A novel protein phosphatase 2A (MA) is involved in the transformation of human protozoan parasite Trypanosoma cruzi
dc.contributor.author | Gonzalez, Jorge | |
dc.contributor.author | Cornejo, Alberto | |
dc.contributor.author | Santos, Marcia Regina Machado [UNIFESP] | |
dc.contributor.author | Cordero, Esteban Mauricio [UNIFESP] | |
dc.contributor.author | Gutierrez, Bessy | |
dc.contributor.author | Porcile, Patricio | |
dc.contributor.author | Mortara, Renato Arruda [UNIFESP] | |
dc.contributor.author | Sagua, Hernan | |
dc.contributor.author | Silveira, José F. da [UNIFESP] | |
dc.contributor.author | Araya, Jorge E. | |
dc.contributor.institution | Univ Antofagasta | |
dc.contributor.institution | Universidade Federal de São Paulo (UNIFESP) | |
dc.date.accessioned | 2016-01-24T12:34:03Z | |
dc.date.available | 2016-01-24T12:34:03Z | |
dc.date.issued | 2003-09-14 | |
dc.description.abstract | Here we provide evidence for a critical role of PP2As (protein phosphatase 2As) in the transformation of Trypanosoma cruzi. in axenic medium at pH 5.0, trypomastigotes rapidly transform into amastigotes, a process blocked by okadaic acid, a potent PP2A inhibitor, at concentrations as low as 0.1 muM. 1-Norokadaone, an inactive okadaic acid analogue, did not affect the transformation. Electron microscopy studies indicated that okadaic acid-treated trypomastigotes had not undergone ultrastructural modifications, reinforcing the idea that PP2A inhibits transformation. Using a microcystin-Sepharose affinity column we purified the native T cruzi PP2A. the enzyme displayed activity against 12 P-labelled phosphorylase a that was inhibited in a dose-dependent manner by okadaic acid. the protein was also submitted to MS and, from the peptides obtained, degenerate primers were used to clone a novel T cruzi PP2A enzyme by PCR. the isolated gene encodes a protein of 303 amino acids, termed TcPP2A, which displayed a high degree of homology (86%) with the catalytic subunit of Trypanosoma brucei PP2A. Northern-blot analysis revealed the presence of a major 2.1-kb mRNA hybridizing in all T cruzi developmental stages. Southern-blot analysis suggested that the TcPP2A gene is present in low copy number in the T cruzi genome. These results are consistent with the mapping of PP2A genes in two chromosomal bands by pulsed-field gel electrophoresis and chromoblot hybridization. Our studies suggest that in T cruzi PP2A is important for the complete transformation of trypomastigotes into amastigotes during the life cycle of this protozoan parasite. | en |
dc.description.affiliation | Univ Antofagasta, Dept Med Technol, Parasitol Unit, Antofagasta, Chile | |
dc.description.affiliation | Universidade Federal de São Paulo, EPM, Dept Microbiol Immunol & Parasitol, BR-04023062 São Paulo, SP, Brazil | |
dc.description.affiliationUnifesp | Universidade Federal de São Paulo, EPM, Dept Microbiol Immunol & Parasitol, BR-04023062 São Paulo, SP, Brazil | |
dc.description.source | Web of Science | |
dc.format.extent | 647-656 | |
dc.identifier | http://dx.doi.org/10.1042/BJ20030215 | |
dc.identifier.citation | Biochemical Journal. London: Portland Press, v. 374, p. 647-656, 2003. | |
dc.identifier.doi | 10.1042/BJ20030215 | |
dc.identifier.issn | 0264-6021 | |
dc.identifier.uri | http://repositorio.unifesp.br/handle/11600/27414 | |
dc.identifier.wos | WOS:000185546800007 | |
dc.language.iso | eng | |
dc.publisher | Portland Press | |
dc.relation.ispartof | Biochemical Journal | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | enzyme purification | en |
dc.subject | expression | en |
dc.subject | gene cloning | en |
dc.subject | genomic organization | en |
dc.subject | phosphatase-specific inhibitor | en |
dc.subject | trypanosome transformation | en |
dc.title | A novel protein phosphatase 2A (MA) is involved in the transformation of human protozoan parasite Trypanosoma cruzi | en |
dc.type | info:eu-repo/semantics/article |