4.4 Article

Mps1 regulates spindle morphology through MCRS1 to promote chromosome alignment

Journal

MOLECULAR BIOLOGY OF THE CELL
Volume 30, Issue 9, Pages 1060-1068

Publisher

AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E18-09-0546

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Funding

  1. NYU-ECNU Center for Computational Chemistry at NYU Shanghai
  2. National Science Foundation of China [31671412]
  3. New York University at Shanghai

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Accurate partitioning of chromosomes during mitosis is essential for genetic stability and requires the assembly of the dynamic mitotic spindle and proper kinetochore-microtubule attachment. The spindle assembly checkpoint (SAC) monitors the incompleteness and errors in kinetochore-microtubule attachment and delays anaphase. The SAC kinase Mps1 regulates the recruitment of downstream effectors to unattached kinetochores. Mps1 also actively promotes chromosome alignment during metaphase, but the underlying mechanism is not completely understood. Here, we show that Mps1 regulates chromosome alignment through MCRS1, a spindle assembly factor that controls the dynamics of the minus end of kinetochore microtubules. Mps1 binds and phosphorylates MCRS1. This mechanism enables KIF2A localization to the minus end of spindle microtubules. Thus, our study reveals a novel role of Mps1 in regulating the dynamics of the minus end of microtubules and expands the functions of Mps1 in genome maintenance.

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