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Effect of Topping on Flowering and Fruit Setting in Lower Nodes of Blueberry Shoots
LUXingyu, WENZhuang, WULiting, CUILingyan, LIUYalan, YANGQin
Chin Agric Sci Bull ›› 2026, Vol. 42 ›› Issue (5) : 69-76.
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Abbreviation (ISO4): Chin Agric Sci Bull
Editor in chief: Yulong YIN
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Effect of Topping on Flowering and Fruit Setting in Lower Nodes of Blueberry Shoots
The development of effective flowering regulation techniques is of great significance for improving blueberry yield. This study investigated the regulatory effects of mild apical dominance suppression on reproductive growth in blueberries, aiming to provide a theoretical basis for optimizing flowering and fruiting management practices. Two consecutive trials were conducted using ‘Premier’ blueberry as plant material, with apical bud removal (topping) and non-removal (non-topping, the control) treatments. Morphological observation, statistical analysis, and quantitative PCR were employed to systematically compare flowering and fruiting performance in lower shoot nodes and to analyze the expression dynamics of key flowering-related genes VcFT and VcFT-like in corresponding leaves. The results showed that flower number, flowering rate, fruit setting number, and fruit setting rate all decreased progressively with lower node positions. Among these, flower number and flowering rate were consistent across both trials, and the flowering rate of topping group was consistently higher than that of the control. However, the number of flowering nodes, fruit setting number, and fruit setting rate showed annual variation: topping significantly increased the number of flowering nodes in the first trial but led to poorer fruit setting, whereas the second trial showed significantly improved fruit setting rate and fruit setting number in the topping group. Gene expression analysis indicated that VcFT expression increased progressively during floral induction, with a more pronounced increase under topping treatment and a delayed expression peak in lower nodes. In contrast, the expression of VcFT-like was high only at the initial stage of induction, then declined continuously and was nearly undetectable at mid-to-late phases, with no significant differences between the two treatments. In conclusion, topping treatment effectively promotes flower bud formation and increases flower number in lower nodes of blueberry branches. However, its effect on fruit setting may be constrained by environmental conditions and management practices, leading to inconsistent results between years. VcFT plays a positive regulatory role in floral induction, influenced by topping treatment and node position, while VcFT-like may be involved mainly in the early stage of floral induction. These findings reveal that mild apical bud removal promotes flower bud formation at lower nodes on blueberry branches, providing a theoretical reference for flowering and fruit setting regulation in blueberry.
blueberry / topping / flowering / fruit setting / node / gene expression
| [1] |
李斌, 谢旭, 孙希云, 等. 国内外蓝莓加工技术与功能性成分研究进展[J]. 食品科学技术学报, 2019, 37(5):16-22.
|
| [2] |
徐艺格, 王兴东, 刘有春, 等. 蓝莓产业现状及技术发展趋势分析与展望[J]. 北方园艺, 2024(8):130-136.
|
| [3] |
李亚东, 刘成, 魏鑫, 等. 2024年中国蓝莓产业发展报告[J]. 吉林农业大学学报, 2025, 47(1):1-14.
|
| [4] |
|
| [5] |
|
| [6] |
吴传宝, 段续伟, 闫国华, 等. 甜樱桃副梢成花特性及促进副梢成花的方法[J]. 落叶果树, 2024, 56(1):75-77.
|
| [7] |
朱维, 林玲, 谢蜀豫, 等. 摘心对一年两收栽培‘夏黑’葡萄不同节位冬芽花芽分化的影响[J]. 果树学报, 2020, 37(2):226-234.
|
| [8] |
谢晓华, 李亚洲, 赵银彦, 等. 新梢留不同叶片摘心对促控桃树生长及成花结果的影响[J]. 农业技术与装备, 2021(2):148-149.
|
| [9] |
李菊馨, 汤狄华, 黄桂香, 等. 蓝莓结果母枝性状与成花的相关性分析[J]. 南方农业学报, 2017, 48(3):465-469.
|
| [10] |
|
| [11] |
刘宣, 陈国双, 唐雪东, 等. 摘心对基质栽培蓝莓生长及花芽形成的影响[J]. 经济林研究, 2022, 40(4):228-238,266.
|
| [12] |
李可, 申朦晓, 潘炜浩, 等. 蓝莓C2H2家族基因在花芽休眠解除中的作用初探[J]. 园艺学报, 2023, 50(4):737-753.
