Tubulin isotypes contribute opposing properties to balance anaphase spindle morphogenesis

J Cell Biol. 2025 Sep 1;224(9):e202301115. doi: 10.1083/jcb.202301115. Epub 2025 Jul 25.

Abstract

Faithful chromosome segregation requires proper function of the mitotic spindle, which is built from, and depends on, the coordinated regulation of many microtubules and the activities of molecular motors and MAPs. In addition, microtubules themselves are assembled from multiple variants, or isotypes of α- and β-tubulin, yet whether they mediate the activities of motors and MAPs required for proper spindle function remains poorly understood. Here, we use budding yeast to reveal that α-tubulin isotypes regulate opposing outward- and inward-directed forces in the spindle midzone that facilitate optimal spindle elongation and length control. Moreover, we show that the isotypes mediate balanced spindle forces by differentially localizing the antagonistic force generators Cin8 (kinesin-5) and Kar3 (kinesin-14) to interpolar microtubules. Our results reveal new roles for tubulin isotypes in orchestrating motor and MAP activities and provide insights into how forces in the spindle are properly calibrated to ensure proper mitotic spindle morphogenesis.

MeSH terms

  • Anaphase*
  • Chromosome Segregation
  • Kinesins / genetics
  • Kinesins / metabolism
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / metabolism
  • Morphogenesis
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Saccharomyces cerevisiae Proteins* / genetics
  • Saccharomyces cerevisiae Proteins* / metabolism
  • Saccharomyces cerevisiae* / genetics
  • Saccharomyces cerevisiae* / metabolism
  • Spindle Apparatus* / genetics
  • Spindle Apparatus* / metabolism
  • Tubulin* / genetics
  • Tubulin* / metabolism

Substances

  • Saccharomyces cerevisiae Proteins
  • Tubulin
  • Kinesins
  • Microtubule-Associated Proteins
  • CIN8 protein, S cerevisiae
  • KAR3 protein, S cerevisiae
  • Protein Isoforms