Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae

Detalhes bibliográficos
Autor(a) principal: Farzana, Sabir
Data de Publicação: 2020
Outros Autores: Gomes, Sara, Loureiro-Dias, Maria C., Soveral, Graça, Prista, Catarina
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.5/19560
Resumo: Plant Nodulin 26-like Intrinsic Proteins (NIPs) are multifunctional membrane channels of the Major Intrinsic Protein (MIP) family. Unlike other homologs, they have low intrinsic water permeability. NIPs possess diverse substrate selectivity, ranging from water to glycerol and to other small solutes, depending on the group-specific amino acid composition at aromatic/Arg (ar/R) constriction. We cloned three NIPs (NIP1;1, NIP5;1, and NIP6;1) from grapevine (cv. Touriga Nacional). Their expression in the membrane of aqy-null Saccharomyces cerevisiae enabled their functional characterization for water and glycerol transport through stopped-flow spectroscopy. VvTnNIP1;1 demonstrated high water as well as glycerol permeability, whereas VvTnNIP6;1 was impermeable to water but presented high glycerol permeability. Their transport activities were declined by cytosolic acidification, implying that internal-pH can regulate NIPs gating. Furthermore, an extension of C-terminal in VvTnNIP6;1M homolog, led to improved channel activity, suggesting that NIPs gating is putatively regulated by C-terminal. Yeast growth assays in the presence of diverse substrates suggest that the transmembrane flux of metalloids (As, B, and Se) and the heavy metal (Cd) are facilitated through grapevine NIPs. This is the first molecular and functional characterization of grapevine NIPs, providing crucial insights into understanding their role for uptake and translocation of small solutes, and extrusion of toxic compounds in grapevine
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spelling Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiaeaquaporingrapevineSaccharomyces cerevisiaeNIPsmetalloidsglycerolPlant Nodulin 26-like Intrinsic Proteins (NIPs) are multifunctional membrane channels of the Major Intrinsic Protein (MIP) family. Unlike other homologs, they have low intrinsic water permeability. NIPs possess diverse substrate selectivity, ranging from water to glycerol and to other small solutes, depending on the group-specific amino acid composition at aromatic/Arg (ar/R) constriction. We cloned three NIPs (NIP1;1, NIP5;1, and NIP6;1) from grapevine (cv. Touriga Nacional). Their expression in the membrane of aqy-null Saccharomyces cerevisiae enabled their functional characterization for water and glycerol transport through stopped-flow spectroscopy. VvTnNIP1;1 demonstrated high water as well as glycerol permeability, whereas VvTnNIP6;1 was impermeable to water but presented high glycerol permeability. Their transport activities were declined by cytosolic acidification, implying that internal-pH can regulate NIPs gating. Furthermore, an extension of C-terminal in VvTnNIP6;1M homolog, led to improved channel activity, suggesting that NIPs gating is putatively regulated by C-terminal. Yeast growth assays in the presence of diverse substrates suggest that the transmembrane flux of metalloids (As, B, and Se) and the heavy metal (Cd) are facilitated through grapevine NIPs. This is the first molecular and functional characterization of grapevine NIPs, providing crucial insights into understanding their role for uptake and translocation of small solutes, and extrusion of toxic compounds in grapevineMDPIRepositório da Universidade de LisboaFarzana, SabirGomes, SaraLoureiro-Dias, Maria C.Soveral, GraçaPrista, Catarina2020-02-04T12:26:38Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.5/19560engInt. J. Mol. Sci. 2020, 21, 66310.3390/ijms21020663info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-12-10T01:31:19Zoai:www.repository.utl.pt:10400.5/19560Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:04:25.968620Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
title Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
spellingShingle Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
Farzana, Sabir
aquaporin
grapevine
Saccharomyces cerevisiae
NIPs
metalloids
glycerol
title_short Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
title_full Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
title_fullStr Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
title_full_unstemmed Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
title_sort Molecular and functional characterization of grapevine NIPs through heterologous expression in aqy-null Saccharomyces cerevisiae
author Farzana, Sabir
author_facet Farzana, Sabir
Gomes, Sara
Loureiro-Dias, Maria C.
Soveral, Graça
Prista, Catarina
author_role author
author2 Gomes, Sara
Loureiro-Dias, Maria C.
Soveral, Graça
Prista, Catarina
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório da Universidade de Lisboa
dc.contributor.author.fl_str_mv Farzana, Sabir
Gomes, Sara
Loureiro-Dias, Maria C.
Soveral, Graça
Prista, Catarina
dc.subject.por.fl_str_mv aquaporin
grapevine
Saccharomyces cerevisiae
NIPs
metalloids
glycerol
topic aquaporin
grapevine
Saccharomyces cerevisiae
NIPs
metalloids
glycerol
description Plant Nodulin 26-like Intrinsic Proteins (NIPs) are multifunctional membrane channels of the Major Intrinsic Protein (MIP) family. Unlike other homologs, they have low intrinsic water permeability. NIPs possess diverse substrate selectivity, ranging from water to glycerol and to other small solutes, depending on the group-specific amino acid composition at aromatic/Arg (ar/R) constriction. We cloned three NIPs (NIP1;1, NIP5;1, and NIP6;1) from grapevine (cv. Touriga Nacional). Their expression in the membrane of aqy-null Saccharomyces cerevisiae enabled their functional characterization for water and glycerol transport through stopped-flow spectroscopy. VvTnNIP1;1 demonstrated high water as well as glycerol permeability, whereas VvTnNIP6;1 was impermeable to water but presented high glycerol permeability. Their transport activities were declined by cytosolic acidification, implying that internal-pH can regulate NIPs gating. Furthermore, an extension of C-terminal in VvTnNIP6;1M homolog, led to improved channel activity, suggesting that NIPs gating is putatively regulated by C-terminal. Yeast growth assays in the presence of diverse substrates suggest that the transmembrane flux of metalloids (As, B, and Se) and the heavy metal (Cd) are facilitated through grapevine NIPs. This is the first molecular and functional characterization of grapevine NIPs, providing crucial insights into understanding their role for uptake and translocation of small solutes, and extrusion of toxic compounds in grapevine
publishDate 2020
dc.date.none.fl_str_mv 2020-02-04T12:26:38Z
2020
2020-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.5/19560
url http://hdl.handle.net/10400.5/19560
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Int. J. Mol. Sci. 2020, 21, 663
10.3390/ijms21020663
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv MDPI
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dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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