China Tobacco Gene Research Center, Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou, 450001, China; College of Agronomy, Northwest A&F University, Yangling, 712100, China.
Chenzhou Branch of Hunan Provincial Tobacco Company, Chenzhou, 423000, China.
Plant Physiol Biochem. 2024 Nov;216:109181. doi: 10.1016/j.plaphy.2024.109181. Epub 2024 Oct 5.
MYB12 is a key regulator that has been shown to promote the accumulation of various phenylpropanoid compounds in plants. However, the regulation of MYB12 gene is largely unknown. In this study, we found that overexpression of the NtMYB59 gene significantly inhibited the accumulation of chlorogenic acid (CGA), flavonols, and anthocyanins in tobacco, while knock-down and knock-out of NtMYB59 significantly increased the contents of these polyphenol compounds. Transcriptome analysis between WT and NtMYB59-OE plants revealed several differentially expressed genes (DEGs) encoding crucial enzymes in the phenylpropanoid pathway and the transcription factor NtMYB12. ChIP-seq assay further indicated that NtMYB12 might be a direct target of NtMYB59. Subsequent yeast one-hybrid, electrophoretic mobility shift assay, and Dual-Luciferase assays confirmed that NtMYB59 directly binds to the promoter of NtMYB12 to inhibit its expression. Moreover, loss-function of NtMYB59 significantly promoted the accumulation of flavonols and anthocyanins in ntmyb59, but their contents in ntmyb59/ntmyb12 double mutants were significantly lower than that of WT and ntmyb59 plants, indicating that the regulation of NtMYB59 on flavonoids biosynthesis depends on the activity of NtMYB12. Our study revealed that NtMYB59 regulates the expression of NtMYB12, and provided new potential strategies for modulating phenylpropanoids biosynthesis in tobacco.
MYB12 是一种关键的调节因子,已被证明能促进植物中各种苯丙素化合物的积累。然而,MYB12 基因的调控在很大程度上是未知的。在这项研究中,我们发现过表达 NtMYB59 基因显著抑制了烟草中绿原酸(CGA)、类黄酮和花青素的积累,而敲低和敲除 NtMYB59 则显著增加了这些多酚化合物的含量。WT 和 NtMYB59-OE 植株之间的转录组分析揭示了几个差异表达的基因(DEGs),这些基因编码苯丙素途径中的关键酶和转录因子 NtMYB12。ChIP-seq 实验进一步表明,NtMYB12 可能是 NtMYB59 的直接靶标。随后的酵母单杂交、电泳迁移率变动分析和双荧光素酶报告基因 assays 证实,NtMYB59 直接结合到 NtMYB12 的启动子上,抑制其表达。此外,NtMYB59 的功能缺失显著促进了 ntmyb59 中类黄酮和花青素的积累,但 ntmyb59/ntmyb12 双突变体中的含量明显低于 WT 和 ntmyb59 植株,表明 NtMYB59 对类黄酮生物合成的调节依赖于 NtMYB12 的活性。我们的研究揭示了 NtMYB59 对 NtMYB12 的表达调控,并为调节烟草中苯丙素生物合成提供了新的潜在策略。