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Cloning and Functional Analysis of RhMYB23 in Rosa hybrida |
FU Ting-Rui, ZHANG Huan-Yu, CUI Yong-Yi, LUO Ping* |
College of Horticulture Science/Key Laboratory of Quality and Safety Control for Subtropical Fruit and Vegetable, Ministry of Agriculture and Rural Affairs/Collaborative Innovation Center for Efficient and Green Production of Agriculture in Mountainous Areas of Zhejiang Province, Zhejiang A&F University, Hangzhou 311300, China |
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Abstract The MYB transcription factors constitute one of the largest families of transcription factors in plants and are extensively involved in plant growth and development as well as the biosynthesis of various secondary metabolites. To explore the regulatory function of MYB transcription factors in the biosynthesis of proanthocyanidins in Rosa hybrida, this study used R. hybrida 'Violet' as the experimental material and isolated RhMYB23 (GenBank No. PQ441876) from its petals. The ORF of RhMYB23 was 771 bp and encoded 256 amino acids. Multiple sequence alignment and phylogenetic analysis revealed that RhMYB23 had a conserved R2R3 domain and was most closely related to Arabidopsis thaliana AtTT2 (transparent testa 2). Expression pattern analysis revealed that RhMYB23 was predominantly expressed in R. hybrida petals. RhMYB23 was localized in the nucleus and possessed transcriptional activation activity. Transient overexpression of RhMYB23 in R. hybrida petals significantly increased the accumulation of proanthocyanidins (P<0.05) and significantly upregulated the expression of key genes involved in proanthocyanidin biosynthesis, RhANR (anthocyanin reductase) and RhLAR (leucoanthocyanidin reductase) (P<0.001). These results suggested that RhMYB23 in R. hybrida might positively regulate proanthocyanidin synthesis. This study reveals the crucial regulatory role of RhMYB23 in proanthocyanidin biosynthesis in R. hybrida, offering theoretical support for R. hybrida flower color improvement.
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Received: 21 October 2024
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Corresponding Authors:
*pingluo@zafu.edu.cn
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