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Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables

Microtubules and actin filaments interact and cooperate in many processes in eukaryotic cells, but the functional implications of such interactions are not well understood. In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed for spindle orientation. In...

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Detalles Bibliográficos
Autores principales: Hwang, Eric, Kusch, Justine, Barral, Yves, Huffaker, Tim C.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172944/
https://www.ncbi.nlm.nih.gov/pubmed/12743102
http://dx.doi.org/10.1083/jcb.200302030
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author Hwang, Eric
Kusch, Justine
Barral, Yves
Huffaker, Tim C.
author_facet Hwang, Eric
Kusch, Justine
Barral, Yves
Huffaker, Tim C.
author_sort Hwang, Eric
collection PubMed
description Microtubules and actin filaments interact and cooperate in many processes in eukaryotic cells, but the functional implications of such interactions are not well understood. In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed for spindle orientation. In addition, this process requires the type V myosin protein Myo2, the microtubule end–binding protein Bim1, and Kar9. Here, we show that fusing Bim1 to the tail of the Myo2 is sufficient to orient spindles in the absence of Kar9, suggesting that the role of Kar9 is to link Myo2 to Bim1. In addition, we show that Myo2 localizes to the plus ends of cytoplasmic microtubules, and that the rate of movement of these cytoplasmic microtubules to the bud neck depends on the intrinsic velocity of Myo2 along actin filaments. These results support a model for spindle orientation in which a Myo2–Kar9–Bim1 complex transports microtubule ends along polarized actin cables. We also present data suggesting that a similar process plays a role in orienting cytoplasmic microtubules in mating yeast cells.
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spelling pubmed-21729442008-05-01 Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables Hwang, Eric Kusch, Justine Barral, Yves Huffaker, Tim C. J Cell Biol Report Microtubules and actin filaments interact and cooperate in many processes in eukaryotic cells, but the functional implications of such interactions are not well understood. In the yeast Saccharomyces cerevisiae, both cytoplasmic microtubules and actin filaments are needed for spindle orientation. In addition, this process requires the type V myosin protein Myo2, the microtubule end–binding protein Bim1, and Kar9. Here, we show that fusing Bim1 to the tail of the Myo2 is sufficient to orient spindles in the absence of Kar9, suggesting that the role of Kar9 is to link Myo2 to Bim1. In addition, we show that Myo2 localizes to the plus ends of cytoplasmic microtubules, and that the rate of movement of these cytoplasmic microtubules to the bud neck depends on the intrinsic velocity of Myo2 along actin filaments. These results support a model for spindle orientation in which a Myo2–Kar9–Bim1 complex transports microtubule ends along polarized actin cables. We also present data suggesting that a similar process plays a role in orienting cytoplasmic microtubules in mating yeast cells. The Rockefeller University Press 2003-05-12 /pmc/articles/PMC2172944/ /pubmed/12743102 http://dx.doi.org/10.1083/jcb.200302030 Text en Copyright © 2003, 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 Report
Hwang, Eric
Kusch, Justine
Barral, Yves
Huffaker, Tim C.
Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title_full Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title_fullStr Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title_full_unstemmed Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title_short Spindle orientation in Saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
title_sort spindle orientation in saccharomyces cerevisiae depends on the transport of microtubule ends along polarized actin cables
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172944/
https://www.ncbi.nlm.nih.gov/pubmed/12743102
http://dx.doi.org/10.1083/jcb.200302030
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