Structure of the RZZ complex and molecular basis of Spindly-driven corona assembly at human kinetochores

EMBO J. 2022 May 2;41(9):e110411. doi: 10.15252/embj.2021110411. Epub 2022 Apr 4.

Abstract

In metazoans, a ≈1 megadalton (MDa) multiprotein complex comprising the dynein-dynactin adaptor Spindly and the ROD-Zwilch-ZW10 (RZZ) complex is the building block of a fibrous biopolymer, the kinetochore fibrous corona. The corona assembles on mitotic kinetochores to promote microtubule capture and spindle assembly checkpoint (SAC) signaling. We report here a high-resolution cryo-EM structure that captures the essential features of the RZZ complex, including a farnesyl-binding site required for Spindly binding. Using a highly predictive in vitro assay, we demonstrate that the SAC kinase MPS1 is necessary and sufficient for corona assembly at supercritical concentrations of the RZZ-Spindly (RZZS) complex, and describe the molecular mechanism of phosphorylation-dependent filament nucleation. We identify several structural requirements for RZZS polymerization in rings and sheets. Finally, we identify determinants of kinetochore localization and corona assembly of Spindly. Our results describe a framework for the long-sought-for molecular basis of corona assembly on metazoan kinetochores.

Keywords: RZZ; centromere; fibrous corona; kinetochore; spindle assembly checkpoint.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / metabolism
  • Cell Cycle Proteins / metabolism
  • Humans
  • Kinetochores* / metabolism
  • Microtubule-Associated Proteins / metabolism
  • Microtubules / metabolism
  • Spindle Apparatus* / metabolism

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • Microtubule-Associated Proteins

Associated data

  • PDB/7QPG