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dc.contributor.advisor李國譚zh_TW
dc.contributor.advisorKuo-Tan Lien
dc.contributor.author杉森未來zh_TW
dc.contributor.authorMiku SUGIMORIen
dc.date.accessioned2024-09-15T16:45:35Z-
dc.date.available2024-09-16-
dc.date.copyright2024-09-14-
dc.date.issued2024-
dc.date.submitted2024-08-12-
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/95678-
dc.description.abstract近年來世界各國藍莓(Vaccinium spp.)的需求量不斷提升。短日照(short day, SD)和低溫是誘導藍莓花芽分化的兩個環境因子。然而,有關藍莓開花的分子機制尚未完全闡明。兔眼藍莓雜交子代‘NTU-15-036-RR’(‘Bonita’ x ‘Climax’) (以下稱為‘036’)在臺灣的亞熱帶氣候下具有不開花的特性,此外,‘036’還具有極度矮小的樹冠。在本文第一個實驗中,將‘Climax’作為對照組,與‘036’盆植植株,自2023年9月至2024年1月,置於三種不同溫度的自然光人工氣候室中(30/25°C、25/20°C和20/15°C),評估對其營養生長和生殖生長的影響。
結果顯示,‘036’在兩個較高溫度的處理下,植株維持不開花及其矮性性狀,但在20/15°C的涼溫中,11月下旬之前枝條明顯伸長。相對地,‘Climax’在25/20°C和20/15°C的溫度下枝條生長較佳;至處理結束,僅有置於20/15°C 的’036’植株開花。結果顯示,’036’之營養生長及開花可能對高溫敏感,因而在臺灣的亞熱帶氣候下,植株矮化且無法開花。
在本文第二個實驗中,於處理期間採樣並分析FT(FLOWERING LOCUS T,重要的開花相關基因)和COL5(CONSTANCE-LIKE 5,與光周期性相關基因)的基因表達量。於處理後一個月,20/15°C 中的‘036’FT表達較‘Climax’高。處理後兩個月 (11月底),‘Climax’在30/25°C和20/15°C的FT表達顯著增高,之後於1月3日,25/20°C中的植株也有顯著的增加。於處理期間,‘036’在涼溫處理下之FT表達量上升的時間點早於‘Climax’,符合其後續開花之表現,但隨後下降並保持較低表達量。總體而言,‘036’的FT表達量在試驗期間內多較‘Climax’低,可以與‘036’在臺灣亞熱帶氣候下不開花有關。
兩個品種在三個溫度處理下的COL5基因表達量皆沒有差異,顯示試驗期間的光周期並未影響‘036’開花特性。
本實驗結果說明,‘036’的營養生長及開花對溫度敏感,且FT 基因表達在高溫下受抑制,是而在臺灣的亞熱帶氣候下表現出矮化及不開花的特性。
zh_TW
dc.description.abstractThe demand for blueberries (Vaccinium spp.) has increased globally in recent years. It is well-known that the floral initiation-induction in blueberries is triggered by two environmental signals: short day length (SD) and cool temperature. However, the molecular mechanisms involved in blueberries’ flowering are not fully elucidated. ‘NTU-15-036-RR’ (hereafter called ‘036’), a rabbiteye blueberry (V. virgatum Aiton) selected from a ‘Bonita’ x ‘Climax’ population in the National Taiwan University blueberry breeding program, was investigated for its non-flowering nature under the subtropical climate in Taiwan. In addition, ‘036’ possesses an extreme dwarfness. In the first experiment, ‘Climax’, as a control, and ‘036’ were subjected to three different temperature treatments (30/25°C, 25/20°C, and 20/15°C) from September 2023 to January 2024, and their vegetative and reproductive growth were evaluated.
The results showed that the shoot growth of ‘036’ maintained its dwarfness in the two warm temperature treatments but was more active in the 20/15°C treatment until late November. On the other hand, shoot growth of ‘Climax’ was normal in the two warm temperature rooms but slow in the cool room. No plant produced flowers during the experimental period except ‘036’ in 20/15°C, suggesting that sensitivity to heat might be the cause of dwarfness and non-flowering in ‘036’ under the warm subtropical climate.
In the second experiment, the expression levels of FLOWERING LOCUS T (FT), an important flowering-related gene, and CONSTANCE Like 5 (COL 5), a key gene involved in photoperiodicity were measured at several time points during experimental period. On November 1st, FT expression was lower in ‘Climax’ than in ‘036’ in all temperature treatments. On November 30th, FT expression in ‘Climax’ was significantly high at 30/25°C and 20/15°C and increased continuously until early January at 25/20°C. The results indicated that the onset timing of FT expression increase in ‘036’ was earlier than in ‘Climax’ in the cool temperature treatment, coinciding with its consequent flowering. Nevertheless, the expression of FT was overall lower in ‘036’ than in ‘Climax’ in all treatments.
The expression levels of COL5 were not different between both cultivars and among all temperature treatments during the experimental period, suggesting that the photoperiodic flowering pathway didn’t affect the flowering trait of ‘036’.
In conclusion, the results suggested that vegetative growth and flowering of ‘036’ could be promoted by cool temperature that encourages FT expression.
