A noncatalytic function of the topoisomerase II CTD in Aurora B recruitment to inner centromeres during mitosis

J Cell Biol. 2016 Jun 20;213(6):651-64. doi: 10.1083/jcb.201511080.

Abstract

Faithful chromosome segregation depends on the precise timing of chromatid separation, which is enforced by checkpoint signals generated at kinetochores. Here, we provide evidence that the C-terminal domain (CTD) of DNA topoisomerase IIα (Topo II) provides a novel function at inner centromeres of kinetochores in mitosis. We find that the yeast CTD is required for recruitment of the tension checkpoint kinase Ipl1/Aurora B to inner centromeres in metaphase but is not required in interphase. Conserved CTD SUMOylation sites are required for Ipl1 recruitment. This inner-centromere CTD function is distinct from the catalytic activity of Topo II. Genetic and biochemical evidence suggests that Topo II recruits Ipl1 via the Haspin-histone H3 threonine 3 phosphorylation pathway. Finally, Topo II and Sgo1 are equally important for Ipl1 recruitment to inner centromeres. This indicates H3 T3-Phos/H2A T120-Phos is a universal epigenetic signature that defines the eukaryotic inner centromere and provides the binding site for Ipl1/Aurora B.

MeSH terms

  • Antigens, Neoplasm / metabolism*
  • Aurora Kinase B / metabolism*
  • Cell Cycle Proteins / metabolism
  • Centromere / metabolism*
  • Centromere / physiology*
  • Chromatids / metabolism
  • Chromosome Segregation / physiology
  • DNA Topoisomerases, Type II / metabolism*
  • DNA-Binding Proteins / metabolism*
  • Fungal Proteins / metabolism
  • Histones / metabolism
  • Kinetochores / metabolism
  • Kinetochores / physiology
  • Metaphase / physiology*
  • Phosphorylation / physiology
  • Protein Serine-Threonine Kinases / metabolism
  • Sumoylation / physiology
  • Yeasts / metabolism
  • Yeasts / physiology

Substances

  • Antigens, Neoplasm
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Fungal Proteins
  • Histones
  • Aurora Kinase B
  • Protein Serine-Threonine Kinases
  • DNA Topoisomerases, Type II