为了解蓝莓C<sub>2</sub>H<sub>2</sub>锌指蛋白在花芽休眠中的功能,通过生物信息鉴定蓝莓C<sub>2</sub>H<sub>2</sub>-ZFP基因家族成员,利用转录组数据和荧光定量PCR分析其在花芽内休眠解除过程和外源脱落酸处理下的表达模式。在蓝莓中共鉴定到VcC<sub>2</sub>H<sub>2</sub>-ZFP家族79个成员,通过系统进化树和保守基序将其分为3组。分析表明:VcC<sub>2</sub>H<sub>2</sub>-ZFP家族成员在蓝莓各器官中均有表达,其中15个在花芽内休眠解除过程中表达存在显著差异,如Vc31g303.5、Vc7g51.6、Vc16g355.5在深度内休眠时期表达量高,而休眠解除后表达量较低。VcC<sub>2</sub>H<sub>2</sub>-ZFP启动子含有大量光反应、防御应激、脱落酸、赤霉素等激素响应元件。外源脱落酸处理花芽能显著促进Vc16g355.5、Vc7g51.6、Vc31g303.5等的表达。本研究结果揭示蓝莓部分VcC<sub>2</sub>H<sub>2</sub>-ZFP可能通过响应脱落酸参与花芽休眠过程的调控。
|
| [13] |
The flowering mechanisms, especially chilling requirement-regulated flowering, in deciduous woody crops remain to be elucidated. Flower buds of northern highbush blueberry cultivar Aurora require approximately 1,000 chilling hours to bloom. Overexpression of a blueberry FLOWERING LOCUS T (VcFT) enabled precocious flowering of transgenic “Aurora” mainly in non-terminated apical buds during flower bud formation, meanwhile, most of the mature flower buds could not break until they received enough chilling hours. In this study, we highlighted two groups of differentially expressed genes (DEGs) in flower buds caused by VcFT overexpression (VcFT-OX) and full chilling. We compared the two groups of DEGs with a focus on flowering pathway genes. We found: 1) In non-chilled flower buds, VcFT-OX drove a high VcFT expression and repressed expression of a major MADS-box gene, blueberry SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (VcSOC1) resulting an increased VcFT/VcSOC1 expression ratio; 2) In fully chilled flower buds that are ready to break, the chilling upregulated VcSOC1 expression in non-transgenic “Aurora” and repressed VcFT expression in VcFT-OX “Aurora”, and each resulted in a decreased ratio of VcFT to VcSOC1; additionally, expression of a blueberry SHORT VEGETATIVE PHASE (VcSVP) was upregulated in chilled flower buds of both transgenic and non-transgenic’ “Aurora”. Together with additional analysis of VcFT and VcSOC1 in the transcriptome data of other genotypes and tissues, we provide evidence to support that VcFT expression plays a significant role in promoting floral initiation and that VcSOC1 expression is a key floral activator. We thus propose a new hypothesis on blueberry flowering mechanism, of which the ratios of VcFT-to-VcSOC1 at transcript levels in the flowering pathways determine flower bud formation and bud breaking. Generally, an increased VcFT/VcSOC1 ratio or increased VcSOC1 in leaf promotes precocious flowering and flower bud formation, and a decreased VcFT/VcSOC1 ratio with increased VcSOC1 in fully chilled flower buds contributes to flower bud breaking.
