Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide

Autores
Calderon Villalobos, Luz Irina; Iglesias, María José; Terrile, Maria Cecilia; Casalongue, Claudia
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The term auxin is derived from the Greek word ?auxein,? which means to grow or to expand and 3 was sealed by Charles Darwin more than a century ago. In ?The Power of Movement in Plants? 4 (1880), Darwin first described the effects of light on the movement of canary grass 5 coleoptiles. He demonstrated that the tip of the seedling was responsible for producing some 6 signal, namely auxin, which was transported to the lower part of the coleoptile, where the 7 physiological response of bending following the light occurred. Auxin is probably the most 8 intensely-studied molecule in plants as it impacts virtually every aspect of growth and 9 development during their life cycle. 10The role of auxin is warranted by the coordination of its synthesis, metabolism, transport, and 11 perception. The plant cell traduces the auxin signal through a well-characterized nuclear 12 signaling pathway, triggering transcriptional responses depending on a specific cell, tissue, or 13 organ. 14Auxin signaling pathway initiates once the hormone moves into the nucleus and is bound by a 15 coreceptor system by the E3 ubiquitin ligase SCFTIR1/AFBs and its degradation substrates 16 AUX/IAAs transcriptional repressors. Upon auxin binding SCFTIR1/AFBs trigger ubiquitylation 17 and further AUX/IAA turnover by the proteasome. AUX/IAAs block the expression of auxin-18 responsive genes, their degradation is essential for auxin pathway activation. 19Since plants are sessile organisms unable to escape changes in the environment, the degradation 20 of pre-synthesized AUX/IAA repressor proteins instead of the de novo synthesis of activation 21 proteins constitutes a more rapid and efficient strategy for the activation of molecular pathways 22 required to adapt to new situations. Thus, the ubiquitin proteasome system via the exquisite 23 action of specific E3 ubiquitin ligases, such as the SCFTIR1/AFBs recruit directly proteins 24 degradation substrates. SCF-type E3 ligases are the most abundant substrate recognition 25 complexes in eukaryotic cells and have been implicated in every major phytohormone signaling 26 pathway. Each individual SCF E3 ligase is a multimer consisting of a scaffold protein Cullin 1, a 27 RING RBX1 for binding an E2 conjugating enzyme loaded with ubiquitin, and a substrate 28 binding module build by the adaptor protein, SKP1 (in Arabidopsis ASK1) and, an 29 interchangeable substrate-recognition unit F-box Protein (FBP). 30In the last decade we have gained tremendous knowledge of how the signal auxin is perceived 31 and transmitted, and now we are starting to unveil a new level of regulation of the system at the 32 level of SCFTIR1/AFB stability. Since the Arabidopsis genome encodes hundreds of FBPs, and 33 ASK is able to associate with diverse FBPs to form multiple SCF complexes, the challenge of 34 regulating SCF assembly is particularly relevant. The SCF complex is therefore an exceptional 35 core in which different levels of post-translational modifications might take place. In addition to 36 auxin, nitric oxide (NO) is considered a ubiquitous signal in plants which contributes to 37 determining the morphology and developmental pattern of roots, in part by the modulation of 38 auxin response. Previously, we gained evidence on the role of the second messenger NO for the 39 regulation of the FBP TIR for auxin sensing. We wondered further whether NO might play a 40 broader role regulating the SCFTIR/AFB and its functionality in the plant cell.
