Genetic mapping in the human malaria parasite Plasmodium falciparum.

Abstract:

:The Plasmodium falciparum genome sequence has boosted hopes for a new era of malaria research and for the application of comprehensive molecular knowledge to disease control, but formidable obstacles remain: approximately 60% of the predicted P. falciparum proteins have no known functions or homologues, and most life cycle stages of this haploid eukaryotic parasite are relatively intractable to cultivation and biochemical manipulation. Genetic mapping based on high-resolution maps saturated with single-nucleotide polymorphisms or microsatellites is now providing effective strategies for discovering candidate genes determining important parasite phenotypes. Here we review classical linkage studies using laboratory crosses and population associations that are now amenable to genome-wide approaches and are revealing multiple candidate genes involved in complex drug responses. Moreover, mapping by linkage disequilibrium is practicable in cases where chromosomal segments flanking drug-selected genes have been preserved in populations during relatively recent P. falciparum evolution. We discuss the advantages and limitations of these various genetic mapping strategies, results from which offer complementary insights to those emerging from gene knockout experiments and/or high-throughput genomic technologies.

journal_name

Mol Microbiol

journal_title

Molecular microbiology

authors

Su XZ,Wootton JC

doi

10.1111/j.1365-2958.2004.04270.x

subject

Has Abstract

pub_date

2004-09-01 00:00:00

pages

1573-82

issue

6

eissn

0950-382X

issn

1365-2958

pii

MMI4270

journal_volume

53

pub_type

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