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Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development

The root of Arabidopsis thaliana is used as a model system to unravel the molecular nature of cell elongation and its arrest. From a micro-array performed on roots that were treated with aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, a Small auxin-up RNA (SAUR)-like gene was f...

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Autores principales: Markakis, Marios Nektarios, Boron, Agnieszka Karolina, Van Loock, Bram, Saini, Kumud, Cirera, Susanna, Verbelen, Jean-Pierre, Vissenberg, Kris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842426/
https://www.ncbi.nlm.nih.gov/pubmed/24312429
http://dx.doi.org/10.1371/journal.pone.0082596
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author Markakis, Marios Nektarios
Boron, Agnieszka Karolina
Van Loock, Bram
Saini, Kumud
Cirera, Susanna
Verbelen, Jean-Pierre
Vissenberg, Kris
author_facet Markakis, Marios Nektarios
Boron, Agnieszka Karolina
Van Loock, Bram
Saini, Kumud
Cirera, Susanna
Verbelen, Jean-Pierre
Vissenberg, Kris
author_sort Markakis, Marios Nektarios
collection PubMed
description The root of Arabidopsis thaliana is used as a model system to unravel the molecular nature of cell elongation and its arrest. From a micro-array performed on roots that were treated with aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, a Small auxin-up RNA (SAUR)-like gene was found to be up regulated. As it appeared as the 76th gene in the family, it was named SAUR76. Root and leaf growth of overexpression lines ectopically expressing SAUR76 indicated the possible involvement of the gene in the division process. Using promoter::GUS and GFP lines strong expression was seen in endodermal and pericycle cells at the end of the elongation zone and during several stages of lateral root primordia development. ACC and IAA/NAA were able to induce a strong up regulation of the gene and changed the expression towards cortical and even epidermal cells at the beginning of the elongation zone. Confirmation of this up regulation of expression was delivered using qPCR, which also indicated that the expression quickly returned to normal levels when the inducing IAA-stimulus was removed, a behaviour also seen in other SAUR genes. Furthermore, confocal analysis of protein-GFP fusions localized the protein in the nucleus, cytoplasm and plasma membrane. SAUR76 expression was quantified in several mutants in ethylene and auxin-related pathways, which led to the conclusion that the expression of SAUR76 is mainly regulated by the increase in auxin that results from the addition of ACC, rather than by ACC itself.
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spelling pubmed-38424262013-12-05 Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development Markakis, Marios Nektarios Boron, Agnieszka Karolina Van Loock, Bram Saini, Kumud Cirera, Susanna Verbelen, Jean-Pierre Vissenberg, Kris PLoS One Research Article The root of Arabidopsis thaliana is used as a model system to unravel the molecular nature of cell elongation and its arrest. From a micro-array performed on roots that were treated with aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, a Small auxin-up RNA (SAUR)-like gene was found to be up regulated. As it appeared as the 76th gene in the family, it was named SAUR76. Root and leaf growth of overexpression lines ectopically expressing SAUR76 indicated the possible involvement of the gene in the division process. Using promoter::GUS and GFP lines strong expression was seen in endodermal and pericycle cells at the end of the elongation zone and during several stages of lateral root primordia development. ACC and IAA/NAA were able to induce a strong up regulation of the gene and changed the expression towards cortical and even epidermal cells at the beginning of the elongation zone. Confirmation of this up regulation of expression was delivered using qPCR, which also indicated that the expression quickly returned to normal levels when the inducing IAA-stimulus was removed, a behaviour also seen in other SAUR genes. Furthermore, confocal analysis of protein-GFP fusions localized the protein in the nucleus, cytoplasm and plasma membrane. SAUR76 expression was quantified in several mutants in ethylene and auxin-related pathways, which led to the conclusion that the expression of SAUR76 is mainly regulated by the increase in auxin that results from the addition of ACC, rather than by ACC itself. Public Library of Science 2013-11-27 /pmc/articles/PMC3842426/ /pubmed/24312429 http://dx.doi.org/10.1371/journal.pone.0082596 Text en © 2013 Markakis et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Markakis, Marios Nektarios
Boron, Agnieszka Karolina
Van Loock, Bram
Saini, Kumud
Cirera, Susanna
Verbelen, Jean-Pierre
Vissenberg, Kris
Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title_full Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title_fullStr Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title_full_unstemmed Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title_short Characterization of a Small Auxin-Up RNA (SAUR)-Like Gene Involved in Arabidopsis thaliana Development
title_sort characterization of a small auxin-up rna (saur)-like gene involved in arabidopsis thaliana development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842426/
https://www.ncbi.nlm.nih.gov/pubmed/24312429
http://dx.doi.org/10.1371/journal.pone.0082596
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