Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Nsamba, Emmanuel T., Bera, Abesh, Costanzo, Michael, Boone, Charles, Gupta, Mohan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
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
_version_ 1784595974234046464
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
work_keys_str_mv AT nsambaemmanuelt tubulinisotypesoptimizedistinctspindlepositioningmechanismsduringyeastmitosis
AT beraabesh tubulinisotypesoptimizedistinctspindlepositioningmechanismsduringyeastmitosis
AT costanzomichael tubulinisotypesoptimizedistinctspindlepositioningmechanismsduringyeastmitosis
AT boonecharles tubulinisotypesoptimizedistinctspindlepositioningmechanismsduringyeastmitosis
AT guptamohanl tubulinisotypesoptimizedistinctspindlepositioningmechanismsduringyeastmitosis