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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.
Afiliación
  • Hengeveld RCC; Department of Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.
  • Vromans MJM; Department of Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.
  • Vleugel M; Department of Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.
  • Hadders MA; Department of Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.
  • Lens SMA; Department of Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Universiteitsweg 100, Utrecht 3584 CG, The Netherlands.
Nat Commun ; 8: 15542, 2017 05 31.
Article en En | MEDLINE | ID: mdl-28561035
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Centrómero / Cinetocoros / Aurora Quinasa B / Proteínas Asociadas a Microtúbulos / Microtúbulos / Mitosis Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Centrómero / Cinetocoros / Aurora Quinasa B / Proteínas Asociadas a Microtúbulos / Microtúbulos / Mitosis Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos