Cargando…

Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants

Gibberellins (GAs) are phytohormones that regulate a wide range of developmental processes in plants. Levels of active GAs are regulated by biosynthetic and catabolic enzymes like the GA 2-oxidases (GA2oxs). In tomato (Solanum lycopersicum L.) C(19) GA2oxs are encoded by a small multigenic family of...

Descripción completa

Detalles Bibliográficos
Autores principales: Martínez-Bello, Liliam, Moritz, Thomas, López-Díaz, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566981/
https://www.ncbi.nlm.nih.gov/pubmed/26093022
http://dx.doi.org/10.1093/jxb/erv300
_version_ 1782389753199460352
author Martínez-Bello, Liliam
Moritz, Thomas
López-Díaz, Isabel
author_facet Martínez-Bello, Liliam
Moritz, Thomas
López-Díaz, Isabel
author_sort Martínez-Bello, Liliam
collection PubMed
description Gibberellins (GAs) are phytohormones that regulate a wide range of developmental processes in plants. Levels of active GAs are regulated by biosynthetic and catabolic enzymes like the GA 2-oxidases (GA2oxs). In tomato (Solanum lycopersicum L.) C(19) GA2oxs are encoded by a small multigenic family of five members with some degree of redundancy. In order to investigate their roles in tomato, the silencing of all five genes in transgenic plants was induced. A significant increase in active GA(4) content was found in the ovaries of transgenic plants. In addition, the transgenic unfertilized ovaries were much bigger than wild-type ovaries (about 30 times) and a certain proportion (5–37%) were able to develop parthenocarpically. Among the GA2ox family, genes GA2ox1 and -2 seem to be the most relevant for this phenotype since their expression was induced in unfertilized ovaries and repressed in developing fruits, inversely correlating with ovary growth. Interestingly, transgenic lines exhibited a significant inhibition of branching and a higher content of active GA(4) in axillary buds. This phenotype was reverted, in transgenic plants, by the application of paclobutrazol, a GA biosynthesis inhibitor, suggesting a role for GAs as repressors of branching. In summary, this work demonstrates that GA 2-oxidases regulate gibberellin levels in ovaries and axillary buds of tomato plants and their silencing is responsible for parthenocarpic fruit growth and branching inhibition.
format Online
Article
Text
id pubmed-4566981
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-45669812015-09-15 Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants Martínez-Bello, Liliam Moritz, Thomas López-Díaz, Isabel J Exp Bot Research Paper Gibberellins (GAs) are phytohormones that regulate a wide range of developmental processes in plants. Levels of active GAs are regulated by biosynthetic and catabolic enzymes like the GA 2-oxidases (GA2oxs). In tomato (Solanum lycopersicum L.) C(19) GA2oxs are encoded by a small multigenic family of five members with some degree of redundancy. In order to investigate their roles in tomato, the silencing of all five genes in transgenic plants was induced. A significant increase in active GA(4) content was found in the ovaries of transgenic plants. In addition, the transgenic unfertilized ovaries were much bigger than wild-type ovaries (about 30 times) and a certain proportion (5–37%) were able to develop parthenocarpically. Among the GA2ox family, genes GA2ox1 and -2 seem to be the most relevant for this phenotype since their expression was induced in unfertilized ovaries and repressed in developing fruits, inversely correlating with ovary growth. Interestingly, transgenic lines exhibited a significant inhibition of branching and a higher content of active GA(4) in axillary buds. This phenotype was reverted, in transgenic plants, by the application of paclobutrazol, a GA biosynthesis inhibitor, suggesting a role for GAs as repressors of branching. In summary, this work demonstrates that GA 2-oxidases regulate gibberellin levels in ovaries and axillary buds of tomato plants and their silencing is responsible for parthenocarpic fruit growth and branching inhibition. Oxford University Press 2015-09 2015-06-19 /pmc/articles/PMC4566981/ /pubmed/26093022 http://dx.doi.org/10.1093/jxb/erv300 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Martínez-Bello, Liliam
Moritz, Thomas
López-Díaz, Isabel
Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title_full Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title_fullStr Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title_full_unstemmed Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title_short Silencing C(19)-GA 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
title_sort silencing c(19)-ga 2-oxidases induces parthenocarpic development and inhibits lateral branching in tomato plants
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4566981/
https://www.ncbi.nlm.nih.gov/pubmed/26093022
http://dx.doi.org/10.1093/jxb/erv300
work_keys_str_mv AT martinezbelloliliam silencingc19ga2oxidasesinducesparthenocarpicdevelopmentandinhibitslateralbranchingintomatoplants
AT moritzthomas silencingc19ga2oxidasesinducesparthenocarpicdevelopmentandinhibitslateralbranchingintomatoplants
AT lopezdiazisabel silencingc19ga2oxidasesinducesparthenocarpicdevelopmentandinhibitslateralbranchingintomatoplants