3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells
- Autores
- Gergely, Zachary; Martinez, Dana Ethel; Donohoe, Bryon S.; Mogelsvang, Soren; Herder, Rachel; Staehelin, L. Andrew
- Año de publicación
- 2018
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Background: The insect-trapping leaves of Dionaea muscipula provide a model for studying the secretory pathway of an inducible plant secretory system. The leaf glands were induced with bovine serum albumin to secrete proteases that were characterized via zymogram activity gels over a 6-day period. The accompanying morphological changes of the endoplasmic reticulum (ER) and Golgi were analyzed using 3D electron tomography of glands preserved by highpressure freezing/freeze substitution methods. Results: Secretion of multiple cysteine and aspartic proteases occurred biphasically. The majority of the Golgi was organized in clusters consisting of 3–6 stacks surrounded by a cage-like system of ER cisternae. In these clusters, all Golgi stacks were oriented with their cis-most C1 cisterna facing an ER export site. The C1 Golgi cisternae varied in size and shape consistent with the hypothesis that they form de novo. Following induction, the number of ER-bound polysomes doubled, but no increase in COPII vesicles was observed. Golgi changes included a reduction in the number of cisternae per stack and a doubling of cisternal volume without increased surface area. Polysaccharide molecules that form the sticky slime cause swelling of the trans and trans Golgi network (TGN) cisternae. Peeling of the trans-most cisternae gives rise to free TGN cisternae. One day after gland stimulation, the free TGNs were frequently associated with loose groups of oriented actin-like flaments which were not seen in any other samples. Conclusions: These fndings suggest that the secretory apparatus of resting gland cells is “overbuilt” to enable the cells to rapidly up-regulate lytic enzyme production and secretion in response to prey trapping.
Fil: Gergely, Zachary. State University of Colorado at Boulder; Estados Unidos
Fil: Martinez, Dana Ethel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Fisiología Vegetal. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Instituto de Fisiología Vegetal; Argentina
Fil: Donohoe, Bryon S.. State University of Colorado at Boulder; Estados Unidos
Fil: Mogelsvang, Soren. State University of Colorado at Boulder; Estados Unidos
Fil: Herder, Rachel. State University of Colorado at Boulder; Estados Unidos
Fil: Staehelin, L. Andrew. State University of Colorado at Boulder; Estados Unidos - Materia
-
VENUS FLY TRAP
GOLGI
ELECTRON TOMOGRAPHY - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/93706
Ver los metadatos del registro completo
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3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cellsGergely, ZacharyMartinez, Dana EthelDonohoe, Bryon S.Mogelsvang, SorenHerder, RachelStaehelin, L. AndrewVENUS FLY TRAPGOLGIELECTRON TOMOGRAPHYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Background: The insect-trapping leaves of Dionaea muscipula provide a model for studying the secretory pathway of an inducible plant secretory system. The leaf glands were induced with bovine serum albumin to secrete proteases that were characterized via zymogram activity gels over a 6-day period. The accompanying morphological changes of the endoplasmic reticulum (ER) and Golgi were analyzed using 3D electron tomography of glands preserved by highpressure freezing/freeze substitution methods. Results: Secretion of multiple cysteine and aspartic proteases occurred biphasically. The majority of the Golgi was organized in clusters consisting of 3–6 stacks surrounded by a cage-like system of ER cisternae. In these clusters, all Golgi stacks were oriented with their cis-most C1 cisterna facing an ER export site. The C1 Golgi cisternae varied in size and shape consistent with the hypothesis that they form de novo. Following induction, the number of ER-bound polysomes doubled, but no increase in COPII vesicles was observed. Golgi changes included a reduction in the number of cisternae per stack and a doubling of cisternal volume without increased surface area. Polysaccharide molecules that form the sticky slime cause swelling of the trans and trans Golgi network (TGN) cisternae. Peeling of the trans-most cisternae gives rise to free TGN cisternae. One day after gland stimulation, the free TGNs were frequently associated with loose groups of oriented actin-like flaments which were not seen in any other samples. Conclusions: These fndings suggest that the secretory apparatus of resting gland cells is “overbuilt” to enable the cells to rapidly up-regulate lytic enzyme production and secretion in response to prey trapping.Fil: Gergely, Zachary. State University of Colorado at Boulder; Estados UnidosFil: Martinez, Dana Ethel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Fisiología Vegetal. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Instituto de Fisiología Vegetal; ArgentinaFil: Donohoe, Bryon S.. State University of Colorado at Boulder; Estados UnidosFil: Mogelsvang, Soren. State University of Colorado at Boulder; Estados UnidosFil: Herder, Rachel. State University of Colorado at Boulder; Estados UnidosFil: Staehelin, L. Andrew. State University of Colorado at Boulder; Estados UnidosBMC2018-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/93706Gergely, Zachary; Martinez, Dana Ethel; Donohoe, Bryon S.; Mogelsvang, Soren; Herder, Rachel; et al.; 3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells; BMC; Journal of Biological Research-Thessaloniki; 25; 1; 8-2018; 1-162241-5793CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://jbiolres.biomedcentral.com/articles/10.1186/s40709-018-0086-2info:eu-repo/semantics/altIdentifier/doi/10.1186/s40709-018-0086-2info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:45:22Zoai:ri.conicet.gov.ar:11336/93706instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:45:22.725CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| title |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| spellingShingle |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells Gergely, Zachary VENUS FLY TRAP GOLGI ELECTRON TOMOGRAPHY |
