Cargando…

MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity

Multiple asters (MAST)/Orbit is a member of a new family of nonmotor microtubule-associated proteins that has been previously shown to be required for the organization of the mitotic spindle. Here we provide evidence that MAST/Orbit is required for functional kinetochore attachment, chromosome congr...

Descripción completa

Detalles Bibliográficos
Autores principales: Maiato, Helder, Sampaio, Paula, Lemos, Catarina L., Findlay, John, Carmena, Mar, Earnshaw, William C., Sunkel, Claudio E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173411/
https://www.ncbi.nlm.nih.gov/pubmed/12034769
http://dx.doi.org/10.1083/jcb.200201101
_version_ 1782145195627773952
author Maiato, Helder
Sampaio, Paula
Lemos, Catarina L.
Findlay, John
Carmena, Mar
Earnshaw, William C.
Sunkel, Claudio E.
author_facet Maiato, Helder
Sampaio, Paula
Lemos, Catarina L.
Findlay, John
Carmena, Mar
Earnshaw, William C.
Sunkel, Claudio E.
author_sort Maiato, Helder
collection PubMed
description Multiple asters (MAST)/Orbit is a member of a new family of nonmotor microtubule-associated proteins that has been previously shown to be required for the organization of the mitotic spindle. Here we provide evidence that MAST/Orbit is required for functional kinetochore attachment, chromosome congression, and the maintenance of spindle bipolarity. In vivo analysis of Drosophila mast mutant embryos undergoing early mitotic divisions revealed that chromosomes are unable to reach a stable metaphase alignment and that bipolar spindles collapse as centrosomes move progressively closer toward the cell center and eventually organize into a monopolar configuration. Similarly, soon after depletion of MAST/Orbit in Drosophila S2 cells by double-stranded RNA interference, cells are unable to form a metaphase plate and instead assemble monopolar spindles with chromosomes localized close to the center of the aster. In these cells, kinetochores either fail to achieve end-on attachment or are associated with short microtubules. Remarkably, when microtubule dynamics is suppressed in MAST-depleted cells, chromosomes localize at the periphery of the monopolar aster associated with the plus ends of well-defined microtubule bundles. Furthermore, in these cells, dynein and ZW10 accumulate at kinetochores and fail to transfer to microtubules. However, loss of MAST/Orbit does not affect the kinetochore localization of D-CLIP-190. Together, these results strongly support the conclusion that MAST/Orbit is required for microtubules to form functional attachments to kinetochores and to maintain spindle bipolarity.
format Text
id pubmed-2173411
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21734112008-05-01 MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity Maiato, Helder Sampaio, Paula Lemos, Catarina L. Findlay, John Carmena, Mar Earnshaw, William C. Sunkel, Claudio E. J Cell Biol Article Multiple asters (MAST)/Orbit is a member of a new family of nonmotor microtubule-associated proteins that has been previously shown to be required for the organization of the mitotic spindle. Here we provide evidence that MAST/Orbit is required for functional kinetochore attachment, chromosome congression, and the maintenance of spindle bipolarity. In vivo analysis of Drosophila mast mutant embryos undergoing early mitotic divisions revealed that chromosomes are unable to reach a stable metaphase alignment and that bipolar spindles collapse as centrosomes move progressively closer toward the cell center and eventually organize into a monopolar configuration. Similarly, soon after depletion of MAST/Orbit in Drosophila S2 cells by double-stranded RNA interference, cells are unable to form a metaphase plate and instead assemble monopolar spindles with chromosomes localized close to the center of the aster. In these cells, kinetochores either fail to achieve end-on attachment or are associated with short microtubules. Remarkably, when microtubule dynamics is suppressed in MAST-depleted cells, chromosomes localize at the periphery of the monopolar aster associated with the plus ends of well-defined microtubule bundles. Furthermore, in these cells, dynein and ZW10 accumulate at kinetochores and fail to transfer to microtubules. However, loss of MAST/Orbit does not affect the kinetochore localization of D-CLIP-190. Together, these results strongly support the conclusion that MAST/Orbit is required for microtubules to form functional attachments to kinetochores and to maintain spindle bipolarity. The Rockefeller University Press 2002-05-28 /pmc/articles/PMC2173411/ /pubmed/12034769 http://dx.doi.org/10.1083/jcb.200201101 Text en Copyright © 2002, The Rockefeller University Press 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 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Maiato, Helder
Sampaio, Paula
Lemos, Catarina L.
Findlay, John
Carmena, Mar
Earnshaw, William C.
Sunkel, Claudio E.
MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title_full MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title_fullStr MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title_full_unstemmed MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title_short MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
title_sort mast/orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173411/
https://www.ncbi.nlm.nih.gov/pubmed/12034769
http://dx.doi.org/10.1083/jcb.200201101
work_keys_str_mv AT maiatohelder mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT sampaiopaula mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT lemoscatarinal mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT findlayjohn mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT carmenamar mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT earnshawwilliamc mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity
AT sunkelclaudioe mastorbithasaroleinmicrotubulekinetochoreattachmentandisessentialforchromosomealignmentandmaintenanceofspindlebipolarity