河南农业科学 ›› 2025, Vol. 54 ›› Issue (11): 109-122.DOI: 10.15933/j.cnki.1004-3268.2025.11.012

• 园艺 • 上一篇    下一篇

基于转录组学分析榅桲响应NaHCO₃碱胁迫分子机制

郭献平1,2,3,吕珍珍1,2,3,王东升1,2,3,蒋卉1,吴中营1,徐凌飞4,韩永平1,郭鹏1,王蛟1
  

  1. (1.河南省农业科学院 园艺研究所,河南 郑州 450002;2.河南省园艺与花卉工程研究中心,河南 郑州 450002;3.河南省特色瓜果工程技术研究中心,河南 郑州 450002;4.西北农林科技大学 园艺学院,陕西 杨凌 712100)
  • 收稿日期:2025-05-04 接受日期:2025-06-26 出版日期:2025-11-15 发布日期:2025-11-24
  • 通讯作者: 王东升(1966-),男,河南武陟人,研究员,硕士,主要从事梨栽培生理研究。E-mail:wdse66@126.com
  • 作者简介:郭献平(1982-),男,河南内黄人,副研究员,博士,主要从事梨栽培生理与分子生物学研究。E-mail:xianping2005@163.com
  • 基金资助:
    河南省科技攻关项目(242102110151,232102110196);河南省农业科学院应用科技攻关专项(2024YY03);河南省重大科技专项(221100110400);河南省农业科学院科技创新团队项目(2024TD41);国家梨产业技术体系项目(CARS-28);河南省农业科学院自主创新项目(2025ZC37,2024ZC032)

Molecular Mechanism of Cydonia oblonga Responding to NaHCO Alkali Stress Based on Transcriptomic Analysis

GUO Xianping1,2,3,LÜ Zhenzhen1,2,3,WANG Dongsheng1,2,3,JIANG Hui1,WU Zhongying1,XU Lingfei4,HAN Yongping1,GUO Peng1,WANG Jiao1   

  1. (1.Horticulture Research Institute,Henan Academy of Agricultural Sciences,Zhengzhou 450002,China;2.Henan Horticulture and Flower Engineering Research Center,Zhengzhou 450002,China;3.Henan Characteristic Melon and Fruit Engineering Technology Research Center,Zhengzhou 450002,China;4.College of Horticulture,Northwest A&F University,Yangling 712100,China)
  • Received:2025-05-04 Accepted:2025-06-26 Published:2025-11-15 Online:2025-11-24

摘要: 为探究梨异属矮化砧木榅桲响应NaHCO3碱胁迫的分子机制,对水培榅桲幼苗进行5(T1)、10 mmol/L(T2)NaHCO3碱胁迫处理,以不加NaHCO3为对照(CK),处理6周后,测定叶片叶绿素含量、净光合速率、根系和叶片K+/Na+等指标,并对根系进行转录组测序和分析。结果表明,榅桲叶片叶绿素含量和净光合速率均随着碱胁迫程度的增加而逐渐降低,T1、T2处理叶绿素a+b含量比CK显著降低,降幅分别为15.71%、45.38%,叶片净光合速率比CK显著降低,降幅分别为15.90%、55.42%。T1、T2处理叶片和根系K+/Na+均比CK显著降低,降幅分别为45.40%和96.69%、92.04%和96.32%。转录组测序结果显示,与CK相比,T1、T2处理共筛选出4 974个差异表达基因,T2的差异表达基因数量显著高于T1。GO(Gene ontology)功能富集和KEGG(Kyoto encyclopedia of genes and genomes)通路富集分析显示,T1和T2处理在生物学过程(BP)主要富集到过氧化氢分解途径、对伤害的反应等条目,KEGG通路主要富集于苯丙烷生物合成等代谢通路。基因集富集分析(GSEA)结果显示,与CK相比,苯丙烷生物合成代谢通路在T1 和T2 碱胁迫处理下活性增强。加权基因共表达网络分析(WGCNA)显示,T1 处理枢纽基因cydonia_oblonga_newGene_11700表达受到碱胁迫的显著诱导,该基因被注释为木质素代谢转录因子。T2处理枢纽基因cydonia_oblonga_newGene_11460cydonia_oblonga_newGene_14681均被注释为碳酸酐酶。选取5个差异表达基因进行qRT-PCR验证,其表达模式与RNA-Seq分析结果一致。综合分析,榅桲在10 mmol/L NaHCO3条件下比5 mmol/L NaHCO3下能调动更多的基因响应碱胁迫,且木质素合成代谢通路和碳酸酐酶在榅桲响应NaHCO3碱胁迫时起到重要作用。

关键词: 榅桲, 碱胁迫, 苯丙烷生物合成代谢通路, 碳酸酐酶, 转录组分析

Abstract: To investigate the molecular mechanisms of pear dwarf rootstock quince(Cydonia oblonga)responding to NaHCO3‑induced alkaline stress,hydroponically cultivated quince seedlings were subjected to mild alkaline stress(T1)with 5 mmol/L NaHCO3 and moderate alkaline stress(T2)with 10 mmol/L NaHCO3,without NaHCO3 as a control(CK). After six weeks of treatment,chlorophyll content,net photosynthetic rate in leaves,and K+/Na+ ratios in leaves and roots were measured. Additionally,transcriptome sequencing and analysis were performed on the roots. The results showed that both chlorophyll content and net photosynthetic rate in quince leaves gradually decreased with alkaline stress increasing. Compared to CK,the chlorophyll a+b content in T1 and T2 decreased significantly by 15.71% and 45.38%,respectively,while the net photosynthetic rate decreased by 15.90% and 55.42%,respectively. The K+/Na+ ratios in leaves and roots of T1 and T2 were significantly reduced by 45.40% and 96.69%,and 92.04% and 96.32%,respectively,compared to CK.Transcriptome sequencing revealed a total of 4 974 differentially expressed genes(DEGs)between T1,T2,and CK,with T2 showing a significantly higher number of DEGs than T1.Gene ontology(GO)and Kyoto encyclopedia of genes and genomes(KEGG)pathway enrichment analyses indicated that the biological processes(BP)in T1 and T2 were mainly enriched in terms such as hydrogen peroxide catabolic process and response to wounding,while KEGG pathways were primarily enriched in phenylpropanoid biosynthesis. Gene set enrichment analysis(GSEA)showed that the phenylpropanoid biosynthesis pathway was more active under T1 and T2 compared to CK.Weighted gene co‑expression network analysis(WGCNA)revealed that the hub gene cydonia_oblonga_newGene_11700,annotated as a lignin metabolism transcription factor,was significantly induced by alkaline stress in T1.In T2,the hub genes cydonia_oblonga_newGene_11460 and cydonia_oblonga_newGene_14681,both annotated as carbonic anhydrases,were identified.The expression patterns of five selected DEGs were validated by qRT‑PCR,and the results were consistent with the RNA‑Seq analysis.In summary,quince mobilizes more genes in response to moderate alkaline stress compared to mild stress,and the lignin biosynthesis pathway and carbonic anhydrases play important roles in quince’s response to NaHCO3‑induced alkaline stress.

Key words: Cydonia oblonga, Alkaline stress, Phenylpropanoid biosynthesis pathway, Carbonic anhydrase, Transcriptomic analysis

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