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Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts

During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the...

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Autores principales: Sulerud, Taylor, Sami, Abdullah Bashar, Li, Guihe, Kloxin, April, Oakey, John, Gatlin, Jesse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851858/
https://www.ncbi.nlm.nih.gov/pubmed/33026931
http://dx.doi.org/10.1091/mbc.E20-01-0088
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author Sulerud, Taylor
Sami, Abdullah Bashar
Li, Guihe
Kloxin, April
Oakey, John
Gatlin, Jesse
author_facet Sulerud, Taylor
Sami, Abdullah Bashar
Li, Guihe
Kloxin, April
Oakey, John
Gatlin, Jesse
author_sort Sulerud, Taylor
collection PubMed
description During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the eventual location of the spindle apparatus and ultimately the cytokinetic furrow. Positioning of the MT aster often results in its movement to the center of a cell, even in large blastomeres hundreds of microns in diameter. This translocation requires positioning forces, yet how these forces are generated and then integrated within cells of various sizes and geometries remains an open question. Here we describe a method that combines microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics of aster movement and centration. We determined that asters were able to find the center of artificial channels and annular cylinders, even when cytoplasmic dynein-dependent pulling mechanisms were inhibited. Characterization of aster movement away from V-shaped hydrogel barriers provided additional evidence for a MT-based pushing mechanism. Importantly, the distance over which this mechanism seemed to operate was longer than that predicted by radial aster growth models, agreeing with recent models of a more complex MT network architecture within the aster.
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spelling pubmed-78518582021-02-18 Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts Sulerud, Taylor Sami, Abdullah Bashar Li, Guihe Kloxin, April Oakey, John Gatlin, Jesse Mol Biol Cell Articles During interphase of the eukaryotic cell cycle, the microtubule (MT) cytoskeleton serves as both a supportive scaffold for organelles and an arborized system of tracks for intracellular transport. At the onset of mitosis, the position of the astral MT network, specifically its center, determines the eventual location of the spindle apparatus and ultimately the cytokinetic furrow. Positioning of the MT aster often results in its movement to the center of a cell, even in large blastomeres hundreds of microns in diameter. This translocation requires positioning forces, yet how these forces are generated and then integrated within cells of various sizes and geometries remains an open question. Here we describe a method that combines microfluidics, hydrogels, and Xenopus laevis egg extract to investigate the mechanics of aster movement and centration. We determined that asters were able to find the center of artificial channels and annular cylinders, even when cytoplasmic dynein-dependent pulling mechanisms were inhibited. Characterization of aster movement away from V-shaped hydrogel barriers provided additional evidence for a MT-based pushing mechanism. Importantly, the distance over which this mechanism seemed to operate was longer than that predicted by radial aster growth models, agreeing with recent models of a more complex MT network architecture within the aster. The American Society for Cell Biology 2020-12-01 /pmc/articles/PMC7851858/ /pubmed/33026931 http://dx.doi.org/10.1091/mbc.E20-01-0088 Text en © 2020 Sulerud et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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.
spellingShingle Articles
Sulerud, Taylor
Sami, Abdullah Bashar
Li, Guihe
Kloxin, April
Oakey, John
Gatlin, Jesse
Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title_full Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title_fullStr Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title_full_unstemmed Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title_short Microtubule-dependent pushing forces contribute to long-distance aster movement and centration in Xenopus laevis egg extracts
title_sort microtubule-dependent pushing forces contribute to long-distance aster movement and centration in xenopus laevis egg extracts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851858/
https://www.ncbi.nlm.nih.gov/pubmed/33026931
http://dx.doi.org/10.1091/mbc.E20-01-0088
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