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Published on: April 29, 2020
Identification and Molecular Dissection of IMC32, a Conserved Toxoplasma Inner Membrane Complex Protein That Is
Juan A Torres1, Rebecca R Pasquarelli2, Peter S Back2
1Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, Los Angeles, California, USA.
Abstract:
The inner membrane complex (IMC) is a unique organelle of apicomplexan parasites that plays critical roles in parasite motility, host cell invasion, and replication. Despite the common functions of the organelle, relatively few IMC proteins are conserved across the phylum and the precise roles of many IMC components remain to be characterized. Here, we identify a novel component of the Toxoplasma gondii IMC (IMC32) that localizes to the body portion of the IMC and is recruited to developing daughter buds early during endodyogeny. IMC32 is essential for parasite survival, as its conditional depletion results in a complete collapse of the IMC that is lethal to the parasite. We demonstrate that localization of IMC32 is dependent on both an N-terminal palmitoylation site and a series of C-terminal coiled-coil domains. Using deletion analyses and functional complementation, we show that two conserved regions within the C-terminal coiled-coil domains play critical roles in protein function during replication. Together, this work reveals an essential component of parasite replication that provides a novel target for therapeutic intervention of T. gondii and related apicomplexan parasites.IMPORTANCE The IMC is an important organelle that apicomplexan parasites use to maintain their intracellular lifestyle. While many IMC proteins have been identified, only a few central players that are essential for internal budding have been described and even fewer are conserved across the phylum. Here, we identify IMC32, a novel component of the Toxoplasma gondii IMC that localizes to very early daughter buds, indicating a role in the early stages of parasite replication. We then demonstrate that IMC32 is essential for parasite survival and pinpoint conserved regions within the protein that are important for membrane association and daughter cell formation. As IMC32 is unique to these parasites and not present in their mammalian hosts, it serves as a new target for the development of drugs that exclusively affect these important intracellular pathogens.
Insights
We identified IMC32, a novel protein essential for the inner membrane complex (IMC) in *Toxoplasma gondii*. Its depletion causes IMC collapse, proving lethal and highlighting IMC32 as a potential therapeutic target for apicomplexan parasites.
Area of Science:
- Cell Biology
- Parasitology
- Molecular Biology
Background:
- The inner membrane complex (IMC) is vital for apicomplexan parasite functions like motility and invasion.
- Few IMC proteins are conserved, and many component roles remain unclear.
Purpose of the Study:
- Identify and characterize novel IMC components in *Toxoplasma gondii*.
- Investigate the function and essentiality of IMC32 in parasite replication.
Main Methods:
- Conditional depletion of IMC32.
- Localization studies using microscopy.
- Analysis of IMC32 domains (palmitoylation, coiled-coil).
- Functional complementation assays.
Main Results:
- IMC32 localizes to the IMC body and early daughter buds during endodyogeny.
- Conditional IMC32 depletion leads to IMC collapse and parasite death.
- N-terminal palmitoylation and C-terminal coiled-coil domains are crucial for IMC32 localization and function.
- Conserved regions within coiled-coil domains are critical for replication.
Conclusions:
- IMC32 is an essential IMC component required for *Toxoplasma gondii* survival and replication.
- IMC32's specific role in early daughter bud formation is critical.
- IMC32 represents a promising, parasite-specific therapeutic target.
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