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Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly

Efficient spindle assembly involves the generation of spatial cues around chromosomes that locally stabilize microtubule (MT) plus-ends. In addition to the small GTPase Ran, there is evidence that Aurora B kinase might also generate a spatial cue around chromosomes but direct proof for this is still...

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Detalles Bibliográficos
Autores principales: Tanenbaum, Marvin E., Medema, René H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223347/
https://www.ncbi.nlm.nih.gov/pubmed/21786106
http://dx.doi.org/10.1007/s00412-011-0334-9
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author Tanenbaum, Marvin E.
Medema, René H.
author_facet Tanenbaum, Marvin E.
Medema, René H.
author_sort Tanenbaum, Marvin E.
collection PubMed
description Efficient spindle assembly involves the generation of spatial cues around chromosomes that locally stabilize microtubule (MT) plus-ends. In addition to the small GTPase Ran, there is evidence that Aurora B kinase might also generate a spatial cue around chromosomes but direct proof for this is still lacking. Here, we find that the Aurora B substrate MCAK localizes to MT plus-ends throughout the mitotic spindle, but its accumulation is strongly reduced on MT plus-ends near chromatin, suggesting that a signal emanating from chromosomes negatively regulates MCAK plus-end binding. Indeed, we show that Aurora B is the kinase responsible for producing this chromosome-derived signal. These results are the first to visualize spatially restricted Aurora B kinase activity around chromosomes on an endogenous substrate and explain how Aurora B could spatially control the dynamics of non-kinetochore MTs during spindle assembly. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00412-011-0334-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-32233472011-12-27 Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly Tanenbaum, Marvin E. Medema, René H. Chromosoma Research Article Efficient spindle assembly involves the generation of spatial cues around chromosomes that locally stabilize microtubule (MT) plus-ends. In addition to the small GTPase Ran, there is evidence that Aurora B kinase might also generate a spatial cue around chromosomes but direct proof for this is still lacking. Here, we find that the Aurora B substrate MCAK localizes to MT plus-ends throughout the mitotic spindle, but its accumulation is strongly reduced on MT plus-ends near chromatin, suggesting that a signal emanating from chromosomes negatively regulates MCAK plus-end binding. Indeed, we show that Aurora B is the kinase responsible for producing this chromosome-derived signal. These results are the first to visualize spatially restricted Aurora B kinase activity around chromosomes on an endogenous substrate and explain how Aurora B could spatially control the dynamics of non-kinetochore MTs during spindle assembly. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00412-011-0334-9) contains supplementary material, which is available to authorized users. Springer-Verlag 2011-07-24 2011 /pmc/articles/PMC3223347/ /pubmed/21786106 http://dx.doi.org/10.1007/s00412-011-0334-9 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Research Article
Tanenbaum, Marvin E.
Medema, René H.
Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title_full Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title_fullStr Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title_full_unstemmed Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title_short Localized Aurora B activity spatially controls non-kinetochore microtubules during spindle assembly
title_sort localized aurora b activity spatially controls non-kinetochore microtubules during spindle assembly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223347/
https://www.ncbi.nlm.nih.gov/pubmed/21786106
http://dx.doi.org/10.1007/s00412-011-0334-9
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