Acetylation of Nup62 by TIP60 ensures accurate chromosome segregation in mitosis

J Mol Cell Biol. 2022 Dec 26;14(8):mjac056. doi: 10.1093/jmcb/mjac056.

Abstract

Stable transmission of genetic information during cell division requires faithful mitotic spindle assembly and chromosome segregation. In eukaryotic cells, nuclear envelope breakdown (NEBD) is required for proper chromosome segregation. Although a list of mitotic kinases has been implicated in NEBD, how they coordinate their activity to dissolve the nuclear envelope and protein machinery such as nuclear pore complexes was unclear. Here, we identified a regulatory mechanism in which Nup62 is acetylated by TIP60 in human cell division. Nup62 is a novel substrate of TIP60, and the acetylation of Lys432 by TIP60 dissolves nucleoporin Nup62-Nup58-Nup54 complex during entry into mitosis. Importantly, this acetylation-elicited remodeling of nucleoporin complex promotes the distribution of Nup62 to the mitotic spindle, which is indispensable for orchestrating correct spindle orientation. Moreover, suppression of Nup62 perturbs accurate chromosome segregation during mitosis. These results establish a previously uncharacterized regulatory mechanism in which TIP60-elicited nucleoporin dynamics promotes chromosome segregation in mitosis.

Keywords: Nup62; TIP60; acetylation; mitosis; spindle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Chromosome Segregation*
  • Humans
  • Lysine Acetyltransferase 5* / metabolism
  • Mitosis
  • Nuclear Envelope / metabolism
  • Nuclear Pore Complex Proteins* / genetics
  • Nuclear Pore Complex Proteins* / metabolism

Substances

  • Nuclear Pore Complex Proteins
  • nuclear pore protein p62
  • KAT5 protein, human
  • Lysine Acetyltransferase 5