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The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex

In budding yeast, the mitotic spindle moves into the neck between the mother and bud via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud. How dynein and microtubules interact with the cortex is unknown. We found that cells lacking Num1p failed to exhibit dynein-depen...

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Autores principales: Heil-Chapdelaine, Richard A., Oberle, Jessica R., Cooper, John A.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190597/
https://www.ncbi.nlm.nih.gov/pubmed/11121446
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author Heil-Chapdelaine, Richard A.
Oberle, Jessica R.
Cooper, John A.
author_facet Heil-Chapdelaine, Richard A.
Oberle, Jessica R.
Cooper, John A.
author_sort Heil-Chapdelaine, Richard A.
collection PubMed
description In budding yeast, the mitotic spindle moves into the neck between the mother and bud via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud. How dynein and microtubules interact with the cortex is unknown. We found that cells lacking Num1p failed to exhibit dynein-dependent microtubule sliding in the bud, resulting in defective mitotic spindle movement and nuclear segregation. Num1p localized to the bud cortex, and that localization was independent of microtubules, dynein, or dynactin. These data are consistent with Num1p being an essential element of the cortical attachment mechanism for dynein-dependent sliding of microtubules in the bud.
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spelling pubmed-21905972008-05-01 The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex Heil-Chapdelaine, Richard A. Oberle, Jessica R. Cooper, John A. J Cell Biol Report In budding yeast, the mitotic spindle moves into the neck between the mother and bud via dynein-dependent sliding of cytoplasmic microtubules along the cortex of the bud. How dynein and microtubules interact with the cortex is unknown. We found that cells lacking Num1p failed to exhibit dynein-dependent microtubule sliding in the bud, resulting in defective mitotic spindle movement and nuclear segregation. Num1p localized to the bud cortex, and that localization was independent of microtubules, dynein, or dynactin. These data are consistent with Num1p being an essential element of the cortical attachment mechanism for dynein-dependent sliding of microtubules in the bud. The Rockefeller University Press 2000-12-11 /pmc/articles/PMC2190597/ /pubmed/11121446 Text en © 2000 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
Heil-Chapdelaine, Richard A.
Oberle, Jessica R.
Cooper, John A.
The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title_full The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title_fullStr The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title_full_unstemmed The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title_short The Cortical Protein Num1p Is Essential for Dynein-Dependent Interactions of Microtubules with the Cortex
title_sort cortical protein num1p is essential for dynein-dependent interactions of microtubules with the cortex
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190597/
https://www.ncbi.nlm.nih.gov/pubmed/11121446
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