SUMOylation stabilizes sister kinetochore biorientation to allow timely anaphase

J Cell Biol. 2021 Jul 5;220(7):e202005130. doi: 10.1083/jcb.202005130.

Abstract

During mitosis, sister chromatids attach to microtubules from opposite poles, called biorientation. Sister chromatid cohesion resists microtubule forces, generating tension, which provides the signal that biorientation has occurred. How tension silences the surveillance pathways that prevent cell cycle progression and correct erroneous kinetochore-microtubule attachments remains unclear. Here we show that SUMOylation dampens error correction to allow stable sister kinetochore biorientation and timely anaphase onset. The Siz1/Siz2 SUMO ligases modify the pericentromere-localized shugoshin (Sgo1) protein before its tension-dependent release from chromatin. Sgo1 SUMOylation reduces its binding to protein phosphatase 2A (PP2A), and weakening of this interaction is important for stable biorientation. Unstable biorientation in SUMO-deficient cells is associated with persistence of the chromosome passenger complex (CPC) at centromeres, and SUMOylation of CPC subunit Bir1 also contributes to timely anaphase onset. We propose that SUMOylation acts in a combinatorial manner to facilitate dismantling of the error correction machinery within pericentromeres and thereby sharpen the metaphase-anaphase transition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / genetics*
  • Chromatids / genetics
  • Chromosome Segregation / genetics*
  • Humans
  • Kinetochores
  • Mitosis / genetics
  • Nuclear Proteins / genetics*
  • Protein Phosphatase 2 / genetics
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae Proteins / genetics*
  • Spindle Apparatus / genetics
  • Sumoylation / genetics
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Bir1 protein, S cerevisiae
  • Carrier Proteins
  • Nuclear Proteins
  • Saccharomyces cerevisiae Proteins
  • Sgo1 protein, S cerevisiae
  • Siz2 protein, S cerevisiae
  • Ubiquitin-Protein Ligases
  • Protein Phosphatase 2
  • Siz1 protein, S cerevisiae