Literature DB >> 15465918

Conditional mutagenesis using site-specific recombination in Plasmodium berghei.

Teresa Gil Carvalho1, Sabine Thiberge, Hiroshi Sakamoto, Robert Ménard.   

Abstract

Reverse genetics in Plasmodium, the genus of parasites that cause malaria, still faces major limitations. Only red blood cell stages of this haploid parasite can be transfected. Consequently, the function of many essential genes in these and subsequent stages, including those encoding vaccine candidates, cannot be addressed genetically. Here, we establish conditional mutagenesis in Plasmodium by using site-specific recombination and the Flp/FRT system of yeast. Site-specific recombination is induced after cross-fertilization in the mosquito vector of two clones containing either the target sequence flanked by two FRT sites or the Flp recombinase. Parasites that have undergone recombination are recognized in the cross progeny through the expression of a fluorescence marker. This approach should permit to dissect the function of any essential gene of Plasmodium during the haploid phase of its life, i.e., during infection of salivary glands in the mosquito and infection of both the liver and red blood cells in the mammal.

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Year:  2004        PMID: 15465918      PMCID: PMC522007          DOI: 10.1073/pnas.0404416101

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

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Review 3.  Talking about a revolution: The impact of site-specific recombinases on genetic analyses in mice.

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4.  Gene targeting in Plasmodium berghei.

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Review 5.  Functional analysis of proteins involved in Plasmodium falciparum merozoite invasion of red blood cells.

Authors:  A F Cowman; D L Baldi; J Healer; K E Mills; R A O'Donnell; M B Reed; T Triglia; M E Wickham; B S Crabb
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  19 in total

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4.  FLP/FRT-mediated conditional mutagenesis in pre-erythrocytic stages of Plasmodium berghei.

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Review 6.  Towards genome-wide experimental genetics in the in vivo malaria model parasite Plasmodium berghei.

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7.  Efficient site-specific integration in Plasmodium falciparum chromosomes mediated by mycobacteriophage Bxb1 integrase.

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9.  Identification and characterization of a liver stage-specific promoter region of the malaria parasite Plasmodium.

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10.  Expression and processing of Plasmodium berghei SERA3 during liver stages.

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