Bub1 and CENP-U redundantly recruit Plk1 to stabilize kinetochore-microtubule attachments and ensure accurate chromosome segregation

Cell Rep. 2021 Sep 21;36(12):109740. doi: 10.1016/j.celrep.2021.109740.

Abstract

Bub1 is required for the kinetochore/centromere localization of two essential mitotic kinases Plk1 and Aurora B. Surprisingly, stable depletion of Bub1 by ∼95% in human cells marginally affects whole chromosome segregation fidelity. We show that CENP-U, which is recruited to kinetochores by the CENP-P and CENP-Q subunits of the CENP-O complex, is required to prevent chromosome mis-segregation in Bub1-depleted cells. Mechanistically, Bub1 and CENP-U redundantly recruit Plk1 to kinetochores to stabilize kinetochore-microtubule attachments, thereby ensuring accurate chromosome segregation. Furthermore, unlike its budding yeast homolog, the CENP-O complex does not regulate centromeric localization of Aurora B. Consistently, depletion of Bub1 or CENP-U sensitizes cells to the inhibition of Plk1 but not Aurora B kinase activity. Taken together, our findings provide mechanistic insight into the regulation of kinetochore function, which may have implications for targeted treatment of cancer cells with mutations perturbing kinetochore recruitment of Plk1 by Bub1 or the CENP-O complex.

Keywords: Bub1; CENP-U; Plk1; chromosome alignment; chromosome segregation; kinetochore; kinetochore-microtubule attachment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aurora Kinase B / metabolism
  • Benzimidazoles / pharmacology
  • CRISPR-Cas Systems / genetics
  • Cell Cycle Proteins / antagonists & inhibitors
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Centromere / metabolism
  • Chromosome Segregation / drug effects
  • Chromosome Segregation / physiology*
  • HeLa Cells
  • Histones / antagonists & inhibitors
  • Histones / genetics
  • Histones / metabolism*
  • Humans
  • Kinetochores / metabolism*
  • Microscopy, Fluorescence
  • Microtubules / metabolism*
  • Polo-Like Kinase 1
  • Poly-ADP-Ribose Binding Proteins / metabolism
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / antagonists & inhibitors
  • Proto-Oncogene Proteins / metabolism*
  • RNA Interference
  • RNA, Guide, CRISPR-Cas Systems
  • RNA, Small Interfering / metabolism
  • Thiophenes / pharmacology
  • Time-Lapse Imaging

Substances

  • BUB3 protein, human
  • Benzimidazoles
  • CENPU protein, human
  • Cell Cycle Proteins
  • GSK 461364
  • Histones
  • Poly-ADP-Ribose Binding Proteins
  • Proto-Oncogene Proteins
  • RNA, Small Interfering
  • Thiophenes
  • Aurora Kinase B
  • BUB1 protein, human
  • Protein Serine-Threonine Kinases