Trypanosoma cruzi is a protozoan parasite that causes a fatal illness called Chagas' disease or American typanosomiasis in humans and many nonhuman mammalian species. The World Health Organization has estimated that 18 million people are infected with T. cruzi and that 50,000 patients die each year of the disease. The basic research on T. cruzi over the past two decades has resulted in many advances in our understanding of these organisms, yet these substantial research efforts have not led to a better way to manage or control this devastating disease. Recently, progress on the human genome project, and the determination of the yeast genomic sequence, have unambiguously demonstrated the value of using genomic sequences as a foundation for designing future research efforts. Our long term goal is to sequence the genome of T. cruzi. This proposal, in conjunction with similar proposed efforts at the Seattle Biomedical Research Institute and Uppsala University, represents a large step towards that goal. We will employ a sequencing strategy consisting of two phases. The purpose of the first phase is to enhance early gene discovery and to provide markers that will be important for construction of a high-resolution sequence-ready map. In this phase we will generate approximately 10 Mb of discontinuous single-pass sequence (23 percent of the 43.5 Mb genome). This will be implemented by end-sequencing 5,000 BAC (Bacterial Artificial Chromosome) clones from an already existing library and another 5,000 BAC clones of randomly-sheared DNA (from a library to be constructed in collaboration with Dr. Pieter deJong). Telomere-proximal sequences will be identified in clones of the sheared genonmic library. During the second phase 12 Mb of contiguous T. cruzi DNA will be sequenced using a chromosome by chromosome approach and a syntenic regions conserved between T. cruzi and a related parasite (Trypanosoma brucei) will be identified and analyzed. This project will provide invaluable information and benefits at many levels, including (1) identification of genes involved in basic functions of the eukaryotic cell, (2) easy, inexpensive and fast cloning of genes encoding proteins being actively studied in laboratories around the world, (3) immediate access to genes and their products for functional/structural studies, (4) prediction of metabolic pathways on the basis of candidate genes, (4) identification of parasite-specific gene products by comparison with other genomes, and (5) a framework for future experiments aimed at comparative and integrative mapping of various trypanosomatid genomes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI045038-05
Application #
6712120
Study Section
Genome Study Section (GNM)
Program Officer
Rogers, Martin J
Project Start
2000-03-15
Project End
2005-08-31
Budget Start
2004-03-01
Budget End
2005-08-31
Support Year
5
Fiscal Year
2004
Total Cost
$286,220
Indirect Cost
Name
Institute for Genomic Research
Department
Type
DUNS #
795140805
City
Rockville
State
MD
Country
United States
Zip Code
20850
Bartholomeu, Daniella C; Cerqueira, Gustavo C; Leão, Ana Carolina A et al. (2009) Genomic organization and expression profile of the mucin-associated surface protein (masp) family of the human pathogen Trypanosoma cruzi. Nucleic Acids Res 37:3407-17
Cerqueira, Gustavo C; Bartholomeu, Daniella C; DaRocha, Wanderson D et al. (2008) Sequence diversity and evolution of multigene families in Trypanosoma cruzi. Mol Biochem Parasitol 157:65-72
Moreno, Valeria Ruiz; Aguero, Fernan; Tekiel, Valeria et al. (2007) The Calcineurin A homologue from Trypanosoma cruzi lacks two important regulatory domains. Acta Trop 101:80-9
Bringaud, Frederic; Ghedin, Elodie; Blandin, Gaelle et al. (2006) Evolution of non-LTR retrotransposons in the trypanosomatid genomes: Leishmania major has lost the active elements. Mol Biochem Parasitol 145:158-70
Bringaud, Frederic; Bartholomeu, Daniella C; Blandin, Gaelle et al. (2006) The Trypanosoma cruzi L1Tc and NARTc non-LTR retrotransposons show relative site specificity for insertion. Mol Biol Evol 23:411-20
Fernandes, Marcelo; Silva, Rosane; Rossle, Shaila C et al. (2005) Gene characterization and predicted protein structure of the mitochondrial chaperonin HSP10 of Trypanosoma cruzi. Gene 349:135-42
El-Sayed, Najib M; Myler, Peter J; Bartholomeu, Daniella C et al. (2005) The genome sequence of Trypanosoma cruzi, etiologic agent of Chagas disease. Science 309:409-15
Araripe, Julia Rolao; Ramos, Fabiane Pereira; Cunha e Silva, Narcisa Leal et al. (2005) Characterization of a RAB5 homologue in Trypanosoma cruzi. Biochem Biophys Res Commun 329:638-45
El-Sayed, Najib M; Myler, Peter J; Blandin, Gaelle et al. (2005) Comparative genomics of trypanosomatid parasitic protozoa. Science 309:404-9
Ramos, Fabiane Pereira; Araripe, Julia Rolao; Urmenyi, Turan Peter et al. (2005) Characterization of RAB-like4, the first identified RAB-like protein from Trypanosoma cruzi with GTPase activity. Biochem Biophys Res Commun 333:808-17

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