Cargando…

Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing

Faithful chromosome segregation during mitosis requires that the kinetochores of all sister chromatids become stably connected to microtubules derived from opposite spindle poles. How stable chromosome bi-orientation is accomplished and coordinated with anaphase onset remains incompletely understood...

Descripción completa

Detalles Bibliográficos
Autores principales: Hengeveld, Rutger C. C., Vromans, Martijn J. M., Vleugel, Mathijs, Hadders, Michael A., Lens, Susanne M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460030/
https://www.ncbi.nlm.nih.gov/pubmed/28561035
http://dx.doi.org/10.1038/ncomms15542
_version_ 1783242082575450112
author Hengeveld, Rutger C. C.
Vromans, Martijn J. M.
Vleugel, Mathijs
Hadders, Michael A.
Lens, Susanne M. A.
author_facet Hengeveld, Rutger C. C.
Vromans, Martijn J. M.
Vleugel, Mathijs
Hadders, Michael A.
Lens, Susanne M. A.
author_sort Hengeveld, Rutger C. C.
collection PubMed
description Faithful chromosome segregation during mitosis requires that the kinetochores of all sister chromatids become stably connected to microtubules derived from opposite spindle poles. How stable chromosome bi-orientation is accomplished and coordinated with anaphase onset remains incompletely understood. Here we show that stable chromosome bi-orientation requires inner centromere localization of the non-enzymatic subunits of the chromosomal passenger complex (CPC) to maintain centromeric cohesion. Precise inner centromere localization of the CPC appears less relevant for Aurora B-dependent resolution of erroneous kinetochore–microtubule (KT–MT) attachments and for the stabilization of bi-oriented KT–MT attachments once sister chromatid cohesion is preserved via knock-down of WAPL. However, Aurora B inner centromere localization is essential for mitotic checkpoint silencing to allow spatial separation from its kinetochore substrate KNL1. Our data infer that the CPC is localized at the inner centromere to sustain centromere cohesion on bi-oriented chromosomes and to coordinate mitotic checkpoint silencing with chromosome bi-orientation.
format Online
Article
Text
id pubmed-5460030
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-54600302017-06-12 Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing Hengeveld, Rutger C. C. Vromans, Martijn J. M. Vleugel, Mathijs Hadders, Michael A. Lens, Susanne M. A. Nat Commun Article Faithful chromosome segregation during mitosis requires that the kinetochores of all sister chromatids become stably connected to microtubules derived from opposite spindle poles. How stable chromosome bi-orientation is accomplished and coordinated with anaphase onset remains incompletely understood. Here we show that stable chromosome bi-orientation requires inner centromere localization of the non-enzymatic subunits of the chromosomal passenger complex (CPC) to maintain centromeric cohesion. Precise inner centromere localization of the CPC appears less relevant for Aurora B-dependent resolution of erroneous kinetochore–microtubule (KT–MT) attachments and for the stabilization of bi-oriented KT–MT attachments once sister chromatid cohesion is preserved via knock-down of WAPL. However, Aurora B inner centromere localization is essential for mitotic checkpoint silencing to allow spatial separation from its kinetochore substrate KNL1. Our data infer that the CPC is localized at the inner centromere to sustain centromere cohesion on bi-oriented chromosomes and to coordinate mitotic checkpoint silencing with chromosome bi-orientation. Nature Publishing Group 2017-05-31 /pmc/articles/PMC5460030/ /pubmed/28561035 http://dx.doi.org/10.1038/ncomms15542 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hengeveld, Rutger C. C.
Vromans, Martijn J. M.
Vleugel, Mathijs
Hadders, Michael A.
Lens, Susanne M. A.
Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title_full Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title_fullStr Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title_full_unstemmed Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title_short Inner centromere localization of the CPC maintains centromere cohesion and allows mitotic checkpoint silencing
title_sort inner centromere localization of the cpc maintains centromere cohesion and allows mitotic checkpoint silencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460030/
https://www.ncbi.nlm.nih.gov/pubmed/28561035
http://dx.doi.org/10.1038/ncomms15542
work_keys_str_mv AT hengeveldrutgercc innercentromerelocalizationofthecpcmaintainscentromerecohesionandallowsmitoticcheckpointsilencing
AT vromansmartijnjm innercentromerelocalizationofthecpcmaintainscentromerecohesionandallowsmitoticcheckpointsilencing
AT vleugelmathijs innercentromerelocalizationofthecpcmaintainscentromerecohesionandallowsmitoticcheckpointsilencing
AT haddersmichaela innercentromerelocalizationofthecpcmaintainscentromerecohesionandallowsmitoticcheckpointsilencing
AT lenssusannema innercentromerelocalizationofthecpcmaintainscentromerecohesionandallowsmitoticcheckpointsilencing