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Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol
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 adde...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655816/ https://www.ncbi.nlm.nih.gov/pubmed/23515222 http://dx.doi.org/10.1091/mbc.E12-12-0850 |
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author | Mitchison, Timothy J. Nguyen, Phuong Coughlin, Margaret Groen, Aaron C. |
author_facet | Mitchison, Timothy J. Nguyen, Phuong Coughlin, Margaret Groen, Aaron C. |
author_sort | Mitchison, Timothy J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3655816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-36558162013-07-30 Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol Mitchison, Timothy J. Nguyen, Phuong Coughlin, Margaret Groen, Aaron C. Mol Biol Cell Articles 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 American Society for Cell Biology 2013-05-15 /pmc/articles/PMC3655816/ /pubmed/23515222 http://dx.doi.org/10.1091/mbc.E12-12-0850 Text en © 2013 Mitchison et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell BD; are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Mitchison, Timothy J. Nguyen, Phuong Coughlin, Margaret Groen, Aaron C. Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title | Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title_full | Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title_fullStr | Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title_full_unstemmed | Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title_short | Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol |
title_sort | self-organization of stabilized microtubules by both spindle and midzone mechanisms in xenopus egg cytosol |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655816/ https://www.ncbi.nlm.nih.gov/pubmed/23515222 http://dx.doi.org/10.1091/mbc.E12-12-0850 |
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