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Journal articles on the topic 'FLOWERING LOCUS T'

Author: Grafiati

Published: 24 April 2022

Last updated: 30 July 2025

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1

Kinoshita, Toshinori, Natsuko Ono, Yuki Hayashi, et al. "FLOWERING LOCUS T Regulates Stomatal Opening." Current Biology 21, no. 14 (2011): 1232–38. http://dx.doi.org/10.1016/j.cub.2011.06.025.

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2

Eckardt, Nancy A. "Dissecting cis-Regulation of FLOWERING LOCUS T." Plant Cell 22, no. 5 (2010): 1422. http://dx.doi.org/10.1105/tpc.110.220511.

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3

Andrés, Fernando, Atsuko Kinoshita, Naveen Kalluri, et al. "The sugar transporter SWEET10 acts downstream of FLOWERING LOCUS T during floral transition of Arabidopsis thaliana." BMC Plant Biology 20, no. 1 (2020): 53. https://doi.org/10.1186/s12870-020-2266-0.

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<strong>Background: </strong>Floral transition initiates reproductive development of plants and occurs in response to environmental and endogenous signals. In <i>Arabidopsis thaliana</i>, this process is accelerated by several environmental cues, including exposure to long days. The photoperiod-dependent promotion of flowering involves the transcriptional induction of <i>FLOWERING LOCUS T</i> (<i>FT</i>) in the phloem of the leaf. <i>FT</i> encodes a mobile protein that is transported from the leaves to the shoot apical meristem, where it forms part of a regulatory complex that induces floweri

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4

Boden, Scott A., David Weiss, John J. Ross, et al. "EARLY FLOWERING3 Regulates Flowering in Spring Barley by Mediating Gibberellin Production and FLOWERING LOCUS T Expression." Plant Cell 26, no. 4 (2014): 1557–69. http://dx.doi.org/10.1105/tpc.114.123794.

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5

Wang, Kangning, Huayu Liu, Fei Wang, et al. "Apple MdbHLH4 promotes the flowering transition through interactions with FLOWERING LOCUS C and transcriptional activation of FLOWERING LOCUS T." Scientia Horticulturae 322 (December 2023): 112444. http://dx.doi.org/10.1016/j.scienta.2023.112444.

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6

Hubbard, Katharine E., and Alex A. R. Webb. "Circadian Rhythms: FLOWERING LOCUS T Extends Opening Hours." Current Biology 21, no. 16 (2011): R636—R638. http://dx.doi.org/10.1016/j.cub.2011.06.058.

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7

郭, 丹丽. "Progress on the Multifaceted Roles of Flowering Control Gene FLOWERING LOCUS T (FT)." Botanical Research 03, no. 06 (2014): 218–26. http://dx.doi.org/10.12677/br.2014.36028.

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8

Su, Qiang, Li Chen, Yupeng Cai, et al. "Functional Redundancy of FLOWERING LOCUS T 3b in Soybean Flowering Time Regulation." International Journal of Molecular Sciences 23, no. 5 (2022): 2497. http://dx.doi.org/10.3390/ijms23052497.

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Photoperiodic flowering is an important agronomic trait that determines adaptability and yield in soybean and is strongly influenced by FLOWERING LOCUS T (FT) genes. Due to the presence of multiple FT homologs in the genome, their functions in soybean are not fully understood. Here, we show that GmFT3b exhibits functional redundancy in regulating soybean photoperiodic flowering. Bioinformatic analysis revealed that GmFT3b is a typical floral inducer FT homolog and that the protein is localized to the nucleus. Moreover, GmFT3b expression was induced by photoperiod and circadian rhythm and was m

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9

Notaguchi, Michitaka, Yasufumi Daimon, Mitsutomo Abe, and Takashi Araki. "Graft-transmissible action of Arabidopsis FLOWERING LOCUS T protein to promote flowering." Plant Signaling & Behavior 4, no. 2 (2009): 123–25. http://dx.doi.org/10.4161/psb.4.2.7558.

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10

Jiang, Danhua, Yuqi Wang, Yizhong Wang, and Yuehui He. "Repression of FLOWERING LOCUS C and FLOWERING LOCUS T by the Arabidopsis Polycomb Repressive Complex 2 Components." PLoS ONE 3, no. 10 (2008): e3404. http://dx.doi.org/10.1371/journal.pone.0003404.

