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The ZIP Code of Vesicle Trafficking in Apicomplexa: SEC1/Munc18 and SNARE Proteins

Hugo Bisio, Rouaa Ben Chaabene, Ricarda Sabitzki, Bohumil Maco, Jean Baptiste Marq, Tim‐Wolf Gilberger, Tobias Spielmann, Dominique Soldati‐Favre

2020mBio46 citationsDOIOpen Access PDF

Abstract

The phylum of Apicomplexa groups medically relevant parasites such as those responsible for malaria and toxoplasmosis. As members of the Alveolata superphylum, these protozoans possess specialized organelles in addition to those found in all members of the eukaryotic kingdom. Vesicular trafficking is the major route of communication between membranous organelles. Neither the molecular mechanism that allows communication between organelles nor the vesicular fusion events that underlie it are completely understood in Apicomplexa. Here, we assessed the function of SEC1/Munc18 and SNARE proteins to identify factors involved in the trafficking of vesicles between these various organelles. We show that SEC1/Munc18 in interaction with SNARE proteins allows targeting of vesicles to the inner membrane complex, prerhoptries, micronemes, apicoplast, and vacuolar compartment from the endoplasmic reticulum, Golgi apparatus, or endosomal-like compartment. These data provide an exciting look at the "ZIP code" of vesicular trafficking in apicomplexans, essential for precise organelle biogenesis, homeostasis, and inheritance.

Topics & Concepts

BiologyEndosomeOrganelleApicomplexaApicoplastEndoplasmic reticulumBiogenesisOrganelle biogenesisCell biologyGolgi apparatusVesicleVesicular transport proteinVesicle fusionSynaptic vesicleGeneticsPlasmodium falciparumGeneMalariaIntracellularMembraneImmunologyToxoplasma gondii Research StudiesCellular transport and secretionProtist diversity and phylogeny
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