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Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process

The parasitic protozoan Leishmania alternates between an invertebrate and a mammalian host. Upon their entry to mammalian macrophages, Leishmania promastigotes differentiate into amastigote forms within the harsh environment of the phagolysosomal compartment. Here, we provide evidence for the import...

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Autores principales: Cloutier, Serge, Laverdière, Maxime, Chou, Marie-Noelle, Boilard, Nathalie, Chow, Conan, Papadopoulou, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365078/
https://www.ncbi.nlm.nih.gov/pubmed/22693545
http://dx.doi.org/10.1371/journal.pone.0035085
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author Cloutier, Serge
Laverdière, Maxime
Chou, Marie-Noelle
Boilard, Nathalie
Chow, Conan
Papadopoulou, Barbara
author_facet Cloutier, Serge
Laverdière, Maxime
Chou, Marie-Noelle
Boilard, Nathalie
Chow, Conan
Papadopoulou, Barbara
author_sort Cloutier, Serge
collection PubMed
description The parasitic protozoan Leishmania alternates between an invertebrate and a mammalian host. Upon their entry to mammalian macrophages, Leishmania promastigotes differentiate into amastigote forms within the harsh environment of the phagolysosomal compartment. Here, we provide evidence for the importance of translational control during the Leishmania differentiation process. We find that exposure of promastigotes to a combined elevated temperature and acidic pH stress, a key signal triggering amastigote differentiation, leads to a marked decrease in global translation initiation, which is associated with eIF2α phosphorylation. Interestingly, we show that amastigotes adapted to grow in a cell-free medium exhibit lower levels of protein synthesis in comparison to promastigotes, suggesting that amastigotes have to enter a slow growth state to adapt to the stressful conditions encountered inside macrophages. Reconversion of amastigotes back to promastigote growth results in upregulation of global translation and a decrease in eIF2α phosphorylation. In addition, we show that while general translation is reduced during amastigote differentiation, translation of amastigote-specific transcripts such as A2 is preferentially upregulated. We find that A2 developmental gene regulation is triggered by temperature changes in the environment and that occurs mainly at the level of translation. Upon elevated temperature, the A2 transcript is stabilized through its association with polyribosomes leading to high levels of translation. When temperature decreases during amastigote to promastigote differentiation, the A2 transcript is not longer associated with translating polyribosomes and is being gradually degraded. Overall, these findings contribute to our better understanding of the adaptive responses of Leishmania to stress during its development and highlight the importance of translational control in promastigote to amastigote differentiation and vice-versa.
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spelling pubmed-33650782012-06-12 Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process Cloutier, Serge Laverdière, Maxime Chou, Marie-Noelle Boilard, Nathalie Chow, Conan Papadopoulou, Barbara PLoS One Research Article The parasitic protozoan Leishmania alternates between an invertebrate and a mammalian host. Upon their entry to mammalian macrophages, Leishmania promastigotes differentiate into amastigote forms within the harsh environment of the phagolysosomal compartment. Here, we provide evidence for the importance of translational control during the Leishmania differentiation process. We find that exposure of promastigotes to a combined elevated temperature and acidic pH stress, a key signal triggering amastigote differentiation, leads to a marked decrease in global translation initiation, which is associated with eIF2α phosphorylation. Interestingly, we show that amastigotes adapted to grow in a cell-free medium exhibit lower levels of protein synthesis in comparison to promastigotes, suggesting that amastigotes have to enter a slow growth state to adapt to the stressful conditions encountered inside macrophages. Reconversion of amastigotes back to promastigote growth results in upregulation of global translation and a decrease in eIF2α phosphorylation. In addition, we show that while general translation is reduced during amastigote differentiation, translation of amastigote-specific transcripts such as A2 is preferentially upregulated. We find that A2 developmental gene regulation is triggered by temperature changes in the environment and that occurs mainly at the level of translation. Upon elevated temperature, the A2 transcript is stabilized through its association with polyribosomes leading to high levels of translation. When temperature decreases during amastigote to promastigote differentiation, the A2 transcript is not longer associated with translating polyribosomes and is being gradually degraded. Overall, these findings contribute to our better understanding of the adaptive responses of Leishmania to stress during its development and highlight the importance of translational control in promastigote to amastigote differentiation and vice-versa. Public Library of Science 2012-05-31 /pmc/articles/PMC3365078/ /pubmed/22693545 http://dx.doi.org/10.1371/journal.pone.0035085 Text en Cloutier et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cloutier, Serge
Laverdière, Maxime
Chou, Marie-Noelle
Boilard, Nathalie
Chow, Conan
Papadopoulou, Barbara
Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title_full Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title_fullStr Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title_full_unstemmed Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title_short Translational Control through eIF2alpha Phosphorylation during the Leishmania Differentiation Process
title_sort translational control through eif2alpha phosphorylation during the leishmania differentiation process
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365078/
https://www.ncbi.nlm.nih.gov/pubmed/22693545
http://dx.doi.org/10.1371/journal.pone.0035085
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