MCRS1 modulates the heterogeneity of microtubule minus-end morphologies in mitotic spindles. Academic Article uri icon

Overview

abstract

  • Faithful chromosome segregation requires the assembly of a bipolar spindle, consisting of two antiparallel microtubule (MT) arrays having most of their minus ends focused at the spindle poles and their plus ends overlapping in the spindle midzone. Spindle assembly, chromosome alignment, and segregation require highly dynamic MTs. The plus ends of MTs have been extensively investigated but their minus-end structure remains poorly characterized. Here, we used large-scale electron tomography to study the morphology of the MT minus ends in three dimensionally reconstructed metaphase spindles in HeLa cells. In contrast to the homogeneous open morphology of the MT plus ends at the kinetochores, we found that MT minus ends are heterogeneous, showing either open or closed morphologies. Silencing the minus end-specific stabilizer, MCRS1 increased the proportion of open MT minus ends. Altogether, these data suggest a correlation between the morphology and the dynamic state of the MT ends. Taking this heterogeneity of the MT minus-end morphologies into account, our work indicates an unsynchronized behavior of MTs at the spindle poles, thus laying the groundwork for further studies on the complexity of MT dynamics regulation.

publication date

  • November 9, 2022

Research

keywords

  • Kinesins
  • Spindle Apparatus

Identity

PubMed Central ID

  • PMC9816640

Scopus Document Identifier

  • 85144586021

Digital Object Identifier (DOI)

  • 10.5281/zenodo.3937716

PubMed ID

  • 36350698

Additional Document Info

volume

  • 34

issue

  • 1