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Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii

BACKGROUND: The lytic cycle of the protozoan parasite Toxoplasma gondii, which involves a brief sojourn in the extracellular space, is characterized by defined transcriptional profiles. For an obligate intracellular parasite that is shielded from the cytosolic host immune factors by a parasitophorou...

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Autores principales: Hassan, Musa A., Vasquez, Juan J., Guo-Liang, Chew, Meissner, Markus, Nicolai Siegel, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725899/
https://www.ncbi.nlm.nih.gov/pubmed/29228904
http://dx.doi.org/10.1186/s12864-017-4362-6
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author Hassan, Musa A.
Vasquez, Juan J.
Guo-Liang, Chew
Meissner, Markus
Nicolai Siegel, T.
author_facet Hassan, Musa A.
Vasquez, Juan J.
Guo-Liang, Chew
Meissner, Markus
Nicolai Siegel, T.
author_sort Hassan, Musa A.
collection PubMed
description BACKGROUND: The lytic cycle of the protozoan parasite Toxoplasma gondii, which involves a brief sojourn in the extracellular space, is characterized by defined transcriptional profiles. For an obligate intracellular parasite that is shielded from the cytosolic host immune factors by a parasitophorous vacuole, the brief entry into the extracellular space is likely to exert enormous stress. Due to its role in cellular stress response, we hypothesize that translational control plays an important role in regulating gene expression in Toxoplasma during the lytic cycle. Unlike transcriptional profiles, insights into genome-wide translational profiles of Toxoplasma gondii are lacking. METHODS: We have performed genome-wide ribosome profiling, coupled with high throughput RNA sequencing, in intracellular and extracellular Toxoplasma gondii parasites to investigate translational control during the lytic cycle. RESULTS: Although differences in transcript abundance were mostly mirrored at the translational level, we observed significant differences in the abundance of ribosome footprints between the two parasite stages. Furthermore, our data suggest that mRNA translation in the parasite is potentially regulated by mRNA secondary structure and upstream open reading frames. CONCLUSION: We show that most of the Toxoplasma genes that are dysregulated during the lytic cycle are translationally regulated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4362-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-57258992017-12-13 Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii Hassan, Musa A. Vasquez, Juan J. Guo-Liang, Chew Meissner, Markus Nicolai Siegel, T. BMC Genomics Research Article BACKGROUND: The lytic cycle of the protozoan parasite Toxoplasma gondii, which involves a brief sojourn in the extracellular space, is characterized by defined transcriptional profiles. For an obligate intracellular parasite that is shielded from the cytosolic host immune factors by a parasitophorous vacuole, the brief entry into the extracellular space is likely to exert enormous stress. Due to its role in cellular stress response, we hypothesize that translational control plays an important role in regulating gene expression in Toxoplasma during the lytic cycle. Unlike transcriptional profiles, insights into genome-wide translational profiles of Toxoplasma gondii are lacking. METHODS: We have performed genome-wide ribosome profiling, coupled with high throughput RNA sequencing, in intracellular and extracellular Toxoplasma gondii parasites to investigate translational control during the lytic cycle. RESULTS: Although differences in transcript abundance were mostly mirrored at the translational level, we observed significant differences in the abundance of ribosome footprints between the two parasite stages. Furthermore, our data suggest that mRNA translation in the parasite is potentially regulated by mRNA secondary structure and upstream open reading frames. CONCLUSION: We show that most of the Toxoplasma genes that are dysregulated during the lytic cycle are translationally regulated. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4362-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-11 /pmc/articles/PMC5725899/ /pubmed/29228904 http://dx.doi.org/10.1186/s12864-017-4362-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hassan, Musa A.
Vasquez, Juan J.
Guo-Liang, Chew
Meissner, Markus
Nicolai Siegel, T.
Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title_full Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title_fullStr Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title_full_unstemmed Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title_short Comparative ribosome profiling uncovers a dominant role for translational control in Toxoplasma gondii
title_sort comparative ribosome profiling uncovers a dominant role for translational control in toxoplasma gondii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725899/
https://www.ncbi.nlm.nih.gov/pubmed/29228904
http://dx.doi.org/10.1186/s12864-017-4362-6
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