• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

黄梁木R2R3-MYB基因鉴定及其在卡丹宾合成中的调控作用

Genome-wide Identification and Cadambine-biosynthesis Association of R2R3-MYB Family in Neolamarckia cadamba

  • 摘要:
    目的 黄梁木(Neolamarckia cadamba)是一种富含药用活性成分卡丹宾的速生乔木。通过系统解析黄梁木R2R3-MYB转录因子家族成员信息,明确其在不同组织器官及植物生长调节剂茉莉酸甲酯(methyl jasmonate, MeJA)和水杨酸(salicylic acid, SA)处理下的表达模式,筛选可能参与调控卡丹宾生物合成的MYB基因。
    方法 利用生物信息学方法对黄梁木R2R3-MYB家族进行全基因组鉴定,系统分析其进化关系、基因结构、理化性质、染色体定位与顺式作用元件,并结合不同组织以及MeJA和SA激素处理的转录组数据进行表达模式分析。
    结果 在黄梁木基因组中共鉴定出148个R2R3-MYB家族成员,分布于20条染色体上,并划分为33个亚组,其中S15亚组成员最多(9个)。蛋白基序与基因结构分析结果表明不同MYB蛋白的基序分布存在差异,同一亚家族成员具有相似的结构特征。启动子区域预测发现激素响应、光响应和胁迫响应等相关顺式作用元件。表达模式分析表明多数NcMYB基因在不同组织中广泛表达,部分基因在卡丹宾富集组织高表达且受MeJA和SA诱导。经表达模式及相关性验证分析,推测NcMYB100是潜在的调控卡丹宾生物合成的核心候选转录因子。
    结论 本研究在全基因组水平上鉴定了黄梁木R2R3-MYB家族成员,为进一步揭示MYB基因在卡丹宾生物合成中的调控作用提供重要依据。

     

    Abstract:
    Objective Neolamarckia cadamba is a fast-growing tree species that is rich in the cadambine, a compound of significant medicinal value. R2R3-MYB family in Neolamarckia cadamba was studied for their associations with cadambine biosynthesis of the tree. The expression patterns across different tissues and under treatments with the plant growth regulators methyl jasmonate (MeJA) and salicylic acid (SA) were analyzed, and candidate NcMYB genes potentially involved in the regulation of cadambine biosynthesis were identified.
    Methods A genome-wide identification of the R2R3-MYB family in N. cadamba was conducted using bioinformatics approaches. Analyses on the phylogenetic relationships, gene structures, physicochemical properties, chromosomal localization, and cis-acting regulatory elements of the genes were conducted. Gene expressions in different tissues on the tree and under hormone treatments of methyl jasmonate (MeJA) and salicylic acid (SA) were examined using RNA-seq data.
    Results A total of 148 R2R3-MYB family members distributing across 20 chromosomes were identified in the N. cadamba genome. Phylogenetically, they belonged to 33 subgroups, of which S15 had the most members of 9. There were differences in motif distribution among the MYB proteins, but conserved structure within the same subfamily. The promoter regions contained mainly cis-elements associated with hormone, light, and stress responses. Most NcMYBs were expressed in various organs, with some of them highly expressed and inducible by MeJA and SA in the cadambine-rich tissues. The expression pattern and correlation with cadambine biosynthesis of the members suggested NcMYB100 to be the responsible transcription factor in N. cadamba.
    Conclusion A genome-wide identification of R2R3-MYBs in N. cadamba was obtained for further studies on the regulatory roles of MYB genes in cadambine biosynthesis.

     

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