Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells

Detalhes bibliográficos
Autor(a) principal: Felipe, Maria Sueli Soares
Data de Publicação: 2005
Outros Autores: Andrade, Rosângela Vieira de, Arraes, Fabrício B. M., Nicola, André Moraes, Maranhão, Andrea Queiroz, Torres, Fernando Araripe Gonçalves, Silva-Pereira, Ildinete, Fonseca, Marcio José Poças, Campos, Elida Geralda, Moraes, Lídia Maria Pepe de, Andrade, Patrícia Albuquerque de, Tavares, Aldo Henrique Fonseca Pacheco, Silva, Simoneide Souza, Kyaw, Cynthia Maria, Souza, Diorge Paulo de, PbGenome, Network, Pereira, Maristela, Jesuíno, Rosália Santos Amorim, Andrade, Edmar Vaz de, Parente, Juliana Alves, Oliveira, Gisele Silva de, Barbosa, Mônica Santiago, Martins, Natalia Florêncio, Saltoratto, Ana Lucia Fachin, Cardoso, Renato Sousa, Passos Júnior, Geraldo Aleixo da Silva, Almeida Junior, Nalvo Franco de, Walter, Maria Emília Machado Telles, Soares, Célia Maria de Almeida, Carvalho, Maria José Albuquerque de, Brigido, Marcelo de Macedo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UCB
Texto Completo: http://twingo.ucb.br:8080/jspui/handle/10869/602
https://repositorio.ucb.br:9443/jspui/handle/123456789/7864
Resumo: Paracoccidioides brasiliensis is the causative agent of paracoccidioidomycosis, a disease that affects 10 million individuals in Latin America. This report depicts the results of the analysis of 6,022 assembled groups from mycelium and yeast phase expressed sequence tags, covering about 80% of the estimated genome of this dimorphic, thermo-regulated fungus. The data provide a comprehensive view of the fungal metabolism, including overexpressed transcripts, stage-specific genes, and also those that are up- or down-regulated as assessed by in silico electronic subtraction and cDNA microarrays. Also, a significant differential expression pattern in mycelium and yeast cells was detected, which was confirmed by Northern blot analysis, providing insights into differential metabolic adaptations. The overall transcriptome analysis provided information about sequences related to the cell cycle, stress response, drug resistance, and signal transduction pathways of the pathogen. Novel P. brasiliensis genes have been identified, probably corresponding to proteins that should be addressed as virulence factor candidates and potential new drug targets.
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spelling Felipe, Maria Sueli SoaresAndrade, Rosângela Vieira deArraes, Fabrício B. M.Nicola, André MoraesMaranhão, Andrea QueirozTorres, Fernando Araripe GonçalvesSilva-Pereira, IldineteFonseca, Marcio José PoçasCampos, Elida GeraldaMoraes, Lídia Maria Pepe deAndrade, Patrícia Albuquerque deTavares, Aldo Henrique Fonseca PachecoSilva, Simoneide SouzaKyaw, Cynthia MariaSouza, Diorge Paulo dePbGenome, NetworkPereira, MaristelaJesuíno, Rosália Santos AmorimAndrade, Edmar Vaz deParente, Juliana AlvesOliveira, Gisele Silva deBarbosa, Mônica SantiagoMartins, Natalia FlorêncioSaltoratto, Ana Lucia FachinCardoso, Renato SousaPassos Júnior, Geraldo Aleixo da SilvaAlmeida Junior, Nalvo Franco deWalter, Maria Emília Machado TellesSoares, Célia Maria de AlmeidaCarvalho, Maria José Albuquerque deBrigido, Marcelo de Macedo2016-10-10T03:52:56Z2016-10-10T03:52:56Z2005FELIPE, Maria Sueli Soares et al. Transcriptional profiles of the human pathogenic fungus Paracoccidioides brasiliensis in mycelium and yeast cells. The Journal of Biological Chemistry, v. 280, n. 26, p. 24706-24714, 2005.00219258http://twingo.ucb.br:8080/jspui/handle/10869/602https://repositorio.ucb.br:9443/jspui/handle/123456789/7864Paracoccidioides brasiliensis is the causative agent of paracoccidioidomycosis, a