The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.

Detalhes bibliográficos
Autor(a) principal: Mathieson, William
Data de Publicação: 2011
Outros Autores: Borges, William de Castro, Wilson, R. Alan
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFOP
Texto Completo: http://www.repositorio.ufop.br/handle/123456789/4650
https://doi.org/10.1016/j.molbiopara.2010.10.005
Resumo: Schistosoma mansoni eggs, consisting of an ovum surrounded by nutritive vitelline cells packaged in a tanned protein shell, are produced by paired worms residing in the mesenteric veins of the human host. The vitelline cells are degraded as the larval miracidium matures, the fully developed egg either crossing the gut wall to escape the host or becoming lodged in the host’s tissues where it dies and disintegrates, inducing a potentially pathological immune response. Thus, the egg is central to both the transmission of the parasite and the aetiology of the disease. Herewepresent the first study investigating protein turnover in the egg. We establish that the ubiquitin-proteasome pathway (UPP) changes with egg development and furthermore, that the morphological components of the fully developed egg (the miracidium and the subshell envelope) also exhibit different proteasome subunit expression profiles. We conclude that the UPP is responsible not only for degrading the vitelline cells but is also more highly developed in the envelope than in the miracidium. The envelope is involved in the defence of the miracidium and produces the proteins that the egg secretes, presumably to facilitate its escape from the host, so the UPP probably has a multi-faceted role in the egg’s biology.
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spelling Mathieson, WilliamBorges, William de CastroWilson, R. Alan2015-03-16T18:53:22Z2015-03-16T18:53:22Z2011MATHIESON, W.; BORGES, W. de C.; WILSON, R. A. The proteasome - ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics. Molecular and Biochemical Parasitology, v. 175, p. 118-125, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0166685110002574>. Acesso em: 08 nov. 2014.0166-6851http://www.repositorio.ufop.br/handle/123456789/4650https://doi.org/10.1016/j.molbiopara.2010.10.005Schistosoma mansoni eggs, consisting of an ovum surrounded by nutritive vitelline cells packaged in a tanned protein shell, are produced by paired worms residing in the mesenteric veins of the human host. The vitelline cells are degraded as the larval miracidium matures, the fully developed egg either crossing the gut wall to escape the host or becoming lodged in the host’s tissues where it dies and disintegrates, inducing a potentially pathological immune response. Thus, the egg is central to both the transmission of the parasite and the aetiology of the disease. Herewepresent the first study investigating protein turnover in the egg. We establish that the ubiquitin-proteasome pathway (UPP) changes with egg development and furthermore, that the morphological components of the fully developed egg (the miracidium and the subshell envelope) also exhibit different proteasome subunit expression profiles. We conclude that the UPP is responsible not only for degrading the vitelline cells but is also more highly developed in the envelope than in the miracidium. The envelope is involved in the defence of the miracidium and produces the proteins that the egg secretes, presumably to facilitate its escape from the host, so the UPP probably has a multi-faceted role in the egg’s biology.Hatch fluidMiracidiumVitelline cellsVitellariaThe proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleO periódico Molecular and Biochemical Parasitology concede permissão para depósito deste artigo no Repositório Institucional da UFOP. 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dc.title.pt_BR.fl_str_mv The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
title The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
spellingShingle The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
Mathieson, William
Hatch fluid
Miracidium
Vitelline cells
Vitellaria
title_short The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
title_full The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
title_fullStr The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
title_full_unstemmed The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
title_sort The proteasome-ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics.
author Mathieson, William
author_facet Mathieson, William
Borges, William de Castro
Wilson, R. Alan
author_role author
author2 Borges, William de Castro
Wilson, R. Alan
author2_role author
author
dc.contributor.author.fl_str_mv Mathieson, William
Borges, William de Castro
Wilson, R. Alan
dc.subject.por.fl_str_mv Hatch fluid
Miracidium
Vitelline cells
Vitellaria
topic Hatch fluid
Miracidium
Vitelline cells
Vitellaria
description Schistosoma mansoni eggs, consisting of an ovum surrounded by nutritive vitelline cells packaged in a tanned protein shell, are produced by paired worms residing in the mesenteric veins of the human host. The vitelline cells are degraded as the larval miracidium matures, the fully developed egg either crossing the gut wall to escape the host or becoming lodged in the host’s tissues where it dies and disintegrates, inducing a potentially pathological immune response. Thus, the egg is central to both the transmission of the parasite and the aetiology of the disease. Herewepresent the first study investigating protein turnover in the egg. We establish that the ubiquitin-proteasome pathway (UPP) changes with egg development and furthermore, that the morphological components of the fully developed egg (the miracidium and the subshell envelope) also exhibit different proteasome subunit expression profiles. We conclude that the UPP is responsible not only for degrading the vitelline cells but is also more highly developed in the envelope than in the miracidium. The envelope is involved in the defence of the miracidium and produces the proteins that the egg secretes, presumably to facilitate its escape from the host, so the UPP probably has a multi-faceted role in the egg’s biology.
publishDate 2011
dc.date.issued.fl_str_mv 2011
dc.date.accessioned.fl_str_mv 2015-03-16T18:53:22Z
dc.date.available.fl_str_mv 2015-03-16T18:53:22Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv MATHIESON, W.; BORGES, W. de C.; WILSON, R. A. The proteasome - ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics. Molecular and Biochemical Parasitology, v. 175, p. 118-125, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0166685110002574>. Acesso em: 08 nov. 2014.
dc.identifier.uri.fl_str_mv http://www.repositorio.ufop.br/handle/123456789/4650
dc.identifier.issn.none.fl_str_mv 0166-6851
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.molbiopara.2010.10.005
identifier_str_mv MATHIESON, W.; BORGES, W. de C.; WILSON, R. A. The proteasome - ubiquitin pathway in the Schistosoma mansoni egg has development - and morphology - specific characteristics. Molecular and Biochemical Parasitology, v. 175, p. 118-125, 2011. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0166685110002574>. Acesso em: 08 nov. 2014.
0166-6851
url http://www.repositorio.ufop.br/handle/123456789/4650
https://doi.org/10.1016/j.molbiopara.2010.10.005
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