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Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis
Microtubules are dynamic cytoskeleton filaments that are essential for a wide range of cellular processes. They are polymerized from tubulin, a heterodimer of α- and β-subunits. Most eukaryotic organisms express multiple isotypes of α- and β-tubulin, yet their functional relevance in any organism re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576917/ https://www.ncbi.nlm.nih.gov/pubmed/34739032 http://dx.doi.org/10.1083/jcb.202010155 |
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author | Nsamba, Emmanuel T. Bera, Abesh Costanzo, Michael Boone, Charles Gupta, Mohan L. |
author_facet | Nsamba, Emmanuel T. Bera, Abesh Costanzo, Michael Boone, Charles Gupta, Mohan L. |
author_sort | Nsamba, Emmanuel T. |
collection | PubMed |
description | Microtubules are dynamic cytoskeleton filaments that are essential for a wide range of cellular processes. They are polymerized from tubulin, a heterodimer of α- and β-subunits. Most eukaryotic organisms express multiple isotypes of α- and β-tubulin, yet their functional relevance in any organism remains largely obscure. The two α-tubulin isotypes in budding yeast, Tub1 and Tub3, are proposed to be functionally interchangeable, yet their individual functions have not been rigorously interrogated. Here, we develop otherwise isogenic yeast strains expressing single tubulin isotypes at levels comparable to total tubulin in WT cells. Using genome-wide screening, we uncover unique interactions between the isotypes and the two major mitotic spindle positioning mechanisms. We further exploit these cells to demonstrate that Tub1 and Tub3 optimize spindle positioning by differentially recruiting key components of the Dyn1- and Kar9-dependent mechanisms, respectively. Our results provide novel mechanistic insights into how tubulin isotypes allow highly conserved microtubules to function in diverse cellular processes. |
format | Online Article Text |
id | pubmed-8576917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85769172022-06-06 Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis Nsamba, Emmanuel T. Bera, Abesh Costanzo, Michael Boone, Charles Gupta, Mohan L. J Cell Biol Article Microtubules are dynamic cytoskeleton filaments that are essential for a wide range of cellular processes. They are polymerized from tubulin, a heterodimer of α- and β-subunits. Most eukaryotic organisms express multiple isotypes of α- and β-tubulin, yet their functional relevance in any organism remains largely obscure. The two α-tubulin isotypes in budding yeast, Tub1 and Tub3, are proposed to be functionally interchangeable, yet their individual functions have not been rigorously interrogated. Here, we develop otherwise isogenic yeast strains expressing single tubulin isotypes at levels comparable to total tubulin in WT cells. Using genome-wide screening, we uncover unique interactions between the isotypes and the two major mitotic spindle positioning mechanisms. We further exploit these cells to demonstrate that Tub1 and Tub3 optimize spindle positioning by differentially recruiting key components of the Dyn1- and Kar9-dependent mechanisms, respectively. Our results provide novel mechanistic insights into how tubulin isotypes allow highly conserved microtubules to function in diverse cellular processes. Rockefeller University Press 2021-11-05 /pmc/articles/PMC8576917/ /pubmed/34739032 http://dx.doi.org/10.1083/jcb.202010155 Text en © 2021 Nsamba et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/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 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Nsamba, Emmanuel T. Bera, Abesh Costanzo, Michael Boone, Charles Gupta, Mohan L. Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title | Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title_full | Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title_fullStr | Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title_full_unstemmed | Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title_short | Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
title_sort | tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576917/ https://www.ncbi.nlm.nih.gov/pubmed/34739032 http://dx.doi.org/10.1083/jcb.202010155 |
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