生物技术通报 ›› 2025, Vol. 41 ›› Issue (7): 139-149.doi: 10.13560/j.cnki.biotech.bull.1985.2024-1269

• 研究报告 • 上一篇    下一篇

Ca2+处理对胡麻种子萌发影响的转录组分析

郭秀娟1(), 冯宇2, 吴瑞香1, 王利琴1, 杨建春1()   

  1. 1.山西农业大学高寒区作物研究所,大同 037000
    2.山西农业大学农学院,太谷 030801
  • 收稿日期:2024-12-27 出版日期:2025-07-26 发布日期:2025-07-22
  • 通讯作者: 杨建春,男,研究员,研究方向 :胡麻育种栽培技术研究及示范推广;E-mail: ghshumazhu@sina.com
  • 作者简介:郭秀娟,女,硕士,副研究员,研究方向 :胡麻育种、栽培及资源鉴定、创新;E-mail: guoxiujuan1118@163.com
  • 基金资助:
    ?:?山西农业大学科技创新提升工程(CXGC2023077);山西省现代农业产业技术体系建设专项(2024CYJSTX05-16);山西农业大学生物育种工程(YZGC076)

Transcriptome Analysis of the Effect of Ca 2+ Treatment on the Seed Germination of Flax

GUO Xiu-juan1(), FENG Yu2, WU Rui-xiang1, WANG Li-qin1, YANG Jian-chun1()   

  1. 1.Shanxi Agricultural University, High Latitude Crops Insitute to Shangxi Academy, Datong 037000
    2.College of Agriculture, Shanxi Agricultural University, Taigu 030801
  • Received:2024-12-27 Published:2025-07-26 Online:2025-07-22

摘要:

目的 探究Ca²⁺对胡麻种子萌发特性的影响,揭示其调控机制,为胡麻种子萌发提供理论支持,拓展对Ca²⁺作用机制的理解。 方法 用0.5%的氯化钙溶液对晋亚10号胡麻种子进行浸种处理,晾干后,进行萌发试验。利用生物信息学方法分析其在5、10和15 h的Ca2+处理前后基因的表达情况。 结果 Ca2+处理的胡麻种子露白率和出芽的时间明显地提前。通过对胡麻种子进行不同时间(5、10、15 h)的Ca²⁺处理,并结合转录组测序分析其基因表达变化,在Ca²⁺处理5 h后,与对照组相比,筛选出1 357个差异基因,其中上调基因558个,下调基因799个。随着处理时间延长,差异基因数量显著减少。在10 h时,差异基因减少至641个(上调385个,下调256个);至15 h时,仅剩168个差异基因(上调151个,下调17个)。此外,进一步通过基因共表达网络分析,筛选出各组中最相关的模块及核心基因。 结论 在Ca²⁺处理胡麻种子5 h组(H5)中,显著相关的Meblue模块包含147个基因,主要富集于碳代谢通路、植物激素信号转导通路及光合生物中的碳固定通路。而在15 h组(H15)中,显著相关的Mebrown模块包含141个基因,主要富集于碳代谢通路、类苯基丙烷生物合成通路和亚麻酸代谢通路。此外,本研究重点筛选出35个与植物激素信号转导通路相关的差异表达基因。

关键词: 转录组, 亚麻, 种子发育, 钙离子, 差异基因表达, 核心基因, 表型变化, 植物激素信号通路

Abstract:

Objective The effect of Ca2 + on the germination characteristics of flax (Linum usitatissimum L.) seeds was identified, and the regulation mechanism of flax seed germination was deeply understood, which may provide a theoretical basis for flax seed germination and new insights for further understanding the influence of Ca2 + on flax seed germination. Method The seeds of the flax variety Jinya 10 were treated with a 0.5% calcium chloride solution and then dried in air for germination experiment. Bioinformatics was used to analyze the expressions of genes before and after Ca2 + treatment at 5, 10 and 15 h. Result The time of dew-white and budding of flax seeds treated with Ca2+ was significantly advanced. Transcriptome sequencing was utilized to analyze gene expression before and after Ca²⁺ treatment at 5, 10, and 15 h time points. Following a 5-hour Ca2 + retreatment of the flax seeds, a total of 1 357 differentially expressed genes were identified compared to the control group, with 558 genes upregulated and 799 genes downregulated. As the duration of Ca2 + treatment extended, the number of differentially expressed genes significantly decreased. After a 10-hour Ca2+ treatment, a total of 641 differentially expressed genes were discovered, with 385 upregulated and 256 downregulated. When the flax seeds were treated with Ca2 + for 15-hour, only 168 genes showed differential expression compared to the control, of which 151 were upregulated and 17 were downregulated. Gene co-expression network analysis was employed to select the most relevant modules and hub genes in each group. Conclusion In the H5 group (seeds treated with Ca2+ for 5 h), the Meblue module was significantly associated, a total of 147 genes were identified and enriched in the pathways of carbon metabolism, plant hormone signaling transduction and carbon fixation in photosynthetic organisms. The Mebrown module in the H15 group (seeds treated with Ca2+ for 15 h) contained a total of 141 genes, which were enriched in carbon metabolism pathway, phenylpropanoid biosynthesis pathway and linolenic acid metabolism pathway. Furthermore, 35 genes related to plant hormone signal transduction pathways in flax seeds are specifically selected for differential expression due to Ca2 + treatment.

Key words: transcriptome, flax, seed germination, Ca2+, differentially expressed gene, core gene, phenotypic change, plant hormone signaling pathway