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11

Kim, Gayeon, Yeonggil Rim, Hyunwoo Cho, and Tae Kyung Hyun. "Identification and Functional Characterization of FLOWERING LOCUS T in Platycodon grandiflorus." Plants 11, no. 3 (2022): 325. http://dx.doi.org/10.3390/plants11030325.

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Platycodon grandiflorus roots have been used as a foodstuff and traditional medicine for thousands of years in East Asia. In order to increase the root development of P. grandiflorus, cultivators removed the inflorescences, suggesting the possible negative effect of flowering on root development. This indicates that the genetic improvement of P. grandiflorus by late flowering is a potential approach to increase productivity. However, nothing is known about key genes integrating multiple flowering pathways in P. grandiflorus. In order to fill this gap, we identified potential homologs of the FL

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12

Vollrath, Paul, Harmeet S. Chawla, Sarah V. Schiessl, et al. "A novel deletion in FLOWERING LOCUS T modulates flowering time in winter oilseed rape." Theoretical and Applied Genetics 134, no. 4 (2021): 1217–31. http://dx.doi.org/10.1007/s00122-021-03768-4.

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Abstract Key message A novel structural variant was discovered in the FLOWERING LOCUS T orthologue BnaFT.A02 by long-read sequencing. Nested association mapping in an elite winter oilseed rape population revealed that this 288 bp deletion associates with early flowering, putatively by modification of binding-sites for important flowering regulation genes. Abstract Perfect timing of flowering is crucial for optimal pollination and high seed yield. Extensive previous studies of flowering behavior in Brassica napus (canola, rapeseed) identified mutations in key flowering regulators which differen

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13

Zhou, Hua, Fang-Yun Cheng, Jing Wu, and Chaoying He. "Isolation and Functional Analysis of Flowering Locus T in Tree Peonies (PsFT)." Journal of the American Society for Horticultural Science 140, no. 3 (2015): 265–71. http://dx.doi.org/10.21273/jashs.140.3.265.

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Arabidopsis thaliana Flowering locus T (FT) homologs have been shown to be sufficient to trigger flowering and to regulate flowering time in a wide range of plants. However, such a homologue for the perennial ornamental shrub tree peony has not yet been characterized. In this study, we isolated PsFT, which is a closely related FT homolog from reblooming [Paeonia ×lemoinei ‘High Noon’ (HN)] and nonreblooming [P. ×suffruticosa ‘Luo Yang Hong’ (LYH)] cultivars of tree peonies, and identified its potential role in the regulation of flowering time. The PsFT alleles from the two cultivars encode the

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14

Navarro, Cristina, José A. Abelenda, Eduard Cruz-Oró, et al. "Control of flowering and storage organ formation in potato by FLOWERING LOCUS T." Nature 478, no. 7367 (2011): 119–22. http://dx.doi.org/10.1038/nature10431.

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15

King, R. W. "Mobile signals in day length-regulated flowering: Gibberellins, flowering locus T, and sucrose." Russian Journal of Plant Physiology 59, no. 4 (2012): 479–90. http://dx.doi.org/10.1134/s1021443712040061.

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16

Lin, Tianyi, QiuXia Chen, Ryan Z. Wichenheiser, and Guo-qing Song. "Constitutive expression of a blueberry FLOWERING LOCUS T gene hastens petunia plant flowering." Scientia Horticulturae 253 (July 2019): 376–81. http://dx.doi.org/10.1016/j.scienta.2019.04.051.

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17

Wang, Shenhao, Hongbo Li, Yangyang Li, et al. "FLOWERING LOCUS T Improves Cucumber Adaptation to Higher Latitudes." Plant Physiology 182, no. 2 (2019): 908–18. http://dx.doi.org/10.1104/pp.19.01215.

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18

Sawa, M., and S. A. Kay. "GIGANTEA directly activates Flowering Locus T in Arabidopsis thaliana." Proceedings of the National Academy of Sciences 108, no. 28 (2011): 11698–703. http://dx.doi.org/10.1073/pnas.1106771108.

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19

Liang, Minting, and David W. Ow. "Nucleocytoplasmic OXIDATIVE STRESS 2 can relocate FLOWERING LOCUS T." Biochemical and Biophysical Research Communications 517, no. 4 (2019): 735–40. http://dx.doi.org/10.1016/j.bbrc.2019.07.124.

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20

Xu, Jingya, Yuzhen Zhang, Hongjia Ren, et al. "VDAC1 Negatively Regulates Floral Transition in Arabidopsis thaliana." International Journal of Molecular Sciences 22, no. 21 (2021): 11603. http://dx.doi.org/10.3390/ijms222111603.

