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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
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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. |
format | Text |
id | pubmed-2173762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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