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Insights from an erroneous kinetochore-microtubule attachment state

Faithful distribution of the genome requires that sister kinetochores, which assemble on each chromatid during cell division, interact with dynamic microtubules from opposite spindle poles in a configuration called chromosome biorientation. Biorientation produces tension that increases the affinity...

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Detalles Bibliográficos
Autores principales: Cane, Stuart, McGilvray, Philip T., Maresca, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782542/
https://www.ncbi.nlm.nih.gov/pubmed/23887229
http://dx.doi.org/10.4161/bioa.25734
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author Cane, Stuart
McGilvray, Philip T.
Maresca, Thomas J.
author_facet Cane, Stuart
McGilvray, Philip T.
Maresca, Thomas J.
author_sort Cane, Stuart
collection PubMed
description Faithful distribution of the genome requires that sister kinetochores, which assemble on each chromatid during cell division, interact with dynamic microtubules from opposite spindle poles in a configuration called chromosome biorientation. Biorientation produces tension that increases the affinity of kinetochores for microtubules via ill-defined mechanisms. Non-bioriented kinetochore-microtubule (kt-MT) interactions are prevalent but short-lived due to an error correction pathway that reduces the affinity of kinetochores for microtubules. Interestingly, incorrect kt-MT interactions can be stabilized by experimentally applying force to misoriented chromosomes. Here, a live-cell force assay is utilized to characterize the molecular composition of a common type of improper kt-MT attachment. Our force-related studies are also discussed in the context of current models for tension-dependent stabilization of kt-MT interactions.
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spelling pubmed-37825422013-09-26 Insights from an erroneous kinetochore-microtubule attachment state Cane, Stuart McGilvray, Philip T. Maresca, Thomas J. Bioarchitecture Short Communication Faithful distribution of the genome requires that sister kinetochores, which assemble on each chromatid during cell division, interact with dynamic microtubules from opposite spindle poles in a configuration called chromosome biorientation. Biorientation produces tension that increases the affinity of kinetochores for microtubules via ill-defined mechanisms. Non-bioriented kinetochore-microtubule (kt-MT) interactions are prevalent but short-lived due to an error correction pathway that reduces the affinity of kinetochores for microtubules. Interestingly, incorrect kt-MT interactions can be stabilized by experimentally applying force to misoriented chromosomes. Here, a live-cell force assay is utilized to characterize the molecular composition of a common type of improper kt-MT attachment. Our force-related studies are also discussed in the context of current models for tension-dependent stabilization of kt-MT interactions. Landes Bioscience 2013-05-01 2013-07-15 /pmc/articles/PMC3782542/ /pubmed/23887229 http://dx.doi.org/10.4161/bioa.25734 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Short Communication
Cane, Stuart
McGilvray, Philip T.
Maresca, Thomas J.
Insights from an erroneous kinetochore-microtubule attachment state
title Insights from an erroneous kinetochore-microtubule attachment state
title_full Insights from an erroneous kinetochore-microtubule attachment state
title_fullStr Insights from an erroneous kinetochore-microtubule attachment state
title_full_unstemmed Insights from an erroneous kinetochore-microtubule attachment state
title_short Insights from an erroneous kinetochore-microtubule attachment state
title_sort insights from an erroneous kinetochore-microtubule attachment state
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782542/
https://www.ncbi.nlm.nih.gov/pubmed/23887229
http://dx.doi.org/10.4161/bioa.25734
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