Modeling a disease-correlated tubulin mutation in budding yeast reveals insight into MAP-mediated dynein function

• Published in: Molecular biology of the cell Vol. 32; no. 20; p. ar10
• Main Authors: Denarier, E, Ecklund, K H, Berthier, G, Favier, A, O'Toole, E T, Gory-Fauré, S, De Macedo, L, Delphin, C, Andrieux, A, Markus, S M, Boscheron, C
• Format: Journal Article
• Language: English
• Published: United States American Society for Cell Biology 01-10-2021; The American Society for Cell Biology
• Subjects: Biochemistry, Molecular Biology; Dyneins - genetics; Dyneins - metabolism; Electron Microscope Tomography - methods; Lectins, C-Type - genetics; Lectins, C-Type - metabolism; Life Sciences; Microtubule-Associated Proteins - metabolism; Microtubules - metabolism; Mutation; Neurodevelopmental Disorders - metabolism; Neurogenesis; Phenotype; Receptors, Mitogen - genetics; Receptors, Mitogen - metabolism; Saccharomyces cerevisiae - metabolism; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism; Saccharomycetales - metabolism; Spindle Apparatus - metabolism; Structural Biology; Tubulin - genetics; Tubulin - metabolism
• ISSN: 1059-1524; 1939-4586
• DOI: 10.1091/mbc.E21-05-0237

Mutations in the genes that encode α- and β-tubulin underlie many neurological diseases, most notably malformations in cortical development. In addition to revealing the molecular basis for disease etiology, studying such mutations can provide insight into microtubule function and the role of the large family of microtubule effectors. In this study, we use budding yeast to model one such mutation-Gly436Arg in α-tubulin, which is causative of malformations in cortical development-in order to understand how it impacts microtubule function in a simple eukaryotic system. Using a combination of in vitro and in vivo methodologies, including live cell imaging and electron tomography, we find that the mutant tubulin is incorporated into microtubules, causes a shift in α-tubulin isotype usage, and dramatically enhances dynein activity, which leads to spindle-positioning defects. We find that the basis for the latter phenotype is an impaired interaction between She1-a dynein inhibitor-and the mutant microtubules. In addition to revealing the natural balance of α-tubulin isotype utilization in cells, our results provide evidence of an impaired interaction between microtubules and a dynein regulator as a consequence of a tubulin mutation and sheds light on a mechanism that may be causative of neurodevelopmental diseases.