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      Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray

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          Abstract

          DNA microarrays based on long oligonucleotides are powerful tools for the functional annotation of the Plasmodium falciparum genome. Expression profiling of trophozoites and schizonts revealed genes associated with stage-specific processes and may serve as the basis for future drug targets and vaccine development.

          Abstract

          Background

          The worldwide persistence of drug-resistant Plasmodium falciparum, the most lethal variety of human malaria, is a global health concern. The P. falciparum sequencing project has brought new opportunities for identifying molecular targets for antimalarial drug and vaccine development.

          Results

          We developed a software package, ArrayOligoSelector, to design an open reading frame (ORF)-specific DNA microarray using the publicly available P. falciparum genome sequence. Each gene was represented by one or more long 70 mer oligonucleotides selected on the basis of uniqueness within the genome, exclusion of low-complexity sequence, balanced base composition and proximity to the 3' end. A first-generation microarray representing approximately 6,000 ORFs of the P. falciparum genome was constructed. Array performance was evaluated through the use of control oligonucleotide sets with increasing levels of introduced mutations, as well as traditional northern blotting. Using this array, we extensively characterized the gene-expression profile of the intraerythrocytic trophozoite and schizont stages of P. falciparum. The results revealed extensive transcriptional regulation of genes specialized for processes specific to these two stages.

          Conclusions

          DNA microarrays based on long oligonucleotides are powerful tools for the functional annotation and exploration of the P. falciparum genome. Expression profiling of trophozoites and schizonts revealed genes associated with stage-specific processes and may serve as the basis for future drug targets and vaccine development.

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          Most cited references45

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              S Altschul (1990)
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                Author and article information

                Journal
                Genome Biol
                Genome Biology
                BioMed Central
                1465-6906
                1465-6914
                2003
                31 January 2003
                : 4
                : 2
                : R9
                Affiliations
                [1 ]Department of Biochemistry and Biophysics, University of California San Francisco, 513 Parnassus Ave, San Francisco, CA 94143-0448, USA
                [2 ]Department of Molecular and Cellular Pharmacology, University of California San Francisco, 513 Parnassus Ave, San Francisco, CA 94143-0448, USA
                Correspondence: Joseph L DeRisi. E-amil: joe@derisilab.ucsf.edu
                Article
                gb-2003-4-2-r9
                10.1186/gb-2003-4-2-r9
                151308
                12620119
                f71e68d3-bb03-466f-8275-5f8992403f5e
                Copyright © 2003 Bozdech et al.; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
                History
                : 23 August 2002
                : 10 October 2002
                : 5 December 2002
                Categories
                Research

                Genetics
                Genetics

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