Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.

Conventional reverse genetic approaches for study of Plasmodium malaria parasite gene function are limited, or not applicable. Hence, new inducible systems are needed. Here we describe a method to control P. falciparum gene expression in which target genes bearing a glmS ribozyme in the 3' untr...

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Autores principales: Parichat Prommana, Chairat Uthaipibull, Chayaphat Wongsombat, Sumalee Kamchonwongpaisan, Yongyuth Yuthavong, Ellen Knuepfer, Anthony A Holder, Philip J Shaw
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Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/cbdb79dbc4e3405a975346b77b49e550
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spelling oai:doaj.org-article:cbdb79dbc4e3405a975346b77b49e5502021-11-18T08:57:31ZInducible knockdown of Plasmodium gene expression using the glmS ribozyme.1932-620310.1371/journal.pone.0073783https://doaj.org/article/cbdb79dbc4e3405a975346b77b49e5502013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24023691/?tool=EBIhttps://doaj.org/toc/1932-6203Conventional reverse genetic approaches for study of Plasmodium malaria parasite gene function are limited, or not applicable. Hence, new inducible systems are needed. Here we describe a method to control P. falciparum gene expression in which target genes bearing a glmS ribozyme in the 3' untranslated region are efficiently knocked down in transgenic P. falciparum parasites in response to glucosamine inducer. Using reporter genes, we show that the glmS ribozyme cleaves reporter mRNA in vivo leading to reduction in mRNA expression following glucosamine treatment. Glucosamine-induced ribozyme activation led to efficient reduction of reporter protein, which could be rapidly reversed by removing the inducer. The glmS ribozyme was validated as a reverse-genetic tool by integration into the essential gene and antifolate drug target dihydrofolate reductase-thymidylate synthase (PfDHFR-TS). Glucosamine treatment of transgenic parasites led to rapid and efficient knockdown of PfDHFR-TS mRNA and protein. PfDHFR-TS knockdown led to a growth/arrest mutant phenotype and hypersensitivity to pyrimethamine. The glmS ribozyme may thus be a tool for study of essential genes in P. falciparum and other parasite species amenable to transfection.Parichat PrommanaChairat UthaipibullChayaphat WongsombatSumalee KamchonwongpaisanYongyuth YuthavongEllen KnuepferAnthony A HolderPhilip J ShawPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 8, p e73783 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Parichat Prommana
Chairat Uthaipibull
Chayaphat Wongsombat
Sumalee Kamchonwongpaisan
Yongyuth Yuthavong
Ellen Knuepfer
Anthony A Holder
Philip J Shaw
Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
description Conventional reverse genetic approaches for study of Plasmodium malaria parasite gene function are limited, or not applicable. Hence, new inducible systems are needed. Here we describe a method to control P. falciparum gene expression in which target genes bearing a glmS ribozyme in the 3' untranslated region are efficiently knocked down in transgenic P. falciparum parasites in response to glucosamine inducer. Using reporter genes, we show that the glmS ribozyme cleaves reporter mRNA in vivo leading to reduction in mRNA expression following glucosamine treatment. Glucosamine-induced ribozyme activation led to efficient reduction of reporter protein, which could be rapidly reversed by removing the inducer. The glmS ribozyme was validated as a reverse-genetic tool by integration into the essential gene and antifolate drug target dihydrofolate reductase-thymidylate synthase (PfDHFR-TS). Glucosamine treatment of transgenic parasites led to rapid and efficient knockdown of PfDHFR-TS mRNA and protein. PfDHFR-TS knockdown led to a growth/arrest mutant phenotype and hypersensitivity to pyrimethamine. The glmS ribozyme may thus be a tool for study of essential genes in P. falciparum and other parasite species amenable to transfection.
format article
author Parichat Prommana
Chairat Uthaipibull
Chayaphat Wongsombat
Sumalee Kamchonwongpaisan
Yongyuth Yuthavong
Ellen Knuepfer
Anthony A Holder
Philip J Shaw
author_facet Parichat Prommana
Chairat Uthaipibull
Chayaphat Wongsombat
Sumalee Kamchonwongpaisan
Yongyuth Yuthavong
Ellen Knuepfer
Anthony A Holder
Philip J Shaw
author_sort Parichat Prommana
title Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
title_short Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
title_full Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
title_fullStr Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
title_full_unstemmed Inducible knockdown of Plasmodium gene expression using the glmS ribozyme.
title_sort inducible knockdown of plasmodium gene expression using the glms ribozyme.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/cbdb79dbc4e3405a975346b77b49e550
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