Bipolarization and poleward flux correlate during xenopus extract spindle assembly

dc.contributor.author Mitchison, Timothy J.
dc.contributor.author Maddox, P.
dc.contributor.author Groen, Aaron C.
dc.contributor.author Cameron, Lisa
dc.contributor.author Perlman, Z.
dc.contributor.author Ohi, Ryoma
dc.contributor.author Desai, Ankur R.
dc.contributor.author Salmon, Edward D.
dc.contributor.author Kapoor, Tarun M.
dc.date.accessioned 2007-10-31T15:36:42Z
dc.date.available 2007-10-31T15:36:42Z
dc.date.issued 2004-09-22
dc.description Author Posting. © American Society for Cell Biology, 2004. This article is posted here by permission of American Society for Cell Biology for personal use, not for redistribution. The definitive version was published in Molecular Biology of the Cell 15 (2004): 5603-5615, doi:10.1091/mbc.E04-05-0440. en
dc.description.abstract 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. en
dc.description.sponsorship This work was funded by National Institutes of Health grants GM39565 (T.J.M.), GM24364 and GM606780 (E.D.S.), and by MBL fellowships from UIC Inc. and Nikon Inc. en
dc.format.mimetype application/pdf
dc.format.mimetype video/quicktime
dc.identifier.citation Molecular Biology of the Cell 15 (2004): 5603-5615 en
dc.identifier.doi 10.1091/mbc.E04-05-0440
dc.identifier.uri https://hdl.handle.net/1912/1844
dc.language.iso en_US en
dc.publisher American Society for Cell Biology en
dc.relation.uri https://doi.org/10.1091/mbc.E04-05-0440
dc.title Bipolarization and poleward flux correlate during xenopus extract spindle assembly en
dc.type Article en
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CSF monopole labeled with X-rhodamine tubulin at speckle levels, before computational alignment
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CSF monopole labeled with X-rhodamine tubulin at speckle levels undergoing spontaneous bipolarization
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