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Translational Repression in Malaria Sporozoites

Malaria is a mosquito-borne infectious disease of humans and other animals. It is caused by the parasitic protozoan, Plasmodium. Sporozoites, the infectious form of malaria parasites, are quiescent when they remain in the salivary glands of the Anopheles mosquito until transmission into a mammalian...

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Autores principales: Turque, Oliver, Tsao, Tiffany, Li, Thomas, Zhang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349151/
https://www.ncbi.nlm.nih.gov/pubmed/28357358
http://dx.doi.org/10.15698/mic2016.05.502
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author Turque, Oliver
Tsao, Tiffany
Li, Thomas
Zhang, Min
author_facet Turque, Oliver
Tsao, Tiffany
Li, Thomas
Zhang, Min
author_sort Turque, Oliver
collection PubMed
description Malaria is a mosquito-borne infectious disease of humans and other animals. It is caused by the parasitic protozoan, Plasmodium. Sporozoites, the infectious form of malaria parasites, are quiescent when they remain in the salivary glands of the Anopheles mosquito until transmission into a mammalian host. Metamorphosis of the dormant sporozoite to its active form in the liver stage requires transcriptional and translational regulations. Here, we summarize recent advances in the translational repression of gene expression in the malaria sporozoite. In sporozoites, many mRNAs that are required for liver stage development are translationally repressed. Phosphorylation of eukaryotic Initiation Factor 2α (eIF2α) leads to a global translational repression in sporozoites. The eIF2α kinase, known as Upregulated in Infectious Sporozoite 1 (UIS1), is dominant in the sporozoite. The eIF2α phosphatase, UIS2, is translationally repressed by the Pumilio protein Puf2. This translational repression is alleviated when sporozoites are delivered into the mammalian host.
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spelling pubmed-53491512017-03-29 Translational Repression in Malaria Sporozoites Turque, Oliver Tsao, Tiffany Li, Thomas Zhang, Min Microb Cell Microbiology Malaria is a mosquito-borne infectious disease of humans and other animals. It is caused by the parasitic protozoan, Plasmodium. Sporozoites, the infectious form of malaria parasites, are quiescent when they remain in the salivary glands of the Anopheles mosquito until transmission into a mammalian host. Metamorphosis of the dormant sporozoite to its active form in the liver stage requires transcriptional and translational regulations. Here, we summarize recent advances in the translational repression of gene expression in the malaria sporozoite. In sporozoites, many mRNAs that are required for liver stage development are translationally repressed. Phosphorylation of eukaryotic Initiation Factor 2α (eIF2α) leads to a global translational repression in sporozoites. The eIF2α kinase, known as Upregulated in Infectious Sporozoite 1 (UIS1), is dominant in the sporozoite. The eIF2α phosphatase, UIS2, is translationally repressed by the Pumilio protein Puf2. This translational repression is alleviated when sporozoites are delivered into the mammalian host. Shared Science Publishers OG 2016-04-05 /pmc/articles/PMC5349151/ /pubmed/28357358 http://dx.doi.org/10.15698/mic2016.05.502 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microbiology
Turque, Oliver
Tsao, Tiffany
Li, Thomas
Zhang, Min
Translational Repression in Malaria Sporozoites
title Translational Repression in Malaria Sporozoites
title_full Translational Repression in Malaria Sporozoites
title_fullStr Translational Repression in Malaria Sporozoites
title_full_unstemmed Translational Repression in Malaria Sporozoites
title_short Translational Repression in Malaria Sporozoites
title_sort translational repression in malaria sporozoites
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349151/
https://www.ncbi.nlm.nih.gov/pubmed/28357358
http://dx.doi.org/10.15698/mic2016.05.502
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