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From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy
BACKGROUND: Bud dormancy is a crucial stage in perennial trees and allows survival over winter to ensure optimal flowering and fruit production. Recent work highlighted physiological and molecular events occurring during bud dormancy in trees. However, they usually examined bud development or bud do...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909552/ https://www.ncbi.nlm.nih.gov/pubmed/31830909 http://dx.doi.org/10.1186/s12864-019-6348-z |
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author | Vimont, Noémie Fouché, Mathieu Campoy, José Antonio Tong, Meixuezi Arkoun, Mustapha Yvin, Jean-Claude Wigge, Philip A. Dirlewanger, Elisabeth Cortijo, Sandra Wenden, Bénédicte |
author_facet | Vimont, Noémie Fouché, Mathieu Campoy, José Antonio Tong, Meixuezi Arkoun, Mustapha Yvin, Jean-Claude Wigge, Philip A. Dirlewanger, Elisabeth Cortijo, Sandra Wenden, Bénédicte |
author_sort | Vimont, Noémie |
collection | PubMed |
description | BACKGROUND: Bud dormancy is a crucial stage in perennial trees and allows survival over winter to ensure optimal flowering and fruit production. Recent work highlighted physiological and molecular events occurring during bud dormancy in trees. However, they usually examined bud development or bud dormancy in isolation. In this work, we aimed to further explore the global transcriptional changes happening throughout bud development and dormancy onset, progression and release. RESULTS: Using next-generation sequencing and modelling, we conducted an in-depth transcriptomic analysis for all stages of flower buds in several sweet cherry (Prunus avium L.) cultivars that are characterized for their contrasted dates of dormancy release. We find that buds in organogenesis, paradormancy, endodormancy and ecodormancy stages are defined by the expression of genes involved in specific pathways, and these are conserved between different sweet cherry cultivars. In particular, we found that DORMANCY ASSOCIATED MADS-box (DAM), floral identity and organogenesis genes are up-regulated during the pre-dormancy stages while endodormancy is characterized by a complex array of signalling pathways, including cold response genes, ABA and oxidation-reduction processes. After dormancy release, genes associated with global cell activity, division and differentiation are activated during ecodormancy and growth resumption. We then went a step beyond the global transcriptomic analysis and we developed a model based on the transcriptional profiles of just seven genes to accurately predict the main bud dormancy stages. CONCLUSIONS: Overall, this study has allowed us to better understand the transcriptional changes occurring throughout the different phases of flower bud development, from bud formation in the summer to flowering in the following spring. Our work sets the stage for the development of fast and cost effective diagnostic tools to molecularly define the dormancy stages. Such integrative approaches will therefore be extremely useful for a better comprehension of complex phenological processes in many species. |
format | Online Article Text |
id | pubmed-6909552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69095522019-12-19 From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy Vimont, Noémie Fouché, Mathieu Campoy, José Antonio Tong, Meixuezi Arkoun, Mustapha Yvin, Jean-Claude Wigge, Philip A. Dirlewanger, Elisabeth Cortijo, Sandra Wenden, Bénédicte BMC Genomics Research Article BACKGROUND: Bud dormancy is a crucial stage in perennial trees and allows survival over winter to ensure optimal flowering and fruit production. Recent work highlighted physiological and molecular events occurring during bud dormancy in trees. However, they usually examined bud development or bud dormancy in isolation. In this work, we aimed to further explore the global transcriptional changes happening throughout bud development and dormancy onset, progression and release. RESULTS: Using next-generation sequencing and modelling, we conducted an in-depth transcriptomic analysis for all stages of flower buds in several sweet cherry (Prunus avium L.) cultivars that are characterized for their contrasted dates of dormancy release. We find that buds in organogenesis, paradormancy, endodormancy and ecodormancy stages are defined by the expression of genes involved in specific pathways, and these are conserved between different sweet cherry cultivars. In particular, we found that DORMANCY ASSOCIATED MADS-box (DAM), floral identity and organogenesis genes are up-regulated during the pre-dormancy stages while endodormancy is characterized by a complex array of signalling pathways, including cold response genes, ABA and oxidation-reduction processes. After dormancy release, genes associated with global cell activity, division and differentiation are activated during ecodormancy and growth resumption. We then went a step beyond the global transcriptomic analysis and we developed a model based on the transcriptional profiles of just seven genes to accurately predict the main bud dormancy stages. CONCLUSIONS: Overall, this study has allowed us to better understand the transcriptional changes occurring throughout the different phases of flower bud development, from bud formation in the summer to flowering in the following spring. Our work sets the stage for the development of fast and cost effective diagnostic tools to molecularly define the dormancy stages. Such integrative approaches will therefore be extremely useful for a better comprehension of complex phenological processes in many species. BioMed Central 2019-12-12 /pmc/articles/PMC6909552/ /pubmed/31830909 http://dx.doi.org/10.1186/s12864-019-6348-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Vimont, Noémie Fouché, Mathieu Campoy, José Antonio Tong, Meixuezi Arkoun, Mustapha Yvin, Jean-Claude Wigge, Philip A. Dirlewanger, Elisabeth Cortijo, Sandra Wenden, Bénédicte From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title | From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title_full | From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title_fullStr | From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title_full_unstemmed | From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title_short | From bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
title_sort | from bud formation to flowering: transcriptomic state defines the cherry developmental phases of sweet cherry bud dormancy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909552/ https://www.ncbi.nlm.nih.gov/pubmed/31830909 http://dx.doi.org/10.1186/s12864-019-6348-z |
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