Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.

Apicomplexan parasites are global killers, being the causative agents of diseases like toxoplasmosis and malaria. These parasites are known to be hypersensitive to redox imbalance, yet little is understood about the cellular roles of their various redox regulators. The apicoplast, an essential plast...

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Main Authors: Marco Biddau, Anne Bouchut, Jack Major, Tracy Saveria, Julie Tottey, Ojore Oka, Marcel van-Lith, Katherine Elizabeth Jennings, Jana Ovciarikova, Amy DeRocher, Boris Striepen, Ross Frederick Waller, Marilyn Parsons, Lilach Sheiner
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-02-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1006836
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spelling doaj-971e47a9d0744ad6bcce81deef63eef62021-04-21T17:54:30ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742018-02-01142e100683610.1371/journal.ppat.1006836Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.Marco BiddauAnne BouchutJack MajorTracy SaveriaJulie TotteyOjore OkaMarcel van-LithKatherine Elizabeth JenningsJana OvciarikovaAmy DeRocherBoris StriepenRoss Frederick WallerMarilyn ParsonsLilach SheinerApicomplexan parasites are global killers, being the causative agents of diseases like toxoplasmosis and malaria. These parasites are known to be hypersensitive to redox imbalance, yet little is understood about the cellular roles of their various redox regulators. The apicoplast, an essential plastid organelle, is a verified apicomplexan drug target. Nuclear-encoded apicoplast proteins traffic through the ER and multiple apicoplast sub-compartments to their place of function. We propose that thioredoxins contribute to the control of protein trafficking and of protein function within these apicoplast compartments. We studied the role of two Toxoplasma gondii apicoplast thioredoxins (TgATrx), both essential for parasite survival. By describing the cellular phenotypes of the conditional depletion of either of these redox regulated enzymes we show that each of them contributes to a different apicoplast biogenesis pathway. We provide evidence for TgATrx1's involvement in ER to apicoplast trafficking and TgATrx2 in the control of apicoplast gene expression components. Substrate pull-down further recognizes gene expression factors that interact with TgATrx2. We use genetic complementation to demonstrate that the function of both TgATrxs is dependent on their disulphide exchange activity. Finally, TgATrx2 is divergent from human thioredoxins. We demonstrate its activity in vitro thus providing scope for drug screening. Our study represents the first functional characterization of thioredoxins in Toxoplasma, highlights the importance of redox regulation of apicoplast functions and provides new tools to study redox biology in these parasites.https://doi.org/10.1371/journal.ppat.1006836
collection DOAJ
language English
format Article
sources DOAJ
author Marco Biddau
Anne Bouchut
Jack Major
Tracy Saveria
Julie Tottey
Ojore Oka
Marcel van-Lith
Katherine Elizabeth Jennings
Jana Ovciarikova
Amy DeRocher
Boris Striepen
Ross Frederick Waller
Marilyn Parsons
Lilach Sheiner
spellingShingle Marco Biddau
Anne Bouchut
Jack Major
Tracy Saveria
Julie Tottey
Ojore Oka
Marcel van-Lith
Katherine Elizabeth Jennings
Jana Ovciarikova
Amy DeRocher
Boris Striepen
Ross Frederick Waller
Marilyn Parsons
Lilach Sheiner
Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
PLoS Pathogens
author_facet Marco Biddau
Anne Bouchut
Jack Major
Tracy Saveria
Julie Tottey
Ojore Oka
Marcel van-Lith
Katherine Elizabeth Jennings
Jana Ovciarikova
Amy DeRocher
Boris Striepen
Ross Frederick Waller
Marilyn Parsons
Lilach Sheiner
author_sort Marco Biddau
title Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
title_short Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
title_full Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
title_fullStr Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
title_full_unstemmed Two essential Thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in Toxoplasma gondii.
title_sort two essential thioredoxins mediate apicoplast biogenesis, protein import, and gene expression in toxoplasma gondii.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2018-02-01
description Apicomplexan parasites are global killers, being the causative agents of diseases like toxoplasmosis and malaria. These parasites are known to be hypersensitive to redox imbalance, yet little is understood about the cellular roles of their various redox regulators. The apicoplast, an essential plastid organelle, is a verified apicomplexan drug target. Nuclear-encoded apicoplast proteins traffic through the ER and multiple apicoplast sub-compartments to their place of function. We propose that thioredoxins contribute to the control of protein trafficking and of protein function within these apicoplast compartments. We studied the role of two Toxoplasma gondii apicoplast thioredoxins (TgATrx), both essential for parasite survival. By describing the cellular phenotypes of the conditional depletion of either of these redox regulated enzymes we show that each of them contributes to a different apicoplast biogenesis pathway. We provide evidence for TgATrx1's involvement in ER to apicoplast trafficking and TgATrx2 in the control of apicoplast gene expression components. Substrate pull-down further recognizes gene expression factors that interact with TgATrx2. We use genetic complementation to demonstrate that the function of both TgATrxs is dependent on their disulphide exchange activity. Finally, TgATrx2 is divergent from human thioredoxins. We demonstrate its activity in vitro thus providing scope for drug screening. Our study represents the first functional characterization of thioredoxins in Toxoplasma, highlights the importance of redox regulation of apicoplast functions and provides new tools to study redox biology in these parasites.
url https://doi.org/10.1371/journal.ppat.1006836
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