| title_short |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| title_full |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| title_fullStr |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| title_full_unstemmed |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| title_sort |
3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells |
| dc.creator.none.fl_str_mv |
Gergely, Zachary Martinez, Dana Ethel Donohoe, Bryon S. Mogelsvang, Soren Herder, Rachel Staehelin, L. Andrew |
| author |
Gergely, Zachary |
| author_facet |
Gergely, Zachary Martinez, Dana Ethel Donohoe, Bryon S. Mogelsvang, Soren Herder, Rachel Staehelin, L. Andrew |
| author_role |
author |
| author2 |
Martinez, Dana Ethel Donohoe, Bryon S. Mogelsvang, Soren Herder, Rachel Staehelin, L. Andrew |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
VENUS FLY TRAP GOLGI ELECTRON TOMOGRAPHY |
| topic |
VENUS FLY TRAP GOLGI ELECTRON TOMOGRAPHY |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
Background: The insect-trapping leaves of Dionaea muscipula provide a model for studying the secretory pathway of an inducible plant secretory system. The leaf glands were induced with bovine serum albumin to secrete proteases that were characterized via zymogram activity gels over a 6-day period. The accompanying morphological changes of the endoplasmic reticulum (ER) and Golgi were analyzed using 3D electron tomography of glands preserved by highpressure freezing/freeze substitution methods. Results: Secretion of multiple cysteine and aspartic proteases occurred biphasically. The majority of the Golgi was organized in clusters consisting of 3–6 stacks surrounded by a cage-like system of ER cisternae. In these clusters, all Golgi stacks were oriented with their cis-most C1 cisterna facing an ER export site. The C1 Golgi cisternae varied in size and shape consistent with the hypothesis that they form de novo. Following induction, the number of ER-bound polysomes doubled, but no increase in COPII vesicles was observed. Golgi changes included a reduction in the number of cisternae per stack and a doubling of cisternal volume without increased surface area. Polysaccharide molecules that form the sticky slime cause swelling of the trans and trans Golgi network (TGN) cisternae. Peeling of the trans-most cisternae gives rise to free TGN cisternae. One day after gland stimulation, the free TGNs were frequently associated with loose groups of oriented actin-like flaments which were not seen in any other samples. Conclusions: These fndings suggest that the secretory apparatus of resting gland cells is “overbuilt” to enable the cells to rapidly up-regulate lytic enzyme production and secretion in response to prey trapping. Fil: Gergely, Zachary. State University of Colorado at Boulder; Estados Unidos Fil: Martinez, Dana Ethel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Fisiología Vegetal. Universidad Nacional de La Plata. Facultad de Ciencias Naturales y Museo. Instituto de Fisiología Vegetal; Argentina Fil: Donohoe, Bryon S.. State University of Colorado at Boulder; Estados Unidos Fil: Mogelsvang, Soren. State University of Colorado at Boulder; Estados Unidos Fil: Herder, Rachel. State University of Colorado at Boulder; Estados Unidos Fil: Staehelin, L. Andrew. State University of Colorado at Boulder; Estados Unidos |
| description |
Background: The insect-trapping leaves of Dionaea muscipula provide a model for studying the secretory pathway of an inducible plant secretory system. The leaf glands were induced with bovine serum albumin to secrete proteases that were characterized via zymogram activity gels over a 6-day period. The accompanying morphological changes of the endoplasmic reticulum (ER) and Golgi were analyzed using 3D electron tomography of glands preserved by highpressure freezing/freeze substitution methods. Results: Secretion of multiple cysteine and aspartic proteases occurred biphasically. The majority of the Golgi was organized in clusters consisting of 3–6 stacks surrounded by a cage-like system of ER cisternae. In these clusters, all Golgi stacks were oriented with their cis-most C1 cisterna facing an ER export site. The C1 Golgi cisternae varied in size and shape consistent with the hypothesis that they form de novo. Following induction, the number of ER-bound polysomes doubled, but no increase in COPII vesicles was observed. Golgi changes included a reduction in the number of cisternae per stack and a doubling of cisternal volume without increased surface area. Polysaccharide molecules that form the sticky slime cause swelling of the trans and trans Golgi network (TGN) cisternae. Peeling of the trans-most cisternae gives rise to free TGN cisternae. One day after gland stimulation, the free TGNs were frequently associated with loose groups of oriented actin-like flaments which were not seen in any other samples. Conclusions: These fndings suggest that the secretory apparatus of resting gland cells is “overbuilt” to enable the cells to rapidly up-regulate lytic enzyme production and secretion in response to prey trapping. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2018-08 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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publishedVersion |
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http://hdl.handle.net/11336/93706 Gergely, Zachary; Martinez, Dana Ethel; Donohoe, Bryon S.; Mogelsvang, Soren; Herder, Rachel; et al.; 3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells; BMC; Journal of Biological Research-Thessaloniki; 25; 1; 8-2018; 1-16 2241-5793 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/93706 |
| identifier_str_mv |
Gergely, Zachary; Martinez, Dana Ethel; Donohoe, Bryon S.; Mogelsvang, Soren; Herder, Rachel; et al.; 3D electron tomographic and biochemical analysis of ER, Golgi and trans Golgi network membrane systems in stimulated Venus flytrap (Dionaea muscipula) glandular cells; BMC; Journal of Biological Research-Thessaloniki; 25; 1; 8-2018; 1-16 2241-5793 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
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eng |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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