia punctulata. J Morphol. 1972 Oct;138(2):207–238. doi: 10.1002/jmor.1051380206. [DOI] [PubMed] [Google Scholar]
- Mar H. Radial cortical fibers and pronuclear migration in fertilized and artificially activated eggs of Lytechinus pictus. Dev Biol. 1980 Jul;78(1):1–13. doi: 10.1016/0012-1606(80)90313-9. [DOI] [PubMed] [Google Scholar]
- Otto J. J., Kane R. E., Bryan J. Redistribution of actin and fascin in sea urchin eggs after fertilization. Cell Motil. 1980;1(1):31–40. doi: 10.1002/cm.970010104. [DOI] [PubMed] [Google Scholar]
- Otto J. J., Schroeder T. E. Microtubule arrays in the cortex and near the germinal vesicle of immature starfish oocytes. Dev Biol. 1984 Feb;101(2):274–281. doi: 10.1016/0012-1606(84)90141-6. [DOI] [PubMed] [Google Scholar]
- Pratt M. M. The identification of a dynein ATPase in unfertilized sea urchin eggs. Dev Biol. 1980 Feb;74(2):364–378. doi: 10.1016/0012-1606(80)90438-8. [DOI] [PubMed] [Google Scholar]
- Schatten G., Schatten H., Bestor T. H., Balczon R. Taxol inhibits the nuclear movements during fertilization and induces asters in unfertilized sea urchin eggs. J Cell Biol. 1982 Aug;94(2):455–465. doi: 10.1083/jcb.94.2.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schatten G. Sperm incorporation, the pronuclear migrations, and their relation to the establishment of the first embryonic axis: time-lapse video microscopy of the movements during fertilization of the sea urchin Lytechinus variegatus. Dev Biol. 1981 Sep;86(2):426–437. doi: 10.1016/0012-1606(81)90201-3. [DOI] [PubMed] [Google Scholar]
- Schroeder T. E., Stricker S. A. Morphological changes during maturation of starfish oocytes: surface ultrastructure and cortical actin. Dev Biol. 1983 Aug;98(2):373–384. doi: 10.1016/0012-1606(83)90366-4. [DOI] [PubMed] [Google Scholar]
- Schroeder T. E. Surface area change at fertilization: resorption of the mosaic membrane. Dev Biol. 1979 Jun;70(2):306–326. doi: 10.1016/0012-1606(79)90030-7. [DOI] [PubMed] [Google Scholar]
- Stephens R. E. A thermodynamic analysis of mitotic spindle equilibrium at active metaphase. J Cell Biol. 1973 Apr;57(1):133–147. doi: 10.1083/jcb.57.1.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
