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First published online November 18, 2003
doi: 10.1242/10.1242/jcs.00796


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Journal of Cell Science 116, 4891-4903 (2003)
doi: 10.1242/jcs.00796


Research Article

Individual microtubule dynamics contribute to the function of mitotic and cytoplasmic arrays in fission yeast

Meredith Johnson Sagolla, Satoru Uzawa and W. Zacheus Cande*

Department of Molecular and Cell Biology and Department of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720-3200, USA

* Author for correspondence (e-mail: zcande{at}uclink4.berkeley.edu)

Accepted 24 July 2003

Schizosaccharomyces pombe is an excellent organism for studying microtubule dynamics owing to the presence of well-defined microtubule arrays that undergo dramatic rearrangements during various stages of the cell cycle. Using sensitive time-lapse video microscopy and kymographic analysis, we have determined the polymerization/depolymerization kinetics of individual microtubules within these arrays throughout the fission yeast cell cycle. Interphase bundles are composed of 4-7 microtubules that act autonomously, demonstrating that individual microtubules are responsible for mediating the functions ascribed to these arrays. The nucleation and growth of cytoplasmic microtubules is inhibited upon cellular transition into mitosis, leading to their gradual disappearance. At the onset of mitosis, microtubules form on the nuclear face of the spindle pole body and exhibit dramatically increased dynamics. The presence of these intra-nuclear astral microtubules (INA) is reminiscent of spindle assembly and the search and chromosome capture mechanism observed in metazoan cells. Consistent with other in vivo studies, we do not observe microtubule flux in the anaphase B spindle. Finally, the depolymerization of individual microtubules alternates between each half-spindle, resulting in spindle collapse during telophase. On the basis of these observations, we conclude that microtubules in these diverse cytoskeletal arrays have autonomous behaviors that are an essential component of any model describing cell-cycle-dependent changes in the behavior and function of microtubule arrays.

Key words: Microtubule, Dynamics, Fission yeast, Mitosis, Spindle


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