Cargando…

Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly

Mitotic spindle disassembly after chromosome separation is as important as spindle assembly, yet the molecular mechanisms for spindle disassembly are unclear. In this study, we investigated how the chromosomal passenger complex (CPC), which contains the Aurora B kinase Ipl1, swiftly concentrates at...

Descripción completa

Detalles Bibliográficos
Autores principales: Ibarlucea-Benitez, Itziar, Ferro, Luke S., Drubin, David G., Barnes, Georjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940302/
https://www.ncbi.nlm.nih.gov/pubmed/29563217
http://dx.doi.org/10.1083/jcb.201708114
_version_ 1783321088517734400
author Ibarlucea-Benitez, Itziar
Ferro, Luke S.
Drubin, David G.
Barnes, Georjana
author_facet Ibarlucea-Benitez, Itziar
Ferro, Luke S.
Drubin, David G.
Barnes, Georjana
author_sort Ibarlucea-Benitez, Itziar
collection PubMed
description Mitotic spindle disassembly after chromosome separation is as important as spindle assembly, yet the molecular mechanisms for spindle disassembly are unclear. In this study, we investigated how the chromosomal passenger complex (CPC), which contains the Aurora B kinase Ipl1, swiftly concentrates at the spindle midzone in late anaphase, and we researched the role of this dramatic relocalization during spindle disassembly. We showed that the kinesins Kip1 and Kip3 are essential for CPC relocalization. In cells lacking Kip1 and Kip3, spindle disassembly is severely delayed until after contraction of the cytokinetic ring. Purified Kip1 and Kip3 interact directly with the CPC and recruit it to microtubules in vitro, and single-molecule experiments showed that the CPC diffuses dynamically on microtubules but that diffusion stops when the CPC encounters a Kip1 molecule. We propose that Kip1 and Kip3 trap the CPC at the spindle midzone in late anaphase to ensure timely spindle disassembly.
format Online
Article
Text
id pubmed-5940302
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-59403022018-11-07 Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly Ibarlucea-Benitez, Itziar Ferro, Luke S. Drubin, David G. Barnes, Georjana J Cell Biol Research Articles Mitotic spindle disassembly after chromosome separation is as important as spindle assembly, yet the molecular mechanisms for spindle disassembly are unclear. In this study, we investigated how the chromosomal passenger complex (CPC), which contains the Aurora B kinase Ipl1, swiftly concentrates at the spindle midzone in late anaphase, and we researched the role of this dramatic relocalization during spindle disassembly. We showed that the kinesins Kip1 and Kip3 are essential for CPC relocalization. In cells lacking Kip1 and Kip3, spindle disassembly is severely delayed until after contraction of the cytokinetic ring. Purified Kip1 and Kip3 interact directly with the CPC and recruit it to microtubules in vitro, and single-molecule experiments showed that the CPC diffuses dynamically on microtubules but that diffusion stops when the CPC encounters a Kip1 molecule. We propose that Kip1 and Kip3 trap the CPC at the spindle midzone in late anaphase to ensure timely spindle disassembly. Rockefeller University Press 2018-05-07 /pmc/articles/PMC5940302/ /pubmed/29563217 http://dx.doi.org/10.1083/jcb.201708114 Text en © 2018 Ibarlucea-Benitez et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Ibarlucea-Benitez, Itziar
Ferro, Luke S.
Drubin, David G.
Barnes, Georjana
Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title_full Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title_fullStr Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title_full_unstemmed Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title_short Kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
title_sort kinesins relocalize the chromosomal passenger complex to the midzone for spindle disassembly
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940302/
https://www.ncbi.nlm.nih.gov/pubmed/29563217
http://dx.doi.org/10.1083/jcb.201708114
work_keys_str_mv AT ibarluceabenitezitziar kinesinsrelocalizethechromosomalpassengercomplextothemidzoneforspindledisassembly
AT ferrolukes kinesinsrelocalizethechromosomalpassengercomplextothemidzoneforspindledisassembly
AT drubindavidg kinesinsrelocalizethechromosomalpassengercomplextothemidzoneforspindledisassembly
AT barnesgeorjana kinesinsrelocalizethechromosomalpassengercomplextothemidzoneforspindledisassembly