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Research Article |
-tubulin at mitosis
Section of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA
* Author for correspondence (e-mail: fjmcnally{at}ucdavis.edu )
Accepted 25 November 2001
Katanin is a microtubule-severing protein that is concentrated at mitotic
spindle poles but katanin's function in the mitotic spindle has not been
previously reported. Inhibition of katanin with either of two
dominant-negative proteins or a subunit-specific antibody prevented the
redistribution of
-tubulin from the centrosome to the spindle in
prometaphase CV-1 cells as assayed by immunofluorescence microscopy. Because
-tubulin complexes can bind to pre-existing microtubule minus ends,
these results could be explained by a model in which the broad distribution of
-tubulin in the mitotic spindle is in part due to cytosolic
-tubulin ring complexes binding to microtubule minus ends generated by
katanin-mediated microtubule severing. Because microtubules depolymerize at
their ends, we hypothesized that a greater number of microtubule ends
generated by severing in the spindle would result in an increased rate of
spindle disassembly when polymerization is blocked with nocodazole. Indeed,
katanin inhibition slowed the rate of spindle microtubule disassembly in the
presence of nocodazole. However, katanin inhibition did not affect the rate of
exchange between polymerized and unpolymerized tubulin as assayed by
fluorescence recovery after photobleaching. These results support a model in
which katanin activity regulates the number of microtubule ends in the
spindle.
Key words: Katanin, Microtubule, Mitosis, Centrosome,
-Tubulin
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