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Vol. 15, Issue 12, 5603-5615, December 2004
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* Cell Division Group, Marine Biological Laboratory, Woods Hole, MA 02543;
Department of Systems Biology, Harvard Medical School, Boston, MA 02115;
|| Department of Biology, University of North Carolina, Chapel Hill, NC 27599;
¶ Rockefeller University, New York, NY 10021; and
# Department of Cellular and Molecular Medicine, University of California at San Diego, La Jolla, CA 92093
Submitted May 31, 2004;
Revised September 2, 2004;
Accepted September 3, 2004
Monitoring Editor: Tim Stearns
We investigated the mechanism by which meiotic spindles become bipolar and the correlation between bipolarity and poleward flux, using Xenopus egg extracts. By speckle microscopy and computational alignment, we find that monopolar sperm asters do not show evidence for flux, partially contradicting previous work. We account for the discrepancy by describing spontaneous bipolarization of sperm asters that was missed previously. During spontaneous bipolarization, onset of flux correlated with onset of bipolarity, implying that antiparallel microtubule organization may be required for flux. Using a probe for TPX2 in addition to tubulin, we describe two pathways that lead to spontaneous bipolarization, new pole assembly near chromatin, and pole splitting. By inhibiting the Ran pathway with excess importin-alpha, we establish a role for chromatin-derived, antiparallel overlap bundles in generating the sliding force for flux, and we examine these bundles by electron microscopy. Our results highlight the importance of two processes, chromatin-initiated microtubule nucleation, and sliding forces generated between antiparallel microtubules, in self-organization of spindle bipolarity and poleward flux.
The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).
These authors contributed equally to this work.
Corresponding author. E-mail address: timothy_mitchison{at}hms.harvard.edu.
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