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A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes

Trypanosoma brucei glutaredoxin 2 (Grx2) is a dithiol glutaredoxin that is specifically located in the mitochondrial intermembrane space. Bloodstream form parasites lacking Grx2 or both, Grx2 and the cytosolic Grx1, are viable in vitro and infectious to mice suggesting that neither oxidoreductase is...

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Autores principales: Ebersoll, Samantha, Musunda, Blessing, Schmenger, Torsten, Dirdjaja, Natalie, Bonilla, Mariana, Manta, Bruno, Ulrich, Kathrin, Comini, Marcelo A., Krauth-Siegel, R. Luise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975080/
https://www.ncbi.nlm.nih.gov/pubmed/29413965
http://dx.doi.org/10.1016/j.redox.2018.01.011
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author Ebersoll, Samantha
Musunda, Blessing
Schmenger, Torsten
Dirdjaja, Natalie
Bonilla, Mariana
Manta, Bruno
Ulrich, Kathrin
Comini, Marcelo A.
Krauth-Siegel, R. Luise
author_facet Ebersoll, Samantha
Musunda, Blessing
Schmenger, Torsten
Dirdjaja, Natalie
Bonilla, Mariana
Manta, Bruno
Ulrich, Kathrin
Comini, Marcelo A.
Krauth-Siegel, R. Luise
author_sort Ebersoll, Samantha
collection PubMed
description Trypanosoma brucei glutaredoxin 2 (Grx2) is a dithiol glutaredoxin that is specifically located in the mitochondrial intermembrane space. Bloodstream form parasites lacking Grx2 or both, Grx2 and the cytosolic Grx1, are viable in vitro and infectious to mice suggesting that neither oxidoreductase is needed for survival or infectivity to mammals. A 37 °C to 39 °C shift changes the cellular redox milieu of bloodstream cells to more oxidizing conditions and induces a significantly stronger growth arrest in wildtype parasites compared to the mutant cells. Grx2-deficient cells ectopically expressing the wildtype form of Grx2 with its C31QFC34 active site, but not the C34S mutant, regain the sensitivity of the parental strain, indicating that the physiological role of Grx2 requires both active site cysteines. In the procyclic insect stage of the parasite, Grx2 is essential. Both alleles can be replaced if procyclic cells ectopically express authentic or C34S, but not C31S/C34S Grx2, pointing to a redox role that relies on a monothiol mechanism. RNA-interference against Grx2 causes a virtually irreversible proliferation defect. The cells adopt an elongated morphology but do not show any significant alteration in the cell cycle. The growth retardation is attenuated by high glucose concentrations. Under these conditions, procyclic cells obtain ATP by substrate level phosphorylation suggesting that Grx2 might regulate a respiratory chain component.
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spelling pubmed-59750802018-05-31 A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes Ebersoll, Samantha Musunda, Blessing Schmenger, Torsten Dirdjaja, Natalie Bonilla, Mariana Manta, Bruno Ulrich, Kathrin Comini, Marcelo A. Krauth-Siegel, R. Luise Redox Biol Research Paper Trypanosoma brucei glutaredoxin 2 (Grx2) is a dithiol glutaredoxin that is specifically located in the mitochondrial intermembrane space. Bloodstream form parasites lacking Grx2 or both, Grx2 and the cytosolic Grx1, are viable in vitro and infectious to mice suggesting that neither oxidoreductase is needed for survival or infectivity to mammals. A 37 °C to 39 °C shift changes the cellular redox milieu of bloodstream cells to more oxidizing conditions and induces a significantly stronger growth arrest in wildtype parasites compared to the mutant cells. Grx2-deficient cells ectopically expressing the wildtype form of Grx2 with its C31QFC34 active site, but not the C34S mutant, regain the sensitivity of the parental strain, indicating that the physiological role of Grx2 requires both active site cysteines. In the procyclic insect stage of the parasite, Grx2 is essential. Both alleles can be replaced if procyclic cells ectopically express authentic or C34S, but not C31S/C34S Grx2, pointing to a redox role that relies on a monothiol mechanism. RNA-interference against Grx2 causes a virtually irreversible proliferation defect. The cells adopt an elongated morphology but do not show any significant alteration in the cell cycle. The growth retardation is attenuated by high glucose concentrations. Under these conditions, procyclic cells obtain ATP by substrate level phosphorylation suggesting that Grx2 might regulate a respiratory chain component. Elsevier 2018-01-31 /pmc/articles/PMC5975080/ /pubmed/29413965 http://dx.doi.org/10.1016/j.redox.2018.01.011 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Ebersoll, Samantha
Musunda, Blessing
Schmenger, Torsten
Dirdjaja, Natalie
Bonilla, Mariana
Manta, Bruno
Ulrich, Kathrin
Comini, Marcelo A.
Krauth-Siegel, R. Luise
A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title_full A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title_fullStr A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title_full_unstemmed A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title_short A glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of African trypanosomes
title_sort glutaredoxin in the mitochondrial intermembrane space has stage-specific functions in the thermo-tolerance and proliferation of african trypanosomes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5975080/
https://www.ncbi.nlm.nih.gov/pubmed/29413965
http://dx.doi.org/10.1016/j.redox.2018.01.011
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