|
| [14] |
|
| [15] |
The rapid development of high-throughput sequencing techniques has led biology into the big-data era. Data analyses using various bioinformatics tools rely on programming and command-line environments, which are challenging and time-consuming for most wet-lab biologists. Here, we present TBtools (a Toolkit for Biologists integrating various biological data-handling tools), a stand-alone software with a user-friendly interface. The toolkit incorporates over 130 functions, which are designed to meet the increasing demand for big-data analyses, ranging from bulk sequence processing to interactive data visualization. A wide variety of graphs can be prepared in TBtools using a new plotting engine ("JIGplot") developed to maximize their interactive ability; this engine allows quick point-and-click modification of almost every graphic feature. TBtools is platform-independent software that can be run under all operating systems with Java Runtime Environment 1.6 or newer. It is freely available to non-commercial users at https://github.com/CJ-Chen/TBtools/releases.Copyright © 2020 The Author. Published by Elsevier Inc. All rights reserved.
|
| [16] |
|
| [17] |
Secondary flowering is the phenomenon in which a tree blooms twice or more times a year. Along with the development of blueberry (Vaccinium corymbosum L.) fruits in spring, a large number of secondary flowers on the strong upright spring shoots were noticed in blueberries planted in the greenhouse. To reveal the cause and possible regulatory mechanism of the phenomenon, we clarified the phenological characteristics of flower bud differentiation and development on the spring shoots by combining phenological phenotype with anatomical observation. Furthermore, the changes in carbohydrates, trehalose-6-phosphate (Tre6P), and the relationship among the key enzyme regulatory genes for Tre6P metabolism and the key regulatory genes for flower formation during the differentiation process of apical buds and axillary buds were investigated. The results showed that the process of flower bud differentiation and flowering of apical and axillary buds was consistent, accompanied by a large amount of carbohydrate consumption. This process was positively correlated with the expression trends of VcTPS1/2, VcSnRK1, VcFT, VcLFY2, VcSPL43, VcAP1, and VcDAM in general, and negatively correlated with that of VcTPP. In addition, there is a certain difference in the differentiation progress of flower buds between the apical and axillary buds. Compared with axillary buds, apical buds had higher contents of sucrose, fructose, glucose, Tre6P, and higher expression levels of VcTPS2, VcFT, VcSPL43, and VcAP1. Moreover, VcTPS1 and VcTPS2 were more closely related to the physiological substances (sucrose and Tre6P) in axillary bud and apical bud differentiation, respectively. It was suggested that sucrose and trehalose-6-phosphate play a crucial role in promoting flower bud differentiation in strong upright spring shoots, and VcTPS1 and VcTPS2 might play a central role in these activities. Our study provided substantial sight for further study on the mechanism of multiple flowering of blueberries and laid a foundation for the regulation and utilization of the phenomenon of multiple flowering in a growing season of perennial woody plants.
|
| [18] |
赫淑华, 侯智霞, 王亚晶, 等. 秋季剪梢对温室蓝莓芽分化及内源激素的影响[J]. 中国农业科技导报, 2024, 26(6):55-62.
|
| [19] |
王金鑫, 张鹤, 邵建柱, 等. ‘天红2号’苹果花芽分化动态发育时期的研究[J]. 河北农业大学学报, 2019, 42(6):45-50.
采用立体解剖观察法对‘天红 2 号’苹果短枝顶芽花芽分化进程进行了观察,研究不同砧木和不同年份对花芽分化进程的影响。结果表明,‘天红 2 号’苹果于短枝停止生长后 40 d 进入转化期(即花的发端),其时间的长短不受砧木和年份的影响。苹果花芽分化过程分为 7 个时期,分别为转化期、花芽分化初期、花序原基发生期、花萼原基发生期、花瓣原基发生期、雄蕊原基发生期和雌蕊原基发生期。随着时间的推移,花芽分化各个时期依次交叉重叠发生,不同砧木和不同年份对各个时期出现时间和持续时间有一定的影响,但对其集中分化期影响不大, 6 月中旬进入转化期,花芽分化初期集中分化于 7 月上旬,花序原基发生期集中分化于 7月中下旬,花萼原基发生期集中分化于 8 月初,花瓣原基发生期集中分化于 8 月中下旬, 9 月份主要为雄蕊原基发生期, 70% 左右的短枝顶芽在 10 月初进入雌蕊原基发生期。
|
| [20] |
武春昊, 王强, 卢明艳, 等. ‘单花’梨花芽特性及其形态分化过程研究[J]. 园艺学报, 2019, 46(7):1373-1378.
