scholarly journals Flower Bud Dormancy in Prunus Species

2015 ◽  
pp. 123-135 ◽  
Author(s):  
Erica Fadón ◽  
Maria Herrero ◽  
Javier Rodrigo
Keyword(s):  
Bud Dormancy ◽  
Prunus Species ◽  
Flower Bud

scholarly journals Monitoring Dormancy Transition in Almond [Prunus Dulcis (Miller) Webb] during Cold and Warm Mediterranean Seasons through the Analysis of a DAM (Dormancy-Associated MADS-Box) Gene

Horticulturae ◽  
2018 ◽  
Vol 4 (4) ◽  
pp. 41 ◽  
Author(s):  
Ángela Prudencio ◽  
Federico Dicenta ◽  
Pedro Martínez-Gómez
Keyword(s):  
Flowering Time ◽  
Quantitative Polymerase Chain Reaction ◽  
Dominant Gene ◽  
Prunus Dulcis ◽  
Bud Dormancy ◽  
Mads Box ◽  
Prunus Species ◽  
Flower Bud ◽  
Japanese Apricot ◽  
Chilling Requirements

For fruit tree (Prunus) species, flower bud dormancy completion determines the quality of bud break and the flowering time. In the present climate change and global warming context, the relationship between dormancy and flowering processes is a fundamental goal in molecular biology of these species. In almond [P. dulcis (Miller) Webb], flowering time is a trait of great interest in the development of new cultivars adapted to different climatic areas. Late flowering is related to a long dormancy period due to high chilling requirements of the cultivar. It is considered a quantitative and highly heritable character but a dominant gene (Late bloom, Lb) was also described. A major QTL (quantitative trait loci) in the linkage group (LG) 4 was associated with Lb, together with other three QTLs in LG1 and LG7. In addition, DAM (Dormancy-Associated MADS-Box) genes located in LG1 have been largely described as a gene family involved in bud dormancy in different Prunus species including peach [P. persica (L.) Batsch] and Japanese apricot (P. mume Sieb. et Zucc.). In this work, a DAM transcript was cloned and its expression was analysed by qPCR (quantitative Polymerase Chain Reaction) in almond flower buds during the dormancy release. For this purpose two almond cultivars (‘Desmayo Largueta’ and ‘Penta’) with different chilling requirements and flowering time were used, and the study was performed along two years. The complete coding sequence, designated PdDAM6 (Prunus dulcis DAM6), was subjected to a phylogenetic analysis with homologous sequences from other Prunus species. Finally, expression dynamics analysed by using qPCR showed a continuous decrease in transcript levels for both cultivars and years during the period analysed. Monitoring almond flower bud dormancy through DAM expression should be used to improve almond production in different climate conditions.

scholarly journals Interplay among Antioxidant System, Hormone Profile and Carbohydrate Metabolism during Bud Dormancy Breaking in a High-Chill Peach Variety

Antioxidants ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 560
Author(s):  
José A. Hernández ◽  
Pedro Díaz-Vivancos ◽  
José Ramón Acosta-Motos ◽  
Nuria Alburquerque ◽  
Domingo Martínez ◽  
...  
Keyword(s):  
Starch Content ◽  
Sugar Metabolism ◽  
Bud Dormancy ◽  
Dormancy Breaking ◽  
Prunus Species ◽  
Physiological Factors ◽  
Antioxidant Metabolism ◽  
Hormone Profile ◽  
Aba Content ◽  
Gas Ratio

(1) Background: Prunus species have the ability to suspend (induce dormancy) and restart growth, in an intricate process in which environmental and physiological factors interact. (2) Methods: In this work, we studied the evolution of sugars, antioxidant metabolism, and abscisic acid (ABA) and gibberellins (GAs) levels during bud dormancy evolution in a high-chill peach variety, grown for two seasons in two different geographical areas with different annual media temperature, a cold (CA) and a temperate area (TA). (3) Results: In both areas, starch content reached a peak at ecodormancy, and then decreased at dormancy release (DR). Sorbitol and sucrose declined at DR, mainly in the CA. In contrast, glucose and fructose levels progressively rose until DR. A decline in ascorbate peroxidase, dehydroascorbate reductase, superoxide dismutase and catalase activities occurred in both seasons at DR. Moreover, the H2O2-sensitive SOD isoenzymes, Fe-SOD and Cu,Zn-SOD, and two novel peroxidase isoenzymes, were detected. Overall, these results suggest the occurrence of a controlled oxidative stress during DR. GA7 was the major bioactive GA in both areas, the evolution of its levels being different between seasons and areas. In contrast, ABA content decreased during the dormancy period in both areas, resulting in a reduction in the ABA/total GAs ratio, being more evident in the CA. (4) Conclusion: A possible interaction sugars-hormones-ROS could take place in high-chill peach buds, favoring the DR process, suggesting that, in addition to sugar metabolism, redox interactions can govern bud DR, regardless of chilling requirements.

scholarly journals Analysis of Evolution, Expression and Genetic Transformation of TCP Transcription Factors in Blueberry Reveal That VcTCP18 Negatively Regulates the Release of Flower Bud Dormancy

2021 ◽  
Vol 12 ◽  
Author(s):  
Yongqiang Li ◽  
Shuang An ◽  
Qiangqiang Cheng ◽  
Yu Zong ◽  
Wenrong Chen ◽  
...  
Keyword(s):  
Transcription Factors ◽  
Plant Growth ◽  
Gene Family ◽  
Fruit Development ◽  
Germination Rate ◽  
Expression Patterns ◽  
Bud Dormancy ◽  
Dormancy Release ◽  
Flower Bud ◽  
Bud Dormancy Release

