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林业科学 ›› 2026, Vol. 62 ›› Issue (6): 166-177.doi: 10.11707/j.1001-7488.LYKX20250570

• 研究论文 • 上一篇    

油橄榄四倍体构建及巨大化关键基因EXP家族鉴定及表达分析

李雨霏1,易刚1,李书媛1,崔祺禛1,樊育彤1,饶国栋1,2,*()   

  1. 1. 林木遗传育种全国重点实验室 中国林业科学研究院林业研究所 北京 100091
    2. 南京林业大学南方现代林业协同创新中心 南京 210037
  • 收稿日期:2025-09-17 修回日期:2025-12-13 出版日期:2026-06-10 发布日期:2026-06-13
  • 通讯作者: 饶国栋 E-mail:rgd@caf.ac.cn
  • 基金资助:
    中央级公益性科研院所专项资金项目(CAFYBB2023PA005-2);国家自然科学基金项目(32371837)。

Construction of Tetraploid Olive (Olea europaea) and Identification and Expression Analysis of Key Genes in the EXP Family for the Cell Enlargement Phenotype

Yufei Li1,Gang Yi1,Shuyuan Li1,Qizhen Cui1,Yutong Fan1,Guodong Rao1,2,*()   

  1. 1. State Key Laboratory of Tree Genetics and Breeding Research Institute of Forestry, Chinese Academy of Forestry Beijing 100091
    2. Co-innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University Nanjing 210037
  • Received:2025-09-17 Revised:2025-12-13 Online:2026-06-10 Published:2026-06-13
  • Contact: Guodong Rao E-mail:rgd@caf.ac.cn

摘要:

目的: 构建油橄榄四倍体植株,分析其与野生型二倍体植株的表型差异,探索油橄榄四倍体巨大化表型形成的基因调控机制。方法: 使用秋水仙素和安磺灵混合溶液,以滴液法诱导植株,应用流式细胞术快速鉴定植株倍性;通过改良苯酚品红溶液染色,检测植株核型;通过振荡切片和甲苯胺蓝溶液染色,观察四倍体植株叶片横切面;通过PI染色,观察四倍体植株叶片表皮细胞;使用Illumina平台对不同倍性的叶片进行基因表达分析和DEGs富集分析;基于T2T油橄榄高质量基因组,利用Blastp、HMM、ProtParam、cello version 2.5、MEGA11、AlphaFold3.0、SAVES、PyMOL等分析平台,分析鉴定EXP基因家族成员,解析其基因表达模式。结果: 共筛选出23株四倍体油橄榄植株,得率为24.46%;四倍体与二倍体相比,植株出现巨大化的表型,表皮细胞和气孔极显著增大(P<0.0001);共筛选到4 743个差异基因,其中2 371个上调,2 372个下调;通过差异基因分析,富集到与细胞巨大化密切相关的生长素信号转导通路,鉴定出2个显著上调的EXP成员,并进行qRT-PCR验证;在全基因组水平上完成了对EXP基因家族的分析。结论: EXP基因家族与四倍体细胞巨大化密切相关,为今后进一步探索多倍体巨大化表型奠定了基础。

关键词: 油橄榄, 四倍体, 巨大化, 转录组, EXP基因家族

Abstract:

Objective: This study aims to generate tetraploid olive plants, analyze their phenotypic differences from wild-type diploids, and explore the genetic regulatory mechanism underlying the cell enlargement phenotype in the tetraploids. Method: Tetraploid induction was performed using a colchicine and oryzalin mixture via a droplet application. Ploidy was rapidly identified by flow cytometry. Karyotype analysis was performed using improved phenol fuchsin staining. Leaf cross-sections of tetraploid plants were made using vibratome sectioning, and observed after toluidine blue staining. Leaf epidermal cells of tetraploids were examined by PI staining. Gene expression profiling and differentially expressed genes (DEGs) enrichment analysis of leaves of different ploidy plants were conducted using the Illumina platform. Based on the T2T high-quality olive genome, EXP gene family members were identified and characterized using Blastp, HMM, ProtParam, Cello version 2.5, MEGA11, AlphaFold3.0, SAVES, and PyMOL, and their expression patterns were further elucidated. Result: A total of 23 tetraploid olive plants were obtained, with an induction efficiency of 24.46%. Compared to diploids, tetraploids exhibited a cell enlargement phenotype, with significantly enlarged epidermal cells and stomata (P<0.000 1). RNA-seq identified 4 743 DEGs (2 371 up-regulated and 2 372 down-regulated). Through differential gene expression analysis, the auxin signaling pathway closely associated with cell enlargement was significantly enriched. Two markedly upregulated EXP members were identified and further validated by qRT-PCR. A comprehensive genome-wide analysis of the EXP gene family was completed. Conclusion: The EXP gene family is closely associated with tetraploid cell enlargement, laying a foundation for further exploration of the gigas phenotype in polyploids in the future.

Key words: Olea europaea, polyploid, cell enlargement, transcriptome, EXP gene family

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