'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves

Autores
Martínez, Dana Ethel; Costa, María Luján; Gomez, Facundo Martin; Otegui, Marisa; Guiamet, Juan José
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Massive degradation of photosynthetic proteins is the hallmark of leaf senescence; however the mechanism involved in chloroplast protein breakdown is not completely understood. As small 'senescence-associated vacuoles' (SAVs) with intense proteolytic activity accumulate in senescing leaves of soybean and Arabidopsis, the main goal of this work was to determine whether SAVs are involved in the degradation of chloroplastic components. SAVs with protease activity were readily detected through confocal microscopy of naturally senescing leaves of tobacco (Nicotiana tabacum L.). In detached leaves incubated in darkness, acceleration of the chloroplast degradation rate by ethylene treatment correlated with a twofold increase in the number of SAVs per cell, compared to untreated leaves. In a tobacco line expressing GFP targeted to plastids, GFP was re-located to SAVs in senescing leaves. SAVs were isolated by sucrose density gradient centrifugation. Isolated SAVs contained chloroplast-targeted GFP and the chloroplast stromal proteins Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) and glutamine synthetase, but lacked the thylakoid proteins D1 and light-harvesting complex II of the photosystem II reaction center and photosystem II antenna, respectively. In SAVs incubated at 30°C, there was a steady decrease in Rubisco levels, which was completely abolished by addition of protease inhibitors. These results indicate that SAVs are involved in degradation of the soluble photosynthetic proteins of the chloroplast stroma during senescence of leaves.
Instituto de Fisiología Vegetal
Materia
Ciencias Naturales
Chloroplast breakdown
Glutamine synthetase
Proteolysis
Rubisco
Senescence-associated vacuoles
Tobacco
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/84235

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network_name_str SEDICI (UNLP)
spelling 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leavesMartínez, Dana EthelCosta, María LujánGomez, Facundo MartinOtegui, MarisaGuiamet, Juan JoséCiencias NaturalesChloroplast breakdownGlutamine synthetaseProteolysisRubiscoSenescence-associated vacuolesTobaccoMassive degradation of photosynthetic proteins is the hallmark of leaf senescence; however the mechanism involved in chloroplast protein breakdown is not completely understood. As small 'senescence-associated vacuoles' (SAVs) with intense proteolytic activity accumulate in senescing leaves of soybean and Arabidopsis, the main goal of this work was to determine whether SAVs are involved in the degradation of chloroplastic components. SAVs with protease activity were readily detected through confocal microscopy of naturally senescing leaves of tobacco (<i>Nicotiana tabacum</i> L.). In detached leaves incubated in darkness, acceleration of the chloroplast degradation rate by ethylene treatment correlated with a twofold increase in the number of SAVs per cell, compared to untreated leaves. In a tobacco line expressing GFP targeted to plastids, GFP was re-located to SAVs in senescing leaves. SAVs were isolated by sucrose density gradient centrifugation. Isolated SAVs contained chloroplast-targeted GFP and the chloroplast stromal proteins Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) and glutamine synthetase, but lacked the thylakoid proteins D1 and light-harvesting complex II of the photosystem II reaction center and photosystem II antenna, respectively. In SAVs incubated at 30°C, there was a steady decrease in Rubisco levels, which was completely abolished by addition of protease inhibitors. These results indicate that SAVs are involved in degradation of the soluble photosynthetic proteins of the chloroplast stroma during senescence of leaves.Instituto de Fisiología Vegetal2008info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf196-206http://sedici.unlp.edu.ar/handle/10915/84235enginfo:eu-repo/semantics/altIdentifier/issn/0960-7412info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1365-313X.2008.03585.xinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:48:31Zoai:sedici.unlp.edu.ar:10915/84235Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:48:31.457SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
title 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
spellingShingle 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
Martínez, Dana Ethel
Ciencias Naturales
Chloroplast breakdown
Glutamine synthetase
Proteolysis
Rubisco
Senescence-associated vacuoles
Tobacco
title_short 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
