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Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly

To function in diverse cellular processes, the dynamic properties of microtubules must be tightly regulated. Cellular microtubules are influenced by a multitude of regulatory proteins, but how their activities are spatiotemporally coordinated within the cell, or on specific microtubules, remains mos...

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Autores principales: Dave, Sandeep, Anderson, Samuel J., Sinha Roy, Pallavi, Nsamba, Emmanuel T., Bunning, Angela R., Fukuda, Yusuke, Gupta, Mohan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085823/
https://www.ncbi.nlm.nih.gov/pubmed/29874146
http://dx.doi.org/10.1091/mbc.E18-03-0199
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author Dave, Sandeep
Anderson, Samuel J.
Sinha Roy, Pallavi
Nsamba, Emmanuel T.
Bunning, Angela R.
Fukuda, Yusuke
Gupta, Mohan L.
author_facet Dave, Sandeep
Anderson, Samuel J.
Sinha Roy, Pallavi
Nsamba, Emmanuel T.
Bunning, Angela R.
Fukuda, Yusuke
Gupta, Mohan L.
author_sort Dave, Sandeep
collection PubMed
description To function in diverse cellular processes, the dynamic properties of microtubules must be tightly regulated. Cellular microtubules are influenced by a multitude of regulatory proteins, but how their activities are spatiotemporally coordinated within the cell, or on specific microtubules, remains mostly obscure. The conserved kinesin-8 motor proteins are important microtubule regulators, and family members from diverse species combine directed motility with the ability to modify microtubule dynamics. Yet how kinesin-8 activities are appropriately deployed in the cellular context is largely unknown. Here we reveal the importance of the nonmotor tail in differentially controlling the physiological functions of the budding yeast kinesin-8, Kip3. We demonstrate that the tailless Kip3 motor domain adequately governs microtubule dynamics at the bud tip to allow spindle positioning in early mitosis. Notably, discrete regions of the tail mediate specific functions of Kip3 on astral and spindle microtubules. The region proximal to the motor domain operates to spatially regulate astral microtubule stability, while the distal tail serves a previously unrecognized role to control the timing of mitotic spindle disassembly. These findings provide insights into how nonmotor tail domains differentially control kinesin functions in cells and the mechanisms that spatiotemporally control the stability of cellular microtubules.
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spelling pubmed-60858232018-10-16 Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly Dave, Sandeep Anderson, Samuel J. Sinha Roy, Pallavi Nsamba, Emmanuel T. Bunning, Angela R. Fukuda, Yusuke Gupta, Mohan L. Mol Biol Cell Articles To function in diverse cellular processes, the dynamic properties of microtubules must be tightly regulated. Cellular microtubules are influenced by a multitude of regulatory proteins, but how their activities are spatiotemporally coordinated within the cell, or on specific microtubules, remains mostly obscure. The conserved kinesin-8 motor proteins are important microtubule regulators, and family members from diverse species combine directed motility with the ability to modify microtubule dynamics. Yet how kinesin-8 activities are appropriately deployed in the cellular context is largely unknown. Here we reveal the importance of the nonmotor tail in differentially controlling the physiological functions of the budding yeast kinesin-8, Kip3. We demonstrate that the tailless Kip3 motor domain adequately governs microtubule dynamics at the bud tip to allow spindle positioning in early mitosis. Notably, discrete regions of the tail mediate specific functions of Kip3 on astral and spindle microtubules. The region proximal to the motor domain operates to spatially regulate astral microtubule stability, while the distal tail serves a previously unrecognized role to control the timing of mitotic spindle disassembly. These findings provide insights into how nonmotor tail domains differentially control kinesin functions in cells and the mechanisms that spatiotemporally control the stability of cellular microtubules. The American Society for Cell Biology 2018-08-01 /pmc/articles/PMC6085823/ /pubmed/29874146 http://dx.doi.org/10.1091/mbc.E18-03-0199 Text en © 2018 Dave et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Dave, Sandeep
Anderson, Samuel J.
Sinha Roy, Pallavi
Nsamba, Emmanuel T.
Bunning, Angela R.
Fukuda, Yusuke
Gupta, Mohan L.
Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title_full Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title_fullStr Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title_full_unstemmed Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title_short Discrete regions of the kinesin-8 Kip3 tail differentially mediate astral microtubule stability and spindle disassembly
title_sort discrete regions of the kinesin-8 kip3 tail differentially mediate astral microtubule stability and spindle disassembly
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085823/
https://www.ncbi.nlm.nih.gov/pubmed/29874146
http://dx.doi.org/10.1091/mbc.E18-03-0199
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