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PAR-dependent and geometry-dependent mechanisms of spindle positioning

During intrinsically asymmetric division, the spindle is oriented onto a polarized axis specified by a group of conserved PAR proteins. Extrinsic geometric asymmetry generated by cell shape also affects spindle orientation in some systems, but how intrinsic and extrinsic mechanisms coexist without i...

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Detalles Bibliográficos
Autores principales: Tsou, Meng-Fu Bryan, Ku, Wei, Hayashi, Adam, Rose, Lesilee S.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173762/
https://www.ncbi.nlm.nih.gov/pubmed/12642612
http://dx.doi.org/10.1083/jcb.200209079
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author Tsou, Meng-Fu Bryan
Ku, Wei
Hayashi, Adam
Rose, Lesilee S.
author_facet Tsou, Meng-Fu Bryan
Ku, Wei
Hayashi, Adam
Rose, Lesilee S.
author_sort Tsou, Meng-Fu Bryan
collection PubMed
description During intrinsically asymmetric division, the spindle is oriented onto a polarized axis specified by a group of conserved PAR proteins. Extrinsic geometric asymmetry generated by cell shape also affects spindle orientation in some systems, but how intrinsic and extrinsic mechanisms coexist without interfering with each other is unknown. In some asymmetrically dividing cells of the wild-type Caenorhabditis elegans embryo, nuclear rotation directed toward the anterior cortex orients the forming spindle. We find that in such cells, a PAR-dependent mechanism dominates and causes rotation onto the polarized axis, regardless of cell shape. However, when geometric asymmetry is removed, free nuclear rotation in the center of the cell is observed, indicating that the anterior-directed nature of rotation in unaltered embryos is an effect of cell shape. This free rotation is inconsistent with the prevailing model for nuclear rotation, the specialized cortical site model. In contrast, in par-3 mutant embryos, a geometry-dependent mechanism becomes active and causes directed nuclear rotation. These results lead to the model that in wild-type embryos both PAR-3 and PAR-2 are essential for nuclear rotation in asymmetrically dividing cells, but that PAR-3 inhibits geometry-dependent rotation in nonpolarized cells, thus preventing cell shape from interfering with spindle orientation.
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spelling pubmed-21737622008-05-01 PAR-dependent and geometry-dependent mechanisms of spindle positioning Tsou, Meng-Fu Bryan Ku, Wei Hayashi, Adam Rose, Lesilee S. J Cell Biol Article During intrinsically asymmetric division, the spindle is oriented onto a polarized axis specified by a group of conserved PAR proteins. Extrinsic geometric asymmetry generated by cell shape also affects spindle orientation in some systems, but how intrinsic and extrinsic mechanisms coexist without interfering with each other is unknown. In some asymmetrically dividing cells of the wild-type Caenorhabditis elegans embryo, nuclear rotation directed toward the anterior cortex orients the forming spindle. We find that in such cells, a PAR-dependent mechanism dominates and causes rotation onto the polarized axis, regardless of cell shape. However, when geometric asymmetry is removed, free nuclear rotation in the center of the cell is observed, indicating that the anterior-directed nature of rotation in unaltered embryos is an effect of cell shape. This free rotation is inconsistent with the prevailing model for nuclear rotation, the specialized cortical site model. In contrast, in par-3 mutant embryos, a geometry-dependent mechanism becomes active and causes directed nuclear rotation. These results lead to the model that in wild-type embryos both PAR-3 and PAR-2 are essential for nuclear rotation in asymmetrically dividing cells, but that PAR-3 inhibits geometry-dependent rotation in nonpolarized cells, thus preventing cell shape from interfering with spindle orientation. The Rockefeller University Press 2003-03-17 /pmc/articles/PMC2173762/ /pubmed/12642612 http://dx.doi.org/10.1083/jcb.200209079 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Tsou, Meng-Fu Bryan
Ku, Wei
Hayashi, Adam
Rose, Lesilee S.
PAR-dependent and geometry-dependent mechanisms of spindle positioning
title PAR-dependent and geometry-dependent mechanisms of spindle positioning
title_full PAR-dependent and geometry-dependent mechanisms of spindle positioning
title_fullStr PAR-dependent and geometry-dependent mechanisms of spindle positioning
title_full_unstemmed PAR-dependent and geometry-dependent mechanisms of spindle positioning
title_short PAR-dependent and geometry-dependent mechanisms of spindle positioning
title_sort par-dependent and geometry-dependent mechanisms of spindle positioning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173762/
https://www.ncbi.nlm.nih.gov/pubmed/12642612
http://dx.doi.org/10.1083/jcb.200209079
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