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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...

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Detalles Bibliográficos
Autores principales: Maney, Todd, Hunter, Andrew W., Wagenbach, Mike, Wordeman, Linda
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
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.
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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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