Author | Ferreira, Keila Adriana Magalhães | |
Author | Ruiz, Jerônimo Conceição | |
Author | Dias, Fabrício César | |
Author | Silva, Eliane Lages | |
Author | Tosi, Luiz Ricardo Orsini | |
Author | Giraldo, Luis Eduardo Ramirez | |
Author | Pedrosa, André Luiz | |
Access date | 2013-09-13T18:06:28Z | |
Available date | 2013-09-13T18:06:28Z | |
Document date | 2010 | |
Citation | FERREIRA, Keila A.M. et al. Genome Survey Sequence Analysis and Identification of Homologs of Major Surface Protease (gp63) Genes inTrypanosoma rangeli. Vector Borne Zoonotic Dis. 2010; 10(9):847-53 | pt_BR |
ISSN | 1530-3667 | |
URI | https://www.arca.fiocruz.br/handle/icict/6891 | |
Language | eng | pt_BR |
Rights | restricted access | pt_BR |
Title | Genome Survey Sequence Analysis and Identification of Homologs of Major Surface Protease (gp63) Genes inTrypanosoma rangeli | pt_BR |
Type | Article | |
DOI | 10.1089/vbz.2009.0128 | |
Abstract | In this study, 222 genome survey sequences were generated for Trypanosoma rangelistrain P07 isolated from anopossum (Didelphis albiventris) in Minas Gerais State, Brazil. T. rangelisequences were compared by BLASTX (Basic Local Alignment Search Tool X) analysis with the assembled contigs of Leishmania braziliensis, Leishmania infantum, Leishmania major, Trypanosoma brucei, and Trypanosoma cruzi. Results revealed that 82% (182=222) of the sequences were associated with predicted proteins described, whereas 18% (40=222) of the sequences did not show significant identity with sequences deposited in databases, suggesting that they may represent T. rangeli-specific sequences. Among the 182 predicted sequences, 179 (80.6%) had the highest similarity with T. cruzi, 2 (0.9%) with T. brucei, and 1 (0.5%) with L. braziliensis. Computer analysis permitted the identification of members of various gene families described for trypanosomatids in the genome ofT. rangeli, such as trans-sialidases, mucin-associated surface proteins, and major surface proteases (MSPorgp63). This is the first report identifying sequences of the MSP family inT. rangeli. Multiple sequence alignments showed that the predicted MSP of T. rangelipresented the typical characteristics of metalloproteases, such as the presence of the HEXXH motif, which corresponds to a region previously associated with the catalytic site of the enzyme, and various cysteine and proline residues, which are conserved among MSPs of different trypanosomatid species. Reverse transcriptase–polymerase chain reaction analysis revealed the presence of MSP transcripts in epimastigote forms of T. rangeli | pt_BR |
Affilliation | Universidade Federal do Triangulo Mineiro. Departamento de Ciencias Biologicas. Disciplina de Biologia Molecular. Uberaba, MG, Brazil | pt_BR |
Affilliation | Fundação Oswaldo Cruz. Centro de Pesquisas Rene Rachou. Belo Horizonte, Minas Gerais, Brazil | pt_BR |
Affilliation | Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Biologia Celular e Molecular e Bioagentes Patogenicos. Ribeirão Preto. São Paulo, Brazil. | pt_BR |
Affilliation | Universidade Federal do Triangulo Mineiro. Departamento de Ciencias Biologicas. Disciplina de Biologia Molecular. Uberaba, MG, Brazil. | pt_BR |
Affilliation | Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Biologia Celular e Molecular e Bioagentes Patogenicos. Ribeirão Preto. São Paulo, Brazil. | pt_BR |
Affilliation | Universidade Federal do Triangulo Mineiro. Departamento de Ciencias Biologicas. Disciplina de Biologia Molecular. Uberaba, MG, Brazil. | pt_BR |
Affilliation | Universidade Federal do Triangulo Mineiro. Departamento de Ciencias Biologicas. Disciplina de Biologia Molecular. Uberaba, MG, Brazil. | pt_BR |
Subject | Genome organization | pt_BR |
Subject | MSP | pt_BR |
Subject | gp63 | pt_BR |
Subject | Major surface protease | pt_BR |
Subject | Trypanosoma rangeli | pt_BR |