对比转录组分析揭示了脱落酸诱导的bHLH转录因子参与柴胡皂苷的生物合成。

Plant signaling & behavior Pub Date : 2025-12-01 Epub Date: 2025-04-21 DOI:10.1080/15592324.2025.2495301
Han Wang, Shanqun Hu, Tong Li, Xuejie Qu, Jiaqi Zhang, Baoshun Wang, Yixuan Sun, Rui Cao, Yutong Yan, Ze Song, Xia'nan Zhang, Rong Luo, Yuru Tong, Changli Liu
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引用次数: 0

摘要

柴胡。作为一种具有解热和保肝作用的药用植物,柴草皂苷(SSs)在生长过程中受到脱落酸(ABA)介导的SS生物合成限制。基本螺旋-环-螺旋(bHLH)转录因子(TFs)被假设参与ABA信号级联反应,但其在SS调控中的机制尚不清楚。在本研究中,通过aba诱导毛状根的转录组学分析鉴定了20个差异表达的BcbHLH基因,其中4个myc家族候选基因(BcbHLH1-BcbHLH4)显示出aba响应调控潜力。ABA暴露(100或200 μmol/L, 24-72 h)诱导了剂量依赖性SS降低,而相关分析显示BcbHLH1-BcHMGR (r = 0.62)和BcbHLH4-BcBAS (r = 0.78)之间的协调表达,确定这些TFs是SS通路调节的关键节点。组织特异性分析显示BcbHLH在茎和幼叶中主要表达,核定位证实了它们的转录调节细胞器。BcbHLH3/4在MYC_N结构域表现出转录激活活性,而分子对接预测HLH结构域的11号精氨酸是G-box DNA结合所必需的。总之,我们的研究结果表明,BcbHLH1-BcbHLH4可能是微调SS生物合成中ABA响应性的潜在开关。通过基因工程方法(如基于crispr的编辑或过表达)对BcbHLH活性进行战略性操纵可以减轻aba介导的生物合成抑制。此外,对BcbHLH的关键功能域进行精确工程设计,可以增强启动子与靶基因的结合活性,提高SS的生物合成效率。这些发现为利用转录调控因子优化柴胡SS的生产提供了参考框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative transcriptome analysis reveals abscisic acid-induced bHLH transcription factors involved in saikosaponin biosynthesis in Bupleurum chinense DC.

Bupleurum chinense DC. a medicinal plant valued for saikosaponins (SSs) with antipyretic and hepatoprotective properties, faces constrained SS biosynthesis mediated by abscisic acid (ABA) during growth. Basic helix-loop-helix (bHLH) transcription factors (TFs) are hypothesized to participate in ABA signaling cascades, but their mechanistic role in SS regulation remains undefined. In this study, 20 differentially expressed BcbHLH genes were identified by transcriptomic profiling of ABA-induced hairy roots, with four MYC-family candidates (BcbHLH1-BcbHLH4) demonstrating ABA-responsive regulatory potential. ABA exposure (100 or 200 μmol/L, 24-72 h) induced dose-dependent SS reduction, while correlation analyses revealed coordinated expression between BcbHLH1-BcHMGR (r = 0.62) and BcbHLH4-BcBAS (r = 0.78), pinpointing these TFs as critical nodes in SS pathway modulation. Tissue-specific profiling showed predominant BcbHLH expression in stems and young leaves, with nuclear localization confirming their transcriptional regulatory organelles. BcbHLH3/4 exhibited transcriptional activation activity in the MYC_N domain, while molecular docking predicted 11th Arginine in the HLH domain as essential for G-box DNA binding. Collectively, our findings suggest that BcbHLH1-BcbHLH4 may serve as potential switches for fine-tuning ABA responsiveness in SS biosynthesis. Strategic manipulation of BcbHLH activity through genetic engineering approaches such as CRISPR-based editing or overexpression could alleviate ABA-mediated biosynthetic repression. Furthermore, precision engineering of the critical functional domain in BcbHLH could enhance promoter-binding activity to target genes and improve SS biosynthesis efficiency. These findings provide a reference framework for harnessing transcriptional regulators to optimize SS production in Bupleurum chinense DC.

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