Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol
Mitchison, Timothy J.
Nguyen, Phuong A.
Groen, Aaron C.
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Previous study of self-organization of Taxol-stabilized microtubules into asters in Xenopus meiotic extracts revealed motor-dependent organizational mechanisms in the spindle. We revisit this approach using clarified cytosol with glycogen added back to supply energy and reducing equivalents. We added probes for NUMA and Aurora B to reveal microtubule polarity. Taxol and dimethyl sulfoxide promote rapid polymerization of microtubules that slowly self-organize into assemblies with a characteristic morphology consisting of paired lines or open circles of parallel bundles. Minus ends align in NUMA-containing foci on the outside, and plus ends in Aurora B–containing foci on the inside. Assemblies have a well-defined width that depends on initial assembly conditions, but microtubules within them have a broad length distribution. Electron microscopy shows that plus-end foci are coated with electron-dense material and resemble similar foci in monopolar midzones in cells. Functional tests show that two key spindle assembly factors, dynein and kinesin-5, act during assembly as they do in spindles, whereas two key midzone assembly factors, Aurora B and Kif4, act as they do in midzones. These data reveal the richness of self-organizing mechanisms that operate on microtubules after they polymerize in meiotic cytoplasm and provide a biochemically tractable system for investigating plus-end organization in midzones.
© The Author(s), 2013. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Molecular Biology of the Cell 24 (2013): 1559-1573, doi:10.1091/mbc.E12-12-0850.
Suggested CitationArticle: Mitchison, Timothy J., Nguyen, Phuong A., Coughlin, Margaret, Groen, Aaron C., "Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol", Molecular Biology of the Cell 24 (2013): 1559-1573, DOI:10.1091/mbc.E12-12-0850, https://hdl.handle.net/1912/6126
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