College of Life Sciences, North China University of Science and Technology, Tangshan, China.
BMC Genomics. 2023 Feb 22;24(1):84. doi: 10.1186/s12864-023-09191-x.
Methyl-binding domain (MBD) is a class of methyl-CpG-binding domain proteins that affects the regulation of gene expression through epigenetic modifications. MBD genes are not only inseparable from DNA methylation but have also been identified and validated in various plants. Although MBD is involved in a group of physiological processes and stress regulation in these plants, MBD genes in Eleutherococcus senticosus remain largely unknown.
Twenty EsMBD genes were identified in E. senticosus. Among the 24 chromosomes of E. senticosus, EsMBD genes were unevenly distributed on 12 chromosomes, and only one tandem repeat gene existed. Collinearity analysis showed that the fragment duplication was the main motif for EsMBD gene expansion. As the species of Araliaceae evolved, MBD genes also evolved and gradually exhibited different functional differentiation. Furthermore, cis-acting element analysis showed that there were numerous cis-acting elements in the EsMBD promoter region, among which light response elements and anaerobic induction elements were dominant. The expression motif analysis revealed that 60% of the EsMBDs were up-regulated in the 30% water content group.
By comparing the transcriptome data of different saponin contents of E. senticosus and integrating them with the outcomes of molecular docking analysis, we hypothesized that EsMBD2 and EsMBD5 jointly affect the secondary metabolic processes of E. senticosus saponins by binding to methylated CpG under conditions of drought stress. The results of this study laid the foundation for subsequent research on the E. senticosus and MBD genes.
甲基结合域(MBD)是一类通过表观遗传修饰影响基因表达调控的甲基-CpG 结合域蛋白。MBD 基因不仅与 DNA 甲基化密不可分,而且在各种植物中也已被鉴定和验证。虽然 MBD 参与了这些植物中的一组生理过程和应激调节,但刺五加中的 MBD 基因在很大程度上仍然未知。
在刺五加中鉴定出 20 个 EsMBD 基因。在刺五加的 24 条染色体中,EsMBD 基因不均匀分布在 12 条染色体上,并且仅存在一个串联重复基因。共线性分析表明,片段重复是 EsMBD 基因扩张的主要模式。随着伞形科物种的进化,MBD 基因也进化并逐渐表现出不同的功能分化。此外,顺式作用元件分析表明,EsMBD 启动子区域存在大量顺式作用元件,其中光反应元件和厌氧诱导元件占主导地位。表达模式分析表明,60%的 EsMBD 在 30%含水量组中上调。
通过比较不同皂苷含量的刺五加转录组数据,并将其与分子对接分析的结果相结合,我们假设 EsMBD2 和 EsMBD5 通过在干旱胁迫下与甲基化 CpG 结合,共同影响刺五加皂苷的次生代谢过程。本研究结果为后续研究刺五加和 MBD 基因奠定了基础。