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Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa

BACKGROUND: Kinesin-5 (Eg-5) motor proteins are essential for maintenance of spindle bipolarity in animals. The roles of Kinesin-5 proteins in other systems, such as Arabidopsis, Dictyostelium, and sea urchin are more varied. We are studying Kinesin-5-like proteins during early development in the br...

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Autores principales: Peters, Nick T, Miller, Anne Catherine, Kropf, Darryl L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706839/
https://www.ncbi.nlm.nih.gov/pubmed/19527496
http://dx.doi.org/10.1186/1756-0500-2-106
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author Peters, Nick T
Miller, Anne Catherine
Kropf, Darryl L
author_facet Peters, Nick T
Miller, Anne Catherine
Kropf, Darryl L
author_sort Peters, Nick T
collection PubMed
description BACKGROUND: Kinesin-5 (Eg-5) motor proteins are essential for maintenance of spindle bipolarity in animals. The roles of Kinesin-5 proteins in other systems, such as Arabidopsis, Dictyostelium, and sea urchin are more varied. We are studying Kinesin-5-like proteins during early development in the brown alga Silvetia compressa. Previously, this motor was shown to be needed to assemble a bipolar spindle, similar to animals. This report builds on those findings by investigating the localization of the motor and probing its function in spindle maintenance. FINDINGS: Anti-Eg5 antibodies were used to investigate localization of Kinesin-5-like proteins in brown algal zygotes. In interphase zygotes, localization was predominantly within the nucleus. As zygotes entered mitosis, these motor proteins strongly associated with spindle poles and, to a lesser degree, with the polar microtubule arrays and the spindle midzone. In order to address whether Kinesin-5-like proteins are required to maintain spindle bipolarity, we applied monastrol to synchronized zygotes containing bipolar spindles. Monastrol is a cell-permeable chemical inhibitor of the Kinesin-5 class of molecular motors. We found that inhibition of motor function in pre-formed spindles induced the formation of multipolar spindles and short bipolar spindles. CONCLUSION: Based upon these localization and inhibitor studies, we conclude that Kinesin-5-like motors in brown algae are more similar to the motors of animals than those of plants or protists. However, Kinesin-5-like proteins in S. compressa serve novel roles in spindle formation and maintenance not observed in animals.
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spelling pubmed-27068392009-07-08 Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa Peters, Nick T Miller, Anne Catherine Kropf, Darryl L BMC Res Notes Short Report BACKGROUND: Kinesin-5 (Eg-5) motor proteins are essential for maintenance of spindle bipolarity in animals. The roles of Kinesin-5 proteins in other systems, such as Arabidopsis, Dictyostelium, and sea urchin are more varied. We are studying Kinesin-5-like proteins during early development in the brown alga Silvetia compressa. Previously, this motor was shown to be needed to assemble a bipolar spindle, similar to animals. This report builds on those findings by investigating the localization of the motor and probing its function in spindle maintenance. FINDINGS: Anti-Eg5 antibodies were used to investigate localization of Kinesin-5-like proteins in brown algal zygotes. In interphase zygotes, localization was predominantly within the nucleus. As zygotes entered mitosis, these motor proteins strongly associated with spindle poles and, to a lesser degree, with the polar microtubule arrays and the spindle midzone. In order to address whether Kinesin-5-like proteins are required to maintain spindle bipolarity, we applied monastrol to synchronized zygotes containing bipolar spindles. Monastrol is a cell-permeable chemical inhibitor of the Kinesin-5 class of molecular motors. We found that inhibition of motor function in pre-formed spindles induced the formation of multipolar spindles and short bipolar spindles. CONCLUSION: Based upon these localization and inhibitor studies, we conclude that Kinesin-5-like motors in brown algae are more similar to the motors of animals than those of plants or protists. However, Kinesin-5-like proteins in S. compressa serve novel roles in spindle formation and maintenance not observed in animals. BioMed Central 2009-06-15 /pmc/articles/PMC2706839/ /pubmed/19527496 http://dx.doi.org/10.1186/1756-0500-2-106 Text en Copyright © 2009 Peters et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Peters, Nick T
Miller, Anne Catherine
Kropf, Darryl L
Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title_full Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title_fullStr Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title_full_unstemmed Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title_short Localization and function of Kinesin-5-like proteins during assembly and maintenance of mitotic spindles in Silvetia compressa
title_sort localization and function of kinesin-5-like proteins during assembly and maintenance of mitotic spindles in silvetia compressa
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706839/
https://www.ncbi.nlm.nih.gov/pubmed/19527496
http://dx.doi.org/10.1186/1756-0500-2-106
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