‘单花’梨是从‘大香水’(Pyrus ussriensis Maxim.)梨单株中选出的具有单花、单果特性的芽变品种。以‘大香水’梨为对照,通过田间调查和显微观察对‘单花’梨花芽特征及花芽分化过程进行了研究。结果表明:与‘大香水’梨混合花芽不同,‘单花’梨花芽表现出不完全混合花芽和纯花芽两种类型;‘单花’梨花序单花出现在花芽分化初期,即花芽形态分化过程中只形成1个花原基,与‘大香水’梨形成多个花原基存在明显差异。
|
| [21] |
Plant species have evolved different requirements for environmental/endogenous cues to induce flowering. Originally, these varying requirements were thought to reflect the action of different molecular mechanisms. Thinking changed when genetic and molecular analysis in Arabidopsis thaliana revealed that a network of environmental and endogenous signaling input pathways converge to regulate a common set of “floral pathway integrators.” Variation in the predominance of the different input pathways within a network can generate the diversity of requirements observed in different species. Many genes identified by flowering time mutants were found to encode general developmental and gene regulators, with their targets having a specific flowering function. Studies of natural variation in flowering were more successful at identifying genes acting as nodes in the network central to adaptation and domestication. Attention has now turned to mechanistic dissection of flowering time gene function and how that has changed during adaptation. This will inform breeding strategies for climate-proof crops and help define which genes act as critical flowering nodes in many other species.
|
| [22] |
|
| [23] |
|
| [24] |
\n In plants, seasonal changes in day length are perceived in leaves, which initiate long-distance signaling that induces flowering at the shoot apex. The identity of the long-distance signal has yet to be determined. In\n Arabidopsis\n, activation of\n FLOWERING LOCUS T\n (\n FT\n ) transcription in leaf vascular tissue (phloem) induces flowering. We found that\n FT\n messenger RNA is required only transiently in the leaf. In addition, FT fusion proteins expressed specifically in phloem cells move to the apex and move long distances between grafted plants. Finally, we provide evidence that FT does not activate an intermediate messenger in leaves. We conclude that FT protein acts as a long-distance signal that induces\n Arabidopsis\n flowering.\n
|
| [25] |
The true identity of florigen – the molecule(s) that migrates from leaves to apical meristem to initiate flowering – was notoriously elusive, having made it almost the “Bigfoot” of plant biology. There was never a lack of drama in the field of florigen study, and florigen researchers have once again experienced such a swing in the last two years. We wrote a minireview last year in this journal (Yu et al. 2006) to excitedly salute, among other discoveries, the notion that the flowering locus T (FT) mRNA might be the molecular form of a florigen. However, this hypothesis was challenged in a little less than two years after its initial proposition, and the original paper proposed that the FT mRNA hypothesis was retracted (Huang et al. 2005; Bohlenius et al. 2007). Interestingly enough, the FT gene previously proposed to encode a florigen was never challenged. Rather, the FT protein, instead of the FT mRNA, is now believed to migrate from leaves to the apical meristem to promote floral initiation. In this update, we will share with our readers some entertaining stories concerning the recent studies of florigen in five different plant species. In addition to the published reports referenced in this update, readers may also refer to our previous minireview and references therein for additional background information (Yu et al. 2006).
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| [26] |
|
| [27] |
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