disease that affects 10 million individuals in Latin America. This report depicts the results of the analysis of 6,022 assembled groups from mycelium and yeast phase expressed sequence tags, covering about 80% of the estimated genome of this dimorphic, thermo-regulated fungus. The data provide a comprehensive view of the fungal metabolism, including overexpressed transcripts, stage-specific genes, and also those that are up- or down-regulated as assessed by in silico electronic subtraction and cDNA microarrays. Also, a significant differential expression pattern in mycelium and yeast cells was detected, which was confirmed by Northern blot analysis, providing insights into differential metabolic adaptations. The overall transcriptome analysis provided information about sequences related to the cell cycle, stress response, drug resistance, and signal transduction pathways of the pathogen. Novel P. brasiliensis genes have been identified, probably corresponding to proteins that should be addressed as virulence factor candidates and potential new drug targets.Made available in DSpace on 2016-10-10T03:52:56Z (GMT). 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dc.title.pt_BR.fl_str_mv Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
title Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
spellingShingle Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
Felipe, Maria Sueli Soares
title_short Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
title_full Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
title_fullStr Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
title_full_unstemmed Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
title_sort Transcriptional Profiles of the Human Pathogenic Fungus Paracoccidioides brasiliensis in Mycelium and Yeast Cells
author Felipe, Maria Sueli Soares
author_facet Felipe, Maria Sueli Soares
Andrade, Rosângela Vieira de
Arraes, Fabrício B. M.
Nicola, André Moraes
Maranhão, Andrea Queiroz
Torres, Fernando Araripe Gonçalves
Silva-Pereira, Ildinete
Fonseca, Marcio José Poças
Campos, Elida Geralda
Moraes, Lídia Maria Pepe de
Andrade, Patrícia Albuquerque de
Tavares, Aldo Henrique Fonseca Pacheco
Silva, Simoneide Souza
Kyaw, Cynthia Maria
Souza, Diorge Paulo de
PbGenome, Network
Pereira, Maristela
Jesuíno, Rosália Santos Amorim
Andrade, Edmar Vaz de
Parente, Juliana Alves
Oliveira, Gisele Silva de
Barbosa, Mônica Santiago
Martins, Natalia Florêncio
Saltoratto, Ana Lucia Fachin
Cardoso, Renato Sousa
Passos Júnior, Geraldo Aleixo da Silva
Almeida Junior, Nalvo Franco de
Walter, Maria Emília Machado Telles
Soares, Célia Maria de Almeida
Carvalho, Maria José Albuquerque de
Brigido, Marcelo de Macedo
author_role author
author2 Andrade, Rosângela Vieira de
Arraes, Fabrício B. M.
Nicola, André Moraes
Maranhão, Andrea Queiroz
Torres, Fernando Araripe Gonçalves
Silva-Pereira, Ildinete
Fonseca, Marcio José Poças
Campos, Elida Geralda
Moraes, Lídia Maria Pepe de
Andrade, Patrícia Albuquerque de
Tavares, Aldo Henrique Fonseca Pacheco
Silva, Simoneide Souza
Kyaw, Cynthia Maria
Souza, Diorge Paulo de
PbGenome, Network
Pereira, Maristela
Jesuíno, Rosália Santos Amorim
Andrade, Edmar Vaz de
Parente, Juliana Alves
Oliveira, Gisele Silva de
Barbosa, Mônica Santiago
Martins, Natalia Florêncio
Saltoratto, Ana Lucia Fachin
Cardoso, Renato Sousa
Passos Júnior, Geraldo Aleixo da Silva
Almeida Junior, Nalvo Franco de
Walter, Maria Emília Machado Telles
Soares, Célia Maria de Almeida
Carvalho, Maria José Albuquerque de
Brigido, Marcelo de Macedo
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Felipe, Maria Sueli Soares
Andrade, Rosângela Vieira de
Arraes, Fabrício B. M.
