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Metabolic signatures of germination triggered by kinetin in Medicago truncatula
In the present work, non-targeted metabolomics was used to investigate the seed response to kinetin, a phytohormone with potential roles in seed germination, still poorly explored. The aim of this study was to elucidate the metabolic signatures of germination triggered by kinetin and explore changes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639397/ https://www.ncbi.nlm.nih.gov/pubmed/31320688 http://dx.doi.org/10.1038/s41598-019-46866-6 |
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author | Araújo, Susana Pagano, Andrea Dondi, Daniele Lazzaroni, Simone Pinela, Eduardo Macovei, Anca Balestrazzi, Alma |
author_facet | Araújo, Susana Pagano, Andrea Dondi, Daniele Lazzaroni, Simone Pinela, Eduardo Macovei, Anca Balestrazzi, Alma |
author_sort | Araújo, Susana |
collection | PubMed |
description | In the present work, non-targeted metabolomics was used to investigate the seed response to kinetin, a phytohormone with potential roles in seed germination, still poorly explored. The aim of this study was to elucidate the metabolic signatures of germination triggered by kinetin and explore changes in metabolome to identify novel vigor/stress hallmarks in Medicago truncatula. Exposure to 0.5 mM kinetin accelerated seed germination but impaired seedling growth. Metabolite composition was investigated in seeds imbibed with water or with 0.5 mM kinetin collected at 2 h and 8 h of imbibition, and at the radicle protrusion stage. According to Principal Component Analysis, inositol pentakisphosphate, agmatine, digalactosylglycerol, inositol hexakisphosphate, and oleoylcholine were the metabolites that mostly contributed to the separation between 2 h, 8 h and radicle protrusion stage, irrespective of the treatment applied. Overall, only 27 metabolites showed significant changes in mean relative contents triggered by kinetin, exclusively at the radicle protrusion stage. The observed metabolite depletion might associate with faster germination or regarded as a stress signature. Results from alkaline comet assay, highlighting the occurrence of DNA damage at this stage of germination, are consistent with the hypothesis that prolonged exposure to kinetin induces stress conditions leading to genotoxic injury. |
format | Online Article Text |
id | pubmed-6639397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66393972019-07-25 Metabolic signatures of germination triggered by kinetin in Medicago truncatula Araújo, Susana Pagano, Andrea Dondi, Daniele Lazzaroni, Simone Pinela, Eduardo Macovei, Anca Balestrazzi, Alma Sci Rep Article In the present work, non-targeted metabolomics was used to investigate the seed response to kinetin, a phytohormone with potential roles in seed germination, still poorly explored. The aim of this study was to elucidate the metabolic signatures of germination triggered by kinetin and explore changes in metabolome to identify novel vigor/stress hallmarks in Medicago truncatula. Exposure to 0.5 mM kinetin accelerated seed germination but impaired seedling growth. Metabolite composition was investigated in seeds imbibed with water or with 0.5 mM kinetin collected at 2 h and 8 h of imbibition, and at the radicle protrusion stage. According to Principal Component Analysis, inositol pentakisphosphate, agmatine, digalactosylglycerol, inositol hexakisphosphate, and oleoylcholine were the metabolites that mostly contributed to the separation between 2 h, 8 h and radicle protrusion stage, irrespective of the treatment applied. Overall, only 27 metabolites showed significant changes in mean relative contents triggered by kinetin, exclusively at the radicle protrusion stage. The observed metabolite depletion might associate with faster germination or regarded as a stress signature. Results from alkaline comet assay, highlighting the occurrence of DNA damage at this stage of germination, are consistent with the hypothesis that prolonged exposure to kinetin induces stress conditions leading to genotoxic injury. Nature Publishing Group UK 2019-07-18 /pmc/articles/PMC6639397/ /pubmed/31320688 http://dx.doi.org/10.1038/s41598-019-46866-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Araújo, Susana Pagano, Andrea Dondi, Daniele Lazzaroni, Simone Pinela, Eduardo Macovei, Anca Balestrazzi, Alma Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title | Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title_full | Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title_fullStr | Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title_full_unstemmed | Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title_short | Metabolic signatures of germination triggered by kinetin in Medicago truncatula |
title_sort | metabolic signatures of germination triggered by kinetin in medicago truncatula |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639397/ https://www.ncbi.nlm.nih.gov/pubmed/31320688 http://dx.doi.org/10.1038/s41598-019-46866-6 |
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