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.
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28 May 2002
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May 28 2002
MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity
Helder Maiato,
Helder Maiato
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
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Paula Sampaio,
Paula Sampaio
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
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Catarina L. Lemos,
Catarina L. Lemos
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
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John Findlay,
John Findlay
4Biological Sciences Electron Microscope Facility, Institute of Cell and Molecular Biology, University of Edinburgh, Scotland, UK
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Mar Carmena,
Mar Carmena
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
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William C. Earnshaw,
William C. Earnshaw
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
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Claudio E. Sunkel
Claudio E. Sunkel
1Instituto de Ciências Biomédicas de Abel Salazar, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
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Helder Maiato
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
Paula Sampaio
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
Catarina L. Lemos
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
John Findlay
4Biological Sciences Electron Microscope Facility, Institute of Cell and Molecular Biology, University of Edinburgh, Scotland, UK
Mar Carmena
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
William C. Earnshaw
3Chromosome Structure Group, Wellcome Trust Centre for Cell Biology
Claudio E. Sunkel
1Instituto de Ciências Biomédicas de Abel Salazar, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
2Laboratório de Genética Molecular, Instituto de Biologia Molecular e Celular, Universidade do Porto, 4150-180 Porto, Portugal
Address correspondence to Claudio E. Sunkel, Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal. Tel.: 351-22-607-4900. Fax: 351-22-609-9157. E-mail: [email protected]
The online version of this article includes supplemental material.
H. Maiato and P. Sampaio contributed equally to this work.
*
Abbreviations used in this paper: ds, double stranded; GFP, green fluorescent protein; MAP, microtubule-associated protein; MAST, multiple asters; RNAi, dsRNA-mediated interference; NEB, nuclear envelope breakdown.
Received:
January 23 2002
Revision Received:
March 28 2002
Accepted:
April 09 2002
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2002
J Cell Biol (2002) 157 (5): 749–760.
Article history
Received:
January 23 2002
Revision Received:
March 28 2002
Accepted:
April 09 2002
Citation
Helder Maiato, Paula Sampaio, Catarina L. Lemos, John Findlay, Mar Carmena, William C. Earnshaw, Claudio E. Sunkel; MAST/Orbit has a role in microtubule–kinetochore attachment and is essential for chromosome alignment and maintenance of spindle bipolarity . J Cell Biol 28 May 2002; 157 (5): 749–760. doi: https://doi.org/10.1083/jcb.200201101
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