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苍术 R2R3-MYB 亚家族转录因子在介导香豆素生物合成中的作用

MYB transcription factors in Peucedanum Praeruptorum Dunn: the diverse roles of the R2R3-MYB subfamily in mediating coumarin biosynthesis.

机构信息

School of Pharmacy, Anhui University of Chinese Medicine, Hefei, 230012, China.

Anhui Dabieshan Academy of Traditional Chinese Medicine, Anhui Engineering Research Center for Eco-agriculture of Traditional Chinese Medicine, College of Biological and Pharmaceutical Engineering, West Anhui University, Lu'an, 237012, China.

出版信息

BMC Plant Biol. 2024 Nov 28;24(1):1135. doi: 10.1186/s12870-024-05864-1.

Abstract

BACKGROUND

The MYB superfamily (v-myb avian myeloblastosis viral oncogene homolog) plays a role in plant growth and development, environmental stress defense, and synthesis of secondary metabolites. Little is known about the regulatory function of MYB genes in Peucedanum praeruptorum Dunn, although many MYB family members, especially R2R3-MYB genes, have been extensively studied in model plants.

RESULTS

A total of 157 R2R3-MYB transcription factors from P. praeruptorum were identified using bioinformatics analysis. Comprehensive analyses including chromosome location, microsynteny, gene structure, conserved motif, phylogenetic tree, and conserved domain were further performed. The length of the 157 transcription factors ranged from 120 to 1,688 amino acids (molecular weight between 14.21 and 182.69 kDa). All proteins were hydrophilic. Subcellular localization predictions showed that 155 PpMYB proteins were localized in the nucleus, with PpMYB12 and PpMYB157 localized in the chloroplasts and mitochondria, respectively. Ten conserved motifs were identified in the PpMYBs, all of which contained typical MYB domains. Transcriptome analysis identified 47,902 unigenes. Kyoto Encyclopedia of Genes and Genomes analysis revealed 136 pathways, of which 524 genes were associated with the phenylpropanoid pathway. Differential expressed genes (DEGs) before and after bolting showed that 11 genes were enriched in the phenylpropanoid pathway. Moreover, the expression patterns of transcription genes were further verified by qRT-PCR. With high-performance liquid chromatography (HPLC), 8 coumarins were quantified from the root, stem, and leaf tissue samples of P. praeruptorum at different stages. Praeruptorin A was found in both roots and leaves before bolting, whereas praeruptorin B was mainly concentrated in the roots, and the content of both decreased in the roots and stems after bolting. Praeruptorin E content was highest in the leaves and increased with plant growth. The correlation analysis between transcription factors and coumarin content showed that the expression patterns of PpMYB3 and PpMYB103 in roots align with the accumulation trends of praeruptorin A, praeruptorin B, praeruptorin E, scopoletin, and isoscopoletin, which declined in content after bolting, suggesting that these genes may positively regulate the biosynthesis of coumarins. Eleven distinct metabolites and 48 DEGs were identified. Correlation analysis revealed that the expression of all DEGs were significantly related to the accumulation of coumarin metabolites, indicating that these genes are involved in the regulation of coumarin biosynthesis.

CONCLUSIONS

R2R3-MYB transcription factors may be involved in the synthesis of coumarin. Our findings provide basic data and a rationale for future an in-depth studies on the role of R2R3-MYB transcription factors in the growth and regulation of coumarin synthesis.

摘要

背景

MYB 超家族(v-myb 禽成髓细胞瘤病毒癌基因同源物)在植物生长发育、环境胁迫防御和次生代谢物合成中发挥作用。尽管许多 MYB 家族成员,特别是 R2R3-MYB 基因,在模式植物中得到了广泛研究,但关于 MYB 基因在白芷中的调控功能知之甚少。

结果

使用生物信息学分析从白芷中鉴定出 157 个 R2R3-MYB 转录因子。进一步进行了包括染色体位置、微同线性、基因结构、保守基序、系统发育树和保守结构域在内的综合分析。157 个转录因子的长度范围为 120 至 1688 个氨基酸(分子量为 14.21 至 182.69 kDa)。所有蛋白质均为亲水性。亚细胞定位预测表明,155 个 PpMYB 蛋白定位于细胞核,PpMYB12 和 PpMYB157 分别定位于叶绿体和线粒体。在 PpMYBs 中鉴定出 10 个保守基序,均包含典型的 MYB 结构域。转录组分析鉴定出 47902 个 unigenes。京都基因与基因组百科全书分析显示,有 136 条途径,其中 524 个基因与苯丙素途径有关。抽薹前后差异表达基因(DEGs)分析表明,11 个基因富集在苯丙素途径中。此外,通过 qRT-PCR 进一步验证了转录基因的表达模式。采用高效液相色谱法(HPLC)从不同阶段白芷的根、茎和叶组织样品中定量了 8 种香豆素。在抽薹前,发现根和叶中均存在前胡素 A,而前胡素 B 主要集中在根中,抽薹后根和茎中的含量均下降。在叶片中前胡素 E 的含量最高,并随植物生长而增加。转录因子与香豆素含量的相关分析表明,根中 PpMYB3 和 PpMYB103 的表达模式与前胡素 A、前胡素 B、前胡素 E、花椒毒素和异花椒毒素的积累趋势一致,这些化合物在抽薹后含量下降,表明这些基因可能正向调控香豆素的生物合成。鉴定出 11 种不同的代谢物和 48 个 DEGs。相关分析表明,所有 DEGs 的表达均与香豆素代谢物的积累显著相关,表明这些基因参与了香豆素生物合成的调控。

结论

R2R3-MYB 转录因子可能参与香豆素的合成。我们的研究结果为进一步研究 R2R3-MYB 转录因子在香豆素生长和调节中的作用提供了基础数据和依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0620/11604020/6c9ff40cbbce/12870_2024_5864_Fig1_HTML.jpg

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