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Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation
Mitotic centromere–associated kinesin (MCAK) is recruited to the centromere at prophase and remains centromere associated until after telophase. MCAK is a homodimer that is encoded by a single gene and has no associated subunits. A motorless version of MCAK that binds centromeres but not microtubule...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148171/ https://www.ncbi.nlm.nih.gov/pubmed/9700166 |
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author | Maney, Todd Hunter, Andrew W. Wagenbach, Mike Wordeman, Linda |
author_facet | Maney, Todd Hunter, Andrew W. Wagenbach, Mike Wordeman, Linda |
author_sort | Maney, Todd |
collection | PubMed |
description | Mitotic centromere–associated kinesin (MCAK) is recruited to the centromere at prophase and remains centromere associated until after telophase. MCAK is a homodimer that is encoded by a single gene and has no associated subunits. A motorless version of MCAK that binds centromeres but not microtubules disrupts chromosome segregation during anaphase. Antisense-induced depletion of MCAK results in the same defect. MCAK overexpression induces centromere-independent bundling and eventual loss of spindle microtubule polymer suggesting that centromere-associated bundling and/or depolymerization activity is required for anaphase. Live cell imaging indicates that MCAK may be required to coordinate the onset of sister centromere separation. |
format | Text |
id | pubmed-2148171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21481712008-05-01 Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation Maney, Todd Hunter, Andrew W. Wagenbach, Mike Wordeman, Linda J Cell Biol Regular Articles Mitotic centromere–associated kinesin (MCAK) is recruited to the centromere at prophase and remains centromere associated until after telophase. MCAK is a homodimer that is encoded by a single gene and has no associated subunits. A motorless version of MCAK that binds centromeres but not microtubules disrupts chromosome segregation during anaphase. Antisense-induced depletion of MCAK results in the same defect. MCAK overexpression induces centromere-independent bundling and eventual loss of spindle microtubule polymer suggesting that centromere-associated bundling and/or depolymerization activity is required for anaphase. Live cell imaging indicates that MCAK may be required to coordinate the onset of sister centromere separation. The Rockefeller University Press 1998-08-10 /pmc/articles/PMC2148171/ /pubmed/9700166 Text en 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 | Regular Articles Maney, Todd Hunter, Andrew W. Wagenbach, Mike Wordeman, Linda Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title | Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title_full | Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title_fullStr | Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title_full_unstemmed | Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title_short | Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation |
title_sort | mitotic centromere–associated kinesin is important for anaphase chromosome segregation |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148171/ https://www.ncbi.nlm.nih.gov/pubmed/9700166 |
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