Toxoplasma ERK7 protects the apical complex from premature degradation

J Cell Biol. 2023 Jun 5;222(6):e202209098. doi: 10.1083/jcb.202209098. Epub 2023 Apr 7.

Abstract

Accurate cellular replication balances the biogenesis and turnover of complex structures. In the apicomplexan parasite Toxoplasma gondii, daughter cells form within an intact mother cell, creating additional challenges to ensuring fidelity of division. The apical complex is critical to parasite infectivity and consists of apical secretory organelles and specialized cytoskeletal structures. We previously identified the kinase ERK7 as required for maturation of the apical complex in Toxoplasma. Here, we define the Toxoplasma ERK7 interactome, including a putative E3 ligase, CSAR1. Genetic disruption of CSAR1 fully suppresses loss of the apical complex upon ERK7 knockdown. Furthermore, we show that CSAR1 is normally responsible for turnover of maternal cytoskeleton during cytokinesis, and that its aberrant function is driven by mislocalization from the parasite residual body to the apical complex. These data identify a protein homeostasis pathway critical for Toxoplasma replication and fitness and suggest an unappreciated role for the parasite residual body in compartmentalizing processes that threaten the fidelity of parasite development.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Division
  • Cytokinesis
  • Cytoskeleton / metabolism
  • Extracellular Signal-Regulated MAP Kinases* / genetics
  • Extracellular Signal-Regulated MAP Kinases* / metabolism
  • Organelles / metabolism
  • Protozoan Proteins* / genetics
  • Protozoan Proteins* / metabolism
  • Toxoplasma* / enzymology
  • Toxoplasma* / genetics
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Protozoan Proteins
  • Extracellular Signal-Regulated MAP Kinases
  • Ubiquitin-Protein Ligases