Nicola, André Moraes
Maranhão, Andrea Queiroz
Torres, Fernando Araripe Gonçalves
Silva-Pereira, Ildinete
Fonseca, Marcio José Poças
Campos, Elida Geralda
Moraes, Lídia Maria Pepe de
Andrade, Patrícia Albuquerque de
Tavares, Aldo Henrique Fonseca Pacheco
Silva, Simoneide Souza
Kyaw, Cynthia Maria
Souza, Diorge Paulo de
PbGenome, Network
Pereira, Maristela
Jesuíno, Rosália Santos Amorim
Andrade, Edmar Vaz de
Parente, Juliana Alves
Oliveira, Gisele Silva de
Barbosa, Mônica Santiago
Martins, Natalia Florêncio
Saltoratto, Ana Lucia Fachin
Cardoso, Renato Sousa
Passos Júnior, Geraldo Aleixo da Silva
Almeida Junior, Nalvo Franco de
Walter, Maria Emília Machado Telles
Soares, Célia Maria de Almeida
Carvalho, Maria José Albuquerque de
Brigido, Marcelo de Macedo
dc.description.abstract.por.fl_txt_mv Paracoccidioides brasiliensis is the causative agent of paracoccidioidomycosis, a disease that affects 10 million individuals in Latin America. This report depicts the results of the analysis of 6,022 assembled groups from mycelium and yeast phase expressed sequence tags, covering about 80% of the estimated genome of this dimorphic, thermo-regulated fungus. The data provide a comprehensive view of the fungal metabolism, including overexpressed transcripts, stage-specific genes, and also those that are up- or down-regulated as assessed by in silico electronic subtraction and cDNA microarrays. Also, a significant differential expression pattern in mycelium and yeast cells was detected, which was confirmed by Northern blot analysis, providing insights into differential metabolic adaptations. The overall transcriptome analysis provided information about sequences related to the cell cycle, stress response, drug resistance, and signal transduction pathways of the pathogen. Novel P. brasiliensis genes have been identified, probably corresponding to proteins that should be addressed as virulence factor candidates and potential new drug targets.
dc.description.version.pt_BR.fl_txt_mv Sim
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description Paracoccidioides brasiliensis is the causative agent of paracoccidioidomycosis, a disease that affects 10 million individuals in Latin America. This report depicts the results of the analysis of 6,022 assembled groups from mycelium and yeast phase expressed sequence tags, covering about 80% of the estimated genome of this dimorphic, thermo-regulated fungus. The data provide a comprehensive view of the fungal metabolism, including overexpressed transcripts, stage-specific genes, and also those that are up- or down-regulated as assessed by in silico electronic subtraction and cDNA microarrays. Also, a significant differential expression pattern in mycelium and yeast cells was detected, which was confirmed by Northern blot analysis, providing insights into differential metabolic adaptations. The overall transcriptome analysis provided information about sequences related to the cell cycle, stress response, drug resistance, and signal transduction pathways of the pathogen. Novel P. brasiliensis genes have been identified, probably corresponding to proteins that should be addressed as virulence factor candidates and potential new drug targets.
publishDate 2005
dc.date.issued.fl_str_mv 2005
dc.date.accessioned.fl_str_mv 2016-10-10T03:52:56Z
dc.date.available.fl_str_mv 2016-10-10T03:52:56Z
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dc.identifier.citation.fl_str_mv FELIPE, Maria Sueli Soares et al. Transcriptional profiles of the human pathogenic fungus Paracoccidioides brasiliensis in mycelium and yeast cells. The Journal of Biological Chemistry, v. 280, n. 26, p. 24706-24714, 2005.
dc.identifier.uri.fl_str_mv http://twingo.ucb.br:8080/jspui/handle/10869/602
https://repositorio.ucb.br:9443/jspui/handle/123456789/7864
dc.identifier.issn.none.fl_str_mv 00219258
identifier_str_mv FELIPE, Maria Sueli Soares et al. Transcriptional profiles of the human pathogenic fungus Paracoccidioides brasiliensis in mycelium and yeast cells. The Journal of Biological Chemistry, v. 280, n. 26, p. 24706-24714, 2005.
00219258
url http://twingo.ucb.br:8080/jspui/handle/10869/602
https://repositorio.ucb.br:9443/jspui/handle/123456789/7864
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