生物技术通报 ›› 2024, Vol. 40 ›› Issue (6): 251-259.doi: 10.13560/j.cnki.biotech.bull.1985.2024-0034

• 研究报告 • 上一篇    下一篇

比利时杜鹃花类黄酮3'-羟化酶(F3'H)基因克隆及功能分析

吴泽航1(), 杨中义1, 鄢毅铖1, 贾永红1, 吴月燕1, 谢晓鸿2()   

  1. 1.浙江万里学院生物与环境学院,宁波 315100
    2.浙江万里学院设计艺术与建筑学院,宁波 315100
  • 收稿日期:2024-01-11 出版日期:2024-06-26 发布日期:2024-06-24
  • 通讯作者: 谢晓鸿,男,硕士,教授,研究方向:园林植物生理生化;E-mail: zwuxxh@zwu.edu.cn
  • 作者简介:吴泽航,男,硕士研究生,研究方向:杜鹃花花色分子改良;E-mail: wzh881018@163.com
  • 基金资助:
    宁波市科技创新2025现代种业重大专项(2021Z005);浙江省重点研发计划(2021C02053);省一流学科学生创新项目(CX2022023)

Cloning and Functional Analysis of Flavonoid 3'-hydroxylase(F3'H)Gene in Rhododendron hybridum Hort

WU Ze-hang1(), YANG Zhong-yi1, YAN Yi-cheng1, JIA Yong-hong1, WU Yue-yan1, XIE Xiao-hong2()   

  1. 1. College of Biological and Environmental Sciences, Zhejiang Wanli University, Ningbo 315100
    2. Faculty of Design and Architecture, Zhejiang Wanli University, Ningbo 315100
  • Received:2024-01-11 Published:2024-06-26 Online:2024-06-24

摘要:

【目的】 类黄酮3'-羟化酶(flavanone 3'-hydroxylase,F3'H)是植物花青素合成过程中的关键酶,探究比利时杜鹃花(Rhododendron hybridum Hort)F3'H基因的功能及表达特性。【方法】 以比利时杜鹃花不同发育时期的花瓣及盛花期的根、茎、叶为实验材料,从比利时杜鹃花转录本数据库中筛选类黄酮生物合成通路关键酶类黄酮3'-羟化酶基因序列信息并进行生物信息学分析,利用反转录(RT-PCR)技术克隆RhF3'H基因;利用紫外分光光度计测定了比利时杜鹃花花瓣不同时期的花青素含量,利用RT-qPCR技术对不同发育时期花瓣和成熟期的不同组织进行RhF3'H基因表达量分析;采用Gateway技术构建过表达载体35S:RhF3'H-GFP重组载体进行亚细胞定位验证;构建p1302-RhF3'H过表达载体对比利时杜鹃花花瓣进行侵染。【结果】 成功获得比利时杜鹃花RhF3'H基因长度为1 557 bp,编码518个氨基酸,具有保守的F3'H结构域,属于P450超家族;系统进化树分析显示,比利时杜鹃花RhF3'H与龙眼和荔枝F3'H蛋白亲缘关系最近;RT-qPCR结果显示,RhF3'H在比利时杜鹃花不同花瓣时期和根、茎、叶组织中均有表达,在不同花瓣发育时期中,盛开期和衰败期中RhF3'H基因的表达量较高,与花青素含量结果相一致;亚细胞定位分析显示,RhF3'H主要存在于细胞膜上;成功构建P1302-RhF3'H瞬时过表达载体,相较于CK和p1302,p1302-RhF3'H在杜鹃花花瓣中显著高表达,其花青素含量也显著增加。【结论】 RhF3'H基因在花瓣细胞膜中表达,表达模式与花青素积累趋势一致;过表达RhF3'H基因促进了花青素的合成。

关键词: 比利时杜鹃花, 类黄酮3'-羟化酶(F3'H), 花青素, 亚细胞定位, 瞬时表达

Abstract:

【Objective】 The flavonoid 3'-hydroxylase(F3'H)is a key enzyme in the synthesis of anthocyanins in plants, and the function and expression characteristics of F3'H gene in Rhododendron hybridum Hort were investigated.【Method】 The petals and roots, stems and leaves of R. hybridum Hort at different developmental stages were used as experimental materials. The flavonoid 3'-hydroxylase gene sequence information of flavonoid biosynthesis pathway was screened from the R. hybridum Hort transcript database and bioinformatics analysis was performed, and the RhF3'H gene was cloned by reverse transcription(RT-PCR)technology. The anthocyanin content in the petals of R. hybridum Hort at different stages was determined by ultraviolet spectrophotometer, and the expression of RhF3'H gene was analyzed by RT-qPCR technology on different tissues of petals at different development stages and maturity stages. The overexpression vector 35S:RhF3'H-GFP recombinant vector was constructed by Gateway technology for subcellular localization verification, and p1302-RhF3'H overexpression vector was constructed to infect the petals of R. hybridum Hort.【Result】 The RhF3'H gene was 1 557 bp in length and encoded 518 amino acids, and the protein encoded by RhF3'H belonged to the P450 superfamily with a conserved F3'H domain. Phylogenetic tree analysis showed that RhF3'H was the most closely related to Dimocarpus longan and Litchi chinensis F3'H proteins. The results of RT-qPCR showed that RhF3'H was expressed in different petal stages and roots, stems, and leaf tissues of R. hybridum Hort. The expressions of RhF3'H gene were higher in the blooming and decaying stages of different petal development stages, which was consistent with the anthocyanin content, and subcellular localization analysis showed that RhF3'H mainly existed on the cell membrane. Compared with CK and p1302, p1302-RhF3'H was significantly higher in the petals of R. hybridum Hort and its anthocyanin content significantly increased.【Conclusion】 The RhF3'H gene was expressed in the petal cell membrane, and the expression pattern was consistent with the accumulation trend of anthocyanins. Overexpression of the RhF3'H gene promotes the synthesis of anthocyanins.

Key words: Rhododendron hybridum Hort, flavanone 3'-hydroxylase, anthocyanidin, subcellular localization, instantaneous expression.