title_full 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
title_fullStr 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
title_full_unstemmed 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
title_sort 'Senescence-associated vacuoles' are involved in the degradation of chloroplast proteins in tobacco leaves
dc.creator.none.fl_str_mv Martínez, Dana Ethel
Costa, María Luján
Gomez, Facundo Martin
Otegui, Marisa
Guiamet, Juan José
author Martínez, Dana Ethel
author_facet Martínez, Dana Ethel
Costa, María Luján
Gomez, Facundo Martin
Otegui, Marisa
Guiamet, Juan José
author_role author
author2 Costa, María Luján
Gomez, Facundo Martin
Otegui, Marisa
Guiamet, Juan José
author2_role author
author
author
author
dc.subject.none.fl_str_mv Ciencias Naturales
Chloroplast breakdown
Glutamine synthetase
Proteolysis
Rubisco
Senescence-associated vacuoles
Tobacco
topic Ciencias Naturales
Chloroplast breakdown
Glutamine synthetase
Proteolysis
Rubisco
Senescence-associated vacuoles
Tobacco
dc.description.none.fl_txt_mv Massive degradation of photosynthetic proteins is the hallmark of leaf senescence; however the mechanism involved in chloroplast protein breakdown is not completely understood. As small 'senescence-associated vacuoles' (SAVs) with intense proteolytic activity accumulate in senescing leaves of soybean and Arabidopsis, the main goal of this work was to determine whether SAVs are involved in the degradation of chloroplastic components. SAVs with protease activity were readily detected through confocal microscopy of naturally senescing leaves of tobacco (<i>Nicotiana tabacum</i> L.). In detached leaves incubated in darkness, acceleration of the chloroplast degradation rate by ethylene treatment correlated with a twofold increase in the number of SAVs per cell, compared to untreated leaves. In a tobacco line expressing GFP targeted to plastids, GFP was re-located to SAVs in senescing leaves. SAVs were isolated by sucrose density gradient centrifugation. Isolated SAVs contained chloroplast-targeted GFP and the chloroplast stromal proteins Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) and glutamine synthetase, but lacked the thylakoid proteins D1 and light-harvesting complex II of the photosystem II reaction center and photosystem II antenna, respectively. In SAVs incubated at 30°C, there was a steady decrease in Rubisco levels, which was completely abolished by addition of protease inhibitors. These results indicate that SAVs are involved in degradation of the soluble photosynthetic proteins of the chloroplast stroma during senescence of leaves.
Instituto de Fisiología Vegetal
description Massive degradation of photosynthetic proteins is the hallmark of leaf senescence; however the mechanism involved in chloroplast protein breakdown is not completely understood. As small 'senescence-associated vacuoles' (SAVs) with intense proteolytic activity accumulate in senescing leaves of soybean and Arabidopsis, the main goal of this work was to determine whether SAVs are involved in the degradation of chloroplastic components. SAVs with protease activity were readily detected through confocal microscopy of naturally senescing leaves of tobacco (<i>Nicotiana tabacum</i> L.). In detached leaves incubated in darkness, acceleration of the chloroplast degradation rate by ethylene treatment correlated with a twofold increase in the number of SAVs per cell, compared to untreated leaves. In a tobacco line expressing GFP targeted to plastids, GFP was re-located to SAVs in senescing leaves. SAVs were isolated by sucrose density gradient centrifugation. Isolated SAVs contained chloroplast-targeted GFP and the chloroplast stromal proteins Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) and glutamine synthetase, but lacked the thylakoid proteins D1 and light-harvesting complex II of the photosystem II reaction center and photosystem II antenna, respectively. In SAVs incubated at 30°C, there was a steady decrease in Rubisco levels, which was completely abolished by addition of protease inhibitors. These results indicate that SAVs are involved in degradation of the soluble photosynthetic proteins of the chloroplast stroma during senescence of leaves.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/84235
url http://sedici.unlp.edu.ar/handle/10915/84235
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0960-7412
info:eu-repo/semantics/altIdentifier/doi/10.1111/j.1365-313X.2008.03585.x
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
196-206
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instname:Universidad Nacional de La Plata
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instname_str Universidad Nacional de La Plata
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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