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Kinetochore–microtubule error correction is driven by differentially regulated interaction modes

For proper chromosome segregation, sister kinetochores must interact with microtubules from opposite spindle poles (bi-orientation). To establish bi-orientation, aberrant kinetochore–microtubule attachments are disrupted (error correction) by Aurora B kinase (Ipl1 in budding yeast). Paradoxically, d...

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Autores principales: Kalantzaki, Maria, Kitamura, Etsushi, Zhang, Tongli, Mino, Akihisa, Novák, Béla, Tanaka, Tomoyuki U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380510/
https://www.ncbi.nlm.nih.gov/pubmed/25751138
http://dx.doi.org/10.1038/ncb3128
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author Kalantzaki, Maria
Kitamura, Etsushi
Zhang, Tongli
Mino, Akihisa
Novák, Béla
Tanaka, Tomoyuki U.
author_facet Kalantzaki, Maria
Kitamura, Etsushi
Zhang, Tongli
Mino, Akihisa
Novák, Béla
Tanaka, Tomoyuki U.
author_sort Kalantzaki, Maria
collection PubMed
description For proper chromosome segregation, sister kinetochores must interact with microtubules from opposite spindle poles (bi-orientation). To establish bi-orientation, aberrant kinetochore–microtubule attachments are disrupted (error correction) by Aurora B kinase (Ipl1 in budding yeast). Paradoxically, during this disruption, new attachments are still formed efficiently to allow fresh attempts at bi-orientation. How this is possible remains an enigma. Here we show that kinetochore attachment to the microtubule lattice (lateral attachment) is impervious to Aurora B regulation, but attachment to the microtubule plus-end (end-on attachment) is disrupted by this kinase. Thus, a new lateral attachment is formed without interference, then converted to end-on attachment and released if incorrect. This process continues until bi-orientation is established and stabilized by tension across sister kinetochores. We reveal how Aurora B specifically promotes disruption of the end-on attachment through phospho-regulation of kinetochore components Dam1 and Ndc80. Our results reveal fundamental mechanisms for promoting error correction for bi-orientation.
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spelling pubmed-43805102015-10-01 Kinetochore–microtubule error correction is driven by differentially regulated interaction modes Kalantzaki, Maria Kitamura, Etsushi Zhang, Tongli Mino, Akihisa Novák, Béla Tanaka, Tomoyuki U. Nat Cell Biol Article For proper chromosome segregation, sister kinetochores must interact with microtubules from opposite spindle poles (bi-orientation). To establish bi-orientation, aberrant kinetochore–microtubule attachments are disrupted (error correction) by Aurora B kinase (Ipl1 in budding yeast). Paradoxically, during this disruption, new attachments are still formed efficiently to allow fresh attempts at bi-orientation. How this is possible remains an enigma. Here we show that kinetochore attachment to the microtubule lattice (lateral attachment) is impervious to Aurora B regulation, but attachment to the microtubule plus-end (end-on attachment) is disrupted by this kinase. Thus, a new lateral attachment is formed without interference, then converted to end-on attachment and released if incorrect. This process continues until bi-orientation is established and stabilized by tension across sister kinetochores. We reveal how Aurora B specifically promotes disruption of the end-on attachment through phospho-regulation of kinetochore components Dam1 and Ndc80. Our results reveal fundamental mechanisms for promoting error correction for bi-orientation. 2015-03-09 2015-04 /pmc/articles/PMC4380510/ /pubmed/25751138 http://dx.doi.org/10.1038/ncb3128 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kalantzaki, Maria
Kitamura, Etsushi
Zhang, Tongli
Mino, Akihisa
Novák, Béla
Tanaka, Tomoyuki U.
Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title_full Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title_fullStr Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title_full_unstemmed Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title_short Kinetochore–microtubule error correction is driven by differentially regulated interaction modes
title_sort kinetochore–microtubule error correction is driven by differentially regulated interaction modes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380510/
https://www.ncbi.nlm.nih.gov/pubmed/25751138
http://dx.doi.org/10.1038/ncb3128
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