植物学报 ›› 2026, Vol. 61 ›› Issue (5): 791-806.DOI: 10.11983/CBB25132  cstr: 32102.14.CBB25132

• 研究论文 • 上一篇    下一篇

宁夏枸杞果皮蜡质合成关键基因LbCER3的克隆与功能验证

赵娟红, 李治刚, 郑国琦*, 刘展飞, 刘祥婷, 寇莉蓉, 王文秀, 周甜甜, 杨涓   

  1. 宁夏大学生命科学学院, 林木资源高效生产全国重点实验室, 银川 750021
  • 收稿日期:2025-07-24 接受日期:2025-12-06 发布日期:2025-12-08
  • 通讯作者: *郑国琦, 宁夏大学生命科学学院教授, 博士生导师, 主要从事植物逆境生理生态和资源植物学方面的教学和研究工作。团队主要开展药用植物种质资源抗逆性评价, 药用植物有效成分积累与环境因子的关系以及盐碱地生物改良和利用等方面的工作。先后主持完成国家自然科学基金项目和省部级项目10余项。作为主要完成人获省部级科技进步一等奖、二等奖、三等奖各1项, 发表论文80余篇, 部分论文发表在Food Chemistry、International Journal of Biological Macromolecules和BMC Genomics等期刊, 出版学术专著2部。E-mail: Zhengguoqi1977@163.com
  • 基金资助:
    国家自然科学基金(No.32260409)、宁夏自然科学基金(No.2025AAC020034)和宁夏回族自治区重点研发计划(No. 2026BBF02017); *通讯作者; 郑国琦, 宁夏大学生命科学学院教授, 博士生导师, 主要从事植物逆境生理生态和资源植物学方面的教学和研究工作; 团队主要开展药用植物种质资源抗逆性评价, 药用植物有效成分积累与环境因子的关系以及盐碱地生物改良和利用等方面的工作; 先后主持完成国家自然科学基金项目和省部级项目10余项; 作为主要完成人获省部级科技进步一等奖、二等奖、三等奖各1项, 发表论文80余篇, 部分论文发表在Food Chemistry、International Journal of Biological Macromolecules和BMC Genomics等期刊, 出版学术专著2部; E-mail: Zhengguoqi1977@163.com

Cloning and Functional Validation of the Key Gene LbCER3 Involved in Waxy Cuticle Synthesis of Lycium barbarum

Zhao Juanhong, Li Zhigang, Zheng Guoqi*, Liu Zhanfei, Liu Xiangting, Kou Lirong, Wang Wenxiu, Zhou Tiantian, Yang Juan   

  1. State Key Laboratory of Efficient Production of Forest Resources, School of Life Sciences, Ningxia University, Yinchuan 750021, China
  • Received:2025-07-24 Accepted:2025-12-06 Published:2025-12-08
  • Contact: *E-mail: Zhengguoqi1977@163.com

摘要: 宁夏枸杞(Lycium barbarum)果皮蜡质是果实制干过程中水分正常散失的限制因子。为验证蜡质合成关键基因LbCER3的功能, 以宁夏主栽品种宁杞1号和宁杞5号为试材, 采用气相色谱-质谱联用(GC-MS)、转录组学和分子生物学等方法, 开展了不同发育时期果实角质层外蜡和内蜡含量与组分变化规律研究, 并进行果实蜡质关键基因筛选与克隆及功能验证。结果表明, 果实发育和成熟过程中2种材料的角质层内蜡和外蜡含量均逐渐降低, 但宁杞1号总蜡质含量显著高于宁杞5号。基于转录组学和加权基因共表达网络分析(WGCNA)将LbCER3确定为关键基因, LbCER3基因编码序列(CDS)全长1 884 bp, 编码628个氨基酸, 含有1个C端WAX2结构域(Wax2_C)以及脂肪酸羟化酶结构域(FA_hydroxylase)。进一步构建LbCER3过表达载体, 在番茄(Solanum lycopersicum)中成功转化, 转基因株系T1代叶片的叶绿素浸出率显著降低, 叶片蜡质含量显著增加, 蜡质组分烷烃和酸类含量显著增加, 表明LbCER3是枸杞果实蜡质合成的关键基因。

关键词: 功能验证, LbCER3, 宁夏枸杞, 蜡质

Abstract: INTRODUCTION: Waxes are protective substances found on the surface of plants, especially on fruits and leaves, which help prevent non-stomatal water loss from plant tissues. Lycium barbarum is a characteristic economic forest species of Ningxia. Its fruit is a berry with a high-water content, and the surface of the fruit skin is covered with wax, which hinders the normal loss of moisture during the drying process. Alkanes are the main components of the wax on L. barbarum, and the CER3 gene is a key gene involved in alkane biosynthesis. Therefore, an in-depth study of the function of CER3 in L. barbarum provides a theoretical basis for revealing the metabolic synthesis of wax in goji fruits and the molecular mechanism of LbCER3.
RATIONALE: Research on the waxy coating of L. barbarum fruit skin has mainly focused on the structure and composition of the epicuticular wax, with relatively little attention given to its molecular mechanisms. Using the main cultivated varieties of L. barbarum, Ningqi No.1 and Ningqi No.5, as test materials, this study employed methods such as GC-MS, transcriptomics, and molecular biology to investigate the changes in the content and composition of cuticular waxes on the outer and inner layers of the fruit at different developmental stages. It also involved the screening, cloning, and functional validation of key genes related to fruit wax.
RESULTS: During the development and maturation of the fruit, the content of inner and outer cuticular waxes in Ningqi No.1 and Ningqi No.5 gradually decreased, with the total wax content in Ningqi No.1 being significantly higher than that in Ningqi No.5. The outer and inner wax components of both varieties were the same, primarily consisting of alkanes, esters, and acids. Transcriptomic analysis and weighted gene co-expression network analysis (WGCNA) identified LbCER3 as a key gene. The full-length CDS of the LbCER3 gene is 1 884 bp, encoding 628 amino acids, and contains a C-terminal WAX2 domain (Wax2_C) and a fatty acid hydroxylase domain (FA_hydroxylase). An LbCER3 overexpression vector was constructed and successfully transformed into tomato, resulting in a significant reduction in chlorophyll leaching rate in the T1 generation transgenic lines, along with a notable increase in leaf wax content and significant increases in the wax components of alkanes and acids.
CONCLUSION: These findings indicate that LbCER3 is a key gene in the synthesis of wax in L. barbarum.

Key words: functional verification, LbCER3, Lycium barbarum, wax