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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2018
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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. |
format | Online Article Text |
id | pubmed-6085823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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