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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...

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Detalles Bibliográficos
Autores principales: Field, Christine M., Groen, Aaron C., Nguyen, Phuong A., Mitchison, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2015
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.
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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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