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A TRYPANOSOMA CRUZI ZINC FINGER PROTEIN THAT IS IMPLICATED IN THE CONTROL OF EPIMASTIGOTE-SPECIFIC GENE EXPRESSION AND METACYCLOGENESIS
RNA binding proteins
Trypanosoma cruzi
post-transcriptional control
transcriptome analyses
Autor(es)
Tavares, Thais Silva
Mügge, Fernanda Lins Brandão
Silva, Viviane Grazielle
Valente, Bruna Mattioly
Wanessa Moreira Goes, Wanessa Moreira Goes
Oliveira, Antonio Edson Rocha
Belew, Ashton T
Guarneri, Alessandra Aparecida
Pais, Fabiano Sviatopolk Mirsky
El-Sayed, Najib M
Teixeira, Santuza Maria Ribeiro
Mügge, Fernanda Lins Brandão
Silva, Viviane Grazielle
Valente, Bruna Mattioly
Wanessa Moreira Goes, Wanessa Moreira Goes
Oliveira, Antonio Edson Rocha
Belew, Ashton T
Guarneri, Alessandra Aparecida
Pais, Fabiano Sviatopolk Mirsky
El-Sayed, Najib M
Teixeira, Santuza Maria Ribeiro
Afiliação
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil/Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA/Center for Molecular Biology of Heidelberg University. Heidelberg, Germany.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA.
Fundação Oswaldo Cruz. Instituto René Rachou. Belo Horizonte, MG, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Belo Horizonte, MG, Brazil.
Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil/Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA/Center for Molecular Biology of Heidelberg University. Heidelberg, Germany.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA.
Fundação Oswaldo Cruz. Instituto René Rachou. Belo Horizonte, MG, Brazil.
Fundação Oswaldo Cruz. Instituto René Rachou. Belo Horizonte, MG, Brazil.
Department of Cell Biology and Molecular Genetics and Center for Bioinformatics and Computational Biology. University of Maryland. Maryland, USA.
Universidade Federal de Minas Gerais. Departamento de Bioquímica e Imunologia. Belo Horizonte, MG, Brazil.
Resumo em Inglês
Trypanosoma cruzi has three biochemically and morphologically distinct developmental stages that are programmed to rapidly respond to environmental changes the parasite faces during its life cycle. Unlike other eukaryotes, Trypanosomatid genomes contain protein coding genes that are transcribed into polycistronic pre-mRNAs and have their expression controlled by post-transcriptional mechanisms. Transcriptome analyses comparing three stages of the T. cruzi life cycle revealed changes in gene expression that reflect the parasite adaptation to distinct environments. Several genes encoding RNA binding proteins (RBPs), known to act as key post-transcriptional regulatory factors, were also differentially expressed. We characterized one T. cruzi RBP, named TcZH3H12, which contains a zinc finger domain and is up-regulated in epimastigotes compared to trypomastigotes and amastigotes. TcZC3H12 knockout (KO) epimastigotes showed decreased growth rates and increased capacity to differentiate into metacyclic trypomastigotes. Transcriptome analyses comparing wild type and TcZC3H12 KOs revealed a TcZC3H12-dependent expression of epimastigote-specific genes such as genes encoding amino acid transporters and proteins associated with differentiation (PADs). RNA immunoprecipitation assays showed that transcripts from the PAD family interact with TcZC3H12. Taken together, these findings suggest that TcZC3H12 positively regulates the expression of genes involved in epimastigote proliferation and also acts as a negative regulator of metacyclogenesis
Palavras-chave em inglês
Parasite differentiationRNA binding proteins
Trypanosoma cruzi
post-transcriptional control
transcriptome analyses
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