Aurora B kinase activity-dependent and -independent functions of the chromosomal passenger complex in regulating sister chromatid cohesion

J Biol Chem. 2019 Feb 8;294(6):2021-2035. doi: 10.1074/jbc.RA118.005978. Epub 2018 Dec 6.

Abstract

The chromosomal passenger complex (CPC) is a master regulator of mitosis. CPC consists of inner centromere protein (INCENP), Survivin, Borealin, and the kinase Aurora B and plays key roles in regulating kinetochore-microtubule attachments and spindle assembly checkpoint signaling. However, the role of CPC in sister chromatid cohesion, mediated by the cohesin complex, remains incompletely understood. Here, we show that Aurora B kinase activity contributes to centromeric cohesion protection partly through promoting kinetochore localization of the kinase Bub1. Interestingly, disrupting the interaction of INCENP with heterochromatin protein 1 (HP1) in HeLa cells selectively weakens cohesion at mitotic centromeres without detectably reducing the kinase activity of Aurora B. Thus, through this INCENP-HP1 interaction, the CPC also protects centromeric cohesion independently of Aurora B kinase activity. Moreover, the requirement for the INCENP-HP1 interaction in centromeric cohesion protection can be bypassed by tethering HP1 to centromeres or by depleting the cohesin release factor Wapl. We provide further evidence suggesting that the INCENP-HP1 interaction protects centromeric cohesion by promoting the centromere localization of Haspin, a protein kinase that antagonizes Wapl activity at centromeres. Taken together, this study identifies Aurora B kinase activity-dependent and -independent roles for the CPC in regulating centromeric cohesion during mitosis in human cells.

Keywords: Aurora B; Haspin; INCENP; cell cycle; centromere; chromosomal passenger complex; cohesin; heterochromatin protein 1; histone modification; kinetochore; mitosis; sister chromatid cohesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aurora Kinase B / genetics
  • Aurora Kinase B / metabolism*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Centromere / genetics
  • Centromere / metabolism*
  • Chromatids / genetics
  • Chromatids / metabolism*
  • Chromobox Protein Homolog 5
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosomal Proteins, Non-Histone / metabolism
  • HeLa Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Mitosis / physiology*
  • Multiprotein Complexes / genetics
  • Multiprotein Complexes / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism

Substances

  • Carrier Proteins
  • Chromosomal Proteins, Non-Histone
  • INCENP protein, human
  • Intracellular Signaling Peptides and Proteins
  • Multiprotein Complexes
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • WAPL protein, human
  • Chromobox Protein Homolog 5
  • AURKB protein, human
  • Aurora Kinase B
  • HASPIN protein, human
  • Protein Serine-Threonine Kinases