Toxoplasma gondii is a model system for genetic analyses in parasites belonging to the phylum Apicomplexa, a group that includes malaria and several additional human and animal pathogens. Like other apicomplexans, T. gondii has a complex life cycle although the underlying molecular bases of developmental transitions are poorly understood. Because the genome is relatively large (80 Mb) and contains many introns, EST sequencing is considerably more efficient than genomic sequencing for generating useful data about genes and their expression.
(AIM1) : To facilitate gene discovery in T. gondii, we will generate a comprehensive set of expression site tags (EST) designed to cover the majority of genes expressed by the three invasive stages in the life cycle: tachyzoites, bradyzoites, and sporozoites. Two of these stages, bradyzoites and sporozoites, are currently inadequately represented in the gene databases despite being important in transmission to and chronic infection of humans. By comparison to the existing gene databases, the expanded T. gondii ESTs will identify phylogenetically conserved genes and those unique to the Apicomplexa. They will also identify many strain-specific alleles for single-nucleotide polymorphism mapping.
(AIM2) : The ESTs generated here will be exploited for DNA microarray analyses of stage-specific, gene expression. DNA microarrays will be used to explore changes in gene expression during sporulation and during differentiation from tachyzoite to bradyzoite forms. In combination with the genetic tools available in T. gondii, this will greatly accelerate investigations into the complex developmental biology of apicomplexan parasites.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI045806-03
Application #
6532787
Study Section
Special Emphasis Panel (ZRG1-BIOL-1 (03))
Program Officer
Gottlieb, Michael
Project Start
2000-08-01
Project End
2004-06-30
Budget Start
2002-08-01
Budget End
2003-06-30
Support Year
3
Fiscal Year
2002
Total Cost
$376,952
Indirect Cost
Name
Washington University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Braun, Laurence; Cannella, Dominique; Pinheiro, Alexandre M et al. (2009) The small ubiquitin-like modifier (SUMO)-conjugating system of Toxoplasma gondii. Int J Parasitol 39:81-90
Sautel, Celine F; Ortet, Philippe; Saksouk, Nehme et al. (2009) The histone methylase KMTox interacts with the redox-sensor peroxiredoxin-1 and targets genes involved in Toxoplasma gondii antioxidant defences. Mol Microbiol 71:212-26
Bougdour, Alexandre; Maubon, Daniele; Baldacci, Patricia et al. (2009) Drug inhibition of HDAC3 and epigenetic control of differentiation in Apicomplexa parasites. J Exp Med 206:953-66
Boyle, Jon P; Saeij, Jeroen P J; Harada, Scott Y et al. (2008) Expression quantitative trait locus mapping of toxoplasma genes reveals multiple mechanisms for strain-specific differences in gene expression. Eukaryot Cell 7:1403-14
Seeber, Frank; Limenitakis, Julien; Soldati-Favre, Dominique (2008) Apicomplexan mitochondrial metabolism: a story of gains, losses and retentions. Trends Parasitol 24:468-78
Krucken, Jurgen; Hosse, Ralf J; Mouafo, Aimdip N et al. (2008) Excystation of Eimeria tenella sporozoites impaired by antibody recognizing gametocyte/oocyst antigens GAM22 and GAM56. Eukaryot Cell 7:202-11
El Hajj, Hiba; Lebrun, Maryse; Arold, Stefan T et al. (2007) ROP18 is a rhoptry kinase controlling the intracellular proliferation of Toxoplasma gondii. PLoS Pathog 3:e14
Cook, Tuesday; Roos, David; Morada, Mary et al. (2007) Divergent polyamine metabolism in the Apicomplexa. Microbiology 153:1123-30
Ling, Yan; Li, Zhu-Hong; Miranda, Kildare et al. (2007) The farnesyl-diphosphate/geranylgeranyl-diphosphate synthase of Toxoplasma gondii is a bifunctional enzyme and a molecular target of bisphosphonates. J Biol Chem 282:30804-16
Sautel, Celine F; Cannella, Dominique; Bastien, Olivier et al. (2007) SET8-mediated methylations of histone H4 lysine 20 mark silent heterochromatic domains in apicomplexan genomes. Mol Cell Biol 27:5711-24

Showing the most recent 10 out of 44 publications