生物技术通报 ›› 2025, Vol. 41 ›› Issue (9): 159-167.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0147

• 研究报告 • 上一篇    

荔枝LcTFL1基因的克隆与功能分析

史发超(), 姜永华, 刘海伦, 文英杰, 严倩()   

  1. 广东省农业科学院果树研究所 农业农村部南亚热带果树生物学与遗传资源利用重点实验室 广东省果树科学与技术研究重点实验室,广州 510640
  • 收稿日期:2025-02-13 出版日期:2025-09-26 发布日期:2025-09-24
  • 通讯作者: 严倩,女,博士,副研究员,研究方向 :荔枝资源收集及评价;E-mail: yanqian@gdaas.cn
  • 作者简介:史发超,男,博士,助理研究员,研究方向 :荔枝遗传育种;E-mail: shifachao@126.com
  • 基金资助:
    广州市科技计划项目(2023A04J0137);国家自然科学基金项目(32102333)

Cloning and Functional Analysis of LcTFL1 Gene in Litchi chinensis Sonn.

SHI Fa-chao(), JIANG Yong-hua, LIU Hai-lun, WEN Ying-jie, YAN Qian()   

  1. Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences; Key Laboratory of South Subtropical Fruit Biology and Genetic Resource Utilization, Ministry of Agriculture and Rural Affairs; Guangdong Provincial Key Laboratory of Science and Technology Research on Fruit Tree, Guangzhou 510640
  • Received:2025-02-13 Published:2025-09-26 Online:2025-09-24

摘要:

目的 TFL1基因是植物开花途径中的重要调控基因,克隆荔枝LcTFL1基因并构建系统发育树,分析其表达模式并进行功能研究,为荔枝成花调控提供靶标基因。 方法 基于前期获取的转录组数据,通过设计特异性引物,利用PCR技术从‘妃子笑’荔枝叶片中克隆得到LcTFL1基因,结合生物信息学分析其蛋白保守结构和系统进化关系,通过定量PCR技术选取荔枝不同组织,明确该基因的组织表达模式,利用亚细胞定位确定其蛋白表达位置,通过构建植物双源表达载体,异源过表达拟南芥,统计开花时间表型,分析验证LcTFL1基因功能。 结果 LcTFL1基因编码区全长为513 bp,编码170个氨基酸,为亲水性蛋白,具有保守PEBP家族结构域,启动子区域存在多个响应光、激素和胁迫的顺式作用元件,亚细胞定位显示其蛋白定位在细胞质中。系统进化关系表明荔枝LcTFL1基因和同科的文冠果(Xanthoceras sorbifolium)的JRO89相似性最高。组织表达分析显示,LcTFL1在种子的表达量最高,其次为顶芽和果实。在拟南芥中过表达LcTFL1基因,过表达拟南芥植株表现为始花期莲座叶片数量显著增多,叶片长度和宽度显著降低,且植株出现晚花表型。 结论 LcTFL1高表达会延迟拟南芥开花,作为调控开花的抑制因子存在。

关键词: 荔枝, LcTFL1基因, 表达模式, 过表达, 开花

Abstract:

Objective The TERMINAL FLOWER 1 (TFL1) gene is a crucial regulator in the plant flowering pathway. Our study aims to clone the LcTFL1 gene of litchi (Litchi chinensis Sonn.) and analyze its expression pattern and function, with the goal of identifying a marker gene for litchi flower formation regulation. This helps unlock the genetic mechanisms governing litchi floral development. Method Using previously obtained transcriptome data, we designed specific primers and successfully cloned the LcTFL1 gene from 'Feizixiao' litchi leaves by using the PCR technology. To verify its function, we used bioinformatics for protein structure and phylogenetic analysis. Through quantitative PCR technology, different tissues of litchi were selected to clarify the tissue expression pattern of this gene. Subcellular localization was determined by fusing LcTFL1 with a fluorescent tag and observing with confocal microscopy. By constructing a plant dual-source expression vector, we also overexpressed LcTFL1 in Arabidopsis thaliana to study its impact on flowering. Result The full-length coding region of LcTFL1 is 513 bp, which encodes 170 amino acids. It is a hydrophilic protein with a conserved PEBP domain. The promoter has cis-acting elements responsive to light, hormones, and stress. LcTFL1 localizes to the cytoplasm. Phylogenetically, it is the closest to JRO89 of Xanthoceras sorbifolium. Its expression is the highest in seeds, followed by apical buds and fruits. When the LcTFL1 gene was overexpressed in A. thaliana, the overexpressed A. thaliana plants showed that the number of rosette leaves at the initial flowering stage significantly increased, the length and width of leaves significantly reduced, and the plants demonstrated a late-flowering phenotype. Conclusion High expression of LcTFL1 delays A. thaliana flowering, indicating it acts as an inhibitory factor in flowering regulation. This discovery has implications for understanding plant development and for crop improvement in litchi.

Key words: litchi, LcTFL1 gene, expression pattern, over-expression, flowering