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| Registros recuperados : 6 | |
| 2. |  | THRO, A. M.; WIER, A. T.; TORRES, K. C.; FLORES, H. E.; PILLAY, M. Production of plantlets from tissue cultures of lotonosis, a Southern African veld legume. Journal Grassland Society South Africa, v.4, n.4, p.151-153, 1987.| Biblioteca(s): Embrapa Pantanal. |
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| 4. | | SIMÕES, M.; BAHIA, D.; ZERLOTINI, A.; TORRES, K.; ARTIGUENAVE, F.; NESHICH, G.; KUSER, P.; OLIVEIRA, G. Single nucleotide polymorphisms identification in expressed genes of Schistosoma mansoni. Molecular and Biochemical Parasitology, v. 154, p. 134-140, 2007.| Biblioteca(s): Embrapa Agricultura Digital. |
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| 5. | | SIMÕES, M.; BAHIA, D.; TORRES, K.; ZERLOTINI NETO, A.; ARTIGUENAVE, F.; FALCAO, P. R. K.; NESHICH, G.; OLIVEIRA, G. SNP identification in Schistosoma mansoni expressed genes. In: X-MEETING; INTERNATIONAL CONFERENCE OF THE AB3C, 1., 2005, Caxambu. [Proceedings...]. [S.l.]: Associação Brasileira de Bioinformática e Biologia Computacional, 2005. p. 131. X-meeting 2005. Presented Posters. Na publicação: Paula Kuser.| Biblioteca(s): Embrapa Agricultura Digital. |
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| 6. | | FARIA FILHO, D. E.; TORRES, K. A. A.; VIEIRA, B. S.; ROSA, P. S.; CAMPOS, D. M. B.; MACARI, M.; FURLAN, R. L. Níveis de proteína sobre a digestibilidade de nutrientes e o teor de energia metabolizável para frangos de corte expostos ao calor. In: CONFERÊNCIA APINCO DE CIÊNCIA E TECNOLOGIA AVÍCOLAS, 2007, Santos, SP. Anais... Campinas: FACTA, 2007. Trabalhos de pesquisa. p. 92. Projeto/Plano de Ação: 06.00.30001-16| Biblioteca(s): Embrapa Suínos e Aves. |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Agricultura Digital. Para informações adicionais entre em contato com cnptia.biblioteca@embrapa.br. |
Registro Completo
|
Biblioteca(s): |
Embrapa Agricultura Digital. |
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Data corrente: |
25/04/2006 |
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Data da última atualização: |
17/01/2020 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
SIMÕES, M.; BAHIA, D.; TORRES, K.; ZERLOTINI NETO, A.; ARTIGUENAVE, F.; FALCAO, P. R. K.; NESHICH, G.; OLIVEIRA, G. |
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Afiliação: |
MARIANA SIMÕES, Fiocruz; DIANA BAHIA, Fiocruz; KLEIDER TORRES, Fiocruz; ADHEMAR ZERLOTINI NETO, CNPTIA; FRANÇOIS ARTIGUENAVE, Fiocruz; PAULA REGINA KUSER FALCAO, CNPTIA; GORAN NESIC, CNPTIA; GUILHERME OLIVEIRA, Fiocruz. |
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Título: |
SNP identification in Schistosoma mansoni expressed genes. |
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Ano de publicação: |
2005 |
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Fonte/Imprenta: |
In: X-MEETING; INTERNATIONAL CONFERENCE OF THE AB3C, 1., 2005, Caxambu. [Proceedings...]. [S.l.]: Associação Brasileira de Bioinformática e Biologia Computacional, 2005. |
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Páginas: |
p. 131. |
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Idioma: |
Inglês |
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Notas: |
X-meeting 2005. Presented Posters. Na publicação: Paula Kuser. |
|
Conteúdo: |
Schistosomes are parasitic platyhelminths that cause a chronic. often debilitating disease afflicting over 200 million people worldwide. The study of genetic polymorphisms in Schistosomes is important for vaccine and drug development, in addition to the understanding of the genetic structure of populations. Single nucleotide polymorphisms (SNPs) are the most frequent form of DNA variation, they are abundant and have low mutation rates. SNPs are thought to be the next generation of genetic markers that can be used in many of important biological, genetic, pharmacological and medical applications (Thiel et al, 2004). The aim of this project is to identify in silico SNPs (Useche et al, 2001) in ESTs of Schistosoma mansoni, verify their presence in vaccine and drug target candidates and validate putative SNPs using the cathepsin B gene as a model. The S mansoni cathepin B is a proteolytic enzyme that has been evaluated for development of vaccines and new drugs. It is expressed in the parasite gut and it is believed to function in the digestion of haemoglobin, the main nutrient source for the parasite (Sajid and McKerrow, 2002.) The source of ESTs were 61.002 ESTs generated by Minas Gerais Genome Network, all with quality files base called by Phred (Ewing and Green et al, 2004). The sequences were clustered using Phrap, followed by the identification of putative SNPs applying a novel detection algorithm written by our group, cSNPer. A pre-selection of candidate sequence polymorphisms was conducted and SNPs in the cathepsin B gene, among others, were identified. The quality of the DNA sequences and individual SNPs were assessed by visual inspection with reference to chromatograms. Sixteen SNPs