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Voltage-dependent anion channels (VDACs) are the most important proteins in mitochondria. They localize to the outer mitochondrial membrane and contribute to the metabolite transport between the mitochondria and cytoplasm, which aids plant growth regulation. Here, we report that Arabidopsis thaliana VDAC1 is involved in the floral transition, with the loss of AtVDAC1 function, resulting in an early-flowering phenotype. AtVDAC1 is expressed ubiquitously in Arabidopsis. To identify the flowering pathway integrators that may be responsible for AtVDAC1′s function during the floral transition, an R

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21

Chowdhury, Zulkarnain, Devasantosh Mohanty, Mrunmay K. Giri, et al. "Dehydroabietinal promotes flowering time and plant defense in Arabidopsis via the autonomous pathway genes FLOWERING LOCUS D, FVE, and RELATIVE OF EARLY FLOWERING 6." Journal of Experimental Botany 71, no. 16 (2020): 4903–13. http://dx.doi.org/10.1093/jxb/eraa232.

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Abstract Abietane diterpenoids are tricyclic diterpenes whose biological functions in angiosperms are largely unknown. Here, we show that dehydroabietinal (DA) fosters transition from the vegetative phase to reproductive development in Arabidopsis thaliana by promoting flowering time. DA’s promotion of flowering time was mediated through up-regulation of the autonomous pathway genes FLOWERING LOCUS D (FLD), RELATIVE OF EARLY FLOWERING 6 (REF6), and FVE, which repress expression of FLOWERING LOCUS C (FLC), a negative regulator of the key floral integrator FLOWERING LOCUS T (FT). Our results fur

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22

Gorshkova, D. S., I. A. Getman, L. I. Sergeeva, Vl V. Kuznetsov, and E. S. Pojidaeva. "GRUSP, an Universal Stress Protein, Is Involved in Gibberellin-dependent Induction of Flowering in Arabidopsis thaliana." Doklady Biochemistry and Biophysics 499, no. 1 (2021): 233–37. http://dx.doi.org/10.1134/s1607672921040062.

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Abstract The effect of T-DNA insertion in the 3'-UTR region of Arabidopsis thaliana At3g58450 gene encoding the Germination-Related Universal Stress Protein (GRUSP) was studied. It was found that under a long-day condition this mutation delays transition to flowering of grusp-115 transgenic line that due to a reduced content of endogenous bioactive gibberellins GA1 and GA3 in comparison to the wild-type plants (Col-0). Exogenous GA accelerated flowering of both lines but did not change the time of difference in the onset of flowering between Col-0 and grusp-115. In addition to changes in GA me

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23

Notaguchi, Michitaka, Mitsutomo Abe, Takahiro Kimura, et al. "Long-Distance, Graft-Transmissible Action of Arabidopsis FLOWERING LOCUS T Protein to Promote Flowering." Plant and Cell Physiology 49, no. 11 (2008): 1645–58. http://dx.doi.org/10.1093/pcp/pcn154.

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24

Notaguchi, M., M. Abe, T. Kimura, et al. "Long-Distance, Graft-Transmissible Action of Arabidopsis FLOWERING LOCUS T Protein to Promote Flowering." Plant and Cell Physiology 49, no. 12 (2008): 1922. http://dx.doi.org/10.1093/pcp/pcn176.

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25

Müller-Xing, Ralf, Oliver Clarenz, Lena Pokorny, Justin Goodrich, and Daniel Schubert. "Polycomb-Group Proteins and FLOWERING LOCUS T Maintain Commitment to Flowering in Arabidopsis thaliana." Plant Cell 26, no. 6 (2014): 2457–71. http://dx.doi.org/10.1105/tpc.114.123323.

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26

Laurie, Rebecca E., Payal Diwadkar, Mauren Jaudal, et al. "The Medicago FLOWERING LOCUS T Homolog, MtFTa1, Is a Key Regulator of Flowering Time." Plant Physiology 156, no. 4 (2011): 2207–24. http://dx.doi.org/10.1104/pp.111.180182.

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27

Wang, Lanlan, Jiaping Yan, Xian Zhou, et al. "GbFT, a FLOWERING LOCUS T homolog from Ginkgo biloba, promotes flowering in transgenic Arabidopsis." Scientia Horticulturae 247 (March 2019): 205–15. http://dx.doi.org/10.1016/j.scienta.2018.12.020.