Fil: Calderon Villalobos, Luz Irina. Leibniz Institut Fur Pflanzenbiochemie; Alemania
Fil: Iglesias, María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
Fil: Terrile, Maria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
Fil: Casalongue, Claudia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
Materia
AUXIN
NITRIC OXIDE
PLANTS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/172079

id CONICETDig_a2dacb714e7a7d060bc1f041a4213a03
oai_identifier_str oai:ri.conicet.gov.ar:11336/172079
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric OxideCalderon Villalobos, Luz IrinaIglesias, María JoséTerrile, Maria CeciliaCasalongue, ClaudiaAUXINNITRIC OXIDEPLANTShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The term auxin is derived from the Greek word ?auxein,? which means to grow or to expand and 3 was sealed by Charles Darwin more than a century ago. In ?The Power of Movement in Plants? 4 (1880), Darwin first described the effects of light on the movement of canary grass 5 coleoptiles. He demonstrated that the tip of the seedling was responsible for producing some 6 signal, namely auxin, which was transported to the lower part of the coleoptile, where the 7 physiological response of bending following the light occurred. Auxin is probably the most 8 intensely-studied molecule in plants as it impacts virtually every aspect of growth and 9 development during their life cycle. 10The role of auxin is warranted by the coordination of its synthesis, metabolism, transport, and 11 perception. The plant cell traduces the auxin signal through a well-characterized nuclear 12 signaling pathway, triggering transcriptional responses depending on a specific cell, tissue, or 13 organ. 14Auxin signaling pathway initiates once the hormone moves into the nucleus and is bound by a 15 coreceptor system by the E3 ubiquitin ligase SCFTIR1/AFBs and its degradation substrates 16 AUX/IAAs transcriptional repressors. Upon auxin binding SCFTIR1/AFBs trigger ubiquitylation 17 and further AUX/IAA turnover by the proteasome. AUX/IAAs block the expression of auxin-18 responsive genes, their degradation is essential for auxin pathway activation. 19Since plants are sessile organisms unable to escape changes in the environment, the degradation 20 of pre-synthesized AUX/IAA repressor proteins instead of the de novo synthesis of activation 21 proteins constitutes a more rapid and efficient strategy for the activation of molecular pathways 22 required to adapt to new situations. Thus, the ubiquitin proteasome system via the exquisite 23 action of specific E3 ubiquitin ligases, such as the SCFTIR1/AFBs recruit directly proteins 24 degradation substrates. SCF-type E3 ligases are the most abundant substrate recognition 25 complexes in eukaryotic cells and have been implicated in every major phytohormone signaling 26 pathway. Each individual SCF E3 ligase is a multimer consisting of a scaffold protein Cullin 1, a 27 RING RBX1 for binding an E2 conjugating enzyme loaded with ubiquitin, and a substrate 28 binding module build by the adaptor protein, SKP1 (in Arabidopsis ASK1) and, an 29 interchangeable substrate-recognition unit F-box Protein (FBP). 30In the last decade we have gained tremendous knowledge of how the signal auxin is perceived 31 and transmitted, and now we are starting to unveil a new level of regulation of the system at the 32 level of SCFTIR1/AFB stability. Since the Arabidopsis genome encodes hundreds of FBPs, and 33 ASK is able to associate with diverse FBPs to form multiple SCF complexes, the challenge of 34 regulating SCF assembly is particularly relevant. The SCF complex is therefore an exceptional 35 core in which different levels of post-translational modifications might take place. In addition to 36 auxin, nitric oxide (NO) is considered a ubiquitous signal in plants which contributes to 37 determining the morphology and developmental pattern of roots, in part by the modulation of 38 auxin response. Previously, we gained evidence on the role of the second messenger NO for the 39 regulation of the FBP TIR for auxin sensing. We wondered further whether NO might play a 40 broader role regulating the SCFTIR/AFB and its functionality in the plant cell.Fil: Calderon Villalobos, Luz Irina. Leibniz Institut Fur Pflanzenbiochemie; AlemaniaFil: Iglesias, María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; ArgentinaFil: Terrile, Maria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; ArgentinaFil: Casalongue, Claudia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; ArgentinaPlos2018-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/172079Calderon Villalobos, Luz Irina; Iglesias, María José; Terrile, Maria Cecilia; Casalongue, Claudia; Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide; Plos; Science Trends; 2021; 8-2018; 1-22639-1538CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://sciencetrends.com/plant-strategies-to-control-growth-and-development-integration-of-both-signal-molecules-auxin-and-nitric-oxide/info:eu-repo/semantics/altIdentifier/doi/10.31988/SCITRENDS.29025info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:15:15Zoai:ri.conicet.gov.ar:11336/172079instacron: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:34982025-09-10 13:15:15.356CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
title Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
spellingShingle Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
Calderon Villalobos, Luz Irina
AUXIN
NITRIC OXIDE
PLANTS
title_short Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
title_full Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
title_fullStr Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
title_full_unstemmed Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
title_sort Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide
dc.creator.none.fl_str_mv Calderon Villalobos, Luz Irina
Iglesias, María José
Terrile, Maria Cecilia
Casalongue, Claudia
author Calderon Villalobos, Luz Irina
author_facet Calderon Villalobos, Luz Irina
Iglesias, María José
Terrile, Maria Cecilia
Casalongue, Claudia
author_role author
author2 Iglesias, María José
Terrile, Maria Cecilia
Casalongue, Claudia
author2_role author
author
author
dc.subject.none.fl_str_mv AUXIN
NITRIC OXIDE
PLANTS
topic AUXIN
NITRIC OXIDE
PLANTS
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 term auxin is derived from the Greek word ?auxein,? which means to grow or to expand and 3 was sealed by Charles Darwin more than a century ago. In ?The Power of Movement in Plants? 4 (1880), Darwin first described the effects of light on the movement of canary grass 5 coleoptiles. He demonstrated that the tip of the seedling was responsible for producing some 6 signal, namely auxin, which was transported to the lower part of the coleoptile, where the 7 physiological response of bending following the light occurred. Auxin is probably the most 8 intensely-studied molecule in plants as it impacts virtually every aspect of growth and 9 development during their life cycle. 10The role of auxin is warranted by the coordination of its synthesis, metabolism, transport, and 11 perception. The plant cell traduces the auxin signal through a well-characterized nuclear 12 signaling pathway, triggering transcriptional responses depending on a specific cell, tissue, or 13 organ. 14Auxin signaling pathway initiates once the hormone moves into the nucleus and is bound by a 15 coreceptor system by the E3 ubiquitin ligase SCFTIR1/AFBs and its degradation substrates 16 AUX/IAAs transcriptional repressors. Upon auxin binding SCFTIR1/AFBs trigger ubiquitylation 17 and further AUX/IAA turnover by the proteasome. AUX/IAAs block the expression of auxin-18 responsive genes, their degradation is essential for auxin pathway activation. 19Since plants are sessile organisms unable to escape changes in the environment, the degradation 20 of pre-synthesized AUX/IAA repressor proteins instead of the de novo synthesis of activation 21 proteins constitutes a more rapid and efficient strategy for the activation of molecular pathways 22 required to adapt to new situations. Thus, the ubiquitin proteasome system via the exquisite 23 action of specific E3 ubiquitin ligases, such as the SCFTIR1/AFBs recruit directly proteins 24 degradation substrates. SCF-type E3 ligases are the most abundant substrate recognition 25 complexes in eukaryotic cells and have been implicated in every major phytohormone signaling 26 pathway. Each individual SCF E3 ligase is a multimer consisting of a scaffold protein Cullin 1, a 27 RING RBX1 for binding an E2 conjugating enzyme loaded with ubiquitin, and a substrate 28 binding module build by the adaptor protein, SKP1 (in Arabidopsis ASK1) and, an 29 interchangeable substrate-recognition unit F-box Protein (FBP). 30In the last decade we have gained tremendous knowledge of how the signal auxin is perceived 31 and transmitted, and now we are starting to unveil a new level of regulation of the system at the 32 level of SCFTIR1/AFB stability. Since the Arabidopsis genome encodes hundreds of FBPs, and 33 ASK is able to associate with diverse FBPs to form multiple SCF complexes, the challenge of 34 regulating SCF assembly is particularly relevant. The SCF complex is therefore an exceptional 35 core in which different levels of post-translational modifications might take place. In addition to 36 auxin, nitric oxide (NO) is considered a ubiquitous signal in plants which contributes to 37 determining the morphology and developmental pattern of roots, in part by the modulation of 38 auxin response. Previously, we gained evidence on the role of the second messenger NO for the 39 regulation of the FBP TIR for auxin sensing. We wondered further whether NO might play a 40 broader role regulating the SCFTIR/AFB and its functionality in the plant cell.
