Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.

Genetically-modified mutants are now indispensable Plasmodium gene-function reagents, which are also being pursued as genetically attenuated parasite vaccines. Currently, the generation of transgenic malaria-parasites requires the use of drug-resistance markers. Here we present the development of an...

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Main Authors: Ben C L van Schaijk, Martijn W Vos, Chris J Janse, Robert W Sauerwein, Shahid M Khan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2994908?pdf=render
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spelling doaj-d4ba889c13ea4bb0b1eca8d1024b28ad2020-11-25T02:09:26ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-01511e1512110.1371/journal.pone.0015121Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.Ben C L van SchaijkMartijn W VosChris J JanseRobert W SauerweinShahid M KhanGenetically-modified mutants are now indispensable Plasmodium gene-function reagents, which are also being pursued as genetically attenuated parasite vaccines. Currently, the generation of transgenic malaria-parasites requires the use of drug-resistance markers. Here we present the development of an FRT/FLP-recombinase system that enables the generation of transgenic parasites free of resistance genes. We demonstrate in the human malaria parasite, P. falciparum, the complete and efficient removal of the introduced resistance gene. We targeted two neighbouring genes, p52 and p36, using a construct that has a selectable marker cassette flanked by FRT-sequences. This permitted the subsequent removal of the selectable marker cassette by transient transfection of a plasmid that expressed a 37°C thermostable and enhanced FLP-recombinase. This method of removing heterologous DNA sequences from the genome opens up new possibilities in Plasmodium research to sequentially target multiple genes and for using genetically-modified parasites as live, attenuated malaria vaccines.http://europepmc.org/articles/PMC2994908?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ben C L van Schaijk
Martijn W Vos
Chris J Janse
Robert W Sauerwein
Shahid M Khan
spellingShingle Ben C L van Schaijk
Martijn W Vos
Chris J Janse
Robert W Sauerwein
Shahid M Khan
Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
PLoS ONE
author_facet Ben C L van Schaijk
Martijn W Vos
Chris J Janse
Robert W Sauerwein
Shahid M Khan
author_sort Ben C L van Schaijk
title Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
title_short Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
title_full Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
title_fullStr Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
title_full_unstemmed Removal of heterologous sequences from Plasmodium falciparum mutants using FLPe-recombinase.
title_sort removal of heterologous sequences from plasmodium falciparum mutants using flpe-recombinase.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-01-01
description Genetically-modified mutants are now indispensable Plasmodium gene-function reagents, which are also being pursued as genetically attenuated parasite vaccines. Currently, the generation of transgenic malaria-parasites requires the use of drug-resistance markers. Here we present the development of an FRT/FLP-recombinase system that enables the generation of transgenic parasites free of resistance genes. We demonstrate in the human malaria parasite, P. falciparum, the complete and efficient removal of the introduced resistance gene. We targeted two neighbouring genes, p52 and p36, using a construct that has a selectable marker cassette flanked by FRT-sequences. This permitted the subsequent removal of the selectable marker cassette by transient transfection of a plasmid that expressed a 37°C thermostable and enhanced FLP-recombinase. This method of removing heterologous DNA sequences from the genome opens up new possibilities in Plasmodium research to sequentially target multiple genes and for using genetically-modified parasites as live, attenuated malaria vaccines.
url http://europepmc.org/articles/PMC2994908?pdf=render
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