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28

Bull, Simon, Adrian Alder, Cristina Barsan, et al. "FLOWERING LOCUS T Triggers Early and Fertile Flowering in Glasshouse Cassava (Manihot esculenta Crantz)." Plants 6, no. 4 (2017): 22. http://dx.doi.org/10.3390/plants6020022.

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29

Lu, Hongfeng, Tao Lin, Joël Klein, et al. "QTL-seq identifies an early flowering QTL located near Flowering Locus T in cucumber." Theoretical and Applied Genetics 127, no. 7 (2014): 1491–99. http://dx.doi.org/10.1007/s00122-014-2313-z.

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30

Satake, Akiko, Kazutaka Kawatsu, Yukako Chiba, Keiko Kitamura, and Qingmin Han. "Synchronized expression of FLOWERING LOCUS T between branches underlies mass flowering in Fagus crenata." Population Ecology 61, no. 1 (2018): 5–13. http://dx.doi.org/10.1002/1438-390x.1010.

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31

Fukazawa, Jutarou, Yuki Ohashi, Ryuhei Takahashi, Kanako Nakai, and Yohsuke Takahashi. "DELLA degradation by gibberellin promotes flowering via GAF1-TPR-dependent repression of floral repressors in Arabidopsis." Plant Cell 33, no. 7 (2021): 2258–72. http://dx.doi.org/10.1093/plcell/koab102.

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Abstract Flowering is the developmental transition from the vegetative to the reproductive phase. FLOWERING LOCUS T (FT), SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), and LEAFY (LFY) are floral integrators. These genes are repressed by several floral repressors including EARLY FLOWERING3 (ELF3), SHORT VEGETATIVE PHASE (SVP), TEMPRANILLO1 (TEM1), and TEM2. Although gibberellin (GA) promotes flowering by activating the floral integrator genes, the exact molecular mechanism remains unclear. DELLAs are negative regulators in GA signaling and act as coactivators of the transcription factor GAI

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32

Kang, Junmei, Tiejun Zhang, Tao Guo, et al. "Isolation and Functional Characterization of MsFTa, a FLOWERING LOCUS T Homolog from Alfalfa (Medicago sativa)." International Journal of Molecular Sciences 20, no. 8 (2019): 1968. http://dx.doi.org/10.3390/ijms20081968.

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The production of hay and seeds of alfalfa, an important legume forage for the diary industry worldwide, is highly related to flowering time, which has been widely reported to be integrated by FLOWERING LOCUS T (FT). However, the function of FT(s) in alfalfa is largely unknown. Here, we identified MsFTa, an FT ortholog in alfalfa, and characterized its role in flowering regulation. MsFTa shares the conserved exon/intron structure of FTs, and MsFTa is 98% identical to MtFTa1 in Medicago trucatula. MsFTa was diurnally regulated with a peak before the dark period, and was preferentially expressed

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33

Bellinazzo, Francesca. "Advances in virus-induced flowering in tomato." Journal of Experimental Botany 75, no. 1 (2023): 1–4. http://dx.doi.org/10.1093/jxb/erad407.

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This article comments on: Deng Y, Yarur-Thys A, Baulcombe DC. 2024. Virus-induced overexpression of heterologous FLOWERING LOCUS T for efficient speed breeding in tomato. Journal of Experimental Botany 75, 36–44.

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34

Xu, Feng, Xiaofeng Rong, Xiaohua Huang, and Shuiyuan Cheng. "Recent Advances of Flowering Locus T Gene in Higher Plants." International Journal of Molecular Sciences 13, no. 3 (2012): 3773–81. http://dx.doi.org/10.3390/ijms13033773.

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35

Kim, Soo-Jin, Sung Myun Hong, Seong Jeon Yoo, Suhyun Moon, Hye Seung Jung, and Ji Hoon Ahn. "Post-Translational Regulation of FLOWERING LOCUS T Protein in Arabidopsis." Molecular Plant 9, no. 2 (2016): 308–11. http://dx.doi.org/10.1016/j.molp.2015.11.001.

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36

PIN, P. A., and O. NILSSON. "The multifaceted roles of FLOWERING LOCUS T in plant development." Plant, Cell & Environment 35, no. 10 (2012): 1742–55. http://dx.doi.org/10.1111/j.1365-3040.2012.02558.x.

