中国农业科技导报 ›› 2024, Vol. 26 ›› Issue (10): 98-109.DOI: 10.13304/j.nykjdb.2024.0022

• 生物技术 生命科学 • 上一篇    下一篇

基于转录组和代谢组解析川芎对镉胁迫的响应机制

徐皖菁1,2(), 彭芳1, 赵豆豆1,2, 罗姣姣1, 陶珊1, 廖海浪1, 毛常清1, 吴宇1, 朱秀3, 徐正君2(), 张超1()   

  1. 1.四川省农业科学院经济作物研究所,成都 610300
    2.四川农业大学水稻研究所,成都 611130
    3.贵州师范大学,贵阳 550025
  • 收稿日期:2024-01-09 接受日期:2024-03-11 出版日期:2024-10-15 发布日期:2024-10-18
  • 通讯作者: 徐正君,张超
  • 作者简介:徐皖菁 E-mail:1315024678@qq.com
  • 基金资助:
    四川省育种攻关项目(2021YFYZ0012);四川省财政自主创新专项(2022ZZCX076)

Analysis of Response Mechanism of Ligusticum chuanxiong to Cadmium Stress Based on Transcriptome and Metabolome

Wanjing XU1,2(), Fang PENG1, Doudou ZHAO1,2, Jiaojiao LUO1, Shan TAO1, Hailang LIAO1, Changqing MAO1, Yu WU1, Xiu ZHU3, Zhengjun XU2(), Chao ZHANG1()   

  1. 1.Institute of Cash Crop,Sichuan Academy of Agricultural Sciences,Chengdu 610300,China
    2.Rice Research Institute,Sichuan Agricultural University,Chengdu 611130,China
    3.Guizhou Normal University,Guiyang 550025,China
  • Received:2024-01-09 Accepted:2024-03-11 Online:2024-10-15 Published:2024-10-18
  • Contact: Zhengjun XU,Chao ZHANG

摘要:

为了解不同水平镉(Cd)胁迫下川芎基因表达和代谢产物的变化规律,探究川芎对Cd胁迫的响应机制,利用盆栽试验,以不添加Cd溶液的清洁土壤为对照,设置1、3、6、10 mg·kg-1共4个Cd胁迫处理水平,采用转录组学测序(RNA sequencing,RNA-seq)和超高效液相色谱质谱联用(ultra performance liquid chromatography tandem mass spectrometry,UPLC-MS/MS)技术,筛选川芎抗Cd胁迫的关键基因与代谢通路。结果表明,共筛选到8 569个差异表达基因,包括上调基因6 859个,下调基因1 710个。与对照相比,4个Cd处理组的共有差异基因仅1个,为CML19,可能是川芎抗Cd胁迫的关键基因。代谢组共标注和定量了1 238种差异代谢物,在KEGG数据库中注释得到76条代谢通路,其中包括氨基酸代谢、氨酰基-tRNA的生物合成和脂肪酸的生物合成等。联合分析表明,当受到不同水平Cd胁迫时,川芎通过调节不同种类氨基酸来维持自身代谢平衡,在川芎抗Cd胁迫中发挥重要作用。研究结果为川芎抗Cd胁迫提供科学支撑与理论依据,为针对川芎资源的栽培育种及缓解Cd胁迫等相关研究提供基础。

关键词: 川芎, 镉胁迫, 转录组, 代谢组

Abstract:

In order to understand the changes of gene expression and metabolites of Ligusticum chuanxiong under different levels of cadmium (Cd) stress, and explore the response mechanism of Ligusticum Chuanxiong to Cd stress, a pot experiment was conducted, and 4 Cd stress treatment levels of 1, 3, 6, 9 mg·kg-1 were set with clean soil without adding Cd solution as control group,and RNA sequencing(RNA-seq) and ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) were used to identify key genes and metabolic pathways for resistance to Cd stress in Ligusticum chuanxiong. The results showed that a total of 8 569 differentially expressed genes were screened, including 6 859 up-regulated genes and 1 710 down-regulated genes. Compared with the control group, there was only 1 common differential gene in the 4 Cd-treated groups, CML19, which might be the key gene for resistance to Cd stress in Ligusticum chuanxiong. The metabolome labeled and quantized 1 238 different metabolites, and 76 metabolic pathways were annotated in the KEGG database, including amino acid metabolism, biosynthesis of aminoacyl-tRNA and biosynthesis of fatty acids. The joint analysis showed that Ligusticum chuanxiong played an important role in the resistance to Cd stress by regulating different amino acids to maintain its own metabolic balance when subjected to different levels of Cd stress. Above results provided scientific support and theoretical basis for the resistance of Ligusticum chuanxiong to Cd stress, and provided a basis for the subsequent cultivation and breeding of Ligusticum chuanxiong resources and related research on alleviating Cd stress.

Key words: Ligusticum chuanxiong, cadmium stress, transcriptome, metabolome

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