Login / Signup

Characterization of a MOB1 Homolog in the Apicomplexan Parasite Toxoplasma gondii .

Inês L S DelgadoAlexandra TavaresSamuel FranciscoDulce SantosJoão CoelhoAfonso P BastoSara ZúqueteJoachim MüllerAndrew HemphillMarkus MeissnerHelena SoaresAlexandre LeitãoSofia Nolasco
Published in: Biology (2021)
Monopolar spindle One Binder1 (MOB1) proteins are conserved components of the tumor-suppressing Hippo pathway, regulating cellular processes such as cytokinesis. Apicomplexan parasites present a life cycle that relies on the parasites' ability to differentiate between stages and regulate their proliferation; thus, Hippo signaling pathways could play an important role in the regulation of the apicomplexan life cycle. Here, we report the identification of one MOB1 protein in the apicomplexan Toxoplasma gondii . To characterize the function of MOB1, we generated gain-of-function transgenic lines with a ligand-controlled destabilization domain, and loss-of-function clonal lines obtained through CRISPR/Cas9 technology. Contrary to what has been characterized in other eukaryotes, MOB1 is not essential for cytokinesis in T. gondii . However, this picture is complex since we found MOB1 localized between the newly individualized daughter nuclei at the end of mitosis. Moreover, we detected a significant delay in the replication of overexpressing tachyzoites, contrasting with increased replication rates in knockout tachyzoites. Finally, using the proximity-biotinylation method, BioID, we identified novel members of the MOB1 interactome, a probable consequence of the observed lack of conservation of some key amino acid residues. Altogether, the results point to a complex evolutionary history of MOB1 roles in apicomplexans, sharing properties with other eukaryotes but also with divergent features, possibly associated with their complex life cycle.
Keyphrases
  • life cycle
  • toxoplasma gondii
  • signaling pathway
  • crispr cas
  • amino acid
  • healthcare
  • oxidative stress
  • genome editing
  • plasmodium falciparum
  • transcription factor
  • binding protein
  • cell proliferation
  • induced apoptosis