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dc.description.tableofcontentsMASTER’S THESIS ACCEPTANCE CERTIFICATE i
Acknowledgment iii
摘要 v
Abstract vii
Chapter 1: Introduction 1
1.1. General introduction of blueberries 1
1.2. Background information about the plant material in this research 2
1.3. Environmental factors determining the flower initiation in blueberries 3
1.4. Genetic regulation of flowering in the model plant, Arabidopsis thaliana 4
1.5. Previous research about the genetic regulation of flowering in blueberries 6
1.6. Research objectives and hypotheses 11
Chapter 2: Materials and Methods 13
2.1. Plant materials and the management of plants 13
2.2. Temperature treatments in NTU Phytotron 13
2.3. Characterization of vegetative growth and reproductive growth 14
2.4. RNA extraction 15
2.5. cDNA synthesis and qPCR analysis 16
Chapter 3: Characterization of vegetative and reproductive growth 19
3.1. Introduction 19
3.2. Changes after the temperature treatment in phytotron 19
3.3. Leaf color 20
3.4. Flowering 21
3.5. Flower bud formation 26
3.6. Shoot termination 26
3.7. The length of internodes and leaves 27
3.8. The appearance of the plants around each sampling date 29
3.9. Summary 30
Chapter 4: Measurement of transcription levels of flowering-related genes 33
4.1. Introduction 33
4.2. Changes in expression along the time series 34
4.3. Flowering-related gene expression on November 1st, 2023 35
4.4. Flowering-related gene expression on November 30th, 2023 36
4.5. Flowering-related gene expression on January 3rd, 2024 37
4.6. Flowering-related gene expression on January 29th, 2024 37
4.7. Discussion of the result of qPCR 38
4.8. Summary 40
Chapter 5: Conclusions 43
Chapter 6: References 45


 
List of Figures
Figure 1. Plant Materials 55
Figure 2. Blueberry flowering model created based on the newest research 56
Figure 3. The workflow of the temperature treatment 57
Figure 4. The appearance of the experiment materials before the temperature treatment 58
Figure 5. The length of internode and leaf length sites measured in this experiment 59
Figure 6. Identification of flower buds in this experiment 60
Figure 7. Identification of terminated shoots in this experiment 61
Figure 8. The appearance of the experiment materials after the 4 months of temperature treatments 62
Figure 9. Leaf color of ’036’ and ‘Climax’ rabbiteye under three temperature treatments. 63
Figure 10. Differences in color and rate of color change between ‘036’ and ‘Climax’ at L (20/15°C) 64
Figure 11. Result of the number of blooming individuals after about four months of temperature treatment. 65
Figure 12. Flower buds of ‘036’-M / H and the off-season flower of ‘Climax’-L 66
Figure 13. Buds of ‘Climax’ 67
Figure 14. Percentage of flower buds 68
Figure 15. Percentage of terminated shoots 69
Figure 16. The phenotyping result of internode length of ‘Climax’ and ‘036’ from the end of October to the beginning of January. 70
Figure 17. The phenotyping result of leaf length of ‘Climax’ and ‘036’ from the end of October to the beginning of January. 71
Figure 18. Leaves and nearby buds similar to those used for sampling at each temperature condition and cultivar around November 1st 72
Figure 19. Leaves and nearby buds similar to those used for sampling at each temperature condition and cultivar around November 30th 73
Figure 20. Leaves and nearby buds similar to those used for sampling at each temperature condition and cultivar around January 3rd 74
Figure 21. Leaves and nearby buds similar to those used for sampling at each temperature condition and cultivar around January 29th 75
Figure 22. Changes in VvFT expression along time series for each cultivar and each temperature condition 76
Figure 23. Changes in VvCOL5 expression along time series for each cultivar and each temperature condition 77
Figure 24. The result of FT and COL5 gene expression measurement from the leaves sampled on November 1st, 2023 78
Figure 25. The result of FT and COL5 gene expression measurement from the leaves sampled on November 30th, 2023 79
Figure 26. The result of FT and COL5 gene expression measurement from the leaves sampled on January 3rd, 2024 80
Figure 27. The result of FT and COL5 gene expression measurement from the leaves sampled on January 29th, 2024 81
Appendix 83
Appendix1: Molecular mechanism regulating Floral initiation in Arabidopsis 83
Appendix2: Daylength in Taipei during the experimental period, from September 22nd, 2023 to January 29th, 2024 84
Applendix3: RNA extraction method using PureLink Plant RNA Reagent 85
Appendix4: RNA purification method 87
Appendix5: Protocol of cDNA synthesis for reverse transcription 88
Appendix 6: qPCR method 89
Applendix7: Flowering date of ‘Bonita’ and ‘Climax’, parents of ‘036’ in 2022. 90
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dc.language.isoen-
dc.subject花芽誘導zh_TW
dc.subject溫度zh_TW
dc.subject兔眼藍莓zh_TW
dc.subjectFTzh_TW
dc.subjectCOL5zh_TW
dc.subject開花相關基因zh_TW
dc.subjectCOL5en
dc.subjectrabbiteye blueberryen
dc.subjectflower initiationen
dc.subjecttemperatureen
dc.subjectflowering-related genesen
dc.subjectFTen
dc.title探索臺大選NTU036兔眼藍莓的表型和開花基因表達及其對溫度之反應zh_TW
dc.titleExploring the phenotype and flowering-related gene expression of ‘NTU-15-036-RR’ rabbiteye blueberry and its responses to temperatureen
dc.typeThesis-
dc.date.schoolyear112-2-
dc.description.degree碩士-
dc.contributor.oralexamcommittee許富鈞;林宣佑zh_TW
dc.contributor.oralexamcommitteeFu-Chiun Hsu;Syuan-You Linen
dc.subject.keyword兔眼藍莓,花芽誘導,溫度,開花相關基因,FT,COL5,zh_TW
dc.subject.keywordrabbiteye blueberry,flower initiation,temperature,flowering-related genes,FT,COL5,en
dc.relation.page90-
dc.identifier.doi10.6342/NTU202403012-
dc.rights.note同意授權(限校園內公開)-
dc.date.accepted2024-08-13-
dc.contributor.author-college生物資源暨農學院-
dc.contributor.author-dept園藝暨景觀學系-
dc.date.embargo-lift2029-08-01-
顯示於系所單位:園藝暨景觀學系

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