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.

scholarly journals A Model Describing rRelease of Flower Bud Dormancy in `Prize' and `Gloria' Azaleas

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 760B-760
Author(s):  
William M. Womack ◽  
James E. Barrett ◽  
Terril A. Nell
Keyword(s):  
Growth Regulators ◽  
Bud Dormancy ◽  
Flower Bud ◽  
Cooling Temperature ◽  
Growth Chambers ◽  
Cool Treatment

`Prize' and `Gloria' azaleas were budded at 29C day/24C night without growth regulators. Dormant-budded plants were held at 2, 7, 13, or 18C for 0, 0.5, 1, 2, 4, 6, 8, or 10 weeks and then forced in walk-in growth chambers (29C day/24C night). A model was developed to describe the effect of cooling temperature and duration on days to marketability (eight open flowers) and percent of buds showing color. Holding at temperatures below 7C, increases days to marketability up to 7 days. Extended cooling (beyond 6 weeks) at temperatures <7C increases percent of buds showing color. Extended holding at temperatures >7C decreases buds in color due to development of bypass shoots during cooling and increased bud abortion. Plants not receiving a cool-treatment or cooled for <2 weeks do not flower uniformly. Furthermore, the percentage of plants reaching marketability dramatically decreases for plants held longer than 6 weeks at temperatures >7C. Both cultivars show similar trends, but `Gloria' has greater variability.

scholarly journals AN IN VITRO BIOASSAY FOR THE EVALUATION OF COLD TREATMENT ON FLOWER BUD DORMANCY IN CAMELLIA

2012 ◽  
pp. 607-611
Author(s):  
A. Berruti ◽  
A. Christiaens ◽  
M.C. Van Labeke ◽  
V. Scariot
Keyword(s):  
Cold Treatment ◽  
Bud Dormancy ◽  
In Vitro Bioassay ◽  
Flower Bud

scholarly journals Forcing Irradiance, Temperature, and Fertilization Affect Quality of `Gloria' Azalea

HortScience ◽  
1991 ◽  
Vol 26 (11) ◽  
pp. 1397-1400
Author(s):  
Lori A. Black ◽  
Terril A. Nell ◽  
James E. Barrett
Keyword(s):  
High Temperatures ◽  
Flower Color ◽  
Bud Dormancy ◽  
Harvest Time ◽  
Flower Bud ◽  
Open Flower ◽  
Soluble Fertilizer

Dormant-budded `Gloria' azaleas (Rhododendron sp.) were used to observe the effect of forcing irradiance, temperature, and fertilization on postproduction performance after flower bud dormancy had been broken. Four experiments were conducted during forcing, the treatments for each experiment were: Expt. 1, three forcing irradiances (200,460, and 900 μmol·m-2·s-1) and three postproduction irradiances (4, 8, and 16 μmol·m-z·s-1); Expt. 2, three forcing irradiances (320, 560, and 1110 μmol·m-2s-l); Expt. 3, three controlled day/night temperatures (18/16C, 23/21C, and 29/27C); Expt. 4, fertilizer applied for 7, 14, or 28 days at either 150 or 300 mg N/liter (12% nitrate, 8% ammoniacal) 20N-4.8P-16K soluble fertilizer at every watering, control plants did not receive fertilizer. Days to harvest (time until plants had eight individual open flowers) was less at the high forcing irradiances and temperatures and when fertilizer was applied during forcing. Flower color was less intense at the low forcing irradiance levels, high temperatures, and when duration of fertilization was prolonged and concentration was high. There were more open flower inflorescences at week 2 of postproduction at high forcing irradiance levels, but their number was not affected by forcing temperature or fertilization. Postproduction longevity was shorter when forcing was at 29/27C (day/night) and when plants were fertilized for 28 days at 300 mg N/liter, but was not affected by forcing or postproduction irradiance.

scholarly journals Flower Bud Dormancy, ABA Concentration, and Survival during Frost of Jojoba Genotypes under Water Stress

1992 ◽  
Vol 117 (6) ◽  
pp. 976-980 ◽  
Author(s):  
Aliza Benzioni ◽  
David A. Palzkill ◽  
John M. Nelson
Keyword(s):  
Water Stress ◽  
Frost Damage ◽  
Bud Dormancy ◽  
Flower Bud ◽  
Irrigation Regimes ◽  
Pentadienoic Acid

Flower bud dormancy and anthesis patterns, ABA concentration, and bud survival following frost were studied in eight jojoba [Simmondsia shinensis (Link) Schneider] clones grown under two irrigation regimes (water stress and well irrigated). Several clones broke dormancy in the autumn. Anthesis in the field before winter occurred only in one clone (a male) in the well-irrigated treatment. Buds on water-stressed plants broke dormancy earlier than those on well-watered plants, but anthesis in the field occurred later in the year. Buds on water-stressed plants were less affected by a severe frost than those on control plants (43% vs. 10% survival). There were large differences among clones in the amount of frost damage. ABA levels did not correlate with dormancy patterns or with the amount of frost damage. Chemical name used: S-(Z,E)-5-(1-hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-2,4-pentadienoic acid (ABA).

Sign in / Sign up

Export Citation Format

Share Document