Tools to Study SUMO Conjugation in Caenorhabditis elegans
- Autores
- Pelisch, Federico Gaston; Hay, Ronald T.
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The cell biology of sumoylation has mostly been studied using transformed cultured cells and yeast. Inrecent years, genetic analysis has demonstrated important roles for sumoylation in the biology of C. elegans. Here, we expand the existing set of tools making it possible to address the role of sumoylation in thenematode C. elegans using a combination of genetics, imaging, and biochemistry. Most importantly, thedynamics of SUMO conjugation and deconjugation can be followed very precisely both in space and timewithin living worms. Additionally, the biochemistry of SUMO conjugation and deconjugation can beaddressed using recombinant purifi ed components of the C. elegans sumoylation machinery, including E3ligases and SUMO proteases. These tools and reagents will be useful to gain insights into the biologicalrole of SUMO in the context of a multicellular organism.
Fil: Pelisch, Federico Gaston. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Fisiología, Biología Molecular y Neurociencias. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Fisiología, Biología Molecular y Neurociencias; Argentina. University of Dundee; Reino Unido
Fil: Hay, Ronald T.. University of Dundee; Reino Unido - Materia
-
Sumo
Caenorhabditis Elegans
Cell Cycle
Microscopy - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/45389
Ver los metadatos del registro completo
id |
CONICETDig_2f42b87f711668f929a5c544ecf1ad7a |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/45389 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Tools to Study SUMO Conjugation in Caenorhabditis elegansPelisch, Federico GastonHay, Ronald T.SumoCaenorhabditis ElegansCell CycleMicroscopyhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The cell biology of sumoylation has mostly been studied using transformed cultured cells and yeast. Inrecent years, genetic analysis has demonstrated important roles for sumoylation in the biology of C. elegans. Here, we expand the existing set of tools making it possible to address the role of sumoylation in thenematode C. elegans using a combination of genetics, imaging, and biochemistry. Most importantly, thedynamics of SUMO conjugation and deconjugation can be followed very precisely both in space and timewithin living worms. Additionally, the biochemistry of SUMO conjugation and deconjugation can beaddressed using recombinant purifi ed components of the C. elegans sumoylation machinery, including E3ligases and SUMO proteases. These tools and reagents will be useful to gain insights into the biologicalrole of SUMO in the context of a multicellular organism.Fil: Pelisch, Federico Gaston. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Fisiología, Biología Molecular y Neurociencias. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Fisiología, Biología Molecular y Neurociencias; Argentina. University of Dundee; Reino UnidoFil: Hay, Ronald T.. University of Dundee; Reino UnidoSpringer2016-09-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/45389Pelisch, Federico Gaston; Hay, Ronald T.; Tools to Study SUMO Conjugation in Caenorhabditis elegans; Springer; Methods in Molecular Biology; 1475; 6-9-2016; 233-2561064-3745CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/protocol/10.1007/978-1-4939-6358-4_17info:eu-repo/semantics/altIdentifier/doi/10.1007/978-1-4939-6358-4_17info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:35:38Zoai:ri.conicet.gov.ar:11336/45389instacron: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:34982025-09-29 09:35:39.193CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
title |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
spellingShingle |
Tools to Study SUMO Conjugation in Caenorhabditis elegans Pelisch, Federico Gaston Sumo Caenorhabditis Elegans Cell Cycle Microscopy |
title_short |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
title_full |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
title_fullStr |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
title_full_unstemmed |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
title_sort |
Tools to Study SUMO Conjugation in Caenorhabditis elegans |
dc.creator.none.fl_str_mv |
Pelisch, Federico Gaston Hay, Ronald T. |
author |
Pelisch, Federico Gaston |
author_facet |
Pelisch, Federico Gaston Hay, Ronald T. |
author_role |
author |
author2 |
Hay, Ronald T. |
author2_role |
author |
dc.subject.none.fl_str_mv |
Sumo Caenorhabditis Elegans Cell Cycle Microscopy |
topic |
Sumo Caenorhabditis Elegans Cell Cycle Microscopy |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The cell biology of sumoylation has mostly been studied using transformed cultured cells and yeast. Inrecent years, genetic analysis has demonstrated important roles for sumoylation in the biology of C. elegans. Here, we expand the existing set of tools making it possible to address the role of sumoylation in thenematode C. elegans using a combination of genetics, imaging, and biochemistry. Most importantly, thedynamics of SUMO conjugation and deconjugation can be followed very precisely both in space and timewithin living worms. Additionally, the biochemistry of SUMO conjugation and deconjugation can beaddressed using recombinant purifi ed components of the C. elegans sumoylation machinery, including E3ligases and SUMO proteases. These tools and reagents will be useful to gain insights into the biologicalrole of SUMO in the context of a multicellular organism. Fil: Pelisch, Federico Gaston. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Fisiología, Biología Molecular y Neurociencias. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Fisiología, Biología Molecular y Neurociencias; Argentina. University of Dundee; Reino Unido Fil: Hay, Ronald T.. University of Dundee; Reino Unido |
description |
The cell biology of sumoylation has mostly been studied using transformed cultured cells and yeast. Inrecent years, genetic analysis has demonstrated important roles for sumoylation in the biology of C. elegans. Here, we expand the existing set of tools making it possible to address the role of sumoylation in thenematode C. elegans using a combination of genetics, imaging, and biochemistry. Most importantly, thedynamics of SUMO conjugation and deconjugation can be followed very precisely both in space and timewithin living worms. Additionally, the biochemistry of SUMO conjugation and deconjugation can beaddressed using recombinant purifi ed components of the C. elegans sumoylation machinery, including E3ligases and SUMO proteases. These tools and reagents will be useful to gain insights into the biologicalrole of SUMO in the context of a multicellular organism. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-09-06 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/11336/45389 Pelisch, Federico Gaston; Hay, Ronald T.; Tools to Study SUMO Conjugation in Caenorhabditis elegans; Springer; Methods in Molecular Biology; 1475; 6-9-2016; 233-256 1064-3745 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/45389 |
identifier_str_mv |
Pelisch, Federico Gaston; Hay, Ronald T.; Tools to Study SUMO Conjugation in Caenorhabditis elegans; Springer; Methods in Molecular Biology; 1475; 6-9-2016; 233-256 1064-3745 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/protocol/10.1007/978-1-4939-6358-4_17 info:eu-repo/semantics/altIdentifier/doi/10.1007/978-1-4939-6358-4_17 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
_version_ |
1844613111849418752 |
score |
13.070432 |