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Infection and Immunity, November 1998, p. 5393-5398, Vol. 66, No. 11
Instituto de Investigaciones
Biotecnológicas, Universidad Nacional de General San
Martín, Buenos Aires, Argentina,1
and
Instituto de Biofísica Carlos Chagas Filho,
Universidade Federal do Rio de Janeiro, Rio de Janeiro,
Brazil2
Received 15 May 1998/Returned for modification 2 July 1998/Accepted 10 August 1998
Analysis of expressed sequence tags (ESTs) constitutes a useful
approach for gene identification that, in the case of human pathogens,
might result in the identification of new targets for chemotherapy and
vaccine development. As part of the Trypanosoma cruzi
genome project, we have partially sequenced the 5' ends of 1,949 clones
to generate ESTs. The clones were randomly selected from a normalized
CL Brener epimastigote cDNA library. A total of 14.6% of the clones
were homologous to previously identified T. cruzi genes,
while 18.4% had significant matches to genes from other organisms in
the database. A total of 67% of the ESTs had no matches in the
database, and thus, some of them might be T. cruzi-specific
genes. Functional groups of those sequences with matches in the
database were constructed according to their putative biological
functions. The two largest categories were protein synthesis (23.3%)
and cell surface molecules (10.8%). The information reported in this
paper should be useful for researchers in the field to analyze genes
and proteins of their own interest.
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Gene Discovery through Expressed Sequence Tag
Sequencing in Trypanosoma cruzi
*
Corresponding author. Mailing address: Instituto
de Investigaciones Biotecnológicas, Universidad
Nacional de General San Martín, INTI (Ed. 24), Av. Gral Paz
entre Constituyentes y Albarellos, 1650 San Martín, Provincia
de Buenos Aires, Argentina. Phone: (54-1) 752-0021. Fax: (54-1)
752-9639. E-mail: dsanchez{at}inti.gov.ar.
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