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37

Blanke, M. "Alternanztagung in Palermo: Von Chaostheorie, Flowering Locus T bis Klimawandel." Erwerbs-Obstbau 61, no. 4 (2019): 303–11. http://dx.doi.org/10.1007/s10341-019-00433-5.

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38

Sang, Na, Darun Cai, Chao Li, Yuqiang Sun, and Xianzhong Huang. "Characterization and Activity Analyses of the FLOWERING LOCUS T Promoter in Gossypium Hirsutum." International Journal of Molecular Sciences 20, no. 19 (2019): 4769. http://dx.doi.org/10.3390/ijms20194769.

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Flowering transition is a crucial development process in cotton (Gossypium hirsutum L.), and the flowering time is closely correlated with the timing of FLOWERING LOCUS T (FT) expression. However, the mechanism underlying the coordination of various cis-regulatory elements in the FT promoter of cotton has not been determined. In this study, a 5.9-kb promoter of FT was identified from cotton. A bioinformatics analysis showed that multiple insertion–deletion sites existed in the 5.9-kb promoter. Different expression levels of a reporter gene, and the induction by sequential deletions in GhFT pro

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39

Chen, Hong, Fei Huang, Yanan Liu, et al. "Constitutive expression of chrysanthemum CmBBX29 delays flowering time in transgenic Arabidopsis." Canadian Journal of Plant Science 100, no. 1 (2020): 86–94. http://dx.doi.org/10.1139/cjps-2018-0154.

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BBX transcription factors are known to regulate the flowering time and the plant response to various abiotic stresses, but their functions in chrysanthemum have yet to be thoroughly explored. Here, a chrysanthemum homolog of the Arabidopsis thaliana gene AtBBX29 was isolated and characterized. The gene was transcribed in various plant organs but most strongly in the root and in the ligulate flowers. Its temporal pattern of transcription mirrored that of CmCO, the chrysanthemum homolog of the key flowering regulator CONSTANS (CO). Its constitutive expression in A. thaliana induced a delay to fl

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40

Schwartz, C. J., Joohyun Lee, and Richard Amasino. "Variation in shade-induced flowering in Arabidopsis thaliana results from FLOWERING LOCUS T allelic variation." PLOS ONE 12, no. 11 (2017): e0187768. http://dx.doi.org/10.1371/journal.pone.0187768.

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41

Odipio, John, Beyene Getu, R. D. Chauhan, et al. "Transgenic overexpression of endogenous FLOWERING LOCUS T-like gene MeFT1 produces early flowering in cassava." PLOS ONE 15, no. 1 (2020): e0227199. http://dx.doi.org/10.1371/journal.pone.0227199.

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42

Sun, Hongbo, Zhen Jia, Dong Cao, et al. "GmFT2a, a Soybean Homolog of FLOWERING LOCUS T, Is Involved in Flowering Transition and Maintenance." PLoS ONE 6, no. 12 (2011): e29238. http://dx.doi.org/10.1371/journal.pone.0029238.

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43

Zhang, Xueming, Lin Meng, Bo Liu, et al. "A transposon insertion in FLOWERING LOCUS T is associated with delayed flowering in Brassica rapa." Plant Science 241 (December 2015): 211–20. http://dx.doi.org/10.1016/j.plantsci.2015.10.007.

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44

Groenewald, E. G., and A. J. Van Der Westhuizen. "The florigen mystery." Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie 25, no. 4 (2006): 284–99. http://dx.doi.org/10.4102/satnt.v25i4.173.

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In order to obtain flowering, different applications of chemicals on plants were tested by several researchers. Substances that were tested were, amongst others, auxin, gibberellin, cytokinin, abscisic acid, prostaglandin; melatonin. All had an effect on flowering. With the aid of molecular-genetic research it was established that the product of certain genes, namely CONSTANS (CO) and FLOWERING LOCUS T (FT) could be the flowering stimulus. It could be a peptide or mRNA.

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45

Kalia, Diksha, Joel Jose-Santhi, Ravi Kumar, and Rajesh Singh. "Analysis of PEBP Genes in Saffron Identifies a Flowering Locus T Homologue Involved in Flowering Regulation." Journal of Plant Growth Regulation 42 (July 21, 2022): 2486–505. https://doi.org/10.1007/s00344-022-10721-2.

