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Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs
Mitotic spindles specify cleavage planes in early embryos by communicating their position and orientation to the cell cortex using microtubule asters that grow out from the spindle poles during anaphase. Chromatin also plays a poorly understood role. Polyspermic fertilization provides a natural expe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603933/ https://www.ncbi.nlm.nih.gov/pubmed/26310438 http://dx.doi.org/10.1091/mbc.E15-04-0233 |
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author | Field, Christine M. Groen, Aaron C. Nguyen, Phuong A. Mitchison, Timothy J. |
author_facet | Field, Christine M. Groen, Aaron C. Nguyen, Phuong A. Mitchison, Timothy J. |
author_sort | Field, Christine M. |
collection | PubMed |
description | Mitotic spindles specify cleavage planes in early embryos by communicating their position and orientation to the cell cortex using microtubule asters that grow out from the spindle poles during anaphase. Chromatin also plays a poorly understood role. Polyspermic fertilization provides a natural experiment in which aster pairs from the same spindle (sister asters) have chromatin between them, whereas asters pairs from different spindles (nonsisters) do not. In frogs, only sister aster pairs induce furrows. We found that only sister asters recruited two conserved furrow-inducing signaling complexes, chromosome passenger complex (CPC) and Centralspindlin, to a plane between them. This explains why only sister pairs induce furrows. We then investigated factors that influenced CPC recruitment to microtubule bundles in intact eggs and a cytokinesis extract system. We found that microtubule stabilization, optimal starting distance between asters, and proximity to chromatin all favored CPC recruitment. We propose a model in which proximity to chromatin biases initial CPC recruitment to microtubule bundles between asters from the same spindle. Next a positive feedback between CPC recruitment and microtubule stabilization promotes lateral growth of a plane of CPC-positive microtubule bundles out to the cortex to position the furrow. |
format | Online Article Text |
id | pubmed-4603933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-46039332015-12-30 Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs Field, Christine M. Groen, Aaron C. Nguyen, Phuong A. Mitchison, Timothy J. Mol Biol Cell Articles Mitotic spindles specify cleavage planes in early embryos by communicating their position and orientation to the cell cortex using microtubule asters that grow out from the spindle poles during anaphase. Chromatin also plays a poorly understood role. Polyspermic fertilization provides a natural experiment in which aster pairs from the same spindle (sister asters) have chromatin between them, whereas asters pairs from different spindles (nonsisters) do not. In frogs, only sister aster pairs induce furrows. We found that only sister asters recruited two conserved furrow-inducing signaling complexes, chromosome passenger complex (CPC) and Centralspindlin, to a plane between them. This explains why only sister pairs induce furrows. We then investigated factors that influenced CPC recruitment to microtubule bundles in intact eggs and a cytokinesis extract system. We found that microtubule stabilization, optimal starting distance between asters, and proximity to chromatin all favored CPC recruitment. We propose a model in which proximity to chromatin biases initial CPC recruitment to microtubule bundles between asters from the same spindle. Next a positive feedback between CPC recruitment and microtubule stabilization promotes lateral growth of a plane of CPC-positive microtubule bundles out to the cortex to position the furrow. The American Society for Cell Biology 2015-10-15 /pmc/articles/PMC4603933/ /pubmed/26310438 http://dx.doi.org/10.1091/mbc.E15-04-0233 Text en © 2015 Field 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 for Cell Biology. |
spellingShingle | Articles Field, Christine M. Groen, Aaron C. Nguyen, Phuong A. Mitchison, Timothy J. Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title | Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title_full | Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title_fullStr | Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title_full_unstemmed | Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title_short | Spindle-to-cortex communication in cleaving, polyspermic Xenopus eggs |
title_sort | spindle-to-cortex communication in cleaving, polyspermic xenopus eggs |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603933/ https://www.ncbi.nlm.nih.gov/pubmed/26310438 http://dx.doi.org/10.1091/mbc.E15-04-0233 |
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