were identified, 44% were transitions and 56% transversions, 62% synonym mutations and 38% non-synonym mutations. The majority of the polymorphisms were in the third codon base. We are now pursuing the characterization of the possible effect of the polymorphisms in the structure of the cathepsin B protein. MenosSchistosomes are parasitic platyhelminths that cause a chronic. often debilitating disease afflicting over 200 million people worldwide. The study of genetic polymorphisms in Schistosomes is important for vaccine and drug development, in addition to the understanding of the genetic structure of populations. Single nucleotide polymorphisms (SNPs) are the most frequent form of DNA variation, they are abundant and have low mutation rates. SNPs are thought to be the next generation of genetic markers that can be used in many of important biological, genetic, pharmacological and medical applications (Thiel et al, 2004). The aim of this project is to identify in silico SNPs (Useche et al, 2001) in ESTs of Schistosoma mansoni, verify their presence in vaccine and drug target candidates and validate putative SNPs using the cathepsin B gene as a model. The S mansoni cathepin B is a proteolytic enzyme that has been evaluated for development of vaccines and new drugs. It is expressed in the parasite gut and it is believed to function in the digestion of haemoglobin, the main nutrient source for the parasite (Sajid and McKerrow, 2002.) The source of ESTs were 61.002 ESTs generated by Minas Gerais Genome Network, all with quality files base called by Phred (Ewing and Green et al, 2004). The sequences were clustered using Phrap, followed by the identification of putative SNPs applying a novel detection algorithm written by our group, cSNPer. A pre-selection of candidate sequence polymorph... Mostrar Tudo |
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Palavras-Chave: |
Bioinformática; Polimorfismo de nucleotídeo único. |
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Thesagro: |
Schistosoma mansoni. |
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Thesaurus NAL: |
Bioinformatics; Single nucleotide polymorphism. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
|
Marc: |
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001 1009287
005 2020-01-17
008 2005 bl uuuu u00u1 u #d
100 1 $aSIMÕES, M.
245 $aSNP identification in Schistosoma mansoni expressed genes.$h[electronic resource]
260 $aIn: X-MEETING; INTERNATIONAL CONFERENCE OF THE AB3C, 1., 2005, Caxambu. [Proceedings...]. [S.l.]: Associação Brasileira de Bioinformática e Biologia Computacional$c2005
300 $ap. 131.
500 $aX-meeting 2005. Presented Posters. Na publicação: Paula Kuser.
520 $aSchistosomes are parasitic platyhelminths that cause a chronic. often debilitating disease afflicting over 200 million people worldwide. The study of genetic polymorphisms in Schistosomes is important for vaccine and drug development, in addition to the understanding of the genetic structure of populations. Single nucleotide polymorphisms (SNPs) are the most frequent form of DNA variation, they are abundant and have low mutation rates. SNPs are thought to be the next generation of genetic markers that can be used in many of important biological, genetic, pharmacological and medical applications (Thiel et al, 2004). The aim of this project is to identify in silico SNPs (Useche et al, 2001) in ESTs of Schistosoma mansoni, verify their presence in vaccine and drug target candidates and validate putative SNPs using the cathepsin B gene as a model. The S mansoni cathepin B is a proteolytic enzyme that has been evaluated for development of vaccines and new drugs. It is expressed in the parasite gut and it is believed to function in the digestion of haemoglobin, the main nutrient source for the parasite (Sajid and McKerrow, 2002.) The source of ESTs were 61.002 ESTs generated by Minas Gerais Genome Network, all with quality files base called by Phred (Ewing and Green et al, 2004). The sequences were clustered using Phrap, followed by the identification of putative SNPs applying a novel detection algorithm written by our group, cSNPer. A pre-selection of candidate sequence polymorphisms was conducted and SNPs in the cathepsin B gene, among others, were identified. The quality of the DNA sequences and individual SNPs were assessed by visual inspection with reference to chromatograms. Sixteen SNPs were identified, 44% were transitions and 56% transversions, 62% synonym mutations and 38% non-synonym mutations. The majority of the polymorphisms were in the third codon base. We are now pursuing the characterization of the possible effect of the polymorphisms in the structure of the cathepsin B protein.
650 $aBioinformatics
650 $aSingle nucleotide polymorphism
650 $aSchistosoma mansoni
653 $aBioinformática
653 $aPolimorfismo de nucleotídeo único
700 1 $aBAHIA, D.
700 1 $aTORRES, K.
700 1 $aZERLOTINI NETO, A.
700 1 $aARTIGUENAVE, F.
700 1 $aFALCAO, P. R. K.
700 1 $aNESHICH, G.
700 1 $aOLIVEIRA, G.
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