Metabolic mechanisms underpinning vegetative bud dormancy release and shoot development in sweet cherry

2018 ◽  
Vol 155 ◽  
pp. 1-11 ◽  
Author(s):  
Michail Michailidis ◽  
Evangelos Karagiannis ◽  
Georgia Tanou ◽  
Eirini Sarrou ◽  
Ioannis-Dimosthenis Adamakis ◽  
...  
2015 ◽  
Vol 59 (4) ◽  
pp. 726-734 ◽  
Author(s):  
S. Hussain ◽  
Q. Niu ◽  
F. Yang ◽  
N. Hussain ◽  
Y. Teng

2020 ◽  
Vol 104 (5) ◽  
pp. 1251-1268
Author(s):  
Zhaowan Shi ◽  
Tamar Halaly‐Basha ◽  
Chuanlin Zheng ◽  
Michal Sharabi‐Schwager ◽  
Chen Wang ◽  
...  

Plant Science ◽  
2007 ◽  
Vol 173 (4) ◽  
pp. 446-457 ◽  
Author(s):  
Tsvika Keilin ◽  
Xuequn Pang ◽  
Jaganatha Venkateswari ◽  
Tamar Halaly ◽  
Omer Crane ◽  
...  

BMC Genomics ◽  
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Noémie Vimont ◽  
Mathieu Fouché ◽  
José Antonio Campoy ◽  
Meixuezi Tong ◽  
Mustapha Arkoun ◽  
...  

Abstract 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.


Author(s):  
María Armida Orrantia-Araujo ◽  
Miguel Ángel Martínez-Téllez ◽  
Marisela Rivera-Domínguez ◽  
Miguel Ángel Hernández-Oñate ◽  
Irasema Vargas-Arispuro

2018 ◽  
Vol 98 (6) ◽  
pp. 507-523 ◽  
Author(s):  
Zhaowan Shi ◽  
Tamar Halaly-Basha ◽  
Chuanlin Zheng ◽  
Mira Weissberg ◽  
Ron Ophir ◽  
...  

2011 ◽  
Vol 193 (1) ◽  
pp. 67-80 ◽  
Author(s):  
Carmen Leida ◽  
Ana Conesa ◽  
Gerardo Llácer ◽  
María Luisa Badenes ◽  
Gabino Ríos

2021 ◽  
Vol 12 ◽  
Author(s):  
Yongqiang Li ◽  
Shuang An ◽  
Qiangqiang Cheng ◽  
Yu Zong ◽  
Wenrong Chen ◽  
...  

Plant-specific TEOSINTE BRANCHED 1, CYCLOIDEA, PROLIFERATING CELL FACTORS (TCP) transcription factors have versatile functions in plant growth, development and response to environmental stress. Despite blueberry’s value as an important fruit crop, the TCP gene family has not been systematically studied in this plant. The current study identified blueberry TCP genes (VcTCPs) using genomic data from the tetraploid blueberry variety ‘Draper’; a total of 62 genes were obtained. Using multiple sequence alignment, conserved motif, and gene structure analyses, family members were divided into two subfamilies, of which class II was further divided into two subclasses, CIN and TB1. Synteny analysis showed that genome-wide or segment-based replication played an important role in the expansion of the blueberry TCP gene family. The expression patterns of VcTCP genes during fruit development, flower bud dormancy release, hormone treatment, and tissue-specific expression were analyzed using RNA-seq and qRT-PCR. The results showed that the TB1 subclass members exhibited a certain level of expression in the shoot, leaf, and bud; these genes were not expressed during fruit development, but transcript levels decreased uniformly during the release of flower bud dormancy by low-temperature accumulation. The further transgenic experiments showed the overexpression of VcTCP18 in Arabidopsis significantly decreased the seed germination rate in contrast to the wild type. The bud dormancy phenomena as late-flowering, fewer rosettes and main branches were also observed in transgenic plants. Overall, this study provides the first insight into the evolution, expression, and function of VcTCP genes, including the discovery that VcTCP18 negatively regulated bud dormancy release in blueberry. The results will deepen our understanding of the function of TCPs in plant growth and development.


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