Cargando…
Elevated polar ejection forces stabilize kinetochore–microtubule attachments
Chromosome biorientation promotes congression and generates tension that stabilizes kinetochore–microtubule (kt-MT) interactions. Forces produced by molecular motors also contribute to chromosome alignment, but their impact on kt-MT attachment stability is unclear. A critical force that acts on chro...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549975/ https://www.ncbi.nlm.nih.gov/pubmed/23337118 http://dx.doi.org/10.1083/jcb.201211119 |
_version_ | 1782256512065863680 |
---|---|
author | Cane, Stuart Ye, Anna A. Luks-Morgan, Sasha J. Maresca, Thomas J. |
author_facet | Cane, Stuart Ye, Anna A. Luks-Morgan, Sasha J. Maresca, Thomas J. |
author_sort | Cane, Stuart |
collection | PubMed |
description | Chromosome biorientation promotes congression and generates tension that stabilizes kinetochore–microtubule (kt-MT) interactions. Forces produced by molecular motors also contribute to chromosome alignment, but their impact on kt-MT attachment stability is unclear. A critical force that acts on chromosomes is the kinesin-10–dependent polar ejection force (PEF). PEFs are proposed to facilitate congression by pushing chromosomes away from spindle poles, although knowledge of the molecular mechanisms underpinning PEF generation is incomplete. Here, we describe a live-cell PEF assay in which tension was applied to chromosomes by manipulating levels of the chromokinesin NOD (no distributive disjunction; Drosophila melanogaster kinesin-10). NOD stabilized syntelic kt-MT attachments in a dose- and motor-dependent manner by overwhelming the ability of Aurora B to mediate error correction. NOD-coated chromatin stretched away from the pole via lateral and end-on interactions with microtubules, and NOD chimeras with either plus end–directed motility or tip-tracking activity produced PEFs. Thus, kt-MT attachment stability is modulated by PEFs, which can be generated by distinct force-producing interactions between chromosomes and dynamic spindle microtubules. |
format | Online Article Text |
id | pubmed-3549975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35499752013-07-21 Elevated polar ejection forces stabilize kinetochore–microtubule attachments Cane, Stuart Ye, Anna A. Luks-Morgan, Sasha J. Maresca, Thomas J. J Cell Biol Research Articles Chromosome biorientation promotes congression and generates tension that stabilizes kinetochore–microtubule (kt-MT) interactions. Forces produced by molecular motors also contribute to chromosome alignment, but their impact on kt-MT attachment stability is unclear. A critical force that acts on chromosomes is the kinesin-10–dependent polar ejection force (PEF). PEFs are proposed to facilitate congression by pushing chromosomes away from spindle poles, although knowledge of the molecular mechanisms underpinning PEF generation is incomplete. Here, we describe a live-cell PEF assay in which tension was applied to chromosomes by manipulating levels of the chromokinesin NOD (no distributive disjunction; Drosophila melanogaster kinesin-10). NOD stabilized syntelic kt-MT attachments in a dose- and motor-dependent manner by overwhelming the ability of Aurora B to mediate error correction. NOD-coated chromatin stretched away from the pole via lateral and end-on interactions with microtubules, and NOD chimeras with either plus end–directed motility or tip-tracking activity produced PEFs. Thus, kt-MT attachment stability is modulated by PEFs, which can be generated by distinct force-producing interactions between chromosomes and dynamic spindle microtubules. The Rockefeller University Press 2013-01-21 /pmc/articles/PMC3549975/ /pubmed/23337118 http://dx.doi.org/10.1083/jcb.201211119 Text en © 2013 Cane et al. 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 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Research Articles Cane, Stuart Ye, Anna A. Luks-Morgan, Sasha J. Maresca, Thomas J. Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title | Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title_full | Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title_fullStr | Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title_full_unstemmed | Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title_short | Elevated polar ejection forces stabilize kinetochore–microtubule attachments |
title_sort | elevated polar ejection forces stabilize kinetochore–microtubule attachments |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549975/ https://www.ncbi.nlm.nih.gov/pubmed/23337118 http://dx.doi.org/10.1083/jcb.201211119 |
work_keys_str_mv | AT canestuart elevatedpolarejectionforcesstabilizekinetochoremicrotubuleattachments AT yeannaa elevatedpolarejectionforcesstabilizekinetochoremicrotubuleattachments AT luksmorgansashaj elevatedpolarejectionforcesstabilizekinetochoremicrotubuleattachments AT marescathomasj elevatedpolarejectionforcesstabilizekinetochoremicrotubuleattachments |