生物技术通报 ›› 2023, Vol. 39 ›› Issue (9): 105-116.doi: 10.13560/j.cnki.biotech.bull.1985.2023-0091

• 研究报告 • 上一篇    下一篇

转录组分析转录因子AtbHLH68调控细胞壁发育的分子机制

林红妍1,2,3(), 郭晓蕊1,2,3, 刘迪1,2,3, 李慧1,2,3, 陆海1,2,3()   

  1. 1.林木育种与生态修复国家工程研究中心,北京 100083
    2.树木花卉育种生物工程国家林业和草原局重点实验室,北京 100083
    3.北京林业大学生物科学与技术学院,北京 100083
  • 收稿日期:2023-02-07 出版日期:2023-09-26 发布日期:2023-10-24
  • 通讯作者: 陆海,男,博士,教授,研究方向:树木分子生物学;E-mail: luhai1974@bjfu.edu.cn
  • 作者简介:林红妍,女,硕士研究生,研究方向:树木分子生物学;E-mail: 2638859438@qq.com
  • 基金资助:
    国家自然科学基金面上项目(31971618);国家重点研发计划青年科学家项目(2021YFD2200900)

Molecular Mechanism of Transcriptional Factor AtbHLH68 in Regulating Cell Wall Development by Transcriptome Analysis

LIN Hong-yan1,2,3(), GUO Xiao-rui1,2,3, LIU Di1,2,3, LI Hui1,2,3, LU Hai1,2,3()   

  1. 1. National Engineering Research Center of Tree Breeding and Ecological Retoration, Beijing 100083
    2. The Tree and Ornamental Plant Breeding and Biotechnology Laboratory of National Forestry and Grassland Administration, Beijing 100083
    3. School of Biological Science and Technology, Beijing Forestry University, Beijing 100083
  • Received:2023-02-07 Published:2023-09-26 Online:2023-10-24

摘要:

细胞壁是植物细胞特有的结构,在参与形态建成、水分和营养物质运输以及抵御生物和非生物胁迫中发挥重要作用。前人研究表明AtbHLH68作为bHLH蛋白的第10亚家族成员,在拟南芥茎维管组织中表达。为探究其在细胞壁发育方面的分子机制,本研究建立了雌二醇诱导pER8-AtbHLH68拟南芥表达系统,实时荧光定量PCR(RT-qPCR)结果显示,10 μmol/L雌二醇处理4 h能够有效诱导AtbHLH68的表达,并且随着诱导时间的增加AtbHLH68的mRNA水平进一步积累,处理8 h后达到对照组29倍。利用转录组测序分析得到了在拟南芥茎中AtbHLH68诱导表达后产生的差异基因。与对照组相比,10 μmol/L雌二醇处理8 h后,共得到差异基因2 334个,其中831个基因显著上调,1 503个基因显著下调。显著富集的GO词条主要与细胞壁组分、防御响应、果胶修饰与降解以及激素响应有关。KEGG分析表明DEGs参与了果胶修饰或木质素生物合成代谢等过程。这些结果表明参与以上过程的差异基因可能被AtbHLH68直接或间接调控,从而导致拟南芥茎细胞壁组分相关基因表达量的变化。该研究为阐明转录因子AtbHLH68在细胞壁发育中的分子机制提供了理论依据。

关键词: 诱导表达, AtbHLH68, 转录组, 细胞壁

Abstract:

Cell wall is a plant-specific structure and plays important role in morphogenesis, water and nutrients transportation, and biotic and abiotic resistance. Previous studies have shown that AtbHLH68 as a member of the 10th bHLH protein subfamily, is expressed in the vascular tissue of Arabidopsis thaliana stem. To investigate its molecular mechanism of AtbHLH68 in cell wall development, the estradiol-induced pER8-AtbHLH68 expression system was established in Arabidopsis thaliana. Quantitative real-time PCR(RT-qPCR)results showed that 10 μmol/L estradiol treatment for 4 h can effectively induce the expression of AtbHLH68, and the expression of AtbHLH68 gradually increased with the prolongation of induction time, reaching 29 times after 8 h. The differentially expressed genes(DEGs)induced by AtbHLH68 in Arabidopsis stems were detected by transcriptome analysis. Compared with the control group, after 8 h of treatment with 10 μmol/L estradiol, a total of 2 334 DEGs were detected, among which 831 genes were significantly up-regulated and 1 503 genes were significantly down-regulated. The significantly enrichment GO terms were mainly related to cell wall components, defense response, pectin modification and degradation and hormone response. KEGG analysis showed that DEGs involved in the processes such as pectin modification and lignin biosynthetic metabolism. These results indicated that the DEGs involved in the above processes may be regulated by AtbHLH68 directly or indirectly. This study provided theoretical evidences to clarify the molecular mechanism of transcription factor AtbHLH68 in cell wall development.

Key words: induced expression, AtbHLH68, transcriptome, cell wall