We have developed a method for cutting intact genes out of Plasmodium DNA with mung bean nuclease. The intact genes are then ligated into an expression vector in order to make a recombinant gene bank containing genes from all stages of the parasites life cycle. We have also analyzed what types of DNA structures are involved with mung bean nuclease cleavage and modified the reaction conditions used so that this procedure works with the DNA of many higher eucaryote. From gene banks produced in this fashion we have isolated 1) a gene whose sequence has been useful in the preparation of a trial vaccine for malaria, the circumsporozoite gene on P. falciparum, 2) genes that are specifically produced in the sexual stages of P. falciparum, and 3) a gene that is involved in pyrimethamine resistance.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000208-05
Application #
4688394
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Oakley, Miranda S; Majam, Victoria; Mahajan, Babita et al. (2009) Pathogenic roles of CD14, galectin-3, and OX40 during experimental cerebral malaria in mice. PLoS One 4:e6793
Raj, Dipak Kumar; Mu, Jianbing; Jiang, Hongying et al. (2009) Disruption of a Plasmodium falciparum multidrug resistance-associated protein (PfMRP) alters its fitness and transport of antimalarial drugs and glutathione. J Biol Chem 284:7687-96
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Li, Jian; Zhang, Yanhui; Sullivan, Margery et al. (2007) Typing Plasmodium yoelii microsatellites using a simple and affordable fluorescent labeling method. Mol Biochem Parasitol 155:94-102
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Rathore, Dharmendar; Nagarkatti, Rana; Jani, Dewal et al. (2005) An immunologically cryptic epitope of Plasmodium falciparum circumsporozoite protein facilitates liver cell recognition and induces protective antibodies that block liver cell invasion. J Biol Chem 280:20524-9

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