Tubulin isotypes optimize distinct spindle positioning mechanisms during yeast mitosis

Author:

Nsamba Emmanuel T.1ORCID,Bera Abesh1,Costanzo Michael2ORCID,Boone Charles234,Gupta Mohan L.1ORCID

Affiliation:

1. Genetics, Development, and Cell Biology, Iowa State University, Ames, IA

2. Donnelly Centre, University of Toronto, Toronto, Ontario, Canada

3. Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

4. Chemical Genomics Research Group, RIKEN Center for Sustainable Resource Sciences, Saitama, Japan

Abstract

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.

Funder

Canadian Institutes of Health Research

National Institutes of Health

National Science Foundation

Publisher

Rockefeller University Press

Subject

Cell Biology

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