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Flowering determines the yield of saffron, whereas synchronized sprouting determines plant fitness; thus, their regulation is of utmost importance. In saffron, corm sprouting is marked with the emergence of flowers and leaves simultaneously. PEBP genes have a conserved role in regulating flowering and vegetative growth in plants, but their role in saffron is confined due to the non-availability of genomic resources. In the present study, we isolated their homologues in saffron and examined their alleged role in promoting flowering. Here we report that at least 6 FTs (<em>FLOWERING LOCUS T</em>

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46

Kalia, Diksha, Joel Jose-Santhi, Ravi Kumar, and Singh Rajesh Kumar. "Analysis of PEBP Genes in Saffron Identifies a Flowering Locus T Homologue Involved in Flowering Regulation." Journal of Plant Growth Regulation 2486–2505 (July 21, 2022): 2486–505. https://doi.org/10.5281/zenodo.10018978.

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Flowering determines the yield of saffron, whereas synchronized sprouting determines plant fitness; thus, their regulation is of utmost importance. In saffron, corm sprouting is marked with the emergence of flowers and leaves simultaneously. PEBP genes have a conserved role in regulating flowering and vegetative growth in plants, but their role in saffron is confined due to the non-availability of genomic resources. In the present study, we isolated their homologues in saffron and examined their alleged role in promoting flowering. Here we report that at least 6 FTs (<i>FLOWERING LOCUS T</i>),

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47

Surkova, Svetlana Yu, and Maria G. Samsonova. "Mechanisms of Vernalization-Induced Flowering in Legumes." International Journal of Molecular Sciences 23, no. 17 (2022): 9889. http://dx.doi.org/10.3390/ijms23179889.

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Vernalization is the requirement for exposure to low temperatures to trigger flowering. The best knowledge about the mechanisms of vernalization response has been accumulated for Arabidopsis and cereals. In Arabidopsis thaliana, vernalization involves an epigenetic silencing of the MADS-box gene FLOWERING LOCUS C (FLC), which is a flowering repressor. FLC silencing releases the expression of the main flowering inductor FLOWERING LOCUS T (FT), resulting in a floral transition. Remarkably, no FLC homologues have been identified in the vernalization-responsive legumes, and the mechanisms of cold-

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48

Chen, Min, and Steven Penfield. "Feedback regulation of COOLAIR expression controls seed dormancy and flowering time." Science 360, no. 6392 (2018): 1014–17. http://dx.doi.org/10.1126/science.aar7361.

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Plants integrate seasonal signals, including temperature and day length, to optimize the timing of developmental transitions. Seasonal sensing requires the activity of two proteins, FLOWERING LOCUS C (FLC) and FLOWERING LOCUS T (FT), that control certain developmental transitions in plants. During reproductive development, the mother plant uses FLC and FT to modulate progeny seed dormancy in response to temperature. We found that for regulation of seed dormancy, FLC and FT function in opposite configuration to how those same genes control time to flowering. For seed dormancy, FT regulates seed

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49

Takeshima, Ryoma, Haiyang Nan, Kohei Harigai, et al. "Functional divergence between soybean FLOWERING LOCUS T orthologues FT2a and FT5a in post-flowering stem growth." Journal of Experimental Botany 70, no. 15 (2019): 3941–53. http://dx.doi.org/10.1093/jxb/erz199.

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Abstract Genes in the FLOWERING LOCUS T (FT) family integrate external and internal signals to control various aspects of plant development. In soybean (Glycine max), FT2a and FT5a play a major role in floral induction, but their roles in post-flowering reproductive development remain undetermined. Ectopic overexpression analyses revealed that FT2a and FT5a similarly induced flowering, but FT5a was markedly more effective than FT2a for the post-flowering termination of stem growth. The down-regulation of Dt1, a soybean orthologue of Arabidopsis TERMINAL FLOWER1, in shoot apices in early growin

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50

Song, Guo-qing. "Two Lines Enable FasTrack Breeding in Blueberry." J. Amer. Soc. Hort. Sci. 150, no. 1 (2025): 28–33. https://doi.org/10.21273/jashs05447-24.

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The juvenile period of blueberry seedlings typically lasts ≈3 to 4 years. To shorten this period and facilitate FasTrack breeding, we developed transgenic ‘Aurora’ blueberry plants with constitutive expression of the blueberry FLOWERING LOCUS T gene, enabling flowering of T0 transformants within just 1 year. To evaluate the potential of these transgenic lines in accelerating breeding cycles, we crossed transgenic ‘Aurora’ with transgenic southern highbush blueberry ‘Legacy’, referred to as Mu-Legacy. Mu-Legacy also exhibited early flowering mainly as a result of a transgene insertion, making i

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