Trypanosoma cruzi MSH2: Functional analyses on different parasite strains provide evidences for a role on the oxidative stress response


Autoria(s): CAMPOS, Priscila C.; SILVA, Viviane G.; FURTADO, Carolina; MACHADO-SILVA, Alice; DAROCHA, Wanderson D.; PELOSO, Eduardo F.; GADELHA, Fernanda R.; MEDEIROS, Marisa H. G.; LANA, Gustavo de Carvalho; CHEN, Ying; BARNES, Rebecca L.; PASSOS-SILVA, Danielle Gomes; MCCULLOCH, Richard; MACHADO, Carlos Renato; TEIXEIRA, Santuza M. R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Components of the DNA mismatch repair (MMR) pathway are major players in processes known to generate genetic diversity, such as mutagenesis and DNA recombination. Trypanosoma cruzi, the protozoan parasite that causes Chagas disease has a highly heterogeneous population, composed of a pool of strains with distinct characteristics. Studies with a number of molecular markers identified up to six groups in the T. cruzi population, which showed distinct levels of genetic variability. To investigate the molecular basis for such differences, we analyzed the T. cruzi MSH2 gene, which encodes a key component of MMR, and showed the existence of distinct isoforms of this protein. Here we compared cell survival rates after exposure to genotoxic agents and levels of oxidative stress-induced DNA in different parasite strains. Analyses of msh2 mutants in both T. cruzi and T. brucei were also used to investigate the role of Tcmsh2 in the response to various DNA damaging agents. The results suggest that the distinct MSH2 isoforms have differences in their activity. More importantly, they also indicate that, in addition to its role in MMR, TcMSH2 acts in the parasite response to oxidative stress through a novel mitochondrial function that may be conserved in T. brucei. (C) 2010 Elsevier B.V. All rights reserved.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico - CNPq

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)

Fundacao de Amparo a Pesquisa do Estado de Minas Gerais - FAPEMIG (Brazil)

Howard Hughes Medical Institute (HHMI)

Howard Hughes Medical Institute - HHMI

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo - FAPESP (Brazil)

INCT de Processos Redox em Biomedicina - Redoxoma (Brazil)

INCT de Processos Redox em Biomedicina - Redoxoma (Brazil)

Medical Research Council

Medical Research Council

Wellcome Trust

Wellcome Trust

Identificador

MOLECULAR AND BIOCHEMICAL PARASITOLOGY, v.176, n.1, p.8-16, 2011

0166-6851

http://producao.usp.br/handle/BDPI/30935

10.1016/j.molbiopara.2010.11.001

http://dx.doi.org/10.1016/j.molbiopara.2010.11.001

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Molecular and Biochemical Parasitology

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Trypanosoma cruzi #DNA repair #MSH2 #Oxidative stress #Trypanosoma brucei #DNA MISMATCH REPAIR #SEQUENCE DIVERSITY #GENETIC DIVERSITY #DRUG-RESISTANCE #DAMAGE #EXPRESSION #PROTEIN #FAMILIES #BRUCEI #SITES #Biochemistry & Molecular Biology #Parasitology
Tipo

article

original article

publishedVersion