Fil: Calderon Villalobos, Luz Irina. Leibniz Institut Fur Pflanzenbiochemie; Alemania
Fil: Iglesias, María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
Fil: Terrile, Maria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
Fil: Casalongue, Claudia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones Biológicas. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales. Instituto de Investigaciones Biológicas; Argentina
description The term auxin is derived from the Greek word ?auxein,? which means to grow or to expand and 3 was sealed by Charles Darwin more than a century ago. In ?The Power of Movement in Plants? 4 (1880), Darwin first described the effects of light on the movement of canary grass 5 coleoptiles. He demonstrated that the tip of the seedling was responsible for producing some 6 signal, namely auxin, which was transported to the lower part of the coleoptile, where the 7 physiological response of bending following the light occurred. Auxin is probably the most 8 intensely-studied molecule in plants as it impacts virtually every aspect of growth and 9 development during their life cycle. 10The role of auxin is warranted by the coordination of its synthesis, metabolism, transport, and 11 perception. The plant cell traduces the auxin signal through a well-characterized nuclear 12 signaling pathway, triggering transcriptional responses depending on a specific cell, tissue, or 13 organ. 14Auxin signaling pathway initiates once the hormone moves into the nucleus and is bound by a 15 coreceptor system by the E3 ubiquitin ligase SCFTIR1/AFBs and its degradation substrates 16 AUX/IAAs transcriptional repressors. Upon auxin binding SCFTIR1/AFBs trigger ubiquitylation 17 and further AUX/IAA turnover by the proteasome. AUX/IAAs block the expression of auxin-18 responsive genes, their degradation is essential for auxin pathway activation. 19Since plants are sessile organisms unable to escape changes in the environment, the degradation 20 of pre-synthesized AUX/IAA repressor proteins instead of the de novo synthesis of activation 21 proteins constitutes a more rapid and efficient strategy for the activation of molecular pathways 22 required to adapt to new situations. Thus, the ubiquitin proteasome system via the exquisite 23 action of specific E3 ubiquitin ligases, such as the SCFTIR1/AFBs recruit directly proteins 24 degradation substrates. SCF-type E3 ligases are the most abundant substrate recognition 25 complexes in eukaryotic cells and have been implicated in every major phytohormone signaling 26 pathway. Each individual SCF E3 ligase is a multimer consisting of a scaffold protein Cullin 1, a 27 RING RBX1 for binding an E2 conjugating enzyme loaded with ubiquitin, and a substrate 28 binding module build by the adaptor protein, SKP1 (in Arabidopsis ASK1) and, an 29 interchangeable substrate-recognition unit F-box Protein (FBP). 30In the last decade we have gained tremendous knowledge of how the signal auxin is perceived 31 and transmitted, and now we are starting to unveil a new level of regulation of the system at the 32 level of SCFTIR1/AFB stability. Since the Arabidopsis genome encodes hundreds of FBPs, and 33 ASK is able to associate with diverse FBPs to form multiple SCF complexes, the challenge of 34 regulating SCF assembly is particularly relevant. The SCF complex is therefore an exceptional 35 core in which different levels of post-translational modifications might take place. In addition to 36 auxin, nitric oxide (NO) is considered a ubiquitous signal in plants which contributes to 37 determining the morphology and developmental pattern of roots, in part by the modulation of 38 auxin response. Previously, we gained evidence on the role of the second messenger NO for the 39 regulation of the FBP TIR for auxin sensing. We wondered further whether NO might play a 40 broader role regulating the SCFTIR/AFB and its functionality in the plant cell.
publishDate 2018
dc.date.none.fl_str_mv 2018-08
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/11336/172079
Calderon Villalobos, Luz Irina; Iglesias, María José; Terrile, Maria Cecilia; Casalongue, Claudia; Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide; Plos; Science Trends; 2021; 8-2018; 1-2
2639-1538
CONICET Digital
CONICET
url http://hdl.handle.net/11336/172079
identifier_str_mv Calderon Villalobos, Luz Irina; Iglesias, María José; Terrile, Maria Cecilia; Casalongue, Claudia; Plant Strategies To Control Growth And Development: Integration Of Both Signal Molecules, Auxin And Nitric Oxide; Plos; Science Trends; 2021; 8-2018; 1-2
2639-1538
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://sciencetrends.com/plant-strategies-to-control-growth-and-development-integration-of-both-signal-molecules-auxin-and-nitric-oxide/
info:eu-repo/semantics/altIdentifier/doi/10.31988/SCITRENDS.29025
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
application/pdf
dc.publisher.none.fl_str_mv Plos
publisher.none.fl_str_mv Plos
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_